micro-community-banner
 
Profile Image
  • Saved
Obesity as a chronic disease: Evolving treatment strategies with long-term pharmacologic care.

Obesity is increasingly recognized not merely as a lifestyle issue, but as a chronic, relapsing disease requiring sustained clinical management. Despite rising prevalence and cardiometabolic risks, pharmacologic treatment remains underutilized. While lifestyle interventions are foundational, maintaining weight loss over time through lifestyle changes alone is often challenging. High-intensity behavioral interventions may yield 5–8% total body weight loss, but this often plateaus or regresses by 12 months.

US clinical guidelines recommend anti-obesity medications when BMI is ≥30 kg/m², or ≥27 kg/m² with comorbidities. However, fewer than 2% of eligible patients receive prescriptions. Barriers such as stigma, limited access to specialists, and coverage restrictions may contribute to low treatment rates. GLP-1 receptor agonists, among newer therapies, address the biological drivers of obesity and have demonstrated significant weight loss (>10–20%) and cardiovascular risk reduction in clinical trials.

With an expanding range of therapeutic options, the focus is shifting to identifying the right patients and aligning treatment with their individual clinical needs and goals. Long-term success often depends not just on initiating therapy, but on sustaining it over time.

What clinical factors guide your decision to initiate pharmacologic therapy for obesity, and how do you approach patient selection, support long-term adherence, and identify those most likely to achieve sustained outcomes?

Profile Image
  • 2mo
    Patients with a high burden of obesity-associated disease benefit most: Elevated A1c or prediabetes, Uncontrolled hypertension, Atherogenic dyslipidemia, Evidence of subclinical ASCVD or high 10-yr ASCVD risk
  • 3mo
    I prescribe a lot of weight loss medication. The major barrier is insurance coverage of GLP-1 Agonists. I surprisingly find patients willing to try a once weekly injection. Also once Show More

Show More Comments

  • Saved
infographic
Profile Image
  • Saved
Magnetic Sphincter Augmentation Versus Fundoplication in Non-obese Gastroesophageal Reflux Disease (GERD) Patients: A Systematic Review of Patient-Reported Outcomes and Dysphagia - PubMed

Magnetic Sphincter Augmentation Versus Fundoplication in Non-obese Gastroesophageal Reflux Disease (GERD) Patients: A Systematic Review of Patient-Reported Outcomes and Dysphagia - PubMed

Source : https://pubmed.ncbi.nlm.nih.gov/41179026/

Magnetic sphincter augmentation (MSA) and laparoscopic fundoplication (LF) are established surgical treatments for gastroesophageal reflux disease (GERD). While several comparative studies exist, evidence specifically focusing on non-obese populations remains less...

MSA and fundoplication both improve GERD in non-obese patients; MSA preserves belching and reduces bloating but has more early dysphagia, while long-term control is similar, supporting individualized surgical selection.

Profile Image
  • Saved
Advances in lung health and sleep medicine: Key highlights from CHEST 2025

At CHEST 2025 in Chicago, pulmonology experts shared new insights in asthma, COPD, interstitial lung disease, pulmonary hypertension, and sleep medicine. Dr. Sandhya Khurana highlighted emerging asthma data—such as imaging-based reductions in mucus plugging and outcomes in severe asthma with nasal polyps—while also discussing the future of nanobody therapeutics. Dr. Cosmo Fowler reviewed GLP-1 RA–linked survival benefits in OSA.

Share your thoughts

Profile Image
  • Saved
case study

Patient Background: A 79-year-old woman presented with persistent hypophosphatemia (serum phosphorus 0.8 mg/dL) and multiple stress fractures involving the ribs, spine, and pelvis, consistent with osteomalacia. Her medical history included type 2 diabetes mellitus, hypertension, obesity, osteoarthritis, and anxiety disorder.

Assessment and Diagnosis: Initial evaluation revealed severe hypophosphatemia (0.8 mg/dL; NR: 2.5–4.5 mg/dL), elevated parathyroid hormone (PTH, 169 pg/mL; NR: 10–65 pg/mL), and normal serum calcium levels. Despite vitamin D supplementation, hypophosphatemia persisted (1.7 mg/dL in 2023), and hypercalcemia developed later (10.9 mg/dL; NR: 8.5–10.2 mg/dL). Renal studies showed phosphate wasting (tubular reabsorption of phosphate [TRP] 56.2%) and elevated fibroblast growth factor 23 (FGF-23, 1694 kRU/L). In 2024, ^18F-fluorocholine PET-CT imaging identified two right parathyroid adenomas, confirming a diagnosis of primary hyperparathyroidism (PHPT).

  1. How can chronic hypophosphatemia signal early-stage PHPT?
  2. Why is postoperative monitoring vital in PHPT care?
Profile Image