Infant Colic Represents Gut Inflammation and Dysbiosis

• Published in: The Journal of pediatrics Vol. 203; pp. 55 - 61.e3
• Main Authors: Rhoads, J. Marc, Collins, James, Fatheree, Nicole Y., Hashmi, S. Shahrukh, Taylor, Christopher M., Luo, Meng, Hoang, Thomas K., Gleason, Wallace A., Van Arsdall, Melissa R., Navarro, Fernando, Liu, Yuying
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.12.2018
• Subjects: Acinetobacter - isolation & purification; Breast Feeding; calprotectin; Case-Control Studies; Colic - complications; crying; Dysbiosis - diagnosis; Feces - chemistry; Feces - microbiology; Female; functional bowel disorder; Gastrointestinal Microbiome; Humans; Infant; Infant Formula; Infant, Newborn; Inflammation - diagnosis; intestinal inflammation; Lactobacillus - isolation & purification; Leukocyte L1 Antigen Complex - analysis; Male; microbiota; newborn; microbiota; newborn; intestinal inflammation; functional bowel disorder; crying; calprotectin
• ISSN: 0022-3476; 1097-6833; 1097-6833
• DOI: 10.1016/j.jpeds.2018.07.042

To dissect potential confounding effects of breast milk and formula feeding on crying + fussing, fecal calprotectin, and gut microbiota in babies with colic. We hypothesized that infant colic is associated with gut inflammation linked to intestinal dysbiosis. A nested case-control design of 3 of our studies was used to analyze clinical and laboratory data at presentation, comparing babies with colic with controls. All investigators other than the biostatistician were blinded during data analysis. Subjects were recruited based on their age and crying + fussy time. We screened 65 infants, 37 with colic, as defined by Barr diary (crying + fussing time >3 hours daily), who were compared with 28 noncolicky infants. Fecal calprotectin was elevated in babies with colic. For each mode of infant feeding (breast milk, formula, or breast + formula), infants' fecal calprotectin was higher in babies with colic. Infants with colic had similar levels of fecal alpha diversity (richness) when compared with controls, and alpha diversity was lower in breast-fed babies. Beta diversity at the phylum level revealed significant differences in microbial population. A phylum difference resulted from reduced Actinobacteria (95% of which are Bifidobacilli) in babies with colic. Species significantly associated with colic were Acinetobacter and Lactobacillus iners. Colic is linked with gut inflammation (as determined by fecal calprotectin) and dysbiosis, independent of mode of feeding, with fewer Bifidobacilli. Clinicaltrials.gov: NCT01279265 and NCT01849991.