脂联素-瘦素比值与慢性肾脏病发病率:与性别和身体成分有关

IF 9.4 1区 医学 Q1 GERIATRICS & GERONTOLOGY
Hye-Sun Park, Sang Ho Park, Yeseul Seong, Hyo Jeong Kim, Hoon Young Choi, Yumie Rhee, Hyeong Cheon Park, Jong Hyun Jhee
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引用次数: 0

摘要

背景人们对脂肪连接蛋白与瘦素的比率(A/L 比率)与慢性肾脏病(CKD)发病风险之间的关系知之甚少。本研究旨在调查 A/L 比值与慢性肾脏病发病风险之间的关系,并研究这种关系是否因性别和身体成分而异。方法在这个基于社区的前瞻性队列中,对肾功能正常的参与者(N = 5192)进行了分析。基线时的 A/L 比值与发生 CKD 的风险之间的关系采用多变量 Cox 比例危险度分析进行了评估,CKD 的定义是在随访期间有两次或两次以上估计肾小球滤过率为 <60 mL/min/m2 或用量度尺检测蛋白尿≥1+。根据性别、体重指数(BMI)和是否存在肌肉疏松症进行了分组分析。结果参与者的平均年龄为 57.2 ± 8.3 岁,53.2% 为女性。男性的 A/L 比率高于女性(1.5 [0.8-3.2] 和 0.5 [0.3-0.9] μg/ng,P < 0.001)。在中位随访 9.8 [9.5-10.0] 年期间,共发生了 417 例慢性肾功能衰竭事件(每 1000 人年 8.7 例)。与最低四分位数的男性相比,A/L 比值最高四分位数的男性发生 CKD 的风险较低(调整后危险比 [aHR],0.57;95% 置信区间 [CI],0.33-0.99)。此外,A/L 比值每增加 1.0,男性发生 CKD 的风险就会降低 12%(aHR,0.88;95% 置信区间 [CI],0.80-0.97)。然而,在女性中没有观察到明显的相关性。在按体重指数和是否存在肌肉疏松症进行的亚组分析中,体重指数为 23.0 kg/m2 的男性和存在肌肉疏松症的男性中,A/L 比值高与发生慢性肾脏病的风险降低之间的关系是一致的。结论 A/L比值高是男性发生慢性肾脏病风险降低的一个独立标志,尤其是在体重指数(BMI)≥23.0 kg/m2和患有肌肉疏松症的男性中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Adiponectin-to-leptin ratio and incident chronic kidney disease: Sex and body composition-dependent association

Adiponectin-to-leptin ratio and incident chronic kidney disease: Sex and body composition-dependent association

Background

The association between the adiponectin-to-leptin ratio (A/L ratio) and the risk of incident chronic kidney disease (CKD) is poorly understood. This study aimed to investigate the association between A/L ratio and the risk of incident CKD and to examine whether such a relationship varied according to sex and body composition.

Methods

In this prospective community-based cohort, participants with normal kidney function were analysed (N = 5192). The association between the A/L ratio at baseline and the risk of incident CKD, defined as two or more occasions with an estimated glomerular filtration rate of <60 mL/min/m2 or proteinuria of ≥1+ on a dipstick test during the follow-up period, was evaluated using multivariable Cox proportional hazards analyses. Subgroup analyses were conducted based on sex, body mass index (BMI) and the presence of sarcopenia.

Results

The participants' mean age was 57.2 ± 8.3 years, and 53.2% were women. The A/L ratio was higher in men compared with women (1.5 [0.8–3.2] and 0.5 [0.3–0.9] μg/ng, P < 0.001). During a median follow-up of 9.8 [9.5–10.0] years, 417 incident CKD events occurred (8.7 per 1000 person-years). Men in the highest quartile of A/L ratio had a lower risk of incident CKD (adjusted hazard ratio [aHR], 0.57; 95% confidence interval [CI], 0.33–0.99) than those in the lowest quartile. Additionally, a 1.0 increase in A/L ratio was associated with a 12% decreased risk of incident CKD in men (aHR, 0.88; 95% CI, 0.80–0.97). However, no significant association was observed in women. In subgroup analysis stratified by BMI and the presence of sarcopenia, the association between a high A/L ratio and a reduced risk of incident CKD was consistent in men with a BMI < 23.0 kg/m2 and those with sarcopenia. However, no significant association was observed between men with a BMI ≥ 23.0 kg/m2 and those without sarcopenia.

Conclusions

A high A/L ratio is an independent marker of a reduced risk of incident CKD in men, especially in those with a BMI < 23.0 kg/m2 and sarcopenia.

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来源期刊
Journal of Cachexia Sarcopenia and Muscle
Journal of Cachexia Sarcopenia and Muscle MEDICINE, GENERAL & INTERNAL-
CiteScore
13.30
自引率
12.40%
发文量
234
审稿时长
16 weeks
期刊介绍: The Journal of Cachexia, Sarcopenia and Muscle is a peer-reviewed international journal dedicated to publishing materials related to cachexia and sarcopenia, as well as body composition and its physiological and pathophysiological changes across the lifespan and in response to various illnesses from all fields of life sciences. The journal aims to provide a reliable resource for professionals interested in related research or involved in the clinical care of affected patients, such as those suffering from AIDS, cancer, chronic heart failure, chronic lung disease, liver cirrhosis, chronic kidney failure, rheumatoid arthritis, or sepsis.
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