Suppr超能文献

线粒体 DNA 拷贝数与肾脏疾病进展风险的关联。

Association of Mitochondrial DNA Copy Number with Risk of Progression of Kidney Disease.

机构信息

Boston University School of Medicine, Boston, Massachusetts.

Department of Epidemiology, Tulane University School of Public Health and Tropical Medicine, New Orleans, Louisiana.

出版信息

Clin J Am Soc Nephrol. 2022 Jul;17(7):966-975. doi: 10.2215/CJN.15551121.

Abstract

BACKGROUND AND OBJECTIVES

Mitochondrial DNA copy number is a biomarker of mitochondrial function, which has been hypothesized to contribute to pathogenesis of CKD through podocyte injury, tubular epithelial cell damage, and endothelial dysfunction. The prospective association of mitochondrial DNA copy number with CKD progression has not been previously evaluated.

DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: Chronic Renal Insufficiency Cohort study participants had serum levels of mitochondrial DNA copy number calculated from probe intensities of mitochondrial single nucleotide polymorphisms genotyped on the Illumina HumanOmni 1-Quad Array. CKD progression was defined as kidney failure or halving of eGFR from baseline. Cox proportional hazards models were used to calculate hazard ratios for mitochondrial DNA copy number and risk of CKD progression.

RESULTS

Among 2943 participants, mean age was 58 years, 45% were women, and 48% self-identified as Black. There were 1077 patients who experienced CKD progression over a median follow-up of 6.5 years. The incidence rate of CKD progression was highest for those in the lowest tertile of mitochondrial DNA copy number (tertile 1, 58.1; tertile 2, 50.8; tertile 3, 46.3 per 1000 person-years). Risk for CKD progression was higher for participants with lower levels of mitochondrial DNA copy number after adjustment for established risk factors (for tertile 1 versus 3, hazard ratio, 1.28 [95% confidence interval, 1.10 to 1.50]; for tertile 2 versus 3, hazard ratio, 0.99 [95% confidence interval, 0.85 to 1.16]; trend =0.002). Similar results were seen among those with albuminuria (for tertile 1 versus 3, hazard ratio, 1.24; 95% confidence interval, 1.05 to 1.47), but there were no statistically significant associations among individuals without albuminuria (for tertile 1 versus 3, hazard ratio, 1.04; 95% confidence interval, 0.70 to 1.53; interaction <0.001).

CONCLUSIONS

These findings suggest lower mitochondrial DNA copy number is associated with higher risk of CKD progression, independent of established risk factors among patients with CKD.

摘要

背景和目的

线粒体 DNA 拷贝数是线粒体功能的生物标志物,它通过足细胞损伤、肾小管上皮细胞损伤和内皮功能障碍被假设为导致 CKD 发病机制的原因之一。线粒体 DNA 拷贝数与 CKD 进展的前瞻性关联尚未得到评估。

设计、设置、参与者和测量:慢性肾功能不全队列研究的参与者的血清线粒体 DNA 拷贝数水平是根据在 Illumina HumanOmni 1-Quad 阵列上基因分型的线粒体单核苷酸多态性的探针强度计算得出的。CKD 进展定义为肾功能衰竭或 eGFR 从基线减少一半。Cox 比例风险模型用于计算线粒体 DNA 拷贝数与 CKD 进展风险的风险比。

结果

在 2943 名参与者中,平均年龄为 58 岁,45%为女性,48%自我认定为黑人。在中位随访 6.5 年期间,有 1077 名患者发生 CKD 进展。线粒体 DNA 拷贝数最低三分位组(三分位 1,58.1;三分位 2,50.8;三分位 3,46.3/1000 人年)的 CKD 进展发生率最高。调整既定危险因素后,线粒体 DNA 拷贝数较低的参与者发生 CKD 进展的风险更高(三分位 1 与三分位 3 相比,风险比 1.28[95%置信区间,1.10 至 1.50];三分位 2 与三分位 3 相比,风险比 0.99[95%置信区间,0.85 至 1.16];趋势=0.002)。在有白蛋白尿的患者中也观察到类似的结果(三分位 1 与三分位 3 相比,风险比 1.24[95%置信区间,1.05 至 1.47]),但在没有白蛋白尿的患者中无统计学意义的关联(三分位 1 与三分位 3 相比,风险比 1.04[95%置信区间,0.70 至 1.53];交互作用<0.001)。

结论

这些发现表明,在 CKD 患者中,线粒体 DNA 拷贝数较低与 CKD 进展风险较高独立相关,而与既定的危险因素无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a04/9269623/d00e48102f83/CJN.15551121absf1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验