This document provides an overview of different classes of oral hypoglycemic medications used to treat diabetes mellitus. It discusses the general information, mechanisms of action, dosing, renal adjustments, cardiovascular effects, side effects, and necessary lab investigations for classes including biguanides, sulfonylureas, thiazolidinediones, alpha-glucosidase inhibitors, meglitinides, DPP-4 inhibitors, GLP-1 receptor agonists, and SGLT2 inhibitors. The document aims to educate healthcare providers on optimally managing medications for patients with diabetes.
9. Dose of Metformin
• Maximal dose is 2500-3000 mg.
• 750 mg: used once daily, more tolerable, less GI SE.
• Start the dose 500, and double it every week.
• The practical dose is 1500-2000 mg per day.
11. Doses
• Immediate-release:
Initial dose: 500 mg orally twice a day or 850 mg orally once a day
Maximum dose: 2550 mg/day
Extended-release:
Initial dose: 500 to 1000 mg orally once a day
Maximum dose: 2000 mg/day
12. CVS and Metformin
CV Effects:
• Reduces risk of MI by 39%.
• Diabetes-related death by 42%.
• Mortality by 36%.
• (UK Prospective Diabetes Study UKPDS)
Clinical Use in Patients with CVD:
• Not indicated in the presence of acidosis or
dehydration.
13. Newer CKD guidelines are based on estimated glomerular
filtration rate (eGFR), not on serum creatinine
If 30-45
and not
already on
metformin
> start
insulin
14. Side Effects of Metformin
• Most common: Gastrointestinal side effects
• To decrease side effect: slow release metformin XR 750 mg
•Most serious: Lactic acidosis, andVit B 12 deficiency
17. General Information About SU
• MOA: Inhibit ATP-K channels, stimulating increase Ca and insulin
release and secretion from pancreatic beta cells.
• Mimic normal physiology of glucose.
• Indication: Non pregnant, non obese type 2 DM
• Strong A1C reduction : 0.8-2 %
• Low cost
19. SU: Gliclazide
•Gliclazide:
• Modified release: 30 or 60 mg tablet.
• Maximal dose is 120 mg .
• It mainly affect the fasting blood glucose
• Better to take it before breakfast .
20. Renal adjustments & SU
• Gliclazide:
• Reduce dose if eGFR < 30
• Not recommended if eGFR < 15
• Glimepiride:
• Avoid use if eGFR < 60
• Glipizide:
• No dose adjustment required
• Glibenclamide:
• Avoid use in patients with eGFR < 60
21. Cardiovascular System & SU
• CV Effects:
• Reduction of microvascular complications (UKPDS)
• Increased CV mortality (UGDP trial)
• Precautions should be taken in patients with multiple comorbidities, HF, and advanced CKD
(stages IV andV)
22. Side Effects of SU
•SE: hypoglycemia, weight gain
• High risk for hypoglycemia
•Glibenclamide:
•Most common
•It is the worst for cardiac patients
•Gliclazide: least hypoglycemias
30. Side Effects ofTZD
• Weight gain, mainly by increasing fluids retention
• Edema
• Heart failure exacerbation. (Cardiovascular toxicity)
• Can cause osteoporosis.
• Potential increase in MI ( Rosiglitazone)
• Potential increase in bladder cancer (pioglitazone)
31. Contraindications ofTZD
• Symptomatic HF
• NYHA class III or IV
• Active bladder cancer or H/O bladder cancer
• H/O fracture or high risk for fractures
• (e.g. postmenopausal women with low bone mass)
• Active liver disease
• T1DM
• Pregnancy
32. ForYour Information
• If it is not working by 2 months, patient is compliance,
• Give history of weight loss:
• Suspects insulin deficiency (most common sign for insulin deficiency is weight loss)
• Delayed effect:
• 4-8 weeks to observe effect
• So, follow up with A1C not fasting blood sugar readings.
34. General Information About Acarbose
• Very safe.
• Weight neutral effect.
• Doesn’t cause hypoglycemia.
• Can be used in severe renal cases.
• Decrease HbA1c 0.7– 1.0%.
• Decrease post prandial glucose level.
• Low – moderate cost
35. Mechanism of Action of Acarbose
• Inhibit glucose absorption in the gut
• Delayed absorption of carbohydrates in intestine or prevent breakdown of
polysaccharide to monosaccharide
• So, dosing should be with meal
39. Side Effects of Acarbose
•Gastrointestinal upset: diarrhea and flatulence
•Side effect if taken with carbohydrates
•High serum aminotransferase concentration
42. General Information About Meglitinides
MOA:
• Stimulate insulin secretion (rapidly & for a short duration) in the presence of glucose.
• Taken with meals
Efficacy:
• Decrease peak postprandial glucose level
• Reduce A1C 0.5-2.0%
• Moderate cost
43. Renal Adjustments & Meglitinides
• Repaglinide (Novonorm):
• Initial dose of 0.5 mg before meals when eGFR < 30
• Nateglinide:
• Caution when used with eGFR < 30
• Initiate with 60 mg before meals
46. General Information About DPP4i
• No effects on body weight or risk of hypoglycemia
• Patient call it “”منظم
• Drugs:
• Sitagliptin (Jenovia): need renal adjustment.
• Linagliptin: no need for renal adjustment.
• Saxagliptin
• Vildagliptin
• Alogliptin
47. Mechanism of Action of DPP4i
• MOA:
• Inhibit DPP from degrading GLP 1.
• Increase satiety.
• Decrease emptying.
• Increase insulin secretion.
• Decrease glucagon.
• Efficacy: decrease HbA1c 0.5–0.9%.
• High cost
48. Renal Adjustments & DPP4I
• Sitagliptin:
• 50 mg OD if eGFR 30-50
• 25 mg OD if eGFR < 30
• Saxagliptin:
• 2.5 mg OD if eGFR < 50
• Linagliptin:
• No dose adjustment is required.
Alogliptin:
• 1.25 mg OD if eGFR 30-50
• <0.625 mg OD if eGFR<30 Or on Hemodialysis
49. Dosing and Renal Adjustment (Sitagliptin)
• Based on GFR:
• If GFR > 60:
• 100 mg
• If GFR 30-59:
• 50 mg
• If GFR < 30:
• 25 mg
50. Cardiovascular System & DPP4I
• CV Effects
• Well tolerated
• Increased risk of HF with saxagliptin and alogliptin
51. Side Effects of DPP4I
• Can cause significant appetite loss
• Cause pancreatitis
• Associated with pancreatic cancer ?
• Headache
• Nasopharyngitis
• URTI
• Angioedema – Urtecaria
54. General Information About GLP 1 agonist
• No hypoglycemia.
• Efficacy: reduction of HbA1c by 0.55 – 1.2 %
• Have good weight reduction effect:
• Approved for obesity , Dose: 3 mg .
• Decrease weight by 5-10% in 1 year + exercise and diet .
• Decrease post prandial glucose level
• High cost
55. GLP-1 agonist
• Short – Acting
Exenatide twice daily
Lixisenatide
• Long – Acting
Liraglutide (Victoza)
Exenatide once weekly
Dulaglutide
Semaglutide
56. Liraglutide
T2DM:Victoza
• Dose: 0.6 mg SC daily for 1 week initially, then
increase to 1.2 mg daily. If glycemic control not
achieved, can increase to 1.8 mg daily
• Initial dose of 0.6 mg SC daily: minimizeGI side
effects but it does not provide glycemic
control.
• To reduce the risk of major adverse
cardiovascular events
Obesity: Saxenda
• Indicated as an adjunct to a reduced-calorie diet and
increased physical activity for chronic weight management
in adults
• BMI of ≥30
• BMI of ≥27 + 1 weight-related condition
• E.g, HTN, T2DM, & DLP
• Initiate at 0.6 mg SC daily for 1 week; increase by 0.6
mg/day in weekly intervals until a dose of 3 mg/day is
achieved
• If patients do not tolerate an increased dose during dose
escalation, consider delaying dose escalation for ~1
additional week
• Discontinue if a patient cannot tolerate the 3 mg dose, as
efficacy has not been established at lower doses (eg, 0.6,
1.2, 1.8, 2.4 mg)
57. Liraglutide
T2DM:Victoza
• Dose: 0.6 mg SC daily (No glycemic control effect) for 1 week initially, then increase to 1.2
mg daily.
• If glycemic control not achieved, can increase to 1.8 mg daily.
• To reduce the risk of major adverse cardiovascular events.
58. Liraglutide
Obesity: Saxenda
• Indicated as an adjunct to a reduced-calorie diet and increased physical activity for chronic weight
management in adults:
• BMI of ≥ 30.
• BMI of ≥ 27 + 1 weight-related condition. E.g, HTN,T2DM, & DLP.
• Initiate at 0.6 mg SC daily for 1 week; increase by 0.6 mg/day in weekly intervals until a dose of 3
mg/day is achieved.
• If patients do not tolerate an increased dose during dose escalation, consider delaying dose
escalation for ~1 additional week.
• Discontinue if a patient cannot tolerate the 3 mg dose, as efficacy has not been established at
lower doses (eg, 0.6, 1.2, 1.8, 2.4 mg)
60. Renal Adjustment & GLP-1 Agonist
• Liraglutide (0.6-1.8 mg):
• No restrictions if eGFR > 30
• Once daily injection
• Dulaglutide (0.7-1.5 mg):
• No dose modifications on any renal
impairment.
• Exenatide (QD=5-10 mcg; QW= 2 mg):
• eGFR 30-50 : Dose < 5 mcg Daily
• eGFR< 30: Use with Caution
• Lexisenatide (10,20 mcg):
• - Avoid if eGFR < 50
61. Renal Adjustment & GLP-1 Agonist
• Limited data in patients with advanced CKD (stages IV andV).
• Exenatide is eliminated by renal mechanisms and should not be given in patients
with severe ESRD.
• Liraglutide is not eliminated by renal or hepatic mechanisms, but it should be used
with caution since there are only limited data in patients with renal or hepatic
impairment.
62. Cardiovascular System & GLP-1 agonist
• Significant reduction of composite CV endpoints in LEADER and SUSTAIN-6
trials.
• No significant effects on CV mortality, nonfatal MI, and hospitalization for
HF with Liraglutide and Semaglutide
• Reduced risk of nonfatal stroke with Semaglutide
63. Side Effect of GLP-1 agonist
•Nausea but tolerated with time.
• Disappear in 2 weeks not like Acarbose takes 2 years
• Start low dose 0.6mg then increase till 1.8mg
•Injection site reactions
64. Precautions with GLP-1 agonist
•Patients with history of pancreatitis
•T1DM
•Patients with a personal or family history of Medullary
Thyroid Cancer or Multiple Endocrine Neoplasia 2A or 2B
Very Important
65. ForYour Information
• In animal study: GLP-1 causes Beta cells regeneration
• It is post-prandial effect.
• So, if the patient is on insulin and want to start GLP-1:
• Better to decrease the prandial insulin (Aspart) as it might cause hypoglycemia if
patient is near control.
67. General Information About SGLT2i
• Stop the reabsorption of glucose in the proximal tubule in the kidney and execrating the glucose. (glucose
dependent) .
• Cardio-protective medication:
• Canagliflozin, Empagliflozin.
• Expensive medication
• Weigh loss effect
• Anti hypertension medication effect (Lowers BP by 2-4 mm/Hg).
• Decrease BP, increase LDL and Cr
• A1C effect : 0.6 % , LEAST medication to decrease A1C.
70. Cardiovascular System & SGLT2I
• In the EMPA-REG OUTCOME trial:
• Empagliflozin reduced CV death, HF hospitalization, and total mortality by 38%, 35%,
and 32%, respectively
• No direct effect on the rates of MI or stroke with Empagliflozin
• Reduction of systolic and diastolic BP
71. Side Effects of SGLT2I
• Genitourinary infection
• Masked DKA (euglycemic).
• They have normal glucose while in DKA
• Bladder cancer
• Risk of amputation
• Avoid in case of peripheral vascular disease.
73. Avoid SGLT2I
• Frequent bacterial UTI or genitourinary yeast infections
• High risk of fractures or falls
• Foot ulceration
• Factors predisposing to DKA ( ketosis prone Diabetes, pancreatic
insufficiency, drug or alcohol addiction)
