Multicohort analysis unveils axon guidance pathways linking small for gestational age to spirometric restriction
Recommended Citation
Read JF, Stern DA, Carr TF, Spangenberg AL, Yang M, Luna-Ramirez RI, Guerra S, Morgan WJ, Binder AT, VanWormer JJ, Seroogy CM, Miller RL, Zoratti EM, Ober C, Jackson DJ, Limesand SW, Gold DR, Gern JE, Bosco A, Martinez FD. Multicohort analysis unveils axon guidance pathways linking small for gestational age to spirometric restriction. Nat Commun. 2026;17(1).
Document Type
Article
Publication Date
5-2-2026
Publication Title
Nat Commun
Keywords
Animals, Female, Humans, Axon Guidance, Sheep, Infant, Small for Gestational Age, Genome-Wide Association Study, Lung, Male, Proteomics, Pregnancy, Developmental Origins of Health and Disease
Abstract
Children born small for gestational age (SGA) face elevated risks of metabolic, cardiovascular, respiratory, and neurodevelopmental disorders, as well as premature mortality, yet the underlying mechanisms remain only partly understood. We analyze blood proteomic data from multiple birth cohorts to identify molecular pathways linked to SGA and to later-life lung function. We find that approximately one-third of SGA children exhibit a distinct molecular endotype marked by dysregulation of axon-guidance proteins in cord blood. In peripheral blood collected later in life, these proteins are inversely associated with contemporaneous spirometric restriction. Using GWAS data and an experimental sheep model, we obtain convergent evidence that axon-guidance genes are associated with spirometric indices (FEV(1)/FVC) at genome-wide significance and are broadly expressed during fetal development across multiple organs. These findings offer new insight into the developmental origins of chronic disease and highlight axon-guidance pathways as promising targets for investigating multiorgan morbidity.
Medical Subject Headings
Animals; Female; Humans; Axon Guidance; Sheep; Infant, Small for Gestational Age; Genome-Wide Association Study; Lung; Male; Proteomics; Pregnancy; Developmental Origins of Health and Disease
PubMed ID
42069698
Volume
17
Issue
1
