Introduction
It has recently been suggested that the optimum intake of iodine during pregnancy and lactation should be higher than the amount currently recommended by the WHO, the UNICEF and the ICCIDDReference Delange1, 2. The rationale for this is the increased requirement for thyroxine by the mother, the transfer of thyroxine and iodide from the mother to her foetus and the increased renal clearance of iodideReference Smyth3. Based on an extensive review of the literature, Delange has suggested that the iodine intake during pregnancy should be increased from 200 to 250–300 μg day− 1, and during lactation from 200 to 225–350 μg day− 1.
Neonatal screening for congenital hypothyroidism is not widely used as a monitoring tool to assess the iodine nutrition of populations. We have demonstrated that the concentration of thyroid-stimulating hormone (TSH) in neonates can be used as an indicator of iodine nutritionReference Rajatanavin, Unachak, Winichakoon, Chailurkit, Vilasdecanon, Tananchai and Srinawat4. It is particularly useful when programmes for monitoring, such as the one operating in Thailand, place an emphasis on the iodine status of schoolchildren. However, it is possible that the goitre rate in schoolchildren may not reflect the iodine status of other members of the population, especially neonates. For example, Table 1 shows the change in goitre rate over a period of 4 years among school children in five districts of Thailand in which an iodine supplementation programme was implemented and is compared with the change in the same districts in the odds ratio among neonates of having a TSH concentration greater than neonates born in Bangkok. The changes were not all in the same direction.
The aim of this paper is to present data from Thailand on the relationship between the concentration of TSH in whole blood or serum from neonates and the concentration of iodine in their mother's urine collected at birth to contribute to the contention that the recommended iodine intake during pregnancy should be increased. The paper also presents experience in Thailand of using the neonatal TSH concentration as an indicator of the iodine nutrition of neonates.
Methods
The data were provided by the current programmes of neonatal screening in Bangkok, the capital of Thailand, and from rural areas.
The screening programme for congenital hypothyroidism at Ramathibodi Hospital, Bangkok, which has been in operation since 1993, measures the concentration of TSH in cord serum using an electro-chemiluminescence immunoassay kit from Roche Diagnostics (Mannheim, Germany). The sensitivity of the TSH assay is 0.005 mIU l− 1.
The concentration of TSH in dried whole blood collected on filter paper in rural hospitals in Thailand is measured by an immunoradiometric assay using kits manufactured in Thailand by the Department of Science, Ministry of Public Health, Bangkok. The sensitivity of the assay for TSH is 0.2–0.9 mIU l− 1.
The concentration of iodine in urine samples collected from mothers was measured at the endocrine laboratory, Ramathibodi Hospital using method A, the Sandell–Kolthoff reaction, as recommended by the ICCIDDReference Dunn, Crutchfield, Gute and Dunn5.
Results
Neonatal cord serum TSH concentration
A total of 5144 cord serum samples were collected in 2003 at Ramathibodi Hospital, Bangkok and the TSH concentration was measured. Table 2 shows the reference intervals for neonatal serum TSH concentration using centile ranges for the assessment of univariate reference intervalsReference Koduah, Iles and Nix6.
* 95th percentile.
Neonatal serum TSH and maternal urinary iodine concentrations
In 2000, assays were performed on cord blood and urine samples collected from 203 pairs of infants and their mothers at Ramathibodi Hospital, Bangkok. Figure 1 shows the relationship between the concentration of iodine in the urine of mothers and the concentration of TSH in cord serum.
According to the WHO, the UNICEF and the ICCIDD7, a population has a normal iodine status if < 3% of neonatal whole blood samples have a TSH concentration of >5 mIU l− 1, a value that is equivalent to a serum TSH concentration of 11.2 mIU l− 1. Figure 2 shows the percentage of serum samples from neonates which had a TSH concentration greater than this second value according to the concentration of iodine in the urine of paired samples from mothers.
In total, 31% of serum samples from neonates had a TSH concentration >11.2 mIU l− 1, which was in the range of a moderate iodine deficiency according to the WHO/UNICEF/ICCIDD criteria7. However, the median urinary iodine concentration of mothers of 85 μg l− 1 fell within the range of a mild iodine deficiency2, 7.
Whole blood neonatal TSH concentration
In contrast to the screening programme at Ramathibodi Hospital, the national neonatal screening programme organised by the Ministry of Public Health, which commenced in 1995, uses dried blood spots collected from a heel prick taken 3 days after birth; the assay for TSH therefore uses whole blood, not cord serum.
Figure 3 shows a scatter plot of the TSH and the iodine concentrations on paired samples of blood and urine collected in 2002–03 from 1182 infants and their mothers in six rural provinces. There was no significant correlation between values.
Figure 4 shows that, in contrast to the data presented in Fig. 2, there was no correlation between the concentration of iodine in the urine of mothers and the concentration of TSH in cord serum.
Maternal urinary iodine concentrations in Thailand
Periodic monitoring of the prophylactic iodine programme in Thailand started in 2000, when the concentration of iodine in mother's urine was measured at delivery in 15 provinces each year. The provinces were chosen by random cluster sampling from the whole of Thailand. Table 3 shows the median concentration of urinary iodine.
ND*, not done.
Using a centile chart to assess univariate reference intervalsReference Koduah, Iles and Nix6, the median urinary iodine concentration of samples collected from 1182 mothers in 2002–03 was 103 μg l− 1. Applying this concentration to the data collected on the serum TSH concentration of 203 neonates born at Ramathibodi Hospital in 2000, the odds ratio of having a serum TSH concentration greater than the 95th percentile within the same data set (19.6 mIU l− 1) was 3.2 (95% CI 1.3, 7.8), if the mother's urinary iodine concentration was < 103 μg l− 1. This is shown in Table 4.
In addition, when the odds ratios of having neonatal TSH concentrations >19.6 mIU l− 1 were calculated for each centile of the distribution of maternal urinary iodine concentrations, a dose-response relationship was observed (data not shown). However, it was not a significant difference, probably due to the small sample size.
Maternal urinary iodine and neonatal serum TSH concentrations
Samples of urine from mothers and serum from neonates have been collected at birth on two occasions, 5 years apart, in Dansai district, Loie Province in northern Thailand. It was found that, although the median urinary iodine concentration was 249 μg l− 1 in 1998 and 106 μg l− 1 in 2003, the median neonatal serum TSH concentration at each survey was not different from that of neonates born in Bangkok (see Table 5).
Discussion
According to criteria proposed by the WHO, the UNICEF and the ICCIDD2 to assess iodine nutrition, the urinary iodine concentration of mothers in rural Thailand is adequate, with a median of 103 μg l− 1. However, in 2000, the median urinary iodine concentration of mothers in Bangkok was 85 μg l− 1, which falls in the range of a mild iodine deficiency. The data indicate that a concentration of iodine in the urine of a rural mother of < 103 μg l− 1 was associated with a five-fold greater chance of her neonate having a serum TSH concentration higher than neonates born in Bangkok.
The data shown in Table 5 from Dansai district and Bangkok indicate that there was no substantial difference in the serum TSH concentration of neonates even though the urinary iodine concentration of mothers varied widely from a median of 85 to 249 μg l− 1. These data do not seem to support the contention that the iodine intake in pregnancy should increase to 250 μg l− 1 in order to give a corresponding urinary iodine concentration of 150 μg l− 1.
The data presented in Fig. 3 show that the concentration of TSH in whole blood collected on filter paper from neonates was not sensitive enough to be used as a monitoring tool for iodine nutrition in the neonates, as there was no relationship with the concentration of iodine in the urine of the children's mothers. This was in contrast to the concentration of TSH in serum collected from cord blood. Figure 1 shows a significant relationship between the concentration of TSH in serum from neonates and the concentration of iodine in urine from mothers. In addition, a discrepancy was observed in the same population between two indices of iodine. The proportion of whole blood samples collected from neonates in Bangkok that had a TSH concentration >5 mIU l− 1 suggests that Bangkok is an area of moderate iodine deficiency, whereas the median urinary iodine concentration of the mothers of the same children suggested that it was an area of mild iodine deficiency. These findings suggest that the use of the concentration of TSH in whole blood from neonates should be reassessed as an index of iodine nutrition.
Conclusion
Several conclusions can be drawn from the data from Thailand.
1. Neonatal TSH screening using whole blood collected from a heel prick at 3 days of age is not sensitive enough to assess the iodine nutrition of neonates.
2. Neonatal TSH screening using cord sera can be used to assess iodine nutrition in neonates.
3. The optimum median maternal urinary iodine concentration in Thailand appears to be 103 μg l− 1.
4. The criteria proposed by the WHO, the UNICEF and the ICCIDD to assess iodine nutrition using data on neonatal TSH concentrations should be reassessed.
5. Neonatal TSH screening can be effectively performed by collecting cord serum in district hospitals in Thailand.
Acknowledgement
This work was supported by the Nopparat-Ratanakosin Foundation.