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Micronutrient status during pregnancy is associated with child immune status in rural Bangladesh.
Jung, Da Kyung; Tan, Sophia T; Hemlock, Caitlin; Mertens, Andrew N; Stewart, Christine P; Rahman, Md Ziaur; Ali, Shahjahan; Raqib, Rubhana; Grembi, Jessica A; Karim, Mohammed Rabiul; Shahriar, Sunny; Roy, Anjan Kumar; Abdelrahman, Sarah; Shoab, Abul K; Famida, Syeda L; Hossen, Md Saheen; Mutsuddi, Palash; Akther, Salma; Rahman, Mahbubur; Unicomb, Leanne; Hester, Lisa; Granger, Douglas A; Erhardt, Juergen; Naved, Ruchira Tabassum; Al Mamun, Md Mahfuz; Parvin, Kausar; Colford, John M; Fernald, Lia C H; Luby, Stephen P; Dhabhar, Firdaus S; Lin, Audrie.
Afiliación
  • Jung DK; Division of Epidemiology and Biostatistics, School of Public Health, University of California Berkeley, Berkeley, CA, United States.
  • Tan ST; Division of Infectious Diseases and Geographic Medicine, Stanford University, Stanford, CA, United States.
  • Hemlock C; Division of Epidemiology and Biostatistics, School of Public Health, University of California Berkeley, Berkeley, CA, United States.
  • Mertens AN; Division of Epidemiology and Biostatistics, School of Public Health, University of California Berkeley, Berkeley, CA, United States.
  • Stewart CP; Institute for Global Nutrition, University of California Davis, Davis, CA, United States.
  • Rahman MZ; Environmental Interventions Unit, Infectious Diseases Division, icddr,b, Dhaka 1212, Bangladesh.
  • Ali S; Environmental Interventions Unit, Infectious Diseases Division, icddr,b, Dhaka 1212, Bangladesh.
  • Raqib R; Environmental Interventions Unit, Infectious Diseases Division, icddr,b, Dhaka 1212, Bangladesh.
  • Grembi JA; Division of Infectious Diseases and Geographic Medicine, Stanford University, Stanford, CA, United States.
  • Karim MR; Environmental Interventions Unit, Infectious Diseases Division, icddr,b, Dhaka 1212, Bangladesh.
  • Shahriar S; Environmental Interventions Unit, Infectious Diseases Division, icddr,b, Dhaka 1212, Bangladesh.
  • Roy AK; Environmental Interventions Unit, Infectious Diseases Division, icddr,b, Dhaka 1212, Bangladesh.
  • Abdelrahman S; Division of Epidemiology and Biostatistics, School of Public Health, University of California Berkeley, Berkeley, CA, United States.
  • Shoab AK; Environmental Interventions Unit, Infectious Diseases Division, icddr,b, Dhaka 1212, Bangladesh.
  • Famida SL; Environmental Interventions Unit, Infectious Diseases Division, icddr,b, Dhaka 1212, Bangladesh.
  • Hossen MS; Environmental Interventions Unit, Infectious Diseases Division, icddr,b, Dhaka 1212, Bangladesh.
  • Mutsuddi P; Environmental Interventions Unit, Infectious Diseases Division, icddr,b, Dhaka 1212, Bangladesh.
  • Akther S; Environmental Interventions Unit, Infectious Diseases Division, icddr,b, Dhaka 1212, Bangladesh.
  • Rahman M; Environmental Interventions Unit, Infectious Diseases Division, icddr,b, Dhaka 1212, Bangladesh.
  • Unicomb L; Environmental Interventions Unit, Infectious Diseases Division, icddr,b, Dhaka 1212, Bangladesh.
  • Hester L; Department of Medicine, University of Maryland, Baltimore, MD USA.
  • Granger DA; Institute for Interdisciplinary Salivary Bioscience Research, University of California Irvine, Irvine, CA, United States.
  • Erhardt J; VitMin Lab, Willstätt, Germany.
  • Naved RT; Health System and Population Studies Division, icddr,b, Dhaka, Bangladesh.
  • Al Mamun MM; Health System and Population Studies Division, icddr,b, Dhaka, Bangladesh.
  • Parvin K; Health System and Population Studies Division, icddr,b, Dhaka, Bangladesh.
  • Colford JM; Division of Epidemiology and Biostatistics, School of Public Health, University of California Berkeley, Berkeley, CA, United States.
  • Fernald LCH; Division of Community Health Sciences, School of Public Health, University of California, Berkeley, Berkeley, CA, United States.
  • Luby SP; Division of Infectious Diseases and Geographic Medicine, Stanford University, Stanford, CA, United States.
  • Dhabhar FS; Department of Psychiatry & Behavioral Sciences, Department of Microbiology and Immunology, Sylvester Comprehensive Cancer Center, Miller School of Medicine, University of Miami, Miami, FL, United States.
  • Lin A; Department of Microbiology and Environmental Toxicology, University of California, Santa Cruz, CA, United States.
Curr Dev Nutr ; 7(8): 101969, 2023 Aug.
Article en En | MEDLINE | ID: mdl-37560460
ABSTRACT

Background:

Poor immune function increases children's risk of infection and mortality. Several maternal factors during pregnancy may affect infant immune function during the postnatal period.

Objectives:

We aimed to evaluate whether maternal micronutrients, stress, estriol, and immune status during the first or second trimester of pregnancy were associated with child immune status in the first two years after birth.

Methods:

We conducted observational analyses within the water, sanitation, and hygiene (WASH) Benefits Bangladesh randomized controlled trial. We measured biomarkers in 575 pregnant women and postnatally in their children. Maternal biomarkers measured during the first and second trimester of pregnancy included nutrition status via vitamin D (25-hydroxy-D [25(OH)D]), ferritin, soluble transferrin receptor (sTfR), and retinol-binding protein (RBP); cortisol; estriol. Immune markers were assessed in pregnant women at enrollment and their children at ages 14 and 28 mo, including C-reactive protein (CRP), alpha-1-acid glycoprotein (AGP), and 13 cytokines (including IFN-γ). We generated a standardized sum score of log-transformed cytokines. We analyzed IFN-γ individually because it is a critical immunoregulatory cytokine. All outcomes were prespecified. We used generalized additive models and reported the mean difference and 95% confidence intervals at the 25th and 75th percentiles of exposure distribution.

Results:

At child age 14 mo, concentrations of maternal RBP were inversely associated with the cytokine sum score in children (-0.34 adjusted difference between the 25th and 75th percentile [95% confidence interval -0.61, -0.07]), and maternal vitamin A deficiency was positively associated with the cytokine sum score in children (1.02 [0.13, 1.91]). At child age of 28 mo, maternal RBP was positively associated with IFN-γ in children (0.07 [0.01, 0.14]), whereas maternal vitamin A deficiency was negatively associated with child AGP (-0.07 [-0.13, -0.02]). Maternal iron deficiency was associated with higher AGP concentrations in children at age 14 mo (0.13 [0.04, 0.23]), and maternal sTfR concentrations were positively associated with child CRP concentrations at age 28 mo (0.18 [0, 0.36]).

Conclusion:

Maternal deficiencies in vitamin A or iron during the first 2 trimesters of pregnancy may shape the trajectory of a child's immune status.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Curr Dev Nutr Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Curr Dev Nutr Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos