Life course trajectories of maternal cardiovascular disease risk factors by obstetric history: a UK cohort study using electronic health records.

IF 8.3 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL BMC Medicine Pub Date : 2025-02-14 DOI:10.1186/s12916-025-03937-y
Kate Birnie, Laura D Howe, Timothy Jones, Paul Madley-Dowd, Florence Z Martin, Harriet Forbes, Maria Theresa Redaniel, Rosie Cornish, Maria C Magnus, Neil M Davies, Kate Tilling, Alun D Hughes, Deborah A Lawlor, Abigail Fraser
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Abstract

Background: Women who experience adverse pregnancy outcomes (APOs; gestational hypertension, preeclampsia (PE), gestational diabetes (GD), preterm birth (PTB), small or large for gestational age, miscarriage, multiple miscarriages, stillbirth, and offspring with major congenital anomalies) have increased risk of developing cardiovascular disease (CVD). We aimed to compare cardiometabolic health trajectories across the life course between women with and without APOs.

Methods: We studied 187,186 women with a registered pregnancy in the UK Clinical Practice Research Datalink (CPRD) GOLD linked to Hospital Episode Statistics. Fractional polynomial multilevel models were used to compare trajectories of cardiometabolic risk factors (body mass index [BMI], blood pressure [BP], cholesterol, and glucose) between women with and without a history of APOs (individual APOs in any pregnancy and number of APOs). We explored two underlying time axes: (1) time relative to first pregnancy (from 10 years before first pregnancy to 15 years after) and (2) age. Models controlled for age at first pregnancy, residential area deprivation, non-singleton pregnancy, parity, smoking status, ethnicity, and medications use.

Results: Women with a history of PE, gestational hypertension, or GD had higher BMI, BP, and glucose 10 years before first pregnancy compared to women without these APOs. These differences persisted 15 years post-first pregnancy. Women with a history of GD had a steeper post-partum rise in glucose. Women who experienced multiple (3 +) miscarriage, stillbirth, and/or medically indicated PTB had higher BP and BMI before and after pregnancy, with BP trajectories converging 15 years after first pregnancy. Women who experienced multiple APOs had the most adverse measurements across all cardiometabolic risk factors, with more unfavourable mean levels with each additional APO. There was little difference in cardiometabolic trajectories between women with and without a history of 1 or 2 miscarriages or congenital anomalies.

Conclusions: Women with APOs had adverse cardiometabolic profiles before first pregnancy, persisting up to 15 years post-pregnancy. Findings highlight the potential for targeted public health interventions to promote good cardiometabolic health in young adults transitioning from contraceptive use to planning pregnancies. APOs may identify young women who could benefit from monitoring CVD risk factors and interventions to improve cardiometabolic health.

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产妇心血管疾病风险因素的生命历程轨迹与产科史:一项使用电子健康记录的英国队列研究
背景:经历不良妊娠结局(APOs;妊娠期高血压、先兆子痫(PE)、妊娠期糖尿病(GD)、早产(PTB)、小胎龄或大胎龄、流产、多次流产、死产和有重大先天性异常的后代)都增加了发生心血管疾病(CVD)的风险。我们的目的是比较有和没有apo的女性在整个生命过程中的心脏代谢健康轨迹。方法:我们研究了英国临床实践研究数据链(CPRD) GOLD与医院事件统计相关的187186名登记怀孕的妇女。采用分数多项式多水平模型比较有和没有APOs病史的妇女(任何妊娠期APOs个体和APOs数量)的心脏代谢危险因素(体重指数[BMI]、血压[BP]、胆固醇和葡萄糖)的轨迹。我们研究了两个潜在的时间轴:(1)与第一次怀孕相关的时间(从第一次怀孕前10年到第一次怀孕后15年)和(2)年龄。模型控制了首次怀孕年龄、居住区域剥夺、非单胎妊娠、胎次、吸烟状况、种族和药物使用。结果:与没有这些apo的女性相比,有PE、妊娠期高血压或GD病史的女性在首次妊娠前10年的BMI、血压和血糖水平较高。这些差异在第一次怀孕后15年仍然存在。有GD病史的女性产后血糖升高幅度更大。经历过多次流产、死产和/或医学上指出的PTB的妇女在怀孕前后血压和BMI较高,并且在首次怀孕后15年血压轨迹趋于一致。经历多次APO的女性在所有心脏代谢危险因素中测量结果最不利,每增加一个APO,不利的平均水平就会增加。有1次或2次流产或先天性异常史的妇女和没有1次或2次流产史的妇女的心脏代谢轨迹差别不大。结论:apo患者在首次妊娠前存在不良的心脏代谢特征,并持续至妊娠后15年。研究结果强调了有针对性的公共卫生干预措施的潜力,以促进从使用避孕药具到计划怀孕的年轻人良好的心脏代谢健康。apo可以识别出可以从监测心血管疾病危险因素和干预措施中获益的年轻女性,以改善心脏代谢健康。
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来源期刊
BMC Medicine
BMC Medicine 医学-医学:内科
CiteScore
13.10
自引率
1.10%
发文量
435
审稿时长
4-8 weeks
期刊介绍: BMC Medicine is an open access, transparent peer-reviewed general medical journal. It is the flagship journal of the BMC series and publishes outstanding and influential research in various areas including clinical practice, translational medicine, medical and health advances, public health, global health, policy, and general topics of interest to the biomedical and sociomedical professional communities. In addition to research articles, the journal also publishes stimulating debates, reviews, unique forum articles, and concise tutorials. All articles published in BMC Medicine are included in various databases such as Biological Abstracts, BIOSIS, CAS, Citebase, Current contents, DOAJ, Embase, MEDLINE, PubMed, Science Citation Index Expanded, OAIster, SCImago, Scopus, SOCOLAR, and Zetoc.
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