Yang Zhiwen, Ma Yusheng, Wang Yanbing, Jin Ming, Bin Jianping, Chen Zhiyong, Teng Zhonghua
Department of Cardiology, Guangdong Provincial Key Laboratory of Cardiac Function and Microcirculation, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Department of Cardiology, Yunfu People's Hospital, Southern Medical University, Yunfu, China.
Prev Med Rep. 2024 Apr 16;42:102730. doi: 10.1016/j.pmedr.2024.102730. eCollection 2024 Jun.
α-Klotho is a potential biological marker of aging with satisfactory clinical applicability. However, its prognostic significance in age-related diseases has largely been undermined. Therefore, we aimed to report the prognostic value of serum α-klotho levels in age-related diseases.
Participants with available serum α-klotho data from the National Health and Nutrition Examination Survey (2007-2016) were included. Their survival status was collected at 7.62 ± 2.99 years after serum α-klotho data was collected, and the endpoint was all-cause and cardiovascular mortality. A Cox regression model was established to examine the association between serum α-klotho levels and all-cause and cardiovascular mortality.
The present study included 13,746 U.S. adults with a survey-weighted mean age of 56.19 ± 10.42 years old. Of these, 52.2 % were female and 72.9 % were non-Hispanic whites. The optimal cutoff value of serum α-klotho for predicting all-cause mortality risk in the general population was 603.5 pg/ml. Individuals with low serum α-klotho (<603.5 pg/ml) had a significantly higher risk of all-cause (adjusted HR: 1.34(1.18-1.52), P < 0.001) and cardiovascular mortality (adjusted HR: 1.63(1.27-2.10), P < 0.001). Subgroup analysis showed that low serum α-klotho level was an independent risk factor for all-cause and cardiovascular mortality in people with hypertension, congestive heart failure, diabetes mellitus, and emphysema, while it was an independent risk factor for all-cause mortality in patients with renal insufficiency.
A low serum α-klotho concentration (<603.5 pg/ml) could serve as a marker of all-cause and cardiovascular mortality in the general population and in people with age-related diseases, including hypertension, congestive heart failure, diabetes mellitus, and emphysema.
α-klotho是一种具有良好临床适用性的潜在衰老生物标志物。然而,其在年龄相关疾病中的预后意义在很大程度上被忽视了。因此,我们旨在报告血清α-klotho水平在年龄相关疾病中的预后价值。
纳入来自美国国家健康与营养检查调查(2007 - 2016年)且有可用血清α-klotho数据的参与者。在收集血清α-klotho数据7.62±2.99年后收集他们的生存状况,终点为全因死亡率和心血管死亡率。建立Cox回归模型以检验血清α-klotho水平与全因死亡率和心血管死亡率之间的关联。
本研究纳入了13746名美国成年人,调查加权平均年龄为56.19±10.42岁。其中,52.2%为女性,72.9%为非西班牙裔白人。预测一般人群全因死亡风险的血清α-klotho最佳截断值为603.5 pg/ml。血清α-klotho水平低(<603.5 pg/ml)的个体全因死亡风险显著更高(调整后HR:1.34(1.18 - 1.52),P < 0.001)和心血管死亡风险显著更高(调整后HR:1.63(1.27 - 2.10),P < 0.001)。亚组分析表明,血清α-klotho水平低是高血压、充血性心力衰竭、糖尿病和肺气肿患者全因死亡和心血管死亡的独立危险因素,而在肾功能不全患者中是全因死亡的独立危险因素。
血清α-klotho浓度低(<603.5 pg/ml)可作为一般人群以及患有年龄相关疾病(包括高血压、充血性心力衰竭、糖尿病和肺气肿)的人群全因死亡和心血管死亡的标志物。