GROW, School for Oncology and Developmental Biology, Department of Obstetrics & Gynaecology, Maastricht University Medical Centre, Maastricht, the Netherlands.
Department of Obstetrics and Gynaecology, Radboud University Medical Centre, Nijmegen, the Netherlands.
BJOG. 2015 Dec;122(13):1818-23. doi: 10.1111/1471-0528.13117. Epub 2014 Oct 16.
To study the prevalence of metabolic syndrome in women after a pregnancy complicated by pre-eclampsia or small-for-gestational-age (SGA), both epitomes of placental syndrome.
A retrospective cohort study.
Single tertiary centre for maternal medicine in the Netherlands.
Women with a history of pre-eclampsia in absence of SGA (n = 742) or pregnancy complicated by normotensive SGA (n = 147) between 1996 and 2010.
Women were routinely screened for underlying cardiometabolic and cardiovascular risk factors at least 6 months postpartum. Logistic regression analysis was used to calculate the odds ratio and adjusted odds ratio for each group. Adjustments were made for age, maternal height, smoking, parity, and interval between delivery and measurement.
Prevalence of the metabolic syndrome.
The prevalence of the metabolic syndrome in our population was two-fold higher for women with a history of pre-eclampsia (13.9%) compared with women with a history of SGA (7.6%). Calculated odds ratios for metabolic syndrome, fasting insulin, HOMA, and microalbuminuria were all higher for women with a history of pre-eclampsia compared with women with SGA. This difference persisted after adjustment for confounding factors: metabolic syndrome (adjusted odds ratio, aOR 2.11; 95% confidence interval, 95% CI 1.00-4.47) and hyperinsulinaemia (aOR 1.78; 95% CI 1.13-2.81) insulin resistance (HOMAIR ; aOR 1.80; 95% CI 1.14-2.86). Microalbuminuria (aOR 1.58; 95% CI 0.85-2.93) did not reach the level of significance after adjustment for confounding factors.
A history of pre-eclampsia, rather than SGA, was associated with metabolic syndrome, suggesting that it relates to maternal rather than fetal etiology of placental syndrome.
研究子痫前期或胎儿生长受限(SGA)后妊娠的女性代谢综合征的患病率,这两种情况都是胎盘综合征的典型代表。
回顾性队列研究。
荷兰一家专门从事母胎医学的三级医疗中心。
1996 年至 2010 年间,患有子痫前期且无 SGA(n=742)或妊娠合并正常血压 SGA(n=147)的女性。
女性在产后至少 6 个月常规筛查潜在的心血管代谢和心血管危险因素。采用逻辑回归分析计算每组的优势比和调整后的优势比。调整因素包括年龄、母亲身高、吸烟、产次和分娩与测量之间的间隔。
代谢综合征的患病率。
与 SGA 病史的女性(7.6%)相比,患有子痫前期病史的女性代谢综合征的患病率增加了一倍(13.9%)。与 SGA 病史的女性相比,子痫前期病史的女性代谢综合征、空腹胰岛素、HOMA 和微量白蛋白尿的计算比值比均较高。在调整混杂因素后,这种差异仍然存在:代谢综合征(调整后的比值比,aOR 2.11;95%置信区间,95%CI 1.00-4.47)和高胰岛素血症(aOR 1.78;95%CI 1.13-2.81)胰岛素抵抗(HOMA-IR;aOR 1.80;95%CI 1.14-2.86)。调整混杂因素后,微量白蛋白尿(aOR 1.58;95%CI 0.85-2.93)未达到统计学意义。
子痫前期病史而非 SGA 与代谢综合征相关,表明其与胎盘综合征的母体病因而非胎儿病因有关。