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Lipid Management in Endocrine Disorders

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Other Conditions 16 11. Hypogonadism and Testosterone Replacement and Abuse ➤ 11.1 In patients with low testosterone levels, we suggest testosterone therapy as symptomatically indicated, and not as an approach to improve dyslipidemia or CVD risk. (2|⊕⊕ ) ➤ 11.2 In patients with low HDL (<30 mg/dL [0.8 mmol/L]), especially in the absence of hypertriglyceridemia, we advise clinical or biochemical investigation of anabolic steroid abuse. (UGPS) Technical Remark: Supraphysiological doses of androgens will reduce HDL-C levels. 12. Gender-Affirming Hormone Therapy ➤ 12.1 In transwomen and transmen who have taken or are taking gender- affirming hormone therapy, we advise assessing CV risk by guidelines for non-transgender adults. (UGPS) Technical Remark: There are no data to guide selection of a gender marker in risk calculators for individuals on gender-affirming hormone therapy. Table 4. Statins: LDL-C Reduction by Dose, and Major Drug Interactions Statin Estimated Percent LDL-C Reduction by Dose Major Drug Interactions* High Intensity ≥50% Moderate Intensity 30–50% Low Intensity <30% Gemfibrozil should be avoided in all statins Atorvastatin 40 mg, 80 mg 10 mg, 20 mg ----- Clarithromycin, itraconazole, colchicine, cyclosporine, niacin Rosuvastatin† 20 mg, 40 mg 5 mg, 10 mg ----- Cyclosporine, darolutamide, niacin Simvastatin ----- 20 mg, 40 mg 10 mg Verapamil, diltiazem, amlodipine, macrolide antibiotics, amiodarone, dronedarone, antifungal azoles, nefazodone, danazol, ranolazine, colchicine, cyclosporine, daptomycin, niacin Pravastatin ----- 40 mg, 80 mg 10 mg, 20 mg Macrolide antibiotics, colchicine, cyclosporine

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