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胆碱酯酶抑制剂与阿尔茨海默病痴呆患者肾功能下降之间的关联。

Association between cholinesterase inhibitors and kidney function decline in patients with Alzheimer's dementia.

作者信息

Xu Hong, Garcia-Ptacek Sara, Bruchfeld Annette, Fu Edouard L, Shori Taher Darreh, Lindholm Bengt, Eriksdotter Maria, Carrero Juan Jesus

机构信息

Division of Clinical Geriatrics, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden.

Division of Clinical Geriatrics, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden; Theme Inflammation and Aging, Karolinska University Hospital, Stockholm, Sweden.

出版信息

Kidney Int. 2023 Jan;103(1):166-176. doi: 10.1016/j.kint.2022.09.022. Epub 2022 Oct 28.

Abstract

Preclinical evidence shows that activation of the cholinergic anti-inflammatory pathway (CAP) may have direct and indirect beneficial effects on the kidney. Cholinesterase inhibitors (ChEIs) are specific Alzheimer's dementia (AD) therapies that block the action of cholinesterases and activate CAP. Here, we explored a plausible effect of ChEIs on slowing kidney function decline by comparing the risk of CKD progression among patients with newly diagnosed AD that initiated ChEI or not within 90 days. Using complete information of routine serum creatinine tests, we evaluated changes in estimated glomerular filtration rate (eGFR) and defined the outcome of chronic kidney disease (CKD) progression as the composite of an eGFR decline of over 30%, initiation of dialysis/transplant or death attributed to CKD. A secondary outcome was death. Inverse probability of treatment-weighted Cox regression was used to estimate hazard ratios. Among 11, 898 patients, 6,803 started on ChEIs and 5,095 did not. Mean age was 80 years (64% women) and the mean eGFR was 68 ml/min/1.73m. During a median 3.0 years of follow-up, and compared to non-use, ChEI use was associated with 18% lower risk of CKD progression (1,231 events, adjusted hazard ratio 0.82; 95% confidence interval 0.71-0.96) and a 21% lower risk of death (0.79; 0.72-0.86). Results were consistent across subgroups, ChEI subclasses and after accounting for competing risks. Thus, in patients with AD undergoing routine care, use of ChEI (vs no-use) was associated with lower risk of CKD progression.

摘要

临床前证据表明,胆碱能抗炎通路(CAP)的激活可能对肾脏产生直接和间接的有益影响。胆碱酯酶抑制剂(ChEIs)是治疗阿尔茨海默病(AD)的特效药物,可阻断胆碱酯酶的作用并激活CAP。在此,我们通过比较90天内开始或未开始使用ChEI的新诊断AD患者中慢性肾脏病(CKD)进展的风险,探讨了ChEIs对减缓肾功能下降的可能作用。利用常规血清肌酐检测的完整信息,我们评估了估算肾小球滤过率(eGFR)的变化,并将CKD进展的结局定义为eGFR下降超过30%、开始透析/移植或因CKD死亡的综合情况。次要结局是死亡。采用治疗权重的逆概率Cox回归来估计风险比。在11,898例患者中,6,803例开始使用ChEIs,5,095例未使用。平均年龄为80岁(64%为女性),平均eGFR为68 ml/min/1.73m²。在中位3.0年的随访期间,与未使用ChEIs相比,使用ChEIs与CKD进展风险降低18%相关(1,231例事件,校正风险比0.82;95%置信区间0.71 - 0.96),死亡风险降低21%(0.79;0.72 - 0.86)。各亚组、ChEI亚类以及考虑竞争风险后的结果均一致。因此,在接受常规护理的AD患者中,使用ChEI(与未使用相比)与较低的CKD进展风险相关。

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