Iverson Health Innovation Research Institute and School of Health Sciences, Faculty of Health, Arts and Design, Swinburne University of Technology, Hawthorn, Victoria, Australia.
Department of Econometrics and Business Statistics, Monash University, Clayton, Victoria, Australia.
Am J Physiol Heart Circ Physiol. 2021 Feb 1;320(2):H891-H900. doi: 10.1152/ajpheart.00807.2020. Epub 2020 Dec 31.
People with intellectual disability (ID) experience cardiometabolic-related morbidity and mortality. However, it has been suggested that this population presents and lives with underestimated cardiovascular risk factors at a younger age, hence affecting their overall health and quality of life and contributing to early mortality. We assessed autonomic nervous system function in subjects with ID ( = 39), aged 18-45 yr, through measures of sudomotor function, heart rate and systolic blood pressure variability, and cardiac baroreflex function. Traditional clinical cardiovascular measurements and a biochemical analysis were also undertaken. We found that young adults with ID presented with sudomotor dysfunction, impaired cardiac baroreflex sensitivity, and systolic blood pressure variability, when compared with age-matched control subjects ( = 38). Reduced hand and feet electrochemical skin conductance and asymmetry were significantly associated with having a moderate-profound ID. Autonomic dysfunction in individuals with ID persisted after controlling for age, sex, and other metabolic parameters. Subjects in the ID group also showed significantly increased blood pressure, body mass index, and waist/hip circumference ratio, as well as increased plasma hemoglobin A1c and high-sensitivity C-reactive protein levels. We conclude that autonomic dysfunction is present in young adults with ID and is more marked in those with more severe disability. These finding have important implications in developing preventative strategies to reduce the risk of cardiovascular disease in people with ID. Adults with intellectual disability experience higher risk of premature death than the general population. Our investigation highlights increased cardiovascular risk markers and autonomic dysfunction in young adults with intellectual disability compared with control adults. Autonomic dysfunction was more marked in those with a more severe disability but independent of cardiovascular parameters. Assessment of autonomic nervous system (ANS) function may provide insight into the mechanisms of cardiometabolic disease development and progression in young adults with intellectual disability.
智障人士 (ID) 存在与代谢相关的心血管发病率和死亡率。然而,有人认为,该人群在年轻时就存在被低估的心血管危险因素,从而影响他们的整体健康和生活质量,并导致早逝。我们通过测量自主神经系统功能的汗分泌功能、心率和收缩压变异性以及心脏压力反射功能,评估了 18-45 岁 ID 受试者的自主神经系统功能。还进行了传统的临床心血管测量和生化分析。我们发现,与年龄匹配的对照组( = 38)相比,年轻的 ID 成人存在汗分泌功能障碍、心脏压力反射敏感性受损和收缩压变异性降低。手脚电化学皮肤电导和不对称性降低与中度至重度 ID 显著相关。控制年龄、性别和其他代谢参数后,ID 个体的自主神经功能障碍仍然存在。ID 组的受试者还表现出明显更高的血压、体重指数和腰围/臀围比值,以及更高的血红蛋白 A1c 和高敏 C 反应蛋白水平。我们的结论是,ID 年轻人存在自主神经功能障碍,在残疾程度更严重的人群中更为明显。这些发现对于制定预防策略以降低 ID 人群患心血管疾病的风险具有重要意义。智障成年人比一般人群有更高的早逝风险。我们的研究结果表明,与对照组成年人相比,智障年轻人存在更高的心血管风险标志物和自主神经功能障碍。在残疾程度更严重的人群中,自主神经功能障碍更为明显,但与心血管参数无关。评估自主神经系统 (ANS) 功能可能有助于深入了解智障年轻人发生和发展代谢性疾病的机制。