匹伐他汀对慢性肾病患者红细胞膜脂肪酸含量的影响:双臂平行随机对照试验。

IF 1 Q3 MEDICINE, GENERAL & INTERNAL
Journal of Yeungnam medical science Pub Date : 2024-07-01 Epub Date: 2024-05-08 DOI:10.12701/jyms.2024.00094
Minna Kim, Seong Eun Kim, Su Mi Lee, Won Suk An
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引用次数: 0

摘要

背景:他汀类药物可降低慢性肾脏病(CKD)患者发生心血管事件的风险。尽管糖尿病(DM)是他汀类药物治疗的副作用之一,但一些研究表明,匹伐他汀不会导致糖尿病。本研究调查了匹伐他汀对红细胞膜脂肪酸(FA)含量的影响,FA会影响DM和心血管疾病的发生。此外,还评估了匹伐他汀治疗后脂肪连素和糖化血红蛋白(HbA1c)水平的变化:共招募了 45 名患者,其中 28 人完成了研究。在 24 周的时间里,16 名患者服用 2 毫克匹伐他汀,12 名患者服用 10 毫克阿托伐他汀。如果需要进一步控制血脂,则在 12 周后调整剂量。匹伐他汀组和阿托伐他汀组分别有 10 名和 9 名糖尿病患者。分别采用气相色谱法和酶联免疫吸附法测定红细胞膜脂肪酸和脂肪连素水平:结果:两组的饱和脂肪酸、棕榈酸、反式油酸、总胆固醇和低密度脂蛋白胆固醇水平均显著低于基线水平。在匹伐他汀组中,红细胞膜中的花生四烯酸(AA)含量明显增加,但脂肪连翘素水平未受影响。使用匹伐他汀治疗的患者 HbA1c 水平有所下降。他汀类药物治疗无不良反应:结论:对慢性肾脏病患者进行匹伐他汀治疗可通过改变红细胞膜 AA 水平来改善糖代谢。此外,匹伐他汀不会对慢性肾脏病和糖尿病患者的血糖控制产生不良影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of pitavastatin on erythrocyte membrane fatty acid content in patients with chronic kidney disease: two-arm parallel randomized controlled trial.

Background: Statins reduce the risk of cardiovascular events in patients with chronic kidney disease (CKD). Although diabetes mellitus (DM) is a reported side effect of statin treatment, some studies have indicated that pitavastatin does not cause DM. The present study investigated the effect of pitavastatin on the fatty acid (FA) content of erythrocyte membranes, which affects the occurrence of DM and cardiovascular diseases. In addition, changes in adiponectin and glycated hemoglobin (HbA1c) levels were evaluated after pitavastatin treatment.

Methods: A total of 45 patients were enrolled, 28 of whom completed the study. Over 24 weeks, 16 patients received 2 mg pitavastatin and 12 patients received 10 mg atorvastatin. Dosages were adjusted after 12 weeks if additional lipid control was required. There were 10 and nine patients with DM in the pitavastatin and atorvastatin groups, respectively. Erythrocyte membrane FAs and adiponectin levels were measured using gas chromatography and enzyme-linked immunosorbent assay, respectively.

Results: In both groups, saturated FAs, palmitic acid, trans-oleic acid, total cholesterol, and low-density lipoprotein cholesterol levels were significantly lower than those at baseline. The arachidonic acid (AA) content in the erythrocyte membrane increased significantly in the pitavastatin group, but adiponectin levels were unaffected. HbA1c levels decreased in patients treated with pitavastatin. No adverse effects were associated with statin treatment.

Conclusion: Pitavastatin treatment in patients with CKD may improve glucose metabolism by altering erythrocyte membrane AA levels. In addition, pitavastatin did not adversely affect glucose control in patients with CKD and DM.

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