Gayle C Windham1, Michelle Pearl1, Meredith C Anderson2, Victor Poon2, Darryl Eyles3, Karen L Jones4, Kristen Lyall5, Martin Kharrazi1, Lisa A Croen6. 1. California Department of Public Health, Environmental Health Investigations Branch, Richmond, California. 2. Sequoia Foundation, La Jolla, California. 3. Queensland Brain Institute, University of Queensland, Brisbane, Australia. 4. Division of Rheumatology, Allergy and Clinical Immunology, University of California, Davis, California. 5. AJ Drexel Autism Institute, Drexel University, Philadelphia, Pennsylvania. 6. Kaiser Permanente Division of Research, Oakland, California.
Abstract
Vitamin D deficiency has been increasing concurrently with prevalence of autism spectrum disorders (ASD), and emerging evidence suggests vitamin D is involved in brain development. Most prior studies of ASD examined vitamin D levels in children already diagnosed, but a few examined levels during perinatal development, the more likely susceptibility period. Therefore, we examined newborn vitamin D levels in a case-control study conducted among births in 2000-2003 in southern California. Children with ASD (N = 563) or intellectual disability (ID) (N = 190) were identified from the Department of Developmental Services and compared to population controls (N = 436) identified from birth certificates. 25-hydroxyvitamin D (25(OH)D) was measured in archived newborn dried blood spots by a sensitive assay and corrected to sera equivalents. We categorized 25(OH) D levels as deficient (<50 nmol/L), insufficient (50-74 nmol/L), and sufficient (≥75 nmol/L), and also examined continuous levels, using logistic regression. The adjusted odds ratios (AOR) and 95% confidence intervals for ASD were 0.96 (0.64-1.4) for 25(OH)D deficiency (14% of newborns) and 1.2 (0.86-1.6) for insufficiency (26% of newborns). The AORs for continuous 25(OH)D (per 25 nmol/L) were 1.0 (0.91-1.09) for ASD and 1.14 (1.0-1.30) for ID. Thus, in this relatively large study of measured newborn vitamin D levels, our results do not support the hypothesis of lower 25(OH)D being associated with higher risk of ASD (or ID), although we observed suggestion of interactions with sex and race/ethnicity. 25(OH)D levels were relatively high (median 84 nmol/L in controls), so results may differ in populations with higher prevalence of low vitamin D levels. Autism Res 2019, 12: 989-998.
Vitamin Ddeficiency has been increasing concurrently with prevalence of autism spectrum disorders (ASD), and emerging evidence suggests vitamin D is involved in brain development. Most prior studies of ASD examined vitamin D levels in children already diagnosed, but a few examined levels during perinatal development, the more likely susceptibility period. Therefore, we examined newborn vitamin D levels in a case-control study conducted among births in 2000-2003 in southern California. Children with ASD (N = 563) or intellectual disability (ID) (N = 190) were identified from the Department of Developmental Services and compared to population controls (N = 436) identified from birth certificates. 25-hydroxyvitamin D (25(OH)D) was measured in archived newborn dried blood spots by a sensitive assay and corrected to sera equivalents. We categorized 25(OH) D levels as deficient (<50 nmol/L), insufficient (50-74 nmol/L), and sufficient (≥75 nmol/L), and also examined continuous levels, using logistic regression. The adjusted odds ratios (AOR) and 95% confidence intervals for ASD were 0.96 (0.64-1.4) for 25(OH)D deficiency (14% of newborns) and 1.2 (0.86-1.6) for insufficiency (26% of newborns). The AORs for continuous 25(OH)D (per 25 nmol/L) were 1.0 (0.91-1.09) for ASD and 1.14 (1.0-1.30) for ID. Thus, in this relatively large study of measured newborn vitamin D levels, our results do not support the hypothesis of lower 25(OH)D being associated with higher risk of ASD (or ID), although we observed suggestion of interactions with sex and race/ethnicity. 25(OH)D levels were relatively high (median 84 nmol/L in controls), so results may differ in populations with higher prevalence of low vitamin D levels. Autism Res 2019, 12: 989-998.
Authors: Lisa M Bodnar; Hyagriv N Simhan; Robert W Powers; Michael P Frank; Emily Cooperstein; James M Roberts Journal: J Nutr Date: 2007-02 Impact factor: 4.798
Authors: Darryl Eyles; Cameron Anderson; Pauline Ko; Alun Jones; Andrew Thomas; Thomas Burne; Preben Bo Mortensen; Bent Nørgaard-Pedersen; David Michael Hougaard; John McGrath Journal: Clin Chim Acta Date: 2009-02-14 Impact factor: 3.786
Authors: Lisa A Croen; Daniel Braunschweig; Lori Haapanen; Cathleen K Yoshida; Bruce Fireman; Judith K Grether; Martin Kharrazi; Robin L Hansen; Paul Ashwood; Judy Van de Water Journal: Biol Psychiatry Date: 2008-06-20 Impact factor: 13.382
Authors: C R Gale; S M Robinson; N C Harvey; M K Javaid; B Jiang; C N Martyn; K M Godfrey; C Cooper Journal: Eur J Clin Nutr Date: 2007-02-21 Impact factor: 4.016
Authors: Michela Traglia; Gayle C Windham; Michelle Pearl; Victor Poon; Darryl Eyles; Karen L Jones; Kristen Lyall; Martin Kharrazi; Lisa A Croen; Lauren A Weiss Journal: Genetics Date: 2020-02-11 Impact factor: 4.562
Authors: Kristen Lyall; Jennifer L Ames; Michelle Pearl; Michela Traglia; Lauren A Weiss; Gayle C Windham; Martin Kharrazi; Cathleen K Yoshida; Robert Yolken; Heather E Volk; Paul Ashwood; Judy Van de Water; Lisa A Croen Journal: Mol Autism Date: 2021-03-18 Impact factor: 7.509
Authors: Agnes M Mutua; Margaret Nampijja; Alison M Elliott; John M Pettifor; Thomas N Williams; Amina Abubakar; Emily L Webb; Sarah H Atkinson Journal: Nutrients Date: 2020-06-03 Impact factor: 6.706
Authors: Amina Abubakar; Sarah H Atkinson; Agnes M Mutua; Reagan M Mogire; Alison M Elliott; Thomas N Williams; Emily L Webb Journal: Wellcome Open Res Date: 2020-06-11