Preterm delivery is a maternal risk factor of CVD

28/02/2017

Preterm delivery is independently predictive of CVD which is only partially explained by postpartum development of traditional CVD risk factors.

Preterm delivery and maternal cardiovascular disease in young and middle-aged adult women
Literature - Tanz LJ, Stuart JJ, Williams PL, et al. - Circulation 2017;135:578-589

Background

In the United States ~10% of the deliveries are preterm [1]. It has been hypothesized that pregnancy complications, including preterm delivery, as well as HDP (preeclampsia and gestational hypertension), provide a warning sign of future cardiovascular disease (CVD) risk, that could be useful in identifying high-risk women early in adult life before the appearance of clinical risk factors [2-4]. Prior literature describes a 2-fold increased risk of future CVD events for women who delivered preterm, however, in these studies was not corrected for CVD risk factors and prepregnancy lifestyle such as smoking, physical activity, diet, BMI and family history of CVD [5-7].

Therefore, this study (Nurses’ Health Study II), including 70 182 US registered nurses between 25 and 42 years of age at baseline, evaluated the association between preterm delivery and CVD (myocardial infarction [MI] or stroke) and to what extent this is related to postpartum development of traditional CVD risk factors (chronic hypertension, hypercholesterolemia, type 2 diabetes mellitus [T2DM] and BMI). Preterm delivery was categorized as term (≥37 weeks), moderate preterm (≥32 and <37 weeks) or very preterm (<32 weeks). Follow up was until 50 years of age and started in 1989.

Main results

  • First pregnancy: 2.1% very preterm, 6.7% moderately preterm and 91.2% at term.
  • Women who delivered moderately or very preterm were slightly more like to have a BMI ≥30 kg/m2, pregnancy hypertension and hypercholesterolemia and a family history of CVD. Furthermore, women who delivered very preterm were more likely to be current smokers, experience a stillbirth in first pregnancy and have higher final parity.
  • 949 CVD events occurred; 584 definite and 365 probable.
  • After adjustment for confounding lifestyle and CVD risk factors, women who had a preterm first birth had an increased rate of CVD (HR 1.42, 95% CI 1.16-1.72).
  • When split into 2 categories, the HRs for moderate preterm and very preterm were 1.22 (95% CI 0.96-1.54) and 2.01 (95% CI 1.47-2.75), respectively (trend P<0.0001).
  • When analysing stroke and MI separately, results were slightly stronger for MI.
  • Increased rate of CVD was present in very preterm live birth (HR 1.98, 95% CI 1.27-3.08) as well as very preterm stillbirth (HR 2.07, 95% CI 1.35-3.18).
  • Increased rate of CVD was present in normotensive preterm first pregnancy (HR 1.35, 95% CI 1.06-1.72) but higher in those with both preterm delivery and HDP in first pregnancy (HR 1.66, 95% CI 1.02-2.70).
  • Rate was non-significantly higher in normotensive moderate preterm (HR 1.12, 95% CI 0.83-1.52) than in normotensive very preterm individuals (HR 2.01, 95% CI 1.38-2.93).
  • Women with a preterm first birth and at least 1 later preterm birth had the largest fully adjusted HR (1.65, 95% CI 1.20-2.28).
  • Women with only 1 child (either preterm or term) had an increased rate of CVD compared to women with at least 2 children at term.
  • Increased CVD risk was applicable to both women with preterm delivery in the first pregnancy and later preterm deliveries.
  • Regarding prepregnancy lifestyle, only chronic hypertension before first pregnancy appeared to be a confounder; HR moderate preterm vs. term were 0.21 (95% CI 0.03-1.52) for with and 1.30 (95% CI 1.02-1.64) for without prepregnancy chronic hypertension and HR very preterm with term were 0.57 (95% CI 0.08-4.14) for with and 2.12 (95% CI 1.54-2.92) for without prepregnancy chronic hypertension.
  • 12.8% (95% CI 7.1-21.9) of the association between preterm delivery and CVD was related to postpartum development of chronic hypertension, T2DM, hypercholesterolemia or changes in BMI and was attenuated (5.9%, 95% CI 8.7-27.3) when breastfeeding was also included.

Conclusion

Women who deliver a preterm infant have an increased risk of future CVD events, which was higher for those who deliver before week 32. This risk is only partially explained by the subsequent development of traditional CVD risk factors, but this suggests that modification of these risk factors in these women may decrease the risk of CVD development. As a large part could not be explained by risk factors, additional pathways that link preterm delivery and CVD need to be further explored. Moreover, preterm delivery may be a valuable additional CVD risk marker in screening.

References

1. Hamilton BE, Martin JA, Osterman MJ, Curtin SC, Matthews TJ. Births: final data for 2014. Natl Vital Stat Rep. 2015;64:1–64.

2. Sattar N, Greer IA. Pregnancy complications and maternal cardiovascular risk: opportunities for intervention and screening? BMJ.2002;325:157–160.

3. Rich-Edwards JW. Reproductive health as a sentinel of chronic disease in women. Womens Health (Lond). 2009;5:101–105. doi:10.2217/17455057.5.2.101.

4. Rich-Edwards JW, McElrath TF, Karumanchi SA, Seely EW. Breathing life into the lifecourse approach: pregnancy history and cardiovascular disease in women. Hypertension. 2010;56:331–334.

doi: 10.1161/HYPERTENSIONAHA.110.156810.

5. Smith GC, Pell JP, Walsh D. Pregnancy complications and maternal risk of ischaemic heart disease: a retrospective cohort study of 129,290 births. Lancet. 2001;357:2002–2006. doi:10.1016/S0140-6736(00)05112-6.

6. Bonamy AK, Parikh NI, Cnattingius S, Ludvigsson JF, Ingelsson E. Birth characteristics and subsequent risks of maternal cardiovascular disease: effects of gestational age and fetal growth.

Circulation. 2011;124:2839–2846. doi: 10.1161/CIRCULATIONAHA.111.034884.

7. Hastie CE, Smith GC, Mackay DF, Pell JP. Maternal risk of ischaemic heart disease following elective and spontaneous pre-term delivery: retrospective cohort study of 750 350 singleton pregnancies.

Int J Epidemiol. 2011;40:914–919. doi: 10.1093/ije/dyq270.

Find this publication online at Circulation

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