Infant sex at birth and long‐term maternal mortality. Issue 3 (5th January 2023)

• Record Type: Journal Article
• Authors: Grandi, Sonia M.; Hinkle, Stefanie N.; Mumford, Sunni L.; Sjaarda, Lindsey A.; Grantz, Katherine L.; Mendola, Pauline; Mills, James L.; Pollack, Anna Z.; Yeung, Edwina; Zhang, Cuilin; Schisterman, Enrique F.
• Is Part Of: Paediatric and perinatal epidemiology. Volume 37:Issue 3(2023)
• Page Start: 229
• Page End: 238
• Publication Date: 2023-01-05
• Subjects: infant sex -- male infant -- maternal mortality -- race/ethnicity; Pediatrics -- Periodicals; Perinatology -- Periodicals; Pediatric epidemiology -- Periodicals; Infants (Newborn) -- Diseases -- Periodicals; 618.92
• DOI: 10.1111/ppe.12933
• Languages: English
• ISSNs: 0269-5022

Abstract

Abstract: Background: Maternal adaptations may vary by foetal sex. Whether male infants influence long‐term mortality in mothers remains uncertain. Objective: The objective of the study was to examine whether male infants increase the risk of maternal mortality. Methods: This study included pregnant women enrolled at 12 US sites from 1959 to 1966 in the Collaborative Perinatal Project (CPP). Collaborative Perinatal Project records were linked to the National Death Index and the Social Security Master Death File to ascertain deaths until 2016. Foetal sex was determined by infant sex at birth, defined as the total number of male or female infants in pregnancies prior to or during enrolment in the CPP. In secondary analyses, exposure was defined as infant sex at the last CPP delivery. Outcomes included all‐cause and underlying causes of mortality. We used Cox proportional hazards models weighted by the number of prior live births and stratified our models by parity and race/ethnicity. Results: Among 48, 188 women, 50.8% had a male infant at their last registered CPP pregnancy and 39.0% had a recorded death after a mean follow‐up of 47.8 years (SD 10.5 years). No linear association was found between the number of liveborn males and all‐cause mortality (primipara women: HR 1.02, 95% CI 0.95, 1.09, multipara women, 1 prior live birth: HR 0.96, 95% CI 0.89, 1.03, multipara women, ≥2 prior live births: HR 0.97, 95% CI 0.85, 1.11). A similar trend was noted for cardiovascular‐ and cancer‐related mortality. At the last delivery, women with a male infant did not have an increased risk of all‐cause or cause‐specific mortality compared to women with a female infant. These findings were consistent across racial/ethnic groups. Conclusions: Women who give birth to male infants, regardless of number, are not at increased risk of all‐cause and cause‐specific mortality. These findings suggest that giving birth to male infants may not independently influence the long‐term health of women.