Yu Yu-Ling, An De-Wei, Chori Babangida S, Kaleta Błażej P, Mokwatsi Gontse, Martens Dries S, Abiodun Olugbenga O, Anya Tina, Łebek-Szatańska Agnieszka, Yeh Jong-Shiuan, Mels Catharina M C, Latosinska Agnieszka, Kruger Ruan, Isiguzo Godsent, Narkiewicz Krzystof, Shehu Muhammad N, Salazar Martin, Espeche Walter, Mujaj Blerim, Brgulian-Hitij Jana, Olszanecka Agnieszka, Wojciechowska Wiktoria, Reyskens Peter, Rajzer Marek, Januszewicz Andrzej, Stolarz-Skrzypek Katarzyna, Asayama Kei, Allegaert Karel, Verhamme Peter, Mischak Harald, Nawrot Tim S, Odili Augustine N, Staessen Jan A
Research Unit Environment and Health, KU Leuven Department of Public Health and Primary Care, University of Leuven, Leuven.
Non-Profit Research Association Alliance for the Promotion of Preventive Medicine, Mechelen, Belgium.
J Hypertens. 2025 Mar 1;43(3):481-491. doi: 10.1097/HJH.0000000000003930. Epub 2024 Nov 21.
Greater vulnerability of Black vs. White individuals to cardiovascular disease (CVD) and chronic kidney disease (CKD) is well charted in the United States, but studies involving sub-Saharan blacks are scarce.
Baseline data (2021-2024) were collected in 168 sub-Saharan Blacks and 93 European Whites in an ongoing clinical trial (NCT04299529), using standardized patient selection criteria. Data included clinical and biochemical risk factors, ECG and echocardiographic traits, Framingham CVD risk, CKD grades (KDIGO 2024), self-assessed symptoms (WHO questionnaire), and urinary proteomic profiles predictive of left ventricular dysfunction (LVD) and CKD, HF1, and CKD273, respectively. Racial comparisons rested on unadjusted and multivariable-adjusted analyses.
Despite being younger (60.4 vs. 68.3 years), blacks had a worse risk profile, as evidenced by higher diabetes prevalence, higher BMI, faster heart rate, unfavourable serum cholesterol fractions, lower estimated glomerular filtration rate, microalbuminuria, and sedentary lifestyle. This resulted in blacks having higher 10-year CVD risk, higher heart age (index of vascular ageing with chronological age as reference), and a worse CKD grades. In both races, CKD273 increased with CKD grade, but CKD273 and HF1 were not different by race. These observations were robust in subgroup and adjusted analyses.
This study did not differentiate host (genetic, molecular, and pathogenic) from environmental drivers of disease. Nonetheless, the findings call for a multipronged and comprehensive implementation of innovative health policies in sub-Saharan countries. Education, research, empowerment of stakeholders, and international learned societies connecting experts from a wide array of disciplines should vigorously sustain this effort.
在美国,黑人个体相较于白人个体更容易患心血管疾病(CVD)和慢性肾脏病(CKD),这一点已得到充分记录,但涉及撒哈拉以南黑人的研究却很稀少。
在一项正在进行的临床试验(NCT04299529)中,使用标准化的患者选择标准,收集了168名撒哈拉以南黑人及93名欧洲白人的基线数据(2021 - 2024年)。数据包括临床和生化风险因素、心电图和超声心动图特征、弗雷明汉心血管疾病风险、CKD分级(KDIGO 2024)、自我评估症状(世界卫生组织问卷)以及分别预测左心室功能障碍(LVD)和CKD的尿蛋白质组学图谱HF1和CKD273。种族比较基于未调整和多变量调整分析。
尽管黑人更年轻(60.4岁对68.3岁),但其风险状况更差,表现为糖尿病患病率更高、体重指数更高、心率更快、血清胆固醇组分不利、估计肾小球滤过率更低、微量白蛋白尿以及久坐不动的生活方式。这导致黑人的10年心血管疾病风险更高、心脏年龄更大(以实际年龄为参考的血管老化指数)以及CKD分级更差。在两个种族中,CKD273均随CKD分级增加,但CKD273和HF1在种族上并无差异。这些观察结果在亚组分析和调整分析中均很稳健。
本研究未区分疾病的宿主(遗传、分子和致病)因素与环境驱动因素。尽管如此,研究结果呼吁在撒哈拉以南国家多管齐下、全面实施创新型卫生政策。教育、研究、增强利益相关者的能力以及连接各学科专家的国际学术团体应大力支持这一努力。