Institute of Applied Health Research, University of Birmingham, Birmingham, UK.
Women's Health Research Unit, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
BMJ. 2020 Oct 7;371:m3502. doi: 10.1136/bmj.m3502.
To consolidate evidence from systematic reviews and meta-analyses investigating the association between reproductive factors in women of reproductive age and their subsequent risk of cardiovascular disease.
Umbrella review.
Medline, Embase, and Cochrane databases for systematic reviews and meta-analyses from inception until 31 August 2019.
Two independent reviewers undertook screening, data extraction, and quality appraisal. The population was women of reproductive age. Exposures were fertility related factors and adverse pregnancy outcomes. Outcome was cardiovascular diseases in women, including ischaemic heart disease, heart failure, peripheral arterial disease, and stroke.
32 reviews were included, evaluating multiple risk factors over an average follow-up period of 7-10 years. All except three reviews were of moderate quality. A narrative evidence synthesis with forest plots and tabular presentations was performed. Associations for composite cardiovascular disease were: twofold for pre-eclampsia, stillbirth, and preterm birth; 1.5-1.9-fold for gestational hypertension, placental abruption, gestational diabetes, and premature ovarian insufficiency; and less than 1.5-fold for early menarche, polycystic ovary syndrome, ever parity, and early menopause. A longer length of breastfeeding was associated with a reduced risk of cardiovascular disease. The associations for ischaemic heart disease were twofold or greater for pre-eclampsia, recurrent pre-eclampsia, gestational diabetes, and preterm birth; 1.5-1.9-fold for current use of combined oral contraceptives (oestrogen and progesterone), recurrent miscarriage, premature ovarian insufficiency, and early menopause; and less than 1.5-fold for miscarriage, polycystic ovary syndrome, and menopausal symptoms. For stroke outcomes, the associations were twofold or more for current use of any oral contraceptive (combined oral contraceptives or progesterone only pill), pre-eclampsia, and recurrent pre-eclampsia; 1.5-1.9-fold for current use of combined oral contraceptives, gestational diabetes, and preterm birth; and less than 1.5-fold for polycystic ovary syndrome. The association for heart failure was fourfold for pre-eclampsia. No association was found between cardiovascular disease outcomes and current use of progesterone only contraceptives, use of non-oral hormonal contraceptive agents, or fertility treatment.
From menarche to menopause, reproductive factors were associated with cardiovascular disease in women. In this review, presenting absolute numbers on the scale of the problem was not feasible; however, if these associations are causal, they could account for a large proportion of unexplained risk of cardiovascular disease in women, and the risk might be modifiable. Identifying reproductive risk factors at an early stage in the life of women might facilitate the initiation of strategies to modify potential risks. Policy makers should consider incorporating reproductive risk factors as part of the assessment of cardiovascular risk in clinical guidelines.
PROSPERO CRD42019120076.
对女性生殖年龄段的生殖因素与随后心血管疾病风险之间关联的系统评价和荟萃分析进行综合评估。
伞式综述。
从建立到 2019 年 8 月 31 日,在 Medline、Embase 和 Cochrane 数据库中对系统评价和荟萃分析进行检索。
两名独立的审查员进行筛选、数据提取和质量评估。研究人群为生殖年龄段的女性。暴露因素为与生育相关的因素和不良妊娠结局。研究结果为女性的心血管疾病,包括缺血性心脏病、心力衰竭、外周动脉疾病和中风。
共纳入 32 项研究,平均随访时间为 7-10 年,评估了多种危险因素。除了 3 项研究外,其余研究的质量均为中等。对包含森林图和表格的综合心血管疾病进行了叙述性证据综合分析。复合心血管疾病的关联为:先兆子痫、死胎和早产的风险增加两倍;妊娠高血压、胎盘早剥、妊娠糖尿病和卵巢早衰的风险增加 1.5-1.9 倍;月经初潮提前、多囊卵巢综合征、经产和早绝经的风险低于 1.5 倍。更长的母乳喂养时间与心血管疾病风险降低相关。与缺血性心脏病相关的关联为:先兆子痫、复发性先兆子痫、妊娠糖尿病和早产的风险增加两倍或更高;当前使用复方口服避孕药(雌激素和孕激素)、复发性流产、卵巢早衰和早绝经的风险增加 1.5-1.9 倍;流产、多囊卵巢综合征和绝经症状的风险低于 1.5 倍。对于中风结果,当前使用任何口服避孕药(复方口服避孕药或孕激素仅避孕药)、先兆子痫和复发性先兆子痫的风险增加两倍或更高;当前使用复方口服避孕药、妊娠糖尿病和早产的风险增加 1.5-1.9 倍;多囊卵巢综合征的风险低于 1.5 倍。心力衰竭的风险增加四倍与先兆子痫相关。目前使用孕激素仅避孕药、使用非口服激素避孕药或生育治疗与心血管疾病结局之间没有关联。
从月经初潮到绝经,生殖因素与女性心血管疾病有关。在本综述中,无法呈现问题的绝对数量;但是,如果这些关联是因果关系的,它们可能会解释女性心血管疾病风险中很大一部分无法解释的部分,而且这些风险可能是可以改变的。在女性的生命早期识别生殖危险因素可能有助于启动策略来改变潜在风险。政策制定者应考虑将生殖危险因素纳入临床指南中的心血管风险评估中。
PROSPERO CRD42019120076。