Assessment of the Daily Average Requirement of Iodine in Lactating Women

This study is a single center, randomized, controlled, dose-response metabolic balance study with cross-over design. The study will be conducted in 24 exclusively breastfeeding women and their infants receding in Zürich, Switzerland. The study involves an initial screening, a 2 weeks run-in period and a balance period over 3 weeks. Participating women will be allocated to two groups based on their consumption of dietary iodine supplements during pregnancy. Women who consumed daily iodine supplements during pregnancy will be assigned to group 1 (n=12) and receive daily supplements containing 150 µg iodine for 2 weeks, whereas women who did not will be enrolled in group 2 and will receive no supplement during the run-in period. Breast milk and spot urine samples (mothers and infants) will be collected daily in all participants during two weeks for the measurement of breast milk and urinary iodine concentrations. During the balance period, all women will receive either no supplement, iodine supplements providing 150 µg/day, or 300 µg/day in random order with cross-over design. Each supplement dose will be assessed in a test period of 7 days, including 2 run-in days, 3 balance days and 2 wash-out days. The supplements will be consumed during the first 5 days in each test-period. During the 3 balance days, the daily iodine intake and excretion will be measured in mothers and infants, and the iodine retention will be calculated for each regimen and study group. The minimum daily average requirement will be determined as the iodine intake where the iodine retention is zero.

Mother-infant pairs in good health, free of any acute illness or chronic thyroid disease.

Mothers

Inclusion criteria

• Consent to enroll herself and her baby;
• Age 18 to 49 years;
• Singleton pregnancy;
• Exclusively breastfeeding;
• Self-estimated BMI <30 kg/m2 before conception.

Exclusion criteria

• TSH >6 mIU/L;
• Anemia (Hb <11.7 g/L);
• Pregnancy (self-reported);
• Acute illness (e.g. gastroenteritis);
• History of thyroid disease, diabetes, metabolic disease or inflammatory bowel disease (self-reported);
• Currently smoking (>1 cigarette/day);
• Drug abuse or extensive alcohol intake;
• Exposure to iodine-containing X-ray or computed tomography contrast agents during the past 6 months;
• Adenomatous goiter, dermatitis, anti-C1q-vasculitis.

Infants

Inclusion criteria

• Full term (38-42 weeks);
• Birthweight ≥2.5 kg;
• Exclusively breastfed;
• Age 0-10 weeks at recruitment.

Exclusion criteria

• Age >6 months;
• TSH >10 mIU/L at neonatal screening at 2-5 days after birth (i.e. infants not requested to attend recall assessment);
• Diagnosed or suspected colic.