Tykes, Toddlers, Teens, and Twins of Robust Mothers: Do the Offspring of Twinning Mothers Share in Their Mother’s Robust Phenotype?

  • Alla Chernenko
  • , Michael Hollinghshaus
  • , Shannen Robson
  • , Heidi A. Hanson
  • , Ken R. Smith

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

Women who bear twins may possess a robust phenotype compared to non-twinning mothers. We examine mortality patterns for the singleton offspring of mothers of twins compared to the offspring of non-twinning mothers to determine whether they share the hypothesized robust phenotype of their mothers. Using data from the Utah Population Database, we show that both male and female singleton offspring of twinning mothers experience a survival disadvantage prior to age 5, no survival benefit or penalty between ages 5 and 49, and—for males only—a statistically significant survival advantage after age 50. We further examine the survival effects on singletons born before and after a twinset. We observe a survival disadvantage in early life for singleton offspring of twinning mothers born after the twinset for both sexes. In addition, we find a significant survival advantage at older ages in certain categories of male singleton offspring—a likely reflection of mortality selection. The findings suggest that while bearing twins may reflect a robust maternal phenotype, the toll of bearing twins may disadvantage subsequent offspring, especially during infancy.

Original languageEnglish
Pages (from-to)102-113
Number of pages12
JournalBiodemography and Social Biology
Volume64
Issue number2
DOIs
StatePublished - Apr 3 2018
Externally publishedYes

Funding

We thank the Pedigree and Population Resource of the Huntsman Cancer Institute, University of Utah (funded in part by the Huntsman Cancer Foundation) for its role in the ongoing collection, maintenance, and support of the Utah Population Database (UPDB). We also acknowledge partial support for the UPDB through grant P30 CA2014 from the National Cancer Institute, University of Utah and from the University of Utah’s Program in Personalized Health and Center for Clinical and Translational Science, as well as support for this study through National Institutes of Health grant AG022095 (Early Life Conditions, Survival and Health; Smith PI). In addition, we thank the Friday Demography Mentee Research Group for their feedback on earlier versions of this paper. This work was supported by the National Cancer Institute [Grant Number P30 CA2014];National Institutes of Health [Grant Number AG022095].

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