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Related Subjects: Type 1 DM |Introduction to Type 2 Diabetes |Management of Type 2 Diabetes |Diabetes in Pregnancy |HbA1c |Diabetic Ketoacidosis (DKA) Adults |Hyperglycaemic Hyperosmolar State (HHS) |Diabetic Nephropathy |Diabetic Retinopathy |Diabetic Neuropathy |Diabetic Amyotrophy |Maturity Onset Diabetes of the Young (MODY) |Diabetes: Complications
Management of Type 2 Diabetes requires a patient-centered approach, with regular monitoring, lifestyle intervention, and stepwise pharmacotherapy. Treatment should be individualized based on patient preferences, comorbidities, and the risk of complications. Regular follow-up is essential to adjust therapy and achieve optimal glycaemic control.
Medication Class | Common Drugs | Mechanism of Action | Common Side Effects | Notes |
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Biguanides | Metformin | Reduces hepatic glucose production and improves insulin sensitivity. | Gastrointestinal disturbances (e.g., nausea, diarrhoea), lactic acidosis (rare) | First-line therapy for type 2 diabetes; contraindicated in renal impairment. |
Sulfonylureas | Gliclazide, Glibenclamide, Glipizide | Stimulates pancreatic beta cells to release insulin. | Hypoglycemia, weight gain | Often used as second-line therapy; risk of hypoglycemia. |
DPP-4 Inhibitors | Sitagliptin, Saxagliptin, Linagliptin | Inhibits DPP-4 enzyme, increasing incretin levels and stimulating insulin release. | Nasopharyngitis, headache, pancreatitis (rare) | Weight-neutral; generally well-tolerated. |
SGLT2 Inhibitors | Empagliflozin, Dapagliflozin, Canagliflozin | Inhibits SGLT2 in the kidneys, reducing glucose reabsorption and increasing urinary glucose excretion. | Urinary tract infections, genital infections, dehydration, ketoacidosis (rare) | Benefits in cardiovascular risk reduction; avoid in severe renal impairment. |
Thiazolidinediones (TZDs) | Pioglitazone, Rosiglitazone | Increases insulin sensitivity by activating PPAR-gamma receptors. | Weight gain, fluid retention, risk of heart failure, fractures | Used with caution due to cardiovascular risks; avoid in heart failure. |
Alpha-Glucosidase Inhibitors | Acarbose, Miglitol | Delays carbohydrate absorption in the intestines by inhibiting alpha-glucosidase. | Flatulence, diarrhoea, abdominal pain | Less commonly used; taken with meals to reduce postprandial hyperglycemia. |
Meglitinides | Repaglinide, Nateglinide | Stimulates rapid insulin secretion from the pancreas in response to meals. | Hypoglycemia, weight gain | Short-acting; taken before meals to reduce postprandial glucose levels. |
Bile Acid Sequestrants | Colesevelam | Binds bile acids in the intestine, which reduces glucose production and improves glycaemic control. | Constipation, nausea, bloating | Primarily used for cholesterol management; may also lower blood glucose. |
Long-acting insulin preparations are essential in the management of diabetes mellitus, particularly for maintaining baseline insulin levels and achieving better glycaemic control. These insulins are designed to be released slowly over a prolonged period, typically 24 hours or more, providing a stable insulin level throughout the day and night. In the UK, several long-acting insulin preparations are available for use.
Insulin Type | Brand Names | Onset | Peak | Duration | Notes |
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Insulin Glargine | Lantus, Abasaglar, Toujeo | 1-2 hours | Minimal peak | 24 hours or more |
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Insulin Detemir | Levemir | 1-2 hours | 6-8 hours | Up to 24 hours |
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Insulin Degludec | Tresiba | 1-2 hours | Minimal peak | 42 hours |
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When selecting a long-acting insulin for a patient, several factors should be considered:
Long-acting insulin preparations play a crucial role in the management of diabetes, providing basal insulin coverage to help maintain blood glucose levels within the target range. The choice of insulin should be individualized based on the patient's needs, lifestyle, and response to therapy. Regular follow-up and adjustment of the insulin regimen are essential to achieving optimal glycaemic control.