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Fun Fact! Statin-associated muscle symptoms (SAMS) occur in 10–29% of patients, typically presenting as myalgia or myositis in the thighs or calves. Severe cases like rhabdomyolysis are rare. Genetic variations, especially in the SLCO1B1 gene, have been linked to a higher risk of developing SAMS during statin treatment.

Could SLCO1B1 genetic testing support safer, more personalized statin prescribing?

 NCCN Guidelines

Could SLCO1B1 genetic testing support safer, more personalized statin prescribing?

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A 12-month RCT will assess if adding group-based nutritional education to standard care improves HbA1c in T2D patients. Covering shopping habits, plate planning, and hunger cues, the program targets glycemic control and broader metabolic outcomes.

Learn more about this patient-centered trial

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A Case of Acromegaly With Parasellar Meningioma With Oculomotor Palsy Responding to and Maintained With Oral Octreotide Therapy - PubMed

A Case of Acromegaly With Parasellar Meningioma With Oculomotor Palsy Responding to and Maintained With Oral Octreotide Therapy - PubMed

Source : https://pubmed.ncbi.nlm.nih.gov/41048686/

Current findings from our case may provide evidence for the potential use of somatostatin analogs in treating acromegaly patients diagnosed with meningiomas, particularly those cases that cannot be surgically removed,...

A 65-year-old woman with acromegaly and parasellar meningioma causing oculomotor palsy showed significant neurological and radiological improvement after oral octreotide dose escalation, suggesting somatostatin analogs may benefit non-surgical meningiomas.

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In a cohort of 176 kidney transplant recipients, higher early post-transplant protein intake (≥1.4 g/kg/day) was associated with improved graft function, better lipid and hemoglobin profiles, and overall enhanced recovery outcomes.

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Reassess. Intensify. Protect: Timely LDL-C control post-MI can prevent what comes next

For patients recovering from myocardial infarction (MI), early initiation of high-intensity statin therapy is standard. Yet, sustaining LDL-C control in the months and years that follow is often overlooked despite its potential to reduce recurrent cardiovascular events.

Despite clear guideline targets, real-world data show that many post-MI patients fail to achieve or maintain LDL-C levels below 70 mg/dL. Delays in follow-up testing, therapeutic inertia, and disparities in care contribute to this gap. Real-world data suggest that women and older adults may be less likely to receive high-intensity lipid-lowering therapy (LLT) or timely reassessment, reflecting disparities in access or treatment patterns.

For patients who remain above target despite maximally tolerated statins—or who are unable to tolerate them—adjunctive therapies that enhance LDL receptor activity offer a chance to drive LDL-C lower and reduce residual risk. But these benefits hinge on timely recognition of inadequate response and a proactive approach to intensification.

The 2025 AACE lipid management guidelines recommend a treatment goal of LDL-C <70 mg/dL in adults with ASCVD or at increased risk. Reaching—and maintaining—this threshold has been linked to fewer recurrent events, including MI, stroke, and revascularization. But success depends not just on what we prescribe, but on how closely we monitor, reassess, and adapt over time.

How do you coordinate post-MI lipid management in your practice? What prompts you to intensify treatment when targets aren't met?

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  • 3mo
    When a patient is seen after a cardiac event: • Medication review: • Current medications are reviewed to ensure adherence, tolerance, and appropriate dosing. • Goals of therapy are discussed with the patient, emphasizing the importance Show More
  • 3mo
    When a patient is seen after cardiac event meds are reviewed and discussed regarding goals of treatment and labs to follow up 6-8 weeks later. If LDL is above Show More

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