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Insulin: Dosing Regimen and Adverse Effects01:16

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Insulin-replacement therapy usually includes both long-acting insulin (basal) and short-acting insulin (to cater to postprandial needs). In a diverse group of type 1 diabetes patients, the average daily insulin dose is typically 0.5-0.7 units/kg body weight. However, obese patients and pubertal adolescents may need more due to insulin resistance.
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Insulin preparations are categorized by their duration of action into short-acting and long-acting types. Two strategies are used to modify insulin's absorption and pharmacokinetic profile: slowing the absorption post-subcutaneous injection, or altering human insulin's amino acid sequence or protein structure. These changes retain the insulin's ability to bind to the insulin receptor, but alter its behavior in solution or after injection.
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Incretins include glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP), which stimulate insulin secretion post-meals. In type 2 diabetes, GIP's efficacy is reduced, making GLP-1 a viable drug target. GIP originates from preproGIP.
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The therapy for diabetes aims to alleviate hyperglycemia-related symptoms, prevent acute metabolic decompensation, and reduce chronic end-organ complications. Glycemic control is evaluated through short-term (self-monitoring, continuous glucose monitoring) and long-term (A1c, fructosamine) metrics, enabling near real-time tracking of blood glucose levels and reflecting glycemic control over specific time frames.
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Biguanides, particularly metformin (Glucophage), are insulin sensitizers that enhance glucose uptake, thereby reducing insulin resistance. Unlike sulfonylureas, metformin doesn't prompt insulin secretion, which helps to curb hypoglycemia risk. Metformin is beneficial in treating conditions like polycystic ovary syndrome due to its insulin-resistance reduction capability. The drug's primary action involves curtailing hepatic gluconeogenesis, a significant contributor to high blood...
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[Which insulin for which patients in 2014].

Jacques Philippe

    Revue Medicale Suisse
    |July 10, 2014
    PubMed
    Summary

    Starting insulin therapy for type 2 diabetes involves patient discussion and education. Basal insulin analogues offer improved safety and efficacy over NPH insulin for managing blood sugar.

    Area of Science:

    • Endocrinology
    • Metabolic Diseases
    • Pharmacology

    Context:

    • Type 2 diabetes management often requires the initiation of insulin therapy.
    • Basal insulin is a common starting point, with options including NPH insulin and newer analogues.
    • Patient-physician communication and therapeutic education are crucial for successful insulin initiation.

    Purpose:

    • To outline the standard approach to initiating basal insulin therapy in type 2 diabetes.
    • To compare the benefits and drawbacks of basal insulin analogues versus NPH insulin.
    • To discuss practical considerations for insulin injection timing and continuation of oral antidiabetics.

    Summary:

    • Initiating insulin therapy in type 2 diabetes necessitates shared decision-making and patient education.

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  • Basal insulin analogues (detemir, glargine, degludec) demonstrate advantages over NPH insulin, including fewer side effects, less weight gain, reduced hypoglycemia, and a more predictable, longer-acting profile.
  • Oral antidiabetic agents can often be continued alongside basal insulin, and while more complex regimens exist, they may offer limited additional benefits with increased side effects and lower compliance.
  • Impact:

    • Provides a clear framework for clinicians initiating basal insulin therapy in type 2 diabetes.
    • Highlights the advantages of modern basal insulin analogues for improved patient outcomes and adherence.
    • Emphasizes the importance of individualized treatment plans and patient-centered care in diabetes management.