Tea consumption and attenuation of biological aging: a longitudinal analysis from two cohort studies

IF 7.6 1区 医学 Q1 HEALTH CARE SCIENCES & SERVICES
Yi Xiang , Hao Xu , Hongxiang Chen , Dan Tang , Zitong Huang , Yuan Zhang , Zhenghong Wang , Ziyun Wang , Yangla , Mingming Han , Jianzhong Yin , Xiong Xiao , Xing Zhao
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引用次数: 0

Abstract

Background

The biological aging process can be modified through lifestyle interventions to prevent age-related diseases and extend healthspan. However, evidence from population-based studies on whether tea consumption could delay the biological aging process in humans remains limited.

Methods

This study included 7931 participants aged 30–79 years from the China Multi-Ethnic Cohort (CMEC) Study and 5998 participants aged 37–73 years from the UK Biobank (UKB) who participated in both the baseline and first follow-up surveys. Tea consumption information was collected through questionnaires. Biological age (BA) acceleration was calculated using clinical biomarkers and anthropometric measurements based on the Klemera Doubal method (KDM). Change-to-change analyses were performed to estimate the associations between changes in tea consumption status and changes in BA acceleration using multiple linear models. Follow-up adjusted for baseline analyses were further conducted to examine the prospective exposure-response relationship between tea consumption and BA acceleration among individuals with constant tea consumption status.

Findings

During a median follow-up of 1.98 (1.78, 2.16) years in the CMEC and 4.50 (3.92, 5.00) years in the UKB, tea consumption was consistently associated with attenuated BA acceleration in both cohorts. Transitioning from nondrinking to tea-drinking was associated with decreased BA acceleration (CMEC: β = −0.319, 95% CI: −0.620 to −0.017 years; UKB: β = −0.267, 95% CI: −0.831 to 0.297 years) compared to consistent nondrinking. Even stronger associations were found in consistent tea drinkers. The exposure-response relationship suggested that consuming around 3 cups of tea or 6–8 g of tea leaves per day may offer the most evident anti-aging benefits.

Interpretation

Tea consumption was associated with attenuated BA acceleration measured by KDM, especially for consistent tea drinkers with moderate consumption. Our findings highlight the potential role of tea in developing nutrition-oriented anti-aging interventions and guiding healthy aging policies.

Funding

National Natural Science Foundation of China (Grant No. 82273740).

饮茶与生物衰老的衰减:来自两个队列研究的纵向分析
生物衰老过程可以通过生活方式干预来改变,从而预防与年龄有关的疾病,延长健康寿命。然而,基于人群的研究中关于喝茶是否能延缓人类生物衰老过程的证据仍然有限。方法本研究纳入来自中国多民族队列(CMEC)研究的7931名年龄在30-79岁的参与者和来自英国生物银行(UKB)的5998名年龄在37-73岁的参与者,他们参加了基线调查和第一次随访调查。通过问卷调查收集茶叶消费信息。根据临床生物标志物和基于Klemera双值法(KDM)的人体测量值计算生物年龄(BA)加速。使用多元线性模型进行了变化到变化的分析,以估计茶叶消费状况变化与BA加速变化之间的关系。进一步进行基线分析调整后的随访,以检验恒定饮茶状态个体饮茶与BA加速之间的预期暴露-反应关系。在中位随访期间,CMEC为1.98年(1.78年,2.16年),UKB为4.50年(3.92年,5.00年),在两个队列中,茶的摄入始终与BA加速减弱相关。从不饮酒到喝茶的转变与BA加速降低相关(CMEC: β = - 0.319, 95% CI: - 0.620至- 0.017年;UKB: β = - 0.267, 95% CI: - 0.831至0.297年)。经常喝茶的人甚至发现了更强的关联。暴露-反应关系表明,每天饮用约3杯茶或6-8克茶叶可能具有最明显的抗衰老效果。解释饮茶与KDM测量的BA加速衰减有关,特别是对于适量饮茶的持续饮茶者。我们的研究结果强调了茶在制定以营养为导向的抗衰老干预措施和指导健康老龄化政策方面的潜在作用。国家自然科学基金项目(批准号82273740)。
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来源期刊
The Lancet Regional Health: Western Pacific
The Lancet Regional Health: Western Pacific Medicine-Pediatrics, Perinatology and Child Health
CiteScore
8.80
自引率
2.80%
发文量
305
审稿时长
11 weeks
期刊介绍: The Lancet Regional Health – Western Pacific, a gold open access journal, is an integral part of The Lancet's global initiative advocating for healthcare quality and access worldwide. It aims to advance clinical practice and health policy in the Western Pacific region, contributing to enhanced health outcomes. The journal publishes high-quality original research shedding light on clinical practice and health policy in the region. It also includes reviews, commentaries, and opinion pieces covering diverse regional health topics, such as infectious diseases, non-communicable diseases, child and adolescent health, maternal and reproductive health, aging health, mental health, the health workforce and systems, and health policy.
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