Department of Epidemiology and Biostatistics, School of Public Health, Tianjin Medical University, Tianjin, China.
Tianjin Key Laboratory of Environment, Nutrition and Public Health, Tianjin, China.
BMJ Open. 2021 Jun 28;11(6):e048030. doi: 10.1136/bmjopen-2020-048030.
To examine the association between low birth weight (LBW) and cardiometabolic diseases (CMDs, including heart disease, stroke and type 2 diabetes mellitus) in adulthood, and to explore whether genetic, early-life environmental and healthy lifestyle factors play a role in this association.
A population-based twin study.
Twins from the Swedish Twin Registry who were born in 1958 or earlier participated in the Screening Across the Lifespan Twin (SALT) study for a full-scale screening during 1998-2002 and were followed up until 2014.
19 779 twin individuals in Sweden with birthweight data available (mean age: 55.45 years).
CMDs were assessed based on self-reported medical records, medication use and records from the National Patient Registry. A lifestyle index encompassing smoking status, alcohol consumption, exercise levels and Body Mass Index was derived from the SALT survey and categorised as unfavourable, intermediate or favourable. Data were analysed using generalised estimating equation (GEE) models and conditional logistic regression models.
Of all participants, 3998 (20.2%) had LBW and 5335 (27.0%) had incident CMDs (mean age at onset: 63.64±13.26 years). In GEE models, the OR of any CMD was 1.39 (95% CI 1.27 to 1.52) for LBW. In conditional logistic regression models, the LBW-CMD association became non-significant (OR=1.21, 95% CI 0.94 to 1.56). The difference in ORs from the two models was statistically significant (p<0.001). In the joint effect analysis, the multiadjusted OR of CMDs was 3.47 (95% CI 2.72 to 4.43) for participants with LBW plus an unfavourable lifestyle and 1.25 (95% CI 0.96 to 1.62) for those with LBW plus a favourable lifestyle.
LBW is associated with an increased risk of adult CMDs, and genetic and early-life environmental factors may account for this association. However, a favourable lifestyle profile may modify this risk.
探讨低出生体重(LBW)与成年人心血管代谢疾病(CMD,包括心脏病、中风和 2 型糖尿病)之间的关联,并探讨遗传、生命早期环境和健康生活方式因素是否在这种关联中发挥作用。
基于人群的双胞胎研究。
1958 年或更早出生于瑞典双胞胎登记处的双胞胎参加了跨越生命全程的双胞胎筛查(SALT)研究,在 1998-2002 年进行了全面筛查,并随访至 2014 年。
19779 名在瑞典出生体重数据可用的双胞胎个体(平均年龄:55.45 岁)。
CMD 根据自我报告的医疗记录、药物使用情况和国家患者登记处的记录进行评估。从 SALT 调查中得出了一个包含吸烟状况、饮酒量、运动水平和体重指数的生活方式指数,并分为不利、中等和有利。使用广义估计方程(GEE)模型和条件逻辑回归模型进行数据分析。
在所有参与者中,3998 人(20.2%)有 LBW,5335 人(27.0%)有新发 CMD(发病年龄:63.64±13.26 岁)。在 GEE 模型中,LBW 的任何 CMD 的 OR 为 1.39(95%CI 1.27 至 1.52)。在条件逻辑回归模型中,LBW-CMD 关联变得不显著(OR=1.21,95%CI 0.94 至 1.56)。两个模型的 OR 差异具有统计学意义(p<0.001)。在联合效应分析中,LBW 合并不良生活方式的参与者发生 CMD 的多调整 OR 为 3.47(95%CI 2.72 至 4.43),LBW 合并有利生活方式的参与者为 1.25(95%CI 0.96 至 1.62)。
LBW 与成年人心血管代谢疾病的风险增加有关,遗传和生命早期环境因素可能导致这种关联。然而,有利的生活方式可能会改变这种风险。