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Prevalence of onychomycosis in
patients with diabetes
mellitus: A cross-sectional study from a
tertiary care
hospital in North India
Indian Journal of Dermatology, Venereology and Leprology
Received: April, 2022 Accepted: December, 2022 Published: August, 2023
Sonia Agrawal, Archana Singal, Chander Grover, Shukla Das, V K Arora, S V Madhu
Departments of Dermatology & STD, 1Microbiology, 2Pathology, 3Endocrinology, University College of
Medical Sciences and GTB Hospital, Delhi, India.
Introduction
• Onychomycosis (OM) accounts for 40–50% of all onychopathies with
a worldwide prevalence of 5%.
• India, which is considered the world capital of diabetes has a 0.5–5%
prevalence of OM.
• Risk factors associated with OM include diabetes mellitus (DM),
peripheral arterial disease, immunosuppression, tinea pedis, smoking,
recurrent trauma, psoriasis, sharing of public bathing facilities, etc.
• DM is a metabolic disorder with a rising global prevalence.
• In India, the total number of diabetics is around 61.3 million and this
is further estimated to rise to 101.2 million by the year 2030.
• DM is an established risk factor for OM, its clinico-epidemiological
and mycological characteristics in a diabetic population remain largely
unexplored, in particular from the Indian subcontinent.
Aims and objectives:
• To estimate the prevalence of OM in diabetic patients, to identify and
analyse risk factors
• Correlate the severity of nail changes with glycemic control (HBA1c).
Methods:
• Cross-sectional analytical study was conducted in the Departments of
Dermatology and Endocrinology at the University College of Medical
Sciences, New Delhi, India
• from November 2018 to April 2020
• After getting ethics committee approval.
• Appropriate nail samples were sent for investigations to the
departments of microbiology and pathology.
• 300 consecutive diabetic patients (type 1 and 2) attending the
outpatient Departments of Dermatology and Endocrinology
constituted the study population.
• After written informed consent was obtained, detailed history was
taken (age of onset of DM, duration, type of DM, treatment, risk
factors and co-morbidities)
• followed by thorough examination and haematological investigations,
and findings were recorded on a pre-designed proforma.
• Nails were cleansed with sterile alcohol to look for any clinical
evidence of OM ( onycholysis, subungual hyperkeratosis,
chromonychia, nail plate thickening and dystrophy).
• A representative nail with suspected OM was thus identified and
clinical photographs were taken.
• The severity of nail involvement was calculated based on the number of
affected nails (mild- <3, moderate- 4–6 and severe- >6 nails) and was
correlated with the patient’s glycosylated haemoglobin (HbA1c) level.
Case definition
• The patient was said to have OM if the clinical findings of OM were
corroborated with at least two or more positive tests,
viz onychoscopy, direct microscopic examination (DME) in KOH,
fungal culture and histopathology with PAS staining.
1. Onychoscopy-
• Onychoscopy was performed using Dinolite AM 7515 MZT
dermatoscope on all the nails with isopropyl alcohol as interface
medium.
• The presence of spiked pattern and subungual hyperkeratosis with or
without ruinous aspects were considered to be characteristic features
indicative of the distal and lateral subungual onychomycosis (DLSO)
variant of OM.
• For the endonyx variant, the dendritic pattern was considered a
positive diagnostic feature.
• The diagnostic criteria used for proximal subungual onychomycosis
(PSO) were proximal onycholysis and homogenous opacity.
• Superficial onychomycosis (SO) was diagnosed based on homogenous
opacity without subungual hyperkeratosis.
• Total dystrophic onychomycosis (TDO) was diagnosed by the
presence of both ruinous aspects and longitudinal striae.
2. Nail clippings-
• Nail clippings from appropriate sites were collected for DME in 40%
KOH.
• A part of the nail clipping was sent in a sterile envelope for inoculation
on Sabouraud’s dextrose agar (SDA) with and without
chloramphenicol (0.05 gm/L), gentamycin (20 mg/l) and
cycloheximide (0.5 gm/L), at 25 degrees Celsius for optimal growth.
• In the case of growth, colony characteristics were studied on
lactophenol cotton blue (LPCB) mount preparation.
• The culture was considered negative if no growth was observed after
four weeks of incubation.
• Nail clipping was also sent for histopathology (H&E and PAS
staining); the presence of subungual hyperkeratosis, hyphae in the nail
lamellae and fungal elements in the stratum corneum were considered
diagnostic of onychomycosis.
Statistical analysis
• The data was analysed using SPSS version 20.0 (SPSS Inc., Chicago,
IL, USA).
• Comparative analysis was done using chi-square test of
significance/Fischer’s exact test and P < 0.05 was considered
significant.
• Logistic regression was applied to calculate the significant risk factors
for OM in the studied patients.
Discussion
• Oychomycosis (OM) constitutes the most common nail infection (40–
50% of onychopathies). In our study, 300 diabetic patients were
screened and 102 of these fulfilled the diagnostic criteria for OM,
which translates to a prevalence of 34%.
Results:
• The prevalence of OM in DM patients was 34% (102/300) and
significant risk factors included; age >60 years, male gender, closed
shoes, disease duration >5 years, high BMI (>25) and lack of
awareness about nail changes.
• Distal and lateral subungual OM (78%) was the commonest
presentation followed by proximal subungual OM, superficial OM and
total dystrophic OM.
• Correlation between HbA1c and the number of nails involved was
found to be significant.
Conclusion
• The prevalence of OM is high in patients with diabetes, especially in
males.
• It can be diagnosed with higher certainty using a combination of
investigations.
• Onychomycosis tends to be more severe in patients with poor
glycemic control.
• It is important to diagnose OM early in order to treat and prevent
potential complications.

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onycomycosis.pptx

  • 1. Prevalence of onychomycosis in patients with diabetes mellitus: A cross-sectional study from a tertiary care hospital in North India Indian Journal of Dermatology, Venereology and Leprology Received: April, 2022 Accepted: December, 2022 Published: August, 2023 Sonia Agrawal, Archana Singal, Chander Grover, Shukla Das, V K Arora, S V Madhu Departments of Dermatology & STD, 1Microbiology, 2Pathology, 3Endocrinology, University College of Medical Sciences and GTB Hospital, Delhi, India.
  • 2. Introduction • Onychomycosis (OM) accounts for 40–50% of all onychopathies with a worldwide prevalence of 5%. • India, which is considered the world capital of diabetes has a 0.5–5% prevalence of OM. • Risk factors associated with OM include diabetes mellitus (DM), peripheral arterial disease, immunosuppression, tinea pedis, smoking, recurrent trauma, psoriasis, sharing of public bathing facilities, etc.
  • 3. • DM is a metabolic disorder with a rising global prevalence. • In India, the total number of diabetics is around 61.3 million and this is further estimated to rise to 101.2 million by the year 2030. • DM is an established risk factor for OM, its clinico-epidemiological and mycological characteristics in a diabetic population remain largely unexplored, in particular from the Indian subcontinent.
  • 4. Aims and objectives: • To estimate the prevalence of OM in diabetic patients, to identify and analyse risk factors • Correlate the severity of nail changes with glycemic control (HBA1c).
  • 5. Methods: • Cross-sectional analytical study was conducted in the Departments of Dermatology and Endocrinology at the University College of Medical Sciences, New Delhi, India • from November 2018 to April 2020 • After getting ethics committee approval. • Appropriate nail samples were sent for investigations to the departments of microbiology and pathology.
  • 6. • 300 consecutive diabetic patients (type 1 and 2) attending the outpatient Departments of Dermatology and Endocrinology constituted the study population. • After written informed consent was obtained, detailed history was taken (age of onset of DM, duration, type of DM, treatment, risk factors and co-morbidities) • followed by thorough examination and haematological investigations, and findings were recorded on a pre-designed proforma.
  • 7. • Nails were cleansed with sterile alcohol to look for any clinical evidence of OM ( onycholysis, subungual hyperkeratosis, chromonychia, nail plate thickening and dystrophy). • A representative nail with suspected OM was thus identified and clinical photographs were taken. • The severity of nail involvement was calculated based on the number of affected nails (mild- <3, moderate- 4–6 and severe- >6 nails) and was correlated with the patient’s glycosylated haemoglobin (HbA1c) level.
  • 8. Case definition • The patient was said to have OM if the clinical findings of OM were corroborated with at least two or more positive tests, viz onychoscopy, direct microscopic examination (DME) in KOH, fungal culture and histopathology with PAS staining.
  • 9. 1. Onychoscopy- • Onychoscopy was performed using Dinolite AM 7515 MZT dermatoscope on all the nails with isopropyl alcohol as interface medium. • The presence of spiked pattern and subungual hyperkeratosis with or without ruinous aspects were considered to be characteristic features indicative of the distal and lateral subungual onychomycosis (DLSO) variant of OM. • For the endonyx variant, the dendritic pattern was considered a positive diagnostic feature.
  • 10. • The diagnostic criteria used for proximal subungual onychomycosis (PSO) were proximal onycholysis and homogenous opacity. • Superficial onychomycosis (SO) was diagnosed based on homogenous opacity without subungual hyperkeratosis. • Total dystrophic onychomycosis (TDO) was diagnosed by the presence of both ruinous aspects and longitudinal striae.
  • 11.
  • 12.
  • 13.
  • 14.
  • 15. 2. Nail clippings- • Nail clippings from appropriate sites were collected for DME in 40% KOH. • A part of the nail clipping was sent in a sterile envelope for inoculation on Sabouraud’s dextrose agar (SDA) with and without chloramphenicol (0.05 gm/L), gentamycin (20 mg/l) and cycloheximide (0.5 gm/L), at 25 degrees Celsius for optimal growth. • In the case of growth, colony characteristics were studied on lactophenol cotton blue (LPCB) mount preparation.
  • 16. • The culture was considered negative if no growth was observed after four weeks of incubation. • Nail clipping was also sent for histopathology (H&E and PAS staining); the presence of subungual hyperkeratosis, hyphae in the nail lamellae and fungal elements in the stratum corneum were considered diagnostic of onychomycosis.
  • 17.
  • 18.
  • 19.
  • 20.
  • 21.
  • 22.
  • 23.
  • 24.
  • 25.
  • 26.
  • 27.
  • 28.
  • 29. Statistical analysis • The data was analysed using SPSS version 20.0 (SPSS Inc., Chicago, IL, USA). • Comparative analysis was done using chi-square test of significance/Fischer’s exact test and P < 0.05 was considered significant. • Logistic regression was applied to calculate the significant risk factors for OM in the studied patients.
  • 30. Discussion • Oychomycosis (OM) constitutes the most common nail infection (40– 50% of onychopathies). In our study, 300 diabetic patients were screened and 102 of these fulfilled the diagnostic criteria for OM, which translates to a prevalence of 34%.
  • 31.
  • 32.
  • 33.
  • 34.
  • 35.
  • 36. Results: • The prevalence of OM in DM patients was 34% (102/300) and significant risk factors included; age >60 years, male gender, closed shoes, disease duration >5 years, high BMI (>25) and lack of awareness about nail changes. • Distal and lateral subungual OM (78%) was the commonest presentation followed by proximal subungual OM, superficial OM and total dystrophic OM. • Correlation between HbA1c and the number of nails involved was found to be significant.
  • 37. Conclusion • The prevalence of OM is high in patients with diabetes, especially in males. • It can be diagnosed with higher certainty using a combination of investigations. • Onychomycosis tends to be more severe in patients with poor glycemic control. • It is important to diagnose OM early in order to treat and prevent potential complications.