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Glucagon-like Receptor Agonists01:24

Glucagon-like Receptor Agonists

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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.
GLP-1, when administered in high doses intravenously, triggers insulin secretion, inhibits glucagon release, slows gastric emptying, reduces food intake, and restores normal insulin secretion. However, its rapid inactivation by...
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Atypical antidepressants, including bupropion (Wellbutrin), mirtazapine (Remeron), nefazodone (Serzone), trazodone (Desyrel), and vilazodone (Viibryd), offer unique mechanisms of action. Bupropion weakly inhibits dopamine and norepinephrine reuptake, aiding depression treatment and smoking cessation, with a low risk of sexual dysfunction. Mirtazapine enhances serotonin and norepinephrine neurotransmission, leading to sedation, increased appetite, and weight gain. As a result, it helps treat...
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Dipeptidyl Peptidase 4 Inhibitors01:23

Dipeptidyl Peptidase 4 Inhibitors

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Dipeptidyl peptidase 4 (DPP-4) is a serine protease widely distributed in the body. It's involved in the inactivation of GLP-1 and GIP hormones, which are crucial for insulin regulation. DPP-4 inhibitors, such as sitagliptin (Januvia), saxagliptin (Onglyza), linagliptin (Tradjenta), alogliptin (Nesina), and vildagliptin (Galvus), help increase the proportion of active GLP-1, enhancing insulin secretion. These inhibitors work by competitively binding to DPP-4. This binding causes a...
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Insulin: Dosing Regimen and Adverse Effects01:16

Insulin: Dosing Regimen and Adverse Effects

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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.
The basal dose constitutes about 40%-50% of the total daily dose, with the rest as premeal insulin. The mealtime insulin dose should mirror...
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Oral Hypoglycemic Agents: Biguanides and Glitazones01:26

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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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Drugs for Treatment of Crohn's Disease in IBD Using Glucocorticoids01:21

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Glucocorticoids, a class of anti-inflammatory drugs, are pivotal in treating moderate to severe Crohn's disease by inducing remission. They exhibit their anti-inflammatory action by inhibiting the production of inflammatory cytokines such as tumor necrosis factor (TNF)-α, interleukin (IL)-1, and chemokines like IL-8. In addition, they reduce the expression of inflammatory cell adhesion molecules and inhibit gene transcription of nitric oxide synthase, phospholipase A2, cyclooxygenase-2...
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Multidisciplinary Approach to Obesity Management: A Case Report
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Semaglutide and Tirzepatide in a Remote Weight Management Program: 12-Month Retrospective Observational Study.

Becky Richards1, Will Lunt1, Michael Whitman1

  • 1Second Nature, London, United Kingdom.

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|August 21, 2025
PubMed
Summary

Remote glucagon-like peptide-1 receptor agonist (GLP-1RA) programs show significant weight loss for obesity. These digital interventions are effective, feasible, and cost-saving compared to traditional care.

Keywords:
GLP-1RAbehavioral interventiondigital healthglucagonlike peptide-1 receptor agonistobesityremote health care deliverysemaglutidetelemedicineweight lossweight management

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Area of Science:

  • Obesity Medicine
  • Digital Health Interventions
  • Pharmacological Weight Management

Background:

  • Obesity affects over 890 million adults globally, with traditional interventions often failing long-term.
  • Glucagon-like peptide-1 receptor agonists (GLP-1RAs) demonstrate significant weight loss, but specialist access is limited by cost and capacity.

Purpose of the Study:

  • To evaluate the effectiveness, feasibility, acceptability, and cost-effectiveness of a 12-month remote GLP-1RA-supported weight management program.
  • To compare outcomes between tirzepatide and semaglutide within this remote program.

Main Methods:

  • Retrospective analysis of 339 participants in a 12-month remote weight management program using tirzepatide or semaglutide.
  • Program combined medication, app-based support, dietitian coaching, and clinical oversight with phased behavior change techniques.
  • Primary outcomes: mean weight change and achievement of ≥10% and ≥15% weight loss; secondary outcomes: behavioral changes, side effects, acceptability, feasibility, and cost-effectiveness.

Main Results:

  • Mean weight loss at 12 months was -22.9 kg with tirzepatide and -18.1 kg with semaglutide (P<0.05).
  • ≥10% weight loss achieved by 95.2% (tirzepatide) and 83.1% (semaglutide); ≥15% by 83.7% and 56.2%, respectively.
  • Significant reductions in inactivity and initial side effects (nausea, fatigue, constipation) were observed, with increased reporting of no side effects.

Conclusions:

  • Remotely delivered GLP-1RA programs achieve weight loss comparable to clinical trials and offer significant cost savings (10-70%) versus traditional UK services.
  • Both tirzepatide and semaglutide demonstrated clinically significant weight loss with good safety and positive behavioral changes.
  • Digital delivery models are feasible and effective for expanding access to obesity treatment in resource-constrained systems.