Cardiovascular Division, Department of Medicine, University of California San Francisco, San Francisco, California, USA.
School of Public Health, University of California at Berkeley, Berkeley, California, USA.
J Womens Health (Larchmt). 2020 Oct;29(10):1283-1291. doi: 10.1089/jwh.2018.7560. Epub 2020 Jan 14.
Having a pregnancy complicated by hypertensive disorders of pregnancy (HDP) and/or having a small or preterm baby put a woman at risk for later cardiovascular disease (CVD). It is uncertain if higher maternal CVD risk factors (reflected by increased peripartum CVD biomarker levels) account for this risk, or if experiencing a complicated pregnancy itself increases a woman's CVD risk (reflected by an increase in biomarker trajectories from early pregnancy to postpartum). We conducted a secondary analysis of an 8-week mindful eating and stress reduction intervention in 110 pregnant women. We used mixed linear regression analysis to compare CVD biomarker levels and trajectories, between women with and without a CVD-related pregnancy complication (including HDP [gestational hypertension or preeclampsia] or having a small for gestational age [<10th percentile] or preterm [<37 weeks] baby), at three times: (1) 12-20 weeks of gestation, (2) 3 months postpartum, and (3) 9 months postpartum. CVD biomarkers studied included serum glucose, insulin, homeostasis model assessment of insulin resistance (HOMA-IR), body mass index (BMI), blood pressure (BP), interleukin-6 (IL-6), tumor necrosis factor, and lipids. We adjusted for age, maternal smoking, prepregnancy BMI, BP, age × time, and BMI × time. Women had a mean age of 28 years (standard deviation [SD] 6), mean prior pregnancies of 0.8 (SD 1.0), and 22 women had one or more CVD-related pregnancy complications. HOMA-IR, diastolic BP, triglyceride, high-density lipoprotein cholesterol, and IL-6 average levels, but not trajectories, differed among women with complicated versus normal pregnancy (all values were ≤0.04). Peripartum glucose and systolic BP trajectories were statistically greater in complicated versus normal pregnancies ( values were 0.008 and 0.01, respectively). We conclude that the experience of a complicated pregnancy in addition to elevated CVD risk factor levels may both increase a woman's risk of future CVD. ClinicalTrials.gov Identifier: NCT01307683.
患有妊娠高血压疾病(HDP)和/或有小胎儿或早产儿的孕妇,以后发生心血管疾病(CVD)的风险增加。尚不清楚较高的母体 CVD 风险因素(表现为围产期 CVD 生物标志物水平升高)是否解释了这种风险,还是妊娠并发症本身会增加女性的 CVD 风险(表现为从孕早期到产后的生物标志物轨迹增加)。我们对 110 名孕妇进行了为期 8 周的正念饮食和减压干预的二次分析。我们使用混合线性回归分析比较了患有和不患有与 CVD 相关的妊娠并发症(包括 HDP[妊娠期高血压或先兆子痫]或胎儿小于胎龄[第 10 百分位]或早产[<37 周])的女性之间的 CVD 生物标志物水平和轨迹,共 3 次:(1)妊娠 12-20 周,(2)产后 3 个月,(3)产后 9 个月。研究的 CVD 生物标志物包括血清葡萄糖、胰岛素、胰岛素抵抗稳态模型评估(HOMA-IR)、体重指数(BMI)、血压(BP)、白细胞介素-6(IL-6)、肿瘤坏死因子和脂质。我们调整了年龄、母亲吸烟、孕前 BMI、BP、年龄×时间和 BMI×时间。女性的平均年龄为 28 岁(标准差[SD]6),平均妊娠次数为 0.8(SD 1.0),22 名女性有 1 次或多次与 CVD 相关的妊娠并发症。HOMA-IR、舒张压、三酰甘油、高密度脂蛋白胆固醇和 IL-6 的平均水平,但不是轨迹,在复杂妊娠与正常妊娠的女性中有所不同(所有 P 值均≤0.04)。与正常妊娠相比,复杂妊娠的围产期葡萄糖和收缩压轨迹明显更高(P 值分别为 0.008 和 0.01)。我们的结论是,妊娠并发症的经历加上升高的 CVD 风险因素水平可能都会增加女性未来发生 CVD 的风险。临床试验注册号:NCT01307683。