Jiang Ming-Yan, Wu Wen-Shiann
Department of Internal Medicine, Renal Division, Chi Mei Medical Center, Tainan, Taiwan.
Department of Pharmacy, Chia Nan University of Pharmacy & Science, Tainan, Taiwan.
Medicine (Baltimore). 2025 Jun 27;104(26):e43014. doi: 10.1097/MD.0000000000043014.
Cardiac troponins are prognostic biomarkers for cardiovascular disease (CVD) and mortality, but their significance in individuals with early kidney disease, defined as preserved estimated glomerular filtration rate but albuminuria, remains unclear. This study evaluated the association between high-sensitivity troponin I (hs-TnI) and troponin T (hs-TnT) with all-cause and cardiovascular mortality in this population. This retrospective cohort study used data from the 1999 to 2004 National Health and Nutrition Examination Survey. We included 1296 adults (≥18 years) with estimated glomerular filtration rate ≥ 60 mL/min/1.73 m² and urinary albumin-creatinine ratio ≥ 30 mg/g. Serum hs-TnI and hs-TnT levels were categorized into quintiles. The primary outcomes were all-cause and cardiovascular mortality, determined via National Health and Nutrition Examination Survey-linked National Death Index data through December 31, 2019. The mean age of participants was 51.4 ± 0.7 years, and 45.9% were male. Over a median follow-up of 219 months, 601 participants died, including 185 from CVD. Higher hs-Tn levels were associated with older age, hypertension, diabetes, and greater urinary albumin-creatinine ratio. Each one-quintile increase in hs-TnI was associated with a 26% higher risk of all-cause mortality (hazard ratios [HR]: 1.26; 95% CI: 1.13-1.41; P-trend < .001) and a 33% higher risk of CVD mortality (HR: 1.33; 95% CI: 1.04-1.71; P-trend < .05). Similar associations were observed for hs-TnT (HR: 1.56 for all-cause mortality; 95% CI: 1.37-1.77; P < .001; HR: 1.64 for CVD mortality; 95% CI: 1.33-2.03; P < .001). Sensitivity analyses excluding individuals with preexisting CVD and early deaths confirmed the robustness of these findings. Elevated hs-TnI and hs-TnT independently predict all-cause and cardiovascular mortality in individuals with early kidney disease. These findings highlight the potential role of hs-Tn measurement in enhancing cardiovascular risk stratification. Incorporating hs-Tn testing into routine assessments may help identify individuals who could benefit from earlier preventive interventions to reduce long-term cardiovascular risk; however, further research is needed to validate its clinical utility.
心肌肌钙蛋白是心血管疾病(CVD)和死亡率的预后生物标志物,但其在早期肾病患者(定义为估算肾小球滤过率正常但存在蛋白尿)中的意义仍不明确。本研究评估了高敏肌钙蛋白I(hs-TnI)和肌钙蛋白T(hs-TnT)与该人群全因死亡率和心血管死亡率之间的关联。这项回顾性队列研究使用了1999年至2004年美国国家健康和营养检查调查的数据。我们纳入了1296名成年人(≥18岁),其估算肾小球滤过率≥60 mL/min/1.73 m²且尿白蛋白肌酐比值≥30 mg/g。血清hs-TnI和hs-TnT水平被分为五分位数。主要结局是全因死亡率和心血管死亡率,通过与美国国家健康和营养检查调查相关联的美国国家死亡指数数据确定,截至2019年12月31日。参与者的平均年龄为51.4±0.7岁,45.9%为男性。在中位随访219个月期间,601名参与者死亡,其中185人死于CVD。较高的hs-Tn水平与年龄较大、高血压、糖尿病以及更高的尿白蛋白肌酐比值相关。hs-TnI每增加一个五分位数,全因死亡率风险升高26%(风险比[HR]:1.26;95%置信区间[CI]:1.13 - 1.41;P趋势<0.001),CVD死亡率风险升高33%(HR:1.33;95% CI:1.04 - 1.71;P趋势<0.05)。hs-TnT也观察到类似关联(全因死亡率HR:1.56;95% CI:1.37 - 1.77;P<0.001;CVD死亡率HR:1.64;95% CI:1.33 - 2.03;P<0.001)。排除已患有CVD的个体和早期死亡个体后的敏感性分析证实了这些发现的稳健性。hs-TnI和hs-TnT升高独立预测早期肾病患者的全因死亡率和心血管死亡率。这些发现突出了hs-Tn测量在加强心血管风险分层中的潜在作用。将hs-Tn检测纳入常规评估可能有助于识别那些可从早期预防性干预中获益以降低长期心血管风险的个体;然而,需要进一步研究来验证其临床效用。