Scott M Williams, Aikaterini Eleftheriadou, Uazman Alam, Daniel J Cuthbertson, John P H Wilding
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An estimated global prevalence of the impaired glucose tolerance (IGT) form of pre-DM of 587 million people by 2045 means CAN will become a major clinical problem. CAN is independently associated with silent myocardial ischaemia, major cardiovascular events, myocardial dysfunction and cardiovascular mortality. Screening for CAN in pre-DM using risk scores with analysis of heart rate variability (HRV) or Sudoscan is important to allow earlier treatment at a reversible stage. The link between obesity and CAN highlights the therapeutic potential of lifestyle interventions including diet and physical activity to reverse MetS and prevent CAN. Weight loss achieved using these dietary and exercise lifestyle interventions improves the sympathetic and parasympathetic HRV indices of cardiac autonomic function. Further research is needed to identify high-risk populations of people with pre-DM or obesity that might benefit from targeted pharmacotherapy including metformin, sodium/glucose cotransporter 2 (SGLT2) inhibitors and glucagon-like peptide 1 (GLP-1) analogues. Bariatric surgery also improves HRV through weight loss which might also prevent CAN in severe obesity. 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引用次数: 0
摘要
心脏自主神经病变(CAN)是 1 型和 2 型糖尿病(T1DM 和 T2DM)的主要并发症。大量流行病学研究证实,心脏自主神经病变会增加发病率、心血管疾病死亡率和全因死亡率。然而,CAN 在糖尿病前期(pre-DM)和代谢综合征(MetS)患者中的发病率越来越高,据报道分别高达 11% 和 24%。CAN 与高血压和肥胖等代谢综合征的组成部分有关,早于高血糖。CAN 的病因是多因素的,与胰岛素抵抗和 MetS 存在互为因果的关系。阻塞性睡眠呼吸暂停(OSA)也可能通过代谢紊乱和独立机制与 CAN 相关。据估计,到 2045 年,全球糖耐量受损(IGT)形式的糖尿病前期患者将达到 5.87 亿人,这意味着 CAN 将成为一个主要的临床问题。糖耐量异常与无声心肌缺血、重大心血管事件、心肌功能障碍和心血管死亡率密切相关。通过分析心率变异性(HRV)或Sudoscan进行风险评分,对DM前期的CAN进行筛查非常重要,以便在可逆阶段进行早期治疗。肥胖与 CAN 之间的联系凸显了生活方式干预(包括饮食和体育锻炼)在逆转 MetS 和预防 CAN 方面的治疗潜力。利用这些饮食和运动生活方式干预措施实现减肥,可改善心脏自主神经功能的交感和副交感心率变异指数。还需要开展进一步的研究,以确定可从二甲双胍、钠/葡萄糖共转运体 2 (SGLT2) 抑制剂和胰高血糖素样肽 1 (GLP-1) 类似物等靶向药物疗法中获益的先心病或肥胖症高危人群。减肥手术也能通过减轻体重来改善心率变异,这也可以预防重度肥胖症患者出现心率变异。本文回顾了有关肥胖、DM 前期和 MetS 中 CAN 的文献,以帮助确定筛查、早期干预治疗的基本原理,并针对这一高发疾病提出未来的研究问题。
Cardiac Autonomic Neuropathy in Obesity, the Metabolic Syndrome and Prediabetes: A Narrative Review.
Cardiac autonomic neuropathy (CAN) is a major complication of type 1 and type 2 diabetes mellitus (T1DM and T2DM). The increased morbidity, cardiovascular and all-cause mortality associated with CAN is established from numerous epidemiological studies. However, CAN is increasingly recognised in people with prediabetes (pre-DM) and the metabolic syndrome (MetS) with a reported prevalence up to 11% and 24% respectively. CAN is associated with components of MetS including hypertension and obesity, predating hyperglycaemia. The aetiology of CAN is multifactorial and there is a reciprocal relationship with insulin resistance and MetS. Obstructive sleep apnoea (OSA) is also associated with CAN possibly through MetS and an independent mechanism. An estimated global prevalence of the impaired glucose tolerance (IGT) form of pre-DM of 587 million people by 2045 means CAN will become a major clinical problem. CAN is independently associated with silent myocardial ischaemia, major cardiovascular events, myocardial dysfunction and cardiovascular mortality. Screening for CAN in pre-DM using risk scores with analysis of heart rate variability (HRV) or Sudoscan is important to allow earlier treatment at a reversible stage. The link between obesity and CAN highlights the therapeutic potential of lifestyle interventions including diet and physical activity to reverse MetS and prevent CAN. Weight loss achieved using these dietary and exercise lifestyle interventions improves the sympathetic and parasympathetic HRV indices of cardiac autonomic function. Further research is needed to identify high-risk populations of people with pre-DM or obesity that might benefit from targeted pharmacotherapy including metformin, sodium/glucose cotransporter 2 (SGLT2) inhibitors and glucagon-like peptide 1 (GLP-1) analogues. Bariatric surgery also improves HRV through weight loss which might also prevent CAN in severe obesity. This article reviews the literature on CAN in obesity, pre-DM and MetS, to help determine a rationale for screening, early intervention treatment and formulate future research questions in this highly prevalent condition.
期刊介绍:
Diabetes Therapy is an international, peer reviewed, rapid-publication (peer review in 2 weeks, published 3–4 weeks from acceptance) journal dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of therapeutics and interventions (including devices) across all areas of diabetes. Studies relating to diagnostics and diagnosis, pharmacoeconomics, public health, epidemiology, quality of life, and patient care, management, and education are also encouraged.
The journal is of interest to a broad audience of healthcare professionals and publishes original research, reviews, communications and letters. The journal is read by a global audience and receives submissions from all over the world. Diabetes Therapy will consider all scientifically sound research be it positive, confirmatory or negative data. Submissions are welcomed whether they relate to an international and/or a country-specific audience, something that is crucially important when researchers are trying to target more specific patient populations. This inclusive approach allows the journal to assist in the dissemination of all scientifically and ethically sound research.