In vitro maturation and In vitro FertilizationAsadullah Babar
Immature eggs are retrieved from the ovary through aspiration or slicing and matured in the laboratory. The eggs are then fertilized in vitro through incubation with sperm for 8-10 hours. Finally, the presumed zygotes are cultured for 9 days to allow embryonic development. This process involves collection, transportation, in vitro maturation of eggs, in vitro fertilization through sperm treatment and incubation, and in vitro culture of the resulting embryos.
1. There are four main types of regeneration: stem cell mediated, epimorphosis, morphallaxis, and compensatory regeneration.
2. Epimorphosis involves de-differentiation of cells forming a blastema which then re-differentiates, as seen in salamander limb regeneration.
3. Morphallaxis involves re-patterning of existing tissues with little new growth, as seen when hydra fragments regenerate entire organisms.
This document discusses embryo transfer as the final step of assisted reproductive technology where embryos are placed in the female uterus. It describes factors that affect embryo transfer success including implantation capacity, endometrial receptivity, and technique. The document outlines techniques for embryo transfer including assisted hatching, embryo glue, catheter type and loading, ultrasound guidance, and ensuring no blood or mucus blockage. Successful embryo transfer requires a gentle, non-traumatic procedure performed with attention to numerous technical details.
This document outlines a proposed transdisciplinary study to assess in vitro maturation (IVM) of oocytes as an alternative infertility treatment compared to conventional in vitro fertilization (IVF). The study would have three pillars: 1) comparing the biology of IVM and IVF through animal studies; 2) evaluating the clinical efficacy, safety, costs and psychological impacts of IVM versus IVF through human studies; and 3) studying pregnancy complications and birth outcomes from IVM, IVF and spontaneous pregnancies using population health data. The goal is to provide a comprehensive evaluation of IVM across biological, clinical, economic and population levels to determine its potential as a treatment option for infertile couples.
In vitro fertilization and embryo transfer in humansHasnahana Chetia
The document discusses infertility treatment techniques like in vitro fertilization (IVF) and embryo transfer. It describes the IVF process which involves collecting eggs and sperm, fertilizing the eggs in vitro, and implanting the resulting embryos into the uterus. Embryo transfer is defined as implanting embryos developed in vitro or from another female's uterus. The success rates of IVF depend on factors like the woman's age and number of eggs collected. IVF has led to the birth of the first "test tube baby" and advances in reproductive technology.
This document discusses methods of embryo sexing. It begins with a brief history of embryo sexing and introduces invasive and non-invasive methods. For invasive methods, it describes cytological/karyotyping methods, identification of sex chromatin, use of Y-chromosome probes, and PCR. Advantages include low cost and accuracy, while disadvantages include potential harm to embryo viability. For non-invasive methods, it outlines detection of X-linked enzymes and H-Y antigens, noting advantages of maintaining embryo integrity but challenges around accuracy and availability of reagents. The document concludes by discussing applications and constraints of embryo sexing technologies.
Embryo transfer is a step in assisted reproduction where embryos are placed in the uterus to establish a pregnancy. There are two types of embryo transfer - fresh and frozen. For frozen transfers, the uterus is prepared with estrogen and progesterone to make it receptive. During the procedure, a catheter is used to insert embryos through the cervix under ultrasound guidance. Patients then wait two weeks before a blood test checks for human chorionic gonadotropin, which would confirm a pregnancy.
Polyspermy describes an egg that has been fertilized by more than one sperm. Diploid organisms normally contain two copies of each chromosome, one from each parent. The cell resulting from polyspermy
The first issue that an egg and a sperm of any organism type face in successfully producing an embryo is the possibility of polyspermy. Polyspermy is the fertilization of an egg by multiple sperm, and the results of such unions are lethal.
If multiple sperm fertilize an egg, the embryo inherits multiple paternal centrioles. This causes competition for extra chromosomes and results in the disruption of the creation of the cleavage furrow, thus causing the zygote to die. As an important model organism in the study of fertilization and embryonic development, polyspermy in sea urchins has been studied in detail. The sea urchin’s methods of polyspermy prevention have been broken down into two main pathways. These two primary pathways are known as the fast block and the slow block to polyspermy
After the sperm’s receptors come into contact with the egg’s jelly layer and the acrosomal enzymes are released and break down the jelly layer, the sperm head comes into contact with the vitelline and plasma membranes of the egg. When the two plasma membranes contact one another, signals in the egg are initiated.
First, Na+ channels in the egg open, allowing Na+ to flood into the egg. This causes a depolarization of the egg from it’s normal resting potential of -70 mV.
While depolarization is occurring, the remainder of the jelly layer is dissolving. With the dissolution of the jelly layer and the depolarization of the plasma membrane, the first block to preventing fertilization by multiple sperm is put into place.
These two simple changes are part of the first block to polyspermy, known as the fast block. Within 1/10th of a second of contact, the fast block t
In vitro maturation and In vitro FertilizationAsadullah Babar
Immature eggs are retrieved from the ovary through aspiration or slicing and matured in the laboratory. The eggs are then fertilized in vitro through incubation with sperm for 8-10 hours. Finally, the presumed zygotes are cultured for 9 days to allow embryonic development. This process involves collection, transportation, in vitro maturation of eggs, in vitro fertilization through sperm treatment and incubation, and in vitro culture of the resulting embryos.
1. There are four main types of regeneration: stem cell mediated, epimorphosis, morphallaxis, and compensatory regeneration.
2. Epimorphosis involves de-differentiation of cells forming a blastema which then re-differentiates, as seen in salamander limb regeneration.
3. Morphallaxis involves re-patterning of existing tissues with little new growth, as seen when hydra fragments regenerate entire organisms.
This document discusses embryo transfer as the final step of assisted reproductive technology where embryos are placed in the female uterus. It describes factors that affect embryo transfer success including implantation capacity, endometrial receptivity, and technique. The document outlines techniques for embryo transfer including assisted hatching, embryo glue, catheter type and loading, ultrasound guidance, and ensuring no blood or mucus blockage. Successful embryo transfer requires a gentle, non-traumatic procedure performed with attention to numerous technical details.
This document outlines a proposed transdisciplinary study to assess in vitro maturation (IVM) of oocytes as an alternative infertility treatment compared to conventional in vitro fertilization (IVF). The study would have three pillars: 1) comparing the biology of IVM and IVF through animal studies; 2) evaluating the clinical efficacy, safety, costs and psychological impacts of IVM versus IVF through human studies; and 3) studying pregnancy complications and birth outcomes from IVM, IVF and spontaneous pregnancies using population health data. The goal is to provide a comprehensive evaluation of IVM across biological, clinical, economic and population levels to determine its potential as a treatment option for infertile couples.
In vitro fertilization and embryo transfer in humansHasnahana Chetia
The document discusses infertility treatment techniques like in vitro fertilization (IVF) and embryo transfer. It describes the IVF process which involves collecting eggs and sperm, fertilizing the eggs in vitro, and implanting the resulting embryos into the uterus. Embryo transfer is defined as implanting embryos developed in vitro or from another female's uterus. The success rates of IVF depend on factors like the woman's age and number of eggs collected. IVF has led to the birth of the first "test tube baby" and advances in reproductive technology.
This document discusses methods of embryo sexing. It begins with a brief history of embryo sexing and introduces invasive and non-invasive methods. For invasive methods, it describes cytological/karyotyping methods, identification of sex chromatin, use of Y-chromosome probes, and PCR. Advantages include low cost and accuracy, while disadvantages include potential harm to embryo viability. For non-invasive methods, it outlines detection of X-linked enzymes and H-Y antigens, noting advantages of maintaining embryo integrity but challenges around accuracy and availability of reagents. The document concludes by discussing applications and constraints of embryo sexing technologies.
Embryo transfer is a step in assisted reproduction where embryos are placed in the uterus to establish a pregnancy. There are two types of embryo transfer - fresh and frozen. For frozen transfers, the uterus is prepared with estrogen and progesterone to make it receptive. During the procedure, a catheter is used to insert embryos through the cervix under ultrasound guidance. Patients then wait two weeks before a blood test checks for human chorionic gonadotropin, which would confirm a pregnancy.
Polyspermy describes an egg that has been fertilized by more than one sperm. Diploid organisms normally contain two copies of each chromosome, one from each parent. The cell resulting from polyspermy
The first issue that an egg and a sperm of any organism type face in successfully producing an embryo is the possibility of polyspermy. Polyspermy is the fertilization of an egg by multiple sperm, and the results of such unions are lethal.
If multiple sperm fertilize an egg, the embryo inherits multiple paternal centrioles. This causes competition for extra chromosomes and results in the disruption of the creation of the cleavage furrow, thus causing the zygote to die. As an important model organism in the study of fertilization and embryonic development, polyspermy in sea urchins has been studied in detail. The sea urchin’s methods of polyspermy prevention have been broken down into two main pathways. These two primary pathways are known as the fast block and the slow block to polyspermy
After the sperm’s receptors come into contact with the egg’s jelly layer and the acrosomal enzymes are released and break down the jelly layer, the sperm head comes into contact with the vitelline and plasma membranes of the egg. When the two plasma membranes contact one another, signals in the egg are initiated.
First, Na+ channels in the egg open, allowing Na+ to flood into the egg. This causes a depolarization of the egg from it’s normal resting potential of -70 mV.
While depolarization is occurring, the remainder of the jelly layer is dissolving. With the dissolution of the jelly layer and the depolarization of the plasma membrane, the first block to preventing fertilization by multiple sperm is put into place.
These two simple changes are part of the first block to polyspermy, known as the fast block. Within 1/10th of a second of contact, the fast block t
The document discusses the process of fertilization in several species. It describes 5 steps for recognition and fusion of egg and sperm cells, including chemoattraction, release of acrosomal enzymes, binding to extracellular envelopes, passage through envelopes, and fusion of nuclei. It also discusses the acrosome reaction, prevention of polyspermy through changes in electric potential and cortical granule reaction, and activation of the egg through calcium signaling and increased metabolism. Finally, it summarizes the process of sperm capacitation required for fertilization competence.
Morphogenetic movements involve the rearrangement of cells during embryonic development through processes like gastrulation, tubulation, and organogenesis. These movements are caused by large-scale cell movements and changes in cell behavior, and result in changes to embryonic shape and structure. Key morphogenetic processes include cell division, size, shape, adhesion, death, and interactions with the extracellular matrix. Critical examples are the invagination of epithelial sheets during gastrulation and selective outgrowth of limb buds through differential proliferation.
cell commitment and differentiation, stem cell,types of differentiationshallu kotwal
Cell commitment and differentiation are important processes in the development of multicellular organisms. There are three main modes of cell specification - autonomous specification, conditional specification, and syncytial specification - which determine cell fate. Cell differentiation involves cells changing from embryonic to specialized cell types through morphological, chemical, and physiological changes. The main factors influencing differentiation are gene expression and environmental conditions. Cell differentiation allows a single cell to develop into the many specialized cell types that make up complex, multicellular organisms.
How 3 germ layers are formed in Chick that are endoderm, mesoderm and ectoderm.As Chick are polylecithal so cell movements are somewhat restricted and gastrulation is modified as compared to frog.
The embryo transfer technique is the final and most crucial step of the IVF cycle. It requires close collaboration between the clinician and embryologist. While around 80% of embryos typically reach the transfer stage, the pregnancy rate remains low due to factors such as poor embryo quality and technique. The success of embryo transfer depends on proper preparation, including evaluating the cervico-uterine axis, clearing mucus from the cervix, and using ultrasound guidance. The embryo must be placed in the optimal location of the uterine cavity to maximize implantation chances. Attention to factors such as catheter type, duration of embryo loading, and prevention of uterine contractions can significantly improve clinical pregnancy outcomes.
1. In vertebrates like amphibians, reptiles, birds, and mammals, germ cells known as primordial germ cells (PGCs) migrate from their origin site to the developing gonads, or genital ridges.
2. In amphibians, PGCs form in the animal pole of the blastula and migrate through the gut epithelium to reach the developing gonads.
3. In mammals, PGCs form in the yolk sac near the hindgut and migrate through the gut and up the dorsal mesentery into the developing gonads in the genital ridges. Monoclonal antibodies are used to identify migrating PGCs in mice embryos.
The document discusses embryonic development from an embryologist's perspective. It covers the overall view of embryonic development from conception through harvest and techniques. The source and significance of embryonic development is also examined at a high level.
The document discusses the process of fertilization and the acrosome reaction. It describes how:
1) Upon contact with the egg's jelly coat, the acrosome reaction is initiated, causing enzymes to be released from the acrosome to digest the coat.
2) This reaction fuses the acrosomal membrane with the sperm cell membrane, releasing enzymes that allow the sperm to penetrate the vitelline envelope and reach the egg.
3) The influx of calcium triggers the extension of the acrosomal process through actin polymerization, allowing the sperm to penetrate the zona pellucida and fuse with the egg membrane.
In vitro fertilization and embryo transfer "IVF"; Overview on the Story FRO...Ahmed Mowafy
The document discusses the history and development of in vitro fertilization (IVF). It mentions:
- Aldous Huxley predicted IVF techniques in his 1931 novel "Brave New World".
- The first reported pregnancies from IVF occurred in the late 1950s and early 1960s involving animals.
- The first reported human pregnancy from IVF was in 1973, though it resulted in miscarriage.
- The first successful human birth from IVF, Louise Brown, occurred in 1978 in the UK from the work of Steptoe and Edwards.
Environmental regulation of animal developmentMerlyn Denesia
1. The environment regulates animal development in several ways, such as requiring certain substrates to trigger metamorphosis or relying on symbiotic bacteria for proper organ development.
2. Environmental conditions can influence development through phenotypic plasticity, inducing different phenotypes from the same genotype. Some species exhibit polyphenisms where the environment determines distinctly different phenotypes.
3. Factors like seasonality, temperature, food availability, and presence of predators can alter development to increase fitness. Temperature also determines sex in some species.
This document outlines a course on developmental biology and teratology. It discusses how pattern formation during embryogenesis is genetically controlled and involves cells responding to morphogen gradients and cell signaling pathways to develop spatial patterns. Key genes involved in pattern formation are homeobox genes, which help specify where anatomical structures will develop. In particular, Hox genes are organized in clusters and control patterning along the anteroposterior body axis. Mutations in genes of pattern formation can lead to various clinical congenital malformations and anomalies.
This document summarizes in vitro fertilization (IVF) and embryo transfer. [1] IVF involves removing eggs from a woman, fertilizing them with sperm in the lab, and then transferring the fertilized eggs (zygotes) into the uterus a few days later. [2] Reasons for IVF include infertility, which is increasingly prevalent worldwide. [3] The history, methodology, success rates, factors, and limitations of IVF are discussed over several stages: ovarian stimulation and monitoring, egg retrieval, fertilization, embryo transfer, and potential outcomes.
Morphogens are signals that form concentration gradients to specify multiple cell types during development. Cells respond to different morphogen thresholds to activate distinct gene expression. Bicoid is a transcription factor that acts as a morphogen gradient in Drosophila, turning on different genes in different embryo regions based on its concentration. It forms a gradient from anterior to posterior, with high concentrations specifying head structures and lower concentrations specifying more posterior structures. This gradient establishes the basic body plan of the fruit fly embryo.
Fertilization involves the fusion of an egg and sperm, combining their genetic material. This process activates the egg and initiates embryonic development. Key events include chemoattraction of sperm to the egg, binding and fusion of gametes, and prevention of polyspermy. Fusion results in the formation of a single cell with a combined genome from both parent cells. This triggers metabolic changes in the egg and causes its nuclei to fuse, forming a zygote ready to begin dividing and developing into an embryo.
1. Natural cloning occurs when an embryo splits into two identical embryos. Artificial cloning involves transferring the nucleus from an adult body cell into an empty egg cell.
2. Dolly the sheep was artificially cloned by transferring the nucleus from a sheep's body cell into an empty sheep egg cell, which was then implanted into a surrogate sheep.
3. More research on artificial cloning is needed because larger animals do not naturally produce clones and cloning technology is still new with unknown risks and implications.
1) Embryo transfer involves placing embryos into the uterus of a female with the intent to establish a pregnancy. This can involve fresh or frozen embryos.
2) The first successful embryo transfers were conducted in rabbits in 1890 and then various livestock including sheep, cattle, pigs, and water buffalo. The first "test tube baby" was born in 1978.
3) The embryo transfer process involves preparing the uterus, using catheters to deposit embryos, and confirming pregnancy. Embryos are typically transferred at the 2-4 cell stage. Applications include genetic improvement and conservation of endangered species.
In Vitro Fertilization (IVF) involves stimulating a woman's ovaries to develop multiple eggs, retrieving the eggs and fertilizing them with sperm in a lab, then transferring the resulting embryo(s) into the uterus. Key aspects of IVF include controlled ovarian hyperstimulation using fertility medications, egg retrieval under ultrasound guidance, fertilization via intracytoplasmic sperm injection if needed, embryo culture until blastocyst stage, and embryo transfer into the uterus. Success rates of IVF depend on factors like the woman's age, cause of infertility, and embryo quality.
1. Teratogenesis is the process by which environmental factors cause birth defects during embryonic and fetal development. The period between weeks 3-8 of development carries the highest risk, as this is when organ systems are forming.
2. Important teratogens include alcohol, retinoic acid, endocrine disruptors, synthetic chemicals, heavy metals, and pathogens. Alcohol is the most devastating teratogen and can cause fetal alcohol spectrum disorder, characterized by reduced brain and body size.
3. Retinoic acid is important for embryonic development but can cause abnormalities if exposure levels are too high, as seen in a study where women were accidentally exposed during pregnancy.
This document discusses various aspects of assisted reproductive technology (ART) including in vitro fertilization (IVF) and intracytoplasmic sperm injection (ICSI). It provides information on the causes of infertility, procedures for IVF such as egg retrieval, embryo transfer, and blastocyst culture. The document also discusses who may benefit from IVF and ICSI, including those with male factor infertility issues or previous IVF failures. Other ART procedures mentioned include zygote intrafallopian transfer, gamete intrafallopian transfer, and potential future techniques like creating artificial gametes.
This document discusses various aspects of assisted reproductive technology (ART) including infertility, its causes, treatments, and specific procedures like in vitro fertilization (IVF) and intracytoplasmic sperm injection (ICSI). It provides information on male and female infertility, decreasing male fertility rates, and drugs to treat male infertility. The document also explains the procedures for IVF such as ovulation induction, egg retrieval, fertilization, embryo culture, and embryo transfer. ICSI is introduced as a technique used to treat male factor infertility.
The document discusses the process of fertilization in several species. It describes 5 steps for recognition and fusion of egg and sperm cells, including chemoattraction, release of acrosomal enzymes, binding to extracellular envelopes, passage through envelopes, and fusion of nuclei. It also discusses the acrosome reaction, prevention of polyspermy through changes in electric potential and cortical granule reaction, and activation of the egg through calcium signaling and increased metabolism. Finally, it summarizes the process of sperm capacitation required for fertilization competence.
Morphogenetic movements involve the rearrangement of cells during embryonic development through processes like gastrulation, tubulation, and organogenesis. These movements are caused by large-scale cell movements and changes in cell behavior, and result in changes to embryonic shape and structure. Key morphogenetic processes include cell division, size, shape, adhesion, death, and interactions with the extracellular matrix. Critical examples are the invagination of epithelial sheets during gastrulation and selective outgrowth of limb buds through differential proliferation.
cell commitment and differentiation, stem cell,types of differentiationshallu kotwal
Cell commitment and differentiation are important processes in the development of multicellular organisms. There are three main modes of cell specification - autonomous specification, conditional specification, and syncytial specification - which determine cell fate. Cell differentiation involves cells changing from embryonic to specialized cell types through morphological, chemical, and physiological changes. The main factors influencing differentiation are gene expression and environmental conditions. Cell differentiation allows a single cell to develop into the many specialized cell types that make up complex, multicellular organisms.
How 3 germ layers are formed in Chick that are endoderm, mesoderm and ectoderm.As Chick are polylecithal so cell movements are somewhat restricted and gastrulation is modified as compared to frog.
The embryo transfer technique is the final and most crucial step of the IVF cycle. It requires close collaboration between the clinician and embryologist. While around 80% of embryos typically reach the transfer stage, the pregnancy rate remains low due to factors such as poor embryo quality and technique. The success of embryo transfer depends on proper preparation, including evaluating the cervico-uterine axis, clearing mucus from the cervix, and using ultrasound guidance. The embryo must be placed in the optimal location of the uterine cavity to maximize implantation chances. Attention to factors such as catheter type, duration of embryo loading, and prevention of uterine contractions can significantly improve clinical pregnancy outcomes.
1. In vertebrates like amphibians, reptiles, birds, and mammals, germ cells known as primordial germ cells (PGCs) migrate from their origin site to the developing gonads, or genital ridges.
2. In amphibians, PGCs form in the animal pole of the blastula and migrate through the gut epithelium to reach the developing gonads.
3. In mammals, PGCs form in the yolk sac near the hindgut and migrate through the gut and up the dorsal mesentery into the developing gonads in the genital ridges. Monoclonal antibodies are used to identify migrating PGCs in mice embryos.
The document discusses embryonic development from an embryologist's perspective. It covers the overall view of embryonic development from conception through harvest and techniques. The source and significance of embryonic development is also examined at a high level.
The document discusses the process of fertilization and the acrosome reaction. It describes how:
1) Upon contact with the egg's jelly coat, the acrosome reaction is initiated, causing enzymes to be released from the acrosome to digest the coat.
2) This reaction fuses the acrosomal membrane with the sperm cell membrane, releasing enzymes that allow the sperm to penetrate the vitelline envelope and reach the egg.
3) The influx of calcium triggers the extension of the acrosomal process through actin polymerization, allowing the sperm to penetrate the zona pellucida and fuse with the egg membrane.
In vitro fertilization and embryo transfer "IVF"; Overview on the Story FRO...Ahmed Mowafy
The document discusses the history and development of in vitro fertilization (IVF). It mentions:
- Aldous Huxley predicted IVF techniques in his 1931 novel "Brave New World".
- The first reported pregnancies from IVF occurred in the late 1950s and early 1960s involving animals.
- The first reported human pregnancy from IVF was in 1973, though it resulted in miscarriage.
- The first successful human birth from IVF, Louise Brown, occurred in 1978 in the UK from the work of Steptoe and Edwards.
Environmental regulation of animal developmentMerlyn Denesia
1. The environment regulates animal development in several ways, such as requiring certain substrates to trigger metamorphosis or relying on symbiotic bacteria for proper organ development.
2. Environmental conditions can influence development through phenotypic plasticity, inducing different phenotypes from the same genotype. Some species exhibit polyphenisms where the environment determines distinctly different phenotypes.
3. Factors like seasonality, temperature, food availability, and presence of predators can alter development to increase fitness. Temperature also determines sex in some species.
This document outlines a course on developmental biology and teratology. It discusses how pattern formation during embryogenesis is genetically controlled and involves cells responding to morphogen gradients and cell signaling pathways to develop spatial patterns. Key genes involved in pattern formation are homeobox genes, which help specify where anatomical structures will develop. In particular, Hox genes are organized in clusters and control patterning along the anteroposterior body axis. Mutations in genes of pattern formation can lead to various clinical congenital malformations and anomalies.
This document summarizes in vitro fertilization (IVF) and embryo transfer. [1] IVF involves removing eggs from a woman, fertilizing them with sperm in the lab, and then transferring the fertilized eggs (zygotes) into the uterus a few days later. [2] Reasons for IVF include infertility, which is increasingly prevalent worldwide. [3] The history, methodology, success rates, factors, and limitations of IVF are discussed over several stages: ovarian stimulation and monitoring, egg retrieval, fertilization, embryo transfer, and potential outcomes.
Morphogens are signals that form concentration gradients to specify multiple cell types during development. Cells respond to different morphogen thresholds to activate distinct gene expression. Bicoid is a transcription factor that acts as a morphogen gradient in Drosophila, turning on different genes in different embryo regions based on its concentration. It forms a gradient from anterior to posterior, with high concentrations specifying head structures and lower concentrations specifying more posterior structures. This gradient establishes the basic body plan of the fruit fly embryo.
Fertilization involves the fusion of an egg and sperm, combining their genetic material. This process activates the egg and initiates embryonic development. Key events include chemoattraction of sperm to the egg, binding and fusion of gametes, and prevention of polyspermy. Fusion results in the formation of a single cell with a combined genome from both parent cells. This triggers metabolic changes in the egg and causes its nuclei to fuse, forming a zygote ready to begin dividing and developing into an embryo.
1. Natural cloning occurs when an embryo splits into two identical embryos. Artificial cloning involves transferring the nucleus from an adult body cell into an empty egg cell.
2. Dolly the sheep was artificially cloned by transferring the nucleus from a sheep's body cell into an empty sheep egg cell, which was then implanted into a surrogate sheep.
3. More research on artificial cloning is needed because larger animals do not naturally produce clones and cloning technology is still new with unknown risks and implications.
1) Embryo transfer involves placing embryos into the uterus of a female with the intent to establish a pregnancy. This can involve fresh or frozen embryos.
2) The first successful embryo transfers were conducted in rabbits in 1890 and then various livestock including sheep, cattle, pigs, and water buffalo. The first "test tube baby" was born in 1978.
3) The embryo transfer process involves preparing the uterus, using catheters to deposit embryos, and confirming pregnancy. Embryos are typically transferred at the 2-4 cell stage. Applications include genetic improvement and conservation of endangered species.
In Vitro Fertilization (IVF) involves stimulating a woman's ovaries to develop multiple eggs, retrieving the eggs and fertilizing them with sperm in a lab, then transferring the resulting embryo(s) into the uterus. Key aspects of IVF include controlled ovarian hyperstimulation using fertility medications, egg retrieval under ultrasound guidance, fertilization via intracytoplasmic sperm injection if needed, embryo culture until blastocyst stage, and embryo transfer into the uterus. Success rates of IVF depend on factors like the woman's age, cause of infertility, and embryo quality.
1. Teratogenesis is the process by which environmental factors cause birth defects during embryonic and fetal development. The period between weeks 3-8 of development carries the highest risk, as this is when organ systems are forming.
2. Important teratogens include alcohol, retinoic acid, endocrine disruptors, synthetic chemicals, heavy metals, and pathogens. Alcohol is the most devastating teratogen and can cause fetal alcohol spectrum disorder, characterized by reduced brain and body size.
3. Retinoic acid is important for embryonic development but can cause abnormalities if exposure levels are too high, as seen in a study where women were accidentally exposed during pregnancy.
This document discusses various aspects of assisted reproductive technology (ART) including in vitro fertilization (IVF) and intracytoplasmic sperm injection (ICSI). It provides information on the causes of infertility, procedures for IVF such as egg retrieval, embryo transfer, and blastocyst culture. The document also discusses who may benefit from IVF and ICSI, including those with male factor infertility issues or previous IVF failures. Other ART procedures mentioned include zygote intrafallopian transfer, gamete intrafallopian transfer, and potential future techniques like creating artificial gametes.
This document discusses various aspects of assisted reproductive technology (ART) including infertility, its causes, treatments, and specific procedures like in vitro fertilization (IVF) and intracytoplasmic sperm injection (ICSI). It provides information on male and female infertility, decreasing male fertility rates, and drugs to treat male infertility. The document also explains the procedures for IVF such as ovulation induction, egg retrieval, fertilization, embryo culture, and embryo transfer. ICSI is introduced as a technique used to treat male factor infertility.
In vitro fertilization (IVF) is the process of fertilizing an egg with sperm outside the body in a
laboratory setting and then implanting and developing the embryo in the woman's uterus, where it
will implant and grow into a baby.
What is IVM – In Vitro Maturation of Oocytes.docx9M Fertility
In vitro maturation (IVM) of oocytes is a relatively new technology that has been developed to help couples struggling with infertility. This innovative approach to assisted reproductive technology (ART) involves maturing eggs outside of the body before fertilization, unlike traditional IVF (in vitro fertilization), which involves collecting mature eggs and fertilizing them in a laboratory. We will explore what IVM is, how it works, who may be a good candidate for IVM, its potential risks and complications, and its benefits.
The document summarizes the history and process of in vitro fertilization (IVF). It discusses how IVF was developed as a treatment for infertility and involves fertilizing an egg outside of the body. The summary includes:
- The key stages of an IVF cycle including ovarian stimulation, egg retrieval, fertilization in vitro, embryo transfer, and indications for IVF such as tubal disease or male factor infertility.
- Milestones in the history of IVF including the first successful case in 1978 and development of techniques like ICSI.
- Risks and side effects of ovarian stimulation and factors considered for embryo transfer like number based on patient age and prior attempts.
This document provides an overview of intracytoplasmic sperm injection (ICSI). ICSI involves injecting a single sperm directly into a mature egg under a microscope, which differs from conventional in vitro fertilization where fertilization occurs outside the body. ICSI may be recommended for couples experiencing issues like low sperm counts, abnormal sperm, or problems with antibodies. The process involves sperm and egg retrieval followed by cleaning and injecting a sperm into an egg's cytoplasm. Success rates vary depending on patient factors, though ICSI enables fertilization when few sperm are available. Potential risks include genetic issues being passed to offspring if the father's sperm is abnormal.
This document provides an overview of in vitro fertilization (IVF). It discusses that IVF involves fertilizing an egg with sperm outside of the body in a laboratory dish. The first successful IVF birth was in 1978 in England. The document outlines the basic IVF process which includes hormonal treatment of the female, egg retrieval, fertilization and embryo culture, and embryo transfer. It also discusses the history of IVF, indications for IVF including tubal disease and male factor infertility, factors that affect IVF success rates like maternal age, and potential side effects and risks of IVF treatment.
Infertility is a growing problem caused by factors like delayed childbearing, diseases, pollution, diet, lack of exercise, and prior contraceptive or abortion procedures. In-vitro fertilization (IVF) involves fertilizing an egg outside the body by mixing it with sperm in a laboratory dish. The fertilized egg is then transferred to the uterus. Key steps in IVF include ovarian stimulation to produce multiple eggs, egg retrieval, fertilizing the eggs with sperm in vitro, embryo culture, and embryo transfer. IVF has allowed many infertile couples to conceive and has resulted in over 5 million births worldwide.
In Vitro fertilization (IVF) involves monitoring and stimulating a woman's ovaries, removing eggs and fertilizing them with sperm in a lab dish. IVF is indicated for blocked or damaged fallopian tubes, sperm abnormalities, advanced maternal age, unsuccessful intrauterine insemination, endometriosis, uterine problems, or unexplained infertility. Eggs are retrieved 34-36 hours after an HCG injection under anesthesia. Sperm is then injected into eggs or mixed with eggs, and embryos are selected for transfer into the uterus 2-5 days later. Side effects may include soreness, nausea, mood swings and fatigue. Success rates are 25-30% but vary depending on maternal age, sperm and
Microinsemination involves directly injecting a single sperm into an egg and can help couples with male factor infertility issues undergo in vitro fertilization successfully. It is performed when sperm have poor motility, low density, defects, or cannot penetrate an egg naturally. The process involves preparing sperm, holding an egg in place with a pipette, drawing up a single sperm into a needle, and injecting it into the egg's cytoplasm. This restores normal fertilization rates. While technical issues or lack of success are risks, data does not suggest an increased risk of birth defects, and it may increase pregnancy chances for those with reduced fertilization through standard IVF.
This document provides an overview of several assisted reproductive technologies (ART) including in vitro fertilization (IVF), intrauterine insemination (IUI), intracytoplasmic sperm injection (ICSI), gamete intrafallopian transfer (GIFT), and zygote intrafallopian transfer (ZIFT). It describes the basic procedures and steps for IVF including ovarian stimulation, egg retrieval, fertilization, embryo culture, and embryo transfer. It notes some common indications for IVF include tubal disease, endometriosis, ovulatory dysfunction, and male factor infertility. Potential complications of IVF like ovarian hyperstimulation syndrome and multiple pregnancies are also outlined. IUI and ICSI procedures
Assisted reproductive technology (ART) is a medical procedure used to address infertility issues.It involves procedures such as in vitro fertilization (IVF), intracytoplasmic sperm injection (ICSI), cryopreservation of gametes or embryos, and/or the use of fertility medication.
How Does In Vitro Fertilization (IVF) Work.pdfKioni
In Vitro Fertilization (IVF) is a medical treatment that helps infertile individuals or couples create a child. Here's an explanation of how IVF works:
The Assisted Reproductive Techniques - ART (IVF, IUI, ZIFT, GIFT, ICSI etc.)Muhammad Anas Shamsi
Assisted reproductive technology (ART) is used to treat infertility. It includes fertility treatments that handle both a woman's egg and a man's sperm. It works by removing eggs from a woman's body. The eggs are then mixed with sperm to make embryos. The embryos are then put back in the woman's body. In vitro fertilization (IVF) is the most common and effective type of ART.
1. Infertility is defined as the inability to conceive after one year of unprotected intercourse. Around 10-15% of the population experiences infertility.
2. There are several requirements for natural conception, including the production of healthy eggs and sperm, unblocked fallopian tubes, fertilization, and implantation. When these requirements are not met, Assisted Reproductive Technologies (ART) may help.
3. ART includes procedures like in vitro fertilization (IVF), intracytoplasmic sperm injection (ICSI), frozen embryo transfer, and pre-implantation genetic screening. The goal is to help sperm fertilize eggs or implant embryos when natural conception is not possible. Selecting an experienced ART
This document provides an overview of IVF and ICSI procedures. It discusses that IVF involves fertilizing eggs with sperm in a lab dish, then transferring embryos into the uterus. ICSI is used for severe male factor infertility and involves injecting a single sperm into each egg. Both aim to increase the chances of fertilization. The document outlines the steps of ovarian stimulation, egg retrieval, sperm preparation, fertilization, embryo culture, and embryo transfer.
This document provides an overview of IVF and ICSI procedures. It discusses that IVF involves fertilizing eggs with sperm in a lab dish, then transferring embryos into the uterus. ICSI is used for severe male factor infertility and involves injecting a single sperm into each egg. Both aim to increase the chances of fertilization and pregnancy by positioning sperm closer to eggs. The document outlines the various steps of IVF including ovarian stimulation, egg retrieval, sperm preparation, fertilization, embryo culture, and embryo transfer.
Similar to IVM (In vitro oocyte maturation).pptx (20)
hematic appreciation test is a psychological assessment tool used to measure an individual's appreciation and understanding of specific themes or topics. This test helps to evaluate an individual's ability to connect different ideas and concepts within a given theme, as well as their overall comprehension and interpretation skills. The results of the test can provide valuable insights into an individual's cognitive abilities, creativity, and critical thinking skills
Deep Behavioral Phenotyping in Systems Neuroscience for Functional Atlasing a...Ana Luísa Pinho
Functional Magnetic Resonance Imaging (fMRI) provides means to characterize brain activations in response to behavior. However, cognitive neuroscience has been limited to group-level effects referring to the performance of specific tasks. To obtain the functional profile of elementary cognitive mechanisms, the combination of brain responses to many tasks is required. Yet, to date, both structural atlases and parcellation-based activations do not fully account for cognitive function and still present several limitations. Further, they do not adapt overall to individual characteristics. In this talk, I will give an account of deep-behavioral phenotyping strategies, namely data-driven methods in large task-fMRI datasets, to optimize functional brain-data collection and improve inference of effects-of-interest related to mental processes. Key to this approach is the employment of fast multi-functional paradigms rich on features that can be well parametrized and, consequently, facilitate the creation of psycho-physiological constructs to be modelled with imaging data. Particular emphasis will be given to music stimuli when studying high-order cognitive mechanisms, due to their ecological nature and quality to enable complex behavior compounded by discrete entities. I will also discuss how deep-behavioral phenotyping and individualized models applied to neuroimaging data can better account for the subject-specific organization of domain-general cognitive systems in the human brain. Finally, the accumulation of functional brain signatures brings the possibility to clarify relationships among tasks and create a univocal link between brain systems and mental functions through: (1) the development of ontologies proposing an organization of cognitive processes; and (2) brain-network taxonomies describing functional specialization. To this end, tools to improve commensurability in cognitive science are necessary, such as public repositories, ontology-based platforms and automated meta-analysis tools. I will thus discuss some brain-atlasing resources currently under development, and their applicability in cognitive as well as clinical neuroscience.
BREEDING METHODS FOR DISEASE RESISTANCE.pptxRASHMI M G
Plant breeding for disease resistance is a strategy to reduce crop losses caused by disease. Plants have an innate immune system that allows them to recognize pathogens and provide resistance. However, breeding for long-lasting resistance often involves combining multiple resistance genes
Travis Hills' Endeavors in Minnesota: Fostering Environmental and Economic Pr...Travis Hills MN
Travis Hills of Minnesota developed a method to convert waste into high-value dry fertilizer, significantly enriching soil quality. By providing farmers with a valuable resource derived from waste, Travis Hills helps enhance farm profitability while promoting environmental stewardship. Travis Hills' sustainable practices lead to cost savings and increased revenue for farmers by improving resource efficiency and reducing waste.
The use of Nauplii and metanauplii artemia in aquaculture (brine shrimp).pptxMAGOTI ERNEST
Although Artemia has been known to man for centuries, its use as a food for the culture of larval organisms apparently began only in the 1930s, when several investigators found that it made an excellent food for newly hatched fish larvae (Litvinenko et al., 2023). As aquaculture developed in the 1960s and ‘70s, the use of Artemia also became more widespread, due both to its convenience and to its nutritional value for larval organisms (Arenas-Pardo et al., 2024). The fact that Artemia dormant cysts can be stored for long periods in cans, and then used as an off-the-shelf food requiring only 24 h of incubation makes them the most convenient, least labor-intensive, live food available for aquaculture (Sorgeloos & Roubach, 2021). The nutritional value of Artemia, especially for marine organisms, is not constant, but varies both geographically and temporally. During the last decade, however, both the causes of Artemia nutritional variability and methods to improve poorquality Artemia have been identified (Loufi et al., 2024).
Brine shrimp (Artemia spp.) are used in marine aquaculture worldwide. Annually, more than 2,000 metric tons of dry cysts are used for cultivation of fish, crustacean, and shellfish larva. Brine shrimp are important to aquaculture because newly hatched brine shrimp nauplii (larvae) provide a food source for many fish fry (Mozanzadeh et al., 2021). Culture and harvesting of brine shrimp eggs represents another aspect of the aquaculture industry. Nauplii and metanauplii of Artemia, commonly known as brine shrimp, play a crucial role in aquaculture due to their nutritional value and suitability as live feed for many aquatic species, particularly in larval stages (Sorgeloos & Roubach, 2021).
The debris of the ‘last major merger’ is dynamically youngSérgio Sacani
The Milky Way’s (MW) inner stellar halo contains an [Fe/H]-rich component with highly eccentric orbits, often referred to as the
‘last major merger.’ Hypotheses for the origin of this component include Gaia-Sausage/Enceladus (GSE), where the progenitor
collided with the MW proto-disc 8–11 Gyr ago, and the Virgo Radial Merger (VRM), where the progenitor collided with the
MW disc within the last 3 Gyr. These two scenarios make different predictions about observable structure in local phase space,
because the morphology of debris depends on how long it has had to phase mix. The recently identified phase-space folds in Gaia
DR3 have positive caustic velocities, making them fundamentally different than the phase-mixed chevrons found in simulations
at late times. Roughly 20 per cent of the stars in the prograde local stellar halo are associated with the observed caustics. Based
on a simple phase-mixing model, the observed number of caustics are consistent with a merger that occurred 1–2 Gyr ago.
We also compare the observed phase-space distribution to FIRE-2 Latte simulations of GSE-like mergers, using a quantitative
measurement of phase mixing (2D causticality). The observed local phase-space distribution best matches the simulated data
1–2 Gyr after collision, and certainly not later than 3 Gyr. This is further evidence that the progenitor of the ‘last major merger’
did not collide with the MW proto-disc at early times, as is thought for the GSE, but instead collided with the MW disc within
the last few Gyr, consistent with the body of work surrounding the VRM.
ESPP presentation to EU Waste Water Network, 4th June 2024 “EU policies driving nutrient removal and recycling
and the revised UWWTD (Urban Waste Water Treatment Directive)”
Phenomics assisted breeding in crop improvementIshaGoswami9
As the population is increasing and will reach about 9 billion upto 2050. Also due to climate change, it is difficult to meet the food requirement of such a large population. Facing the challenges presented by resource shortages, climate
change, and increasing global population, crop yield and quality need to be improved in a sustainable way over the coming decades. Genetic improvement by breeding is the best way to increase crop productivity. With the rapid progression of functional
genomics, an increasing number of crop genomes have been sequenced and dozens of genes influencing key agronomic traits have been identified. However, current genome sequence information has not been adequately exploited for understanding
the complex characteristics of multiple gene, owing to a lack of crop phenotypic data. Efficient, automatic, and accurate technologies and platforms that can capture phenotypic data that can
be linked to genomics information for crop improvement at all growth stages have become as important as genotyping. Thus,
high-throughput phenotyping has become the major bottleneck restricting crop breeding. Plant phenomics has been defined as the high-throughput, accurate acquisition and analysis of multi-dimensional phenotypes
during crop growing stages at the organism level, including the cell, tissue, organ, individual plant, plot, and field levels. With the rapid development of novel sensors, imaging technology,
and analysis methods, numerous infrastructure platforms have been developed for phenotyping.
The ability to recreate computational results with minimal effort and actionable metrics provides a solid foundation for scientific research and software development. When people can replicate an analysis at the touch of a button using open-source software, open data, and methods to assess and compare proposals, it significantly eases verification of results, engagement with a diverse range of contributors, and progress. However, we have yet to fully achieve this; there are still many sociotechnical frictions.
Inspired by David Donoho's vision, this talk aims to revisit the three crucial pillars of frictionless reproducibility (data sharing, code sharing, and competitive challenges) with the perspective of deep software variability.
Our observation is that multiple layers — hardware, operating systems, third-party libraries, software versions, input data, compile-time options, and parameters — are subject to variability that exacerbates frictions but is also essential for achieving robust, generalizable results and fostering innovation. I will first review the literature, providing evidence of how the complex variability interactions across these layers affect qualitative and quantitative software properties, thereby complicating the reproduction and replication of scientific studies in various fields.
I will then present some software engineering and AI techniques that can support the strategic exploration of variability spaces. These include the use of abstractions and models (e.g., feature models), sampling strategies (e.g., uniform, random), cost-effective measurements (e.g., incremental build of software configurations), and dimensionality reduction methods (e.g., transfer learning, feature selection, software debloating).
I will finally argue that deep variability is both the problem and solution of frictionless reproducibility, calling the software science community to develop new methods and tools to manage variability and foster reproducibility in software systems.
Exposé invité Journées Nationales du GDR GPL 2024
1. UNIVERSITY OF
LADAKH
Presentation on:
IN VITRO OOCYTE
MATURATUION (IVM)
SUBMITTED BY:
STANZIN DOLMA
1st semester
M.sc. Zoology
SUBMITTED TO:
Dr. BASHARAT ALI
Department of Zoology
2. INTRODUCTION
• In vitro oocyte maturation (IVM) is a medical
technique used in assisted reproductive
technology.
• It involves the collection of immature
oocytes from a woman’s ovaries, which are
then cultured and matured in a controlled
laboratory environment.
• Once matured, these oocytes can be
fertilized, providing a potential solution for
infertility.
• IVM is particularly useful for individuals who cannot undergo traditional in vitro
fertilization (IVF) or those at risk of ovarian hyperstimulation syndrome (OHSS).
3. HISTORY
• In 1935, Pincus & Enzmann did the first experiment on immature rabbit
oocyte, showing in vitro spontaneous maturation and fertilization. They
showed maturation occurs in isolation from normal follicular
environment.
• In 1965 Edwards then continued IVM studies in mouse, sheep, cow, pig,
rhesus monkey and human.
• In 1991 the first human pregnancy was recorded using IVM followed by IVF.
• In 1994 the first birth using IVM oocytes from polycystic ovarian syndrome
patients was recorded highlighting that PCOS patient’s oocytes are capable
of maturation.
4. • Oocyte maturation is the physiological event that precedes, and is required
for, successful fertilization and embryo development
• During development in the fetal ovary, oocytes in most mammals become
arrested at the diplotene stage of prophase I (the germinal vesicle stage).
• Resumption of meiosis, triggered by the preovulatory surge of luteinizing
hormone, and progression through maturation results in further arrest at the
metaphase II (MII) stage with extrusion of the first polar body (PB) and
establishment of a DNA complement of 1n2C.
• Penetration of the sperm (1n1C) leads to extrusion of the second PB and
establishment of a 1n1C state in the oocyte leading to a diploid embryo (2n2C)
after the first mitotic division following fertilization. All subsequent divisions
are mitotic, resulting in two identical daughter cells.
WHAT IS OOCYTE
MATURATION?
6. PROCEDURE OF IVM
In vitro oocyte maturation is a medical procedure used in assisted reproductive
technology. The process includes are:
• Oocyte Retrieval: IVM typically starts
with ovarian stimulation, but in some
cases, it may involve unstimulated
cycles. Immature oocytes (eggs) are
collected from a woman’s ovaries.When
the follicles are mature, an oocyte
retrieval procedure is performed. This
involves a transvaginal ultrasound-
guided aspiration, where a needle is
used to aspirate the fluid from the
mature follicles. This fluid contains
immature oocytes.
• Oocyte Selection: After retrieval, the fluid is examined in the laboratory
to identify the immature oocytes. Not all collected oocytes are suitable
for IVM, so the best-quality ones are chosen for the next steps.
7. In Vitro Culture: The selected immature oocytes are placed in a culture
medium in a controlled environment within the laboratory.
• The culture conditions mimic the environment within the female body as
closely as possible to encourage maturation.
• There are two kinds of culturing methods:
1. Conventional IVM- In the conventional IVM, immature oocytes
were directly cultured to MII oocytes after oocyte .However,
conventional IVM focuses on nuclear maturation, ignoring the
synchronous maturation of cytoplasm.
1. BIPHASIC IVM- The biphasic IVM culturing system (also known as
capacitation IVM (CAPA-IVM)), which includes a pre-IVM culturing period
(around 24 h) before the IVM culturing has been well developed in animal
IVM.The pre-IVM culturing was mainly applied to inhibit resumption of
meiosis and promote synchronization between the nuclear and
cytoplasmic maturation
8. Maturation Process: Over the course of 24 to 48 hours, the immature oocytes
undergo maturation in the culture medium.
• This involves the development of the oocyte nucleus (germinal vesicle) and
the surrounding layers of cells, ultimately reaching the metaphase II (MII)
stage, where they are ready for fertilization.
• Hormone monitoring and microscopic evaluation are used to assess the
progression of maturation.
• This maturation involves the development of the oocyte nucleus and
surrounding layers of cells, ensuring they exhibit the signs of readiness for
fertilization.
Fertilization- Once the oocytes have reached the MII stage, they can be fertilized.
This can be achieved through traditional IVF, where they are exposed to sperm in
a laboratory dish, or by ICSI, where a single sperm is injected directly into each
mature oocyte. After fertilization, the resulting zygotes are cultured for a few
days.
Embryo Transfer- The best-quality embryos are selected for transfer into the
woman’s uterus. The choice of the number of embryos to transfer depends on
the woman’s age, embryo quality, and other factors.
The embryo transfer procedure is similar to traditional IVF, where one or more
embryos are carefully placed in the uterine cavity with the hope of establishing a
successful pregnancy.
9. WHY IVM IS DONE?
In vitro oocyte maturation (IVM) is done for several reasons:
• Polycystic Ovary Syndrome (PCOS): IVM is often used for women with PCOS, a
condition where multiple immature follicles develop in the ovaries.
Conventional ovarian stimulation in IVF can lead to a higher risk of ovarian
hyperstimulation syndrome (OHSS) in these cases, so IVM is a safer alternative.
• Ovarian Disorders: Women with certain ovarian disorders that prevent the
proper maturation of eggs may benefit from IVM.
• Cancer Patients: Some cancer treatments, such as chemotherapy, can harm a
woman’s ovarian function. In such cases, IVM allows for the retrieval and
preservation of immature oocytes before cancer treatment begins.
• Fertility Preservation: IVM can be used for fertility preservation purposes. For
instance, women who wish to delay childbearing for personal or medical
reasons may opt for IVM to freeze and mature their eggs at a later date.
• Low Ovarian Reserve: Women with a low ovarian reserve may have limited egg
production. IVM can help maximize the use of the few available oocytes.
• Patient Preference: In some cases, women may prefer IVM over conventional
IVF due to personal or medical considerations.
10. Differences IVM IVF
Oocyte Maturation In IVM, immature eggs
are retrieved directly
from the ovaries without
the need for extensive
ovarian stimulation.
In traditional IVF, mature
eggs are retrieved from
the woman’s ovaries after
undergoing ovarian
stimulation with fertility
medications.
Timing of Oocyte
Retrieval
Oocyte retrieval in IVM
takes place while the
oocytes are still
immature. They are
matured in vitro over a
period of 24 to 48 hours.
Oocyte retrieval in IVF
occurs after the eggs
have matured in
response to ovarian
stimulation, typically 36
hours after a trigger
injection.
Indication IVM is often considered
for specific situations,
such as women with
PCOS where ovarian
stimulation might carry a
higher risk of ovarian
hyperstimulation
syndrome (OHSS).
IVF is commonly used for
a wide range of fertility
issues, including male
infertility, tubal
blockages, and
unexplained infertility.
DIFFERENCE BETWEEN
IVM AND IVF
11. DIFFERENCES IVM IVF
Hormonal Stimulation IVM minimizes the use of
hormonal stimulation,
which may be more
suitable for certain
patients, especially those
at risk of OHSS.
IVF involves controlled
ovarian stimulation with
hormonal medications to
induce the growth of
multiple follicles.
Success Rates IVM success rates can be
lower, especially in
certain patient
populations. Not all
immature oocytes may
successfully mature.
IVF typically has higher
success rates compared
to IVM, as mature eggs
are used for fertilization.
Cost and Time
Commitment
IVM may be a more cost-
effective and less time-
consuming option for
some patients, as it
involves fewer days of
treatment.
IVF is often more
expensive due to the
need for hormonal
stimulation and a longer
treatment process.
12. SUCESS RATES OF IVM
The success rates of in vitro oocyte maturation (IVM) can vary widely depending
on several factors, including the patient's specific condition, the clinic's expertise,
and the underlying cause of infertility. In general, the success rates for IVM tend
to be lower than those for traditional in vitro fertilization (IVF) because IVM
involves maturing immature oocytes. However, here are some factors that can
influence the success of IVM:
• Underlying Cause of Infertility: The success of IVM may be higher for certain
conditions, such as polycystic ovary syndrome (PCOS), where it is commonly
used. Success rates can be lower for other causes of infertility.
• Patient Age: As with IVF, the age of the patient is a significant factor. Younger
patients tend to have higher success rates with IVM.
• Quality of Oocytes: The quality of the immature oocytes retrieved and their
ability to mature in vitro can impact success. Not all immature oocytes may
successfully mature.
• Expertise of the Clinic: The experience and expertise of the fertility clinic and
its laboratory team play a crucial role in the success of IVM.
• Fertilization Method: The method used for fertilization, whether traditional
IVF or ICSI (intracytoplasmic sperm injection), can influence outcomes.