Relation between infant microbiota and autism? - Results from a national cohort sibling-design study
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Standard
Relation between infant microbiota and autism? - Results from a national cohort sibling-design study. / Axelsson, Paul Bryde; Clausen, Tine Dalsgaard; Petersen, Anne Helby; Hageman, Ida; Pinborg, Anja; Kessing, Lars Vedel; Bergholt, Thomas; Rasmussen, Steen Christian; Keiding, Niels; Kessing, Lars Vedel.
I: Epidemiology (Cambridge, Mass.), Bind 30, Nr. 1, 2019, s. 52-60.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Harvard
APA
Vancouver
Author
Bibtex
}
RIS
TY - JOUR
T1 - Relation between infant microbiota and autism? - Results from a national cohort sibling-design study
AU - Axelsson, Paul Bryde
AU - Clausen, Tine Dalsgaard
AU - Petersen, Anne Helby
AU - Hageman, Ida
AU - Pinborg, Anja
AU - Kessing, Lars Vedel
AU - Bergholt, Thomas
AU - Rasmussen, Steen Christian
AU - Keiding, Niels
AU - Kessing, Lars Vedel
PY - 2019
Y1 - 2019
N2 - BACKGROUND: Hypotheses concerning adverse effects of changes in microbiota have received much recent attention, but unobserved confounding makes them difficult to test. We investigated whether surrogate markers for potential adverse microbiota changes in infancy affected autism risk, addressing unobserved confounding using a sibling study design.METHODS: This is a population-based, prospective cohort study including all singleton live births in Denmark from 1997 to 2010. The exposure variables were cesarean delivery and antibiotic use in the first 2 years of life. The outcome was a subsequent autism diagnosis. We used the between-within sibling model and compared it with sibling stratified Cox models and simpler standard Cox models that ignored sibship.RESULTS: Of our study population including 671,606 children, who were followed for up to 15 years (7,341,133 person-years), 72% received antibiotics, 17.5% were delivered by cesarean, and 1.2% (8,267) developed autism. The standard Cox models predicted that both cesarean (compared to vaginal) delivery and antibiotics increased the risk of autism. In the sibling-stratified Cox model, only broader spectrum antibiotics were associated with increased risk of autism: hazard ratio (HR) 1.16 (95% confidence interval, 1.01-1.36). The between-within model estimated no exposure effects: intrapartum cesarean HR 1.06 (0.89-1.26); pre-labor cesarean HR 0.97 (0.83-1.15); exclusively penicillin HR 1.05 (0.93-1.18); broader spectrum antibiotics HR 1.05 (0.95-1.16).CONCLUSIONS: The between-within model rendered more precise estimates than sibling-stratified Cox models, and we believe also provided more valid estimates. Results from these preferred models do not support a causal relation between antibiotic treatment during infancy, cesarean delivery, and autism.
AB - BACKGROUND: Hypotheses concerning adverse effects of changes in microbiota have received much recent attention, but unobserved confounding makes them difficult to test. We investigated whether surrogate markers for potential adverse microbiota changes in infancy affected autism risk, addressing unobserved confounding using a sibling study design.METHODS: This is a population-based, prospective cohort study including all singleton live births in Denmark from 1997 to 2010. The exposure variables were cesarean delivery and antibiotic use in the first 2 years of life. The outcome was a subsequent autism diagnosis. We used the between-within sibling model and compared it with sibling stratified Cox models and simpler standard Cox models that ignored sibship.RESULTS: Of our study population including 671,606 children, who were followed for up to 15 years (7,341,133 person-years), 72% received antibiotics, 17.5% were delivered by cesarean, and 1.2% (8,267) developed autism. The standard Cox models predicted that both cesarean (compared to vaginal) delivery and antibiotics increased the risk of autism. In the sibling-stratified Cox model, only broader spectrum antibiotics were associated with increased risk of autism: hazard ratio (HR) 1.16 (95% confidence interval, 1.01-1.36). The between-within model estimated no exposure effects: intrapartum cesarean HR 1.06 (0.89-1.26); pre-labor cesarean HR 0.97 (0.83-1.15); exclusively penicillin HR 1.05 (0.93-1.18); broader spectrum antibiotics HR 1.05 (0.95-1.16).CONCLUSIONS: The between-within model rendered more precise estimates than sibling-stratified Cox models, and we believe also provided more valid estimates. Results from these preferred models do not support a causal relation between antibiotic treatment during infancy, cesarean delivery, and autism.
U2 - 10.1097/EDE.0000000000000928
DO - 10.1097/EDE.0000000000000928
M3 - Journal article
C2 - 30273187
VL - 30
SP - 52
EP - 60
JO - Epidemiology
JF - Epidemiology
SN - 1044-3983
IS - 1
ER -
ID: 203376106