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COMT Variants are Associated With Breast and Nipple Pain

  • Tumilara Aderibigbe
  • , Shannon L. Kelleher
  • , Wendy A. Henderson
  • , Stephanie Prescott
  • , Erin E. Young
  • , Ruth F. Lucas
  • University of Connecticut
  • University of Massachusetts Lowell
  • University of Pennsylvania
  • University of South Florida
  • University of Kansas

Research output: Contribution to journal › Article › peer-review

Abstract

Estimates suggest that only 24.9% of infants born in 2019 were exclusively breastfed before 6 months of age, despite the known health benefits of exclusive breastfeeding. Breast and nipple pain is one of the primary determinants of exclusive breastfeeding. Environmental contributions to breastfeeding success have been reported extensively in the literature, but the contribution(s) of maternal genetics has yet to be discovered. The purpose of the study was to identify an association between pain and lactation-related gene variants with exclusive breastfeeding determinants. We selected 4 genes having single nucleotide polymorphisms (SNPs) with potential functional significance in breastfeeding and pain: prolactin receptor (PRLR), oxytocin receptor (OXTR), catechol-O-methyltransferase (COMT), and milk fat globule epidermal growth factor and factor V/VIII domain containing (MFGE8). We performed a cross-sectional secondary analysis of a longitudinal randomized controlled trial study, Promoting Self-Management of Breast and Nipple Pain with Biomarkers and Technology for Breastfeeding Women (NCT05262920). Breast and nipple pain, perceived insufficient milk, and breastfeeding self-efficacy were examined using total scale scores for the Brief Pain Inventory, Visual Analog Scale, H&H Lactation Scale, and the Breastfeeding Self-efficacy Scale-short form, respectively. Of the candidate genes examined, SNPs within COMT were significantly associated with breastfeeding-related outcomes. Specifically, COMT rs4633 and rs4680 minor allele carriers (T, A) reported higher breast and nipple pain intensity than women homozygous for the major allele (C, G). COMT is the most widely researched “pain gene” and has been linked to cold, postoperative, and postpartum pain. This study is the first to identify a contribution of COMT variants to breast and nipple pain and, as a result, to breastfeeding exclusivity. Perspective: Two SNPs in the pain gene COMT are associated with breast and nipple pain. Clinically, a minor allele in COMT rs4633 and rs4680 may increase a woman's rating of moderate breast and nipple pain. Trial registration: PROMPT was registered in ClinicalTrials.gov (protocol #NCT05262920).

Original languageEnglish
Article number104568
JournalJournal of Pain
Volume25
Issue number9
DOIs
StatePublished - Sep 2024

ASJC Scopus Subject Areas

  • Neurology
  • Clinical Neurology
  • Anesthesiology and Pain Medicine

Keywords

  • breast and nipple pain
  • Breastfeeding
  • genetic
  • postpartum
  • women

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