University of Vienna, Research Platform Active Ageing, Department of Nutritional Sciences, Althanstraße 14, 1090, Vienna, Austria.
Institute for Evidence in Medicine, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Mutat Res Rev Mutat Res. 2021 Jan-Jun;787:108367. doi: 10.1016/j.mrrev.2021.108367. Epub 2021 Jan 20.
Chronic diseases such as cardiovascular diseases, type 2 diabetes or cancer are the global leading cause of mortality. Lifestyle interventions are most effective in reducing metabolic risk factors, disease progression or even side effects of a disease. They are also contributing to decelerate the aging process. Genome instability is very often associated with aging or the above-mentioned diseases, and triggered by inflammation and oxidative stress. An established method to measure chromosomal damage is the cytokinesis block micronucleus (CBMN) cytome assay. The aim of this review and meta-analysis is to collect and analyse the current literature regarding the effects of a lifestyle based (dietary) intervention on changes of micronuclei (MNi), nucleoplasmic bridges (NPBs) and nuclear buds (NBUDs) in elderly subjects or people diagnosed with diabetes, metabolic disorders, cardiovascular disease, cancer or micronutrient deficiency. Although the main important diseases were considered as well as the large topic of aging, the number and methodological quality in terms of samples size, duration and rationale of the intervention or an inclusion of a control group of available intervention studies with these backgrounds was low. Most of the studies used antioxidant vitamins or folate, few investigated the whole diet. Only one study showed a physical activity intervention approach. The interventions did not lead to decreased genomic marker despite a few cancer related studies, where particularly MN frequency in mucosa lesions and leukoplakia was reduced by green tea and antioxidants. The performed meta-analysis of the available RCTs did not show a significant reduction of MNi, NBUDs or NPBs of most of the interventions performed, except for green tea. Data show in general a lack of an appropriate number of sound lifestyle based intervention studies linking cytogenetic damage and chronic diseases.
慢性疾病,如心血管疾病、2 型糖尿病或癌症,是全球主要的死亡原因。生活方式干预在降低代谢危险因素、疾病进展甚至疾病的副作用方面最为有效。它们还有助于减缓衰老过程。基因组不稳定性通常与衰老或上述疾病有关,并且由炎症和氧化应激引发。一种已确立的测量染色体损伤的方法是胞质分裂阻断微核(CBMN)细胞遗传学检测。本综述和荟萃分析的目的是收集和分析目前关于基于生活方式(饮食)干预对老年人或被诊断患有糖尿病、代谢紊乱、心血管疾病、癌症或微量营养素缺乏的个体中微核(MNi)、核质桥(NPBs)和核芽(NBUDs)变化的影响的文献。尽管考虑了主要的重要疾病以及衰老这一大主题,但在具有这些背景的可用干预研究中,考虑样本量、干预持续时间和原理、或纳入对照组的数量和方法学质量方面,研究数量和方法学质量都较低。大多数研究使用抗氧化维生素或叶酸,少数研究调查了整个饮食。只有一项研究采用了体育活动干预方法。尽管一些与癌症相关的研究表明,绿茶和抗氧化剂可以降低黏膜病变和白斑中的 MN 频率,但这些干预措施并没有导致基因组标志物的减少。对现有 RCT 的荟萃分析显示,除了绿茶外,大多数干预措施并未显著降低 MNi、NBUDs 或 NPBs。数据总体上显示,缺乏足够数量的将细胞遗传学损伤与慢性疾病联系起来的合理的基于生活方式的干预研究。