Karashima Shigehiro, Yoneda Takashi, Kometani Mitsuhiro, Ohe Masashi, Mori Shunsuke, Sawamura Toshitaka, Furukawa Kenji, Seta Takashi, Yamagishi Masakazu, Takeda Yoshiyu
Department of Internal Medicine, Graduate School of Medical Science, Kanazawa University, Kanazawa, Japan.
Department of Internal Medicine, Kanazawa Insurance Hospital, Kanazawa, Japan.
Hypertens Res. 2016 Mar;39(3):133-7. doi: 10.1038/hr.2015.129. Epub 2015 Nov 26.
The mineralocorticoid receptor (MR) is expressed in the kidneys and in adipose tissue, and primary aldosteronism (PA) is associated with metabolic syndrome. This study assessed the effects of MR blockade by eplerenone (EPL) and spironolactone (SPL) on blood pressure (BP) and metabolic factors in patients with PA. Fifty-four patients with PA were treated with one of two MRAs, EPL (25-100 mg daily, n=27) or SPL (12.5-100 mg daily, n=27) for 12 months. Visceral (VAT) and subcutaneous adipose tissue were quantified using CT and FatScan imaging analysis software. Body mass index, homeostasis model assessment-insulin resistance (HOMA-IR), serum creatinine, potassium and lipids, urinary albumin excretion (UAE) and plasma aldosterone concentration (PAC) and plasma renin activity (PRA) were measured before and after treatment. EPL and SPL decreased BP and increased serum potassium levels to similar degrees. PAC and PRA did not differ between the two groups. Although treatment with the MRAs did not change HOMA-IR or serum lipids, they significantly decreased UAE and VAT (P<0.05). These results suggest that EPL and SPL are effective and safe for the treatment of PA. The long-term metabolic and renal effects of these MRAs should be further investigated.
盐皮质激素受体(MR)在肾脏和脂肪组织中表达,原发性醛固酮增多症(PA)与代谢综合征相关。本研究评估了依普利酮(EPL)和螺内酯(SPL)阻断MR对PA患者血压(BP)和代谢因子的影响。54例PA患者接受两种盐皮质激素受体拮抗剂之一治疗,EPL(每日25 - 100 mg,n = 27)或SPL(每日12.5 - 100 mg,n = 27),疗程12个月。使用CT和FatScan成像分析软件对内脏(VAT)和皮下脂肪组织进行定量分析。在治疗前后测量体重指数、稳态模型评估胰岛素抵抗(HOMA - IR)、血清肌酐、钾和血脂、尿白蛋白排泄量(UAE)以及血浆醛固酮浓度(PAC)和血浆肾素活性(PRA)。EPL和SPL降低血压和升高血清钾水平的程度相似。两组之间的PAC和PRA无差异。虽然使用盐皮质激素受体拮抗剂治疗并未改变HOMA - IR或血脂,但它们显著降低了UAE和VAT(P<0.05)。这些结果表明,EPL和SPL对PA的治疗有效且安全。这些盐皮质激素受体拮抗剂的长期代谢和肾脏效应应进一步研究。