Integrating genetics with newborn metabolomics in infantile hypertrophic pyloric stenosis

• Published in: Metabolomics Vol. 17; no. 1; p. 7
• Main Authors: Fadista, João, Skotte, Line, Courraud, Julie, Geller, Frank, Gørtz, Sanne, Wohlfahrt, Jan, Melbye, Mads, Cohen, Arieh S., Feenstra, Bjarke
• Format: Journal Article
• Language: English
• Published: New York Springer US 2021; Springer Nature B.V
• Subjects: Biochemistry; Biomedical and Life Sciences; Biomedicine; Breast; Cell Biology; Clinical Medicine; Developmental Biology; Endocrinology and Diabetes; Endokrinologi och diabetes; Genetic diversity; Histidine; Hypertrophy; Klinisk medicin; Lecithin; Life Sciences; Lipid metabolism; Medical and Health Sciences; Medicin och hälsovetenskap; Metabolites; Metabolomics; Molecular Medicine; Neonates; Original; Original Article; Phosphatidylcholine; Pyloric sphincter; Sampling; Sphincter; Stenosis
• ISSN: 1573-3882; 1573-3890
• DOI: 10.1007/s11306-020-01763-2

Introduction Infantile hypertrophic pyloric stenosis (IHPS) is caused by hypertrophy of the pyloric sphincter muscle. Objectives Since previous reports have implicated lipid metabolism, we aimed to (1) investigate associations between IHPS and a wide array of lipid-related metabolites in newborns, and (2) address whether detected differences in metabolite levels were likely to be driven by genetic differences between IHPS cases and controls or by differences in early life feeding patterns. Methods We used population-based random selection of IHPS cases and controls born in Denmark between 1997 and 2014. We randomly took dried blood spots of newborns from 267 pairs of IHPS cases and controls matched by sex and day of birth. We used a mixed-effects linear regression model to evaluate associations between 148 metabolites and IHPS in a matched case–control design. Results The phosphatidylcholine PC(38:4) showed significantly lower levels in IHPS cases ( P  = 4.68 × 10 −8 ) as did six other correlated metabolites (four phosphatidylcholines, acylcarnitine AC(2:0), and histidine). Associations were driven by 98 case–control pairs born before 2009, when median age at sampling was 6 days. No association was seen in 169 pairs born in 2009 or later, when median age at sampling was 2 days. More IHPS cases than controls had a diagnosis for neonatal difficulty in feeding at breast ( P  = 6.15 × 10 −3 ). Genetic variants known to be associated with PC(38:4) levels did not associate with IHPS. Conclusions We detected lower levels of certain metabolites in IHPS, possibly reflecting different feeding patterns in the first days of life.