Sarah El-Heis

and 6 more

A protective influence of maternal inflammatory status on infantile atopic eczema risk has been proposed, but few studies have investigated these potential links. We examined the associations between energy-adjusted dietary inflammatory index (E-DII) scores indicative of an inflammatory dietary pattern, maternal serum neopterin levels, a biomarker elevated in Th1 immune activation, and infantile risk of atopic eczema. Within the UK Southampton Women’s Survey, mothers’ diets were recorded using questionnaires at preconception, early and late pregnancy and E-DII scores derived. Atopic eczema was ascertained using the UK Working Party Diagnostic Criteria at ages 6 and 12 months (n=2955 and 2871, respectively). A sub-sample of 497 mothers had serum neopterin measured in late pregnancy. Unadjusted analyses showed that higher E-DII in preconception and late pregnancy was associated with a lower risk of eczema at ages 6 and 12 months. After adjusting for maternal BMI, age, parity, education, smoking during pregnancy, breastfeeding duration and sex, higher E-DII in late pregnancy was associated with reduced risks of eczema at age 6 and 12 months (OR 0.89 [95%CI 0.81,0.99], p=0.03 and OR 0.91 [0.82,1.00], p=0.05, respectively). Consistent with this, higher maternal serum neopterin was associated with a lower risk of eczema at ages 6 months (OR 0.72 (0.51,1.01), p=0.05) and 12 months (OR 0.71 (0.53,0.96), p=0.03). The findings suggest that a pro-inflammatory maternal diet and an inflammatory maternal environment during pregnancy may protect the developing infant from Th2 driven inflammation and lower the risk of infantile atopic eczema.

Sarah El-Heis

and 9 more

Background Evidence linking prenatal maternal vitamin D supplementation and offspring risk of atopic eczema is inconsistent, with most data coming from observational studies. Methods Within the UK Maternal Vitamin D Osteoporosis Study (MAVIDOS) double-blind, randomised, placebo-controlled trial, we examined the relation of maternal vitamin D supplementation during pregnancy with offspring atopic eczema at ages 12, 24 and 48 months. In MAVIDOS, pregnant women were allocated to either cholecalciferol 1000 IU/day or matched placebo, taken from around 14 weeks’ gestation until delivery, with the primary outcome of neonatal whole-body bone mineral content. The prevalence of atopic eczema in the offspring was ascertained at ages 12 (n=636), 24 (n=611) and 48 (n=450) months, based on the UK Working Party Criteria for the Definition of Atopic Dermatitis. Results Mothers and offspring characteristics were similar between the intervention and placebo groups, apart from longer breastfeeding duration in the intervention group. Adjusting for breastfeeding duration, offspring of mothers who received 1000 IU cholecalciferol daily had a lower odds ratio (OR) of atopic eczema at age 12 months: OR (95%CI) 0.55 (0.32-0.97), p=0.04. The ORs of atopic eczema in the intervention group at ages 24 and 48 months were 0.77 (0.47-1.24) and 0.71 (0.35-1.43), respectively. Conclusion Our data demonstrated a clinically important reduction in offspring risk of atopic eczema in infancy following maternal cholecalciferol supplementation during pregnancy. The findings support a developmental influence on infantile atopic eczema and point to gestational cholecalciferol supplementation as a preventive strategy to reduce the burden of atopic eczema during infancy.