Dynamics of lipid profile in patients with end-stage renal disease depending on the class of antihypertensive drugs

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The aim of the study is to evaluate the effect of antihypertensive therapy on lipid metabolism parameters in patients undergoing maintenance hemodialysis (MHD). Materials and methods. A three-year observational study was conducted involving 719 patients undergoing maintenance hemodialysis (MHD). Subgroups were formed based on the antihypertensive therapy received: calcium channel blockers (CCBs: lercanidipine, amlodipine; n=120), renin-angiotensin-aldosterone system blockers (RAASBs: ramipril, perindopril, valsartan, telmisartan, candesartan, azilsartan; n=49), beta-blockers (BBs: bisoprolol, metoprolol; n=47), CCBs + BBs (n=104), BBs + RAASBs (n=34), CCBs + imidazoline receptor agonist (IRA: moxonidine; n=56), and CCBs + RAASBs (n=81). Lipid profiles were evaluated in all patients. Results. Patients receiving BBs exhibited a decrease in the atherogenic index (AI, p<0.05) and an increase in high-density lipoprotein cholesterol (HDL-C, p<0.01) levels. BB therapy was an independent predictor of lower low-density lipoprotein cholesterol (LDL-C, p<0.001). No statistically significant changes were observed during RAASB therapy. Patients receiving CCBs showed a decrease in TG levels (p<0.001). At the same time there was an increase in LDL-C (p<0.05) and AI (p<0.05). Combined CCB + IRA therapy was associated with higher AI, LDL-C, and non-HDL-C levels (p<0.05). CCB + IRA or CCB + RAASB therapies were associated with a less favorable lipid profile (increased AI and non-HDL-C) compared to CCB + BB therapy (p<0.01). BB + CCB or BB + RAASB therapies reduced TC, HDL-C, and non-HDL-C levels (p<0.05). Conclusion. In hemodialysis patients, the use of CCBs, both as monotherapy and in combination, was associated with more pronounced lipid profile disturbances. BB therapy was associated with a reduction in atherogenicity, while RAASB treatment did not lead to significant changes in the lipid profile.

antihypertensive agents \ lipid profile \ hemodialysis \ chronic kidney disease \ dyslipidemia \ calcium channel blockers \ beta-adrenergic blockers \ renin-angiotensin-aldosterone system blockers

Short address: https://sciup.org/14138356

IDS: 14138356   |   UDC: 616.61; 577.125.8; 615.035.1   |   DOI: 10.34014/2227-1848-2026-2-58-76