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一项关于阿托伐他汀治疗锂剂使用者肾源性尿崩症的双盲、随机、安慰剂对照的初步临床试验。

A double-blind, randomized, placebo-controlled pilot trial of atorvastatin for nephrogenic diabetes insipidus in lithium users.

机构信息

Geri-PARTy Research Group, Jewish General Hospital, Montreal, QC, Canada.

Douglas Mental Health University Institute, Montreal, QC, Canada.

出版信息

Bipolar Disord. 2021 Feb;23(1):66-75. doi: 10.1111/bdi.12973. Epub 2020 Jul 16.

Abstract

OBJECTIVE

Lithium remains an important treatment for mood disorders but is associated with kidney disease. Nephrogenic diabetes insipidus (NDI) is associated with up to 3-fold risk of incident chronic kidney disease among lithium users. There are limited randomized controlled trials (RCT) for treatments of lithium-induced NDI, and existing therapies can be poorly tolerated. Therefore, novel treatments are needed for lithium-induced NDI.

METHOD

We conducted a 12-week double-blind pilot RCT to assess the feasibility and efficacy of 20 mg/d atorvastatin vs placebo in the treatment of NDI in chronic lithium users. Patients, recruited between September 2017 and October 2018, were aged 18 to 85, currently on a stable dose of lithium, and determined to have NDI.

RESULTS

Urinary osmolality (UOsm) at 12 weeks adjusted for baseline was not statistically different between groups (+39.6 mOsm/kg [95% CI, -35.3, 114.5] in atorvastatin compared to placebo groups). Secondary outcomes of fluid intake and aquaporin-2 excretions at 12 weeks adjusted for baseline were -0.13 L [95% CI, -0.54, 0.28] and 98.68 [95% CI, -190.34, 387.70], respectively. A moderate effect size was observed for improvements in baseline UOsm by ≥100 mOsm/kg at 12 weeks in patients who received atorvastatin compared to placebo (38.45% (10/26) vs 22.58% (7/31); Cohen's d = 0.66).

CONCLUSION

Among lithium users with NDI, atorvastatin 20 mg/d did not significantly improve urinary osmolality compared to placebo over a 12-week period. Larger confirmatory trials with longer follow-up periods may help to further assess the effects of statins on NDI, especially within patients with more severe NDI.

摘要

目的

锂仍是治疗心境障碍的重要药物,但与肾脏疾病有关。锂使用者发生慢性肾脏病的风险增加 2-3 倍与肾源性尿崩症(NDI)相关。目前对于锂诱导的 NDI 的治疗方法,随机对照试验(RCT)有限,并且现有的治疗方法可能难以耐受。因此,需要新的治疗方法来治疗锂诱导的 NDI。

方法

我们进行了一项为期 12 周的双盲试验 RCT,以评估 20mg/d 阿托伐他汀与安慰剂在治疗慢性锂使用者 NDI 中的疗效和可行性。患者于 2017 年 9 月至 2018 年 10 月期间招募,年龄 18-85 岁,目前锂稳定剂量,且被诊断为 NDI。

结果

12 周时调整基线后的尿渗透压(UOsm)在两组间无统计学差异(阿托伐他汀组比安慰剂组高 39.6mOsm/kg[95%CI,-35.3,114.5])。12 周时调整基线后的液体摄入和水通道蛋白-2 排泄的次要终点分别为-0.13L[95%CI,-0.54,0.28]和 98.68[95%CI,-190.34,387.70]。阿托伐他汀组与安慰剂组相比,在基线 UOsm 改善≥100mOsm/kg 的患者中,12 周时观察到中等治疗效果大小(38.45%(26/68)vs 22.58%(31/139);Cohen's d=0.66)。

结论

在 NDI 的锂使用者中,阿托伐他汀 20mg/d 在 12 周内与安慰剂相比,并未显著改善尿渗透压。需要更大的、随访时间更长的确认性试验来进一步评估他汀类药物对 NDI 的影响,特别是在 NDI 更严重的患者中。

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