Long‐Term Postpartum Cardiac Function and Its Association With Preeclampsia

Author:

deMartelly Victoria A.1,Dreixler John2,Tung Avery2ORCID,Mueller Ariel3,Heimberger Sarah1ORCID,Fazal Abid A.2,Naseem Heba1,Lang Roberto4,Kruse Eric1,Yamat Megan1,Granger Joey P.5,Bakrania Bhavisha A.5,Rodriguez‐Kovacs Javier1,Rana Sarosh1,Shahul Sajid2ORCID

Affiliation:

1. Department of Obstetrics and Gynecology University of Chicago IL

2. Department of Anesthesia and Critical Care University of Chicago IL

3. Department of Anesthesia Critical Care and Pain Medicine Massachusetts General HospitalHarvard Medical School Boston MA

4. Department of Medicine University of Chicago IL

5. Department of Physiology and Biophysics University of Mississippi Medical Center Jackson MS

Abstract

Background Preeclampsia is a prominent risk factor for long‐term development of cardiovascular disease. Although existing studies report a strong correlation between preeclampsia and heart failure, the underlying mechanisms are poorly understood. One possibility is the glycoprotein growth factor activin A. During pregnancy, elevated activin A levels are associated with impaired cardiac global longitudinal strain at 1 year, but whether these changes persist beyond 1 year is not known. We hypothesized that activin A levels would remain increased more than 1 year after a preeclamptic pregnancy and correlate with impaired cardiac function. Methods and Results To test our hypothesis, we performed echocardiograms and measured activin A levels in women approximately 10 years after an uncomplicated pregnancy (n=25) or a pregnancy complicated by preeclampsia (n=21). Compared with women with a previously normal pregnancy, women with preeclampsia had worse global longitudinal strain (−18.3% versus −21.3%, P =0.001), left ventricular posterior wall thickness (0.91 mm versus 0.80 mm, P =0.003), and interventricular septal thickness (0.96 mm versus 0.81 mm, P =0.0002). Women with preeclampsia also had higher levels of activin A (0.52 versus 0.37 ng/mL, P =0.02) and activin/follistatin‐like 3 ratio (0.03 versus 0.02, P =0.04). In a multivariable model, the relationship between activin A levels and worsening global longitudinal strain persisted after adjusting for age at enrollment, mean arterial pressure, race, and body mass index ( P =0.003). Conclusions Our findings suggest that both activin A levels and global longitudinal strain are elevated 10 years after a pregnancy complicated by preeclampsia. Future studies are needed to better understand the relationship between preeclampsia, activin A, and long‐term cardiac function.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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