Adverse childhood and adulthood experiences and risk of new-onset cardiovascular disease with consideration of social support: a prospective cohort study

• Published in: BMC medicine Vol. 21; no. 1; p. 297
• Main Authors: Wang, Wanxin, Liu, Yifeng, Yang, Yuwei, Jiang, Weiqing, Ni, Yanyan, Han, Xue, Lu, Ciyong, Guo, Lan
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 08.08.2023; BioMed Central; BMC
• Subjects: Adult; Adults; Adverse adulthood experience; Adverse childhood experience; Adverse Childhood Experiences; Aged; Cardiovascular disease; Cardiovascular diseases; Cardiovascular Diseases - epidemiology; Children; Cohort analysis; Cohort study; Demographics; Demography; Diagnosis; Exposure; Female; Health aspects; Health risks; Heart diseases; Humans; Life change events; Longitudinal Studies; Male; Middle Aged; New-onset cardiovascular disease; Older people; Population studies; Prospective Studies; Regression analysis; Regression models; Risk; Risk factors; Sensitivity analysis; Signs and symptoms; Social aspects; Social behavior; Social factors; Social interactions; Social networks; Social support; Subgroups; Surveys; Surveys and Questionnaires; Young Adult; Young adults; China; Adverse childhood experience; Adverse adulthood experience; New-onset cardiovascular disease; Cohort study
• ISSN: 1741-7015; 1741-7015
• DOI: 10.1186/s12916-023-03015-1

The relationship between adverse childhood experiences (ACEs) and adverse adulthood experiences (AAEs) and their association with incident cardiovascular disease (CVD) have not been extensively studied. Considering social support, we evaluated the complex relations of ACEs and AAEs with incident CVD. This prospective cohort study used data from the 2014 life course survey and the 2015 and 2018 surveys of the China Health and Retirement Longitudinal Study, a national survey of Chinese adults aged ≥ 45 years from 28 provinces across China. The study population included 5836 individuals (mean [SD] age, 59.59 [8.22] years, 49.7% were males). Information on ACEs, AAEs, young adulthood social support, health behavior factors, health status factors, and demographics was measured. Cox regression models, the difference method to estimate the mediation proportion, and the additive and multiplicative interactions were performed. Subgroup and sensitivity analyses were also conducted. During follow-up, 789 incident cases of CVD occurred. The fully adjusted model, including demographics, health behaviors, health status factors (e.g., depressive symptoms), and social support as control variables, demonstrated that the overall number of ACEs (Hazard ratio [HR]: 1.11, 95% CI: 1.08 to 1.14) and AAEs (HR: 1.19, 95% CI: 1.16 to 1.22) were associated with an increased risk of incident CVD. A dose-response relationship existed between the number of ACEs or AAEs and incident CVD risk. The overall AAEs were found to mediate 17.7% (95% CI: 8.2 to 34.2%) of the association between ACEs and incident CVD. Moreover, a significant additive interaction between ACEs and AAEs was detected (RERI [95% CI]: 0.32 [0.09 to 0.56]). Compared with adults without exposure to both ACE and AAE, those with exposure to both at least one ACE and one AAE indicator had the highest risk of incident CVD (HR: 1.96, 95% CI: 1.72 to 2.23). Exposure to ACEs or AAEs was independently associated with an increased risk of incident CVD among Chinese middle-aged and older adults in a dose-response manner, and the overall AAEs partially mediated the association between ACEs and incident CVD. Preventive measures aimed at addressing either ACEs or AAEs alone may not significantly reduce the risk of CVD later in life. The necessity of a comprehensive life-course health strategy targeting the prevention of adversity merits increased attention.