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社会经济不平等与心血管死亡率及儿童期社会经济状况和成年期危险因素的作用:一项前瞻性队列研究,随访 17 年。

Socioeconomic inequalities in cardiovascular mortality and the role of childhood socioeconomic conditions and adulthood risk factors: a prospective cohort study with 17-years of follow up.

机构信息

Department of Public Health, Erasmus University Medical Centre, PO Box 2040, Rotterdam, CA 3000, The Netherlands.

出版信息

BMC Public Health. 2012 Dec 5;12:1045. doi: 10.1186/1471-2458-12-1045.

Abstract

BACKGROUND

The mechanisms underlying socioeconomic inequalities in mortality from cardiovascular diseases (CVD) are largely unknown. We studied the contribution of childhood socioeconomic conditions and adulthood risk factors to inequalities in CVD mortality in adulthood.

METHODS

The prospective GLOBE study was carried out in the Netherlands, with baseline data from 1991, and linked with the cause of death register in 2007. At baseline, participants reported on adulthood socioeconomic position (SEP) (own educational level), childhood socioeconomic conditions (occupational level of respondent's father), and a broad range of adulthood risk factors (health behaviours, material circumstances, psychosocial factors). This present study is based on 5,395 men and 6,306 women, and the data were analysed using Cox regression models and hazard ratios (HR).

RESULTS

A low adulthood SEP was associated with increased CVD mortality for men (HR 1.84; 95% CI: 1.41-2.39) and women (HR 1.80; 95%CI: 1.04-3.10). Those with poorer childhood socioeconomic conditions were more likely to die from CVD in adulthood, but this reached statistical significance only among men with the poorest childhood socioeconomic circumstances. About half of the investigated adulthood risk factors showed significant associations with CVD mortality among both men and women, namely renting a house, experiencing financial problems, smoking, physical activity and marital status. Alcohol consumption and BMI showed a U-shaped relationship with CVD mortality among women, with the risk being significantly greater for both abstainers and heavy drinkers, and among women who were underweight or obese. Among men, being single or divorced and using sleep/anxiety drugs increased the risk of CVD mortality. In explanatory models, the largest contributor to adulthood CVD inequalities were material conditions for men (42%; 95% CI: -73 to -20) and behavioural factors for women (55%; 95% CI: -191 to -28). Simultaneous adjustment for adulthood risk factors and childhood socioeconomic conditions attenuated the HR for the lowest adulthood SEP to 1.34 (95% CI: 0.99-1.82) for men and 1.19 (95% CI: 0.65-2.15) for women.

CONCLUSIONS

Adulthood material, behavioural and psychosocial factors played a major role in the explanation of adulthood SEP inequalities in CVD mortality. Childhood socioeconomic circumstances made a modest contribution, mainly via their association with adulthood risk factors. Policies and interventions to reduce health inequalities are likely to be most effective when considering the influence of socioeconomic circumstances across the entire life course and in particular, poor material conditions and unhealthy behaviours in adulthood.

摘要

背景

心血管疾病(CVD)死亡率的社会经济不平等的机制在很大程度上是未知的。我们研究了儿童期社会经济状况和成年期危险因素对成年期 CVD 死亡率不平等的贡献。

方法

GLOBE 前瞻性研究在荷兰进行,基线数据来自 1991 年,并于 2007 年与死因登记处相关联。在基线时,参与者报告了成年期社会经济地位(SEP)(自身教育水平)、儿童期社会经济状况(受访者父亲的职业水平)和广泛的成年期危险因素(健康行为、物质状况、心理社会因素)。本研究基于 5395 名男性和 6306 名女性,使用 Cox 回归模型和危险比(HR)进行数据分析。

结果

低成年 SEP 与男性(HR 1.84;95%CI:1.41-2.39)和女性(HR 1.80;95%CI:1.04-3.10)的 CVD 死亡率增加相关。那些儿童期社会经济状况较差的人更有可能在成年后患 CVD,但这仅在儿童期社会经济状况最差的男性中具有统计学意义。大约一半的成年期危险因素与男性和女性的 CVD 死亡率均有显著关联,即租房、经济问题、吸烟、身体活动和婚姻状况。女性的饮酒量和 BMI 与 CVD 死亡率呈 U 型关系,饮酒量少或酗酒的女性以及体重过轻或肥胖的女性风险明显更高。对于男性,单身或离婚以及使用睡眠/焦虑药物会增加 CVD 死亡率的风险。在解释模型中,对男性 CVD 不平等的最大贡献是物质条件(42%;95%CI:-73 至-20),对女性的最大贡献是行为因素(55%;95%CI:-191 至-28)。同时调整成年期危险因素和儿童期社会经济状况,将最低成年 SEP 的 HR 降低至 1.34(95%CI:0.99-1.82),男性为 1.19(95%CI:0.65-2.15)。

结论

成年期物质、行为和心理社会因素在解释 CVD 死亡率的成年期 SEP 不平等方面发挥了主要作用。儿童期社会经济状况仅通过与成年期危险因素的关联做出了适度贡献。减少健康不平等的政策和干预措施,在考虑整个生命过程中社会经济状况的影响时,特别是在考虑成年期物质条件差和不健康行为时,可能最有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31a2/3539932/77eabb1a34c5/1471-2458-12-1045-1.jpg

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