Skip to main content

Iodine deficiency in Danish pregnant women

Stine Linding Andersen1, Louise Kolding Sørensen1, Anne Krejbjerg1, Margrethe Møller2 & Peter Laurberg1

1. jul. 2013
15 min.

Faktaboks

Fakta

Adequate maternal iodine intake is required for thyroid hormone synthesis, and thyroid hormones, in turn, are essential for foetal growth and development, especially for early brain development [1, 2]. Maternal iodine requirements increase during pregnancy [3]. In their guidelines, the World Health Organization (WHO), the United Nations Children’s Fund (UNICEF) and the International Council for the Control of Iodine Deficiency Disorders (ICCIDD) define an adequate intake of iodine during pregnancy as 250 µg/day, which corresponds to a median urinary iodine concentration of 150-249 µg/l in a population of pregnant women [4]. By contrast, a median urinary iodine concentration in the 100-199 µg/l range is considered a sufficient iodine intake in the non-pregnant state [4].

Iodine intake may stem from drinking water and from dietary iodine contents, from food fortified with iodine (typically salt), or from intake of iodine-containing supplements [5]. Denmark was previously iodine-deficient with regional differences caused by regional variation in the levels of iodine in the drinking water: moderate iodine deficiency was observed in Western Denmark and mild iodine deficiency in Eastern Denmark [6, 7]. A mandatory iodine fortification of salt was introduced in the year 2000 [8], and this programme had increased urinary iodine concentration to the lower threshold of the recommended level in the Danish population in 2004-2005 [9]. On the other hand, a recent study performed in 2008-2010 found that urinary iodine concentration had again decreased in the Danish population [10].

In studies of Danish pregnant women before the year 2000, pregnant women with no intake of iodine-containing supplements had a low urinary iodine concentration corresponding to moderate iodine deficiency, increased thyroid volume and high serum thyroglobulin (Tg), and their serum thyroid-stimulating hormone (TSH) levels increased during pregnancy [11, 12]. In a study conducted in five Danish cities [13], 36% of the pregnant women reported an intake of iodine-containing supplements when asked upon arrival for delivery. No previous study has specifically addressed the iodine intake and the use of iodine supplements during pregnancy in Denmark after the introduction of iodine fortification of salt.

The aim of the present study was to investigate if pregnant women living in an area of Denmark with previously moderate iodine deficiency took iodine-containing supplements, to examine predictors of iodine supplement intake and to evaluate iodine intake during pregnancy by measurement of urinary iodine concentration.

MATERIAL AND METHODS

Study population and design

We conducted a cross-sectional study between 13 June and 10 August 2012 in an area of Denmark with previously moderate iodine deficiency [8]. We consecutively recruited healthy, pregnant women referred to Aalborg University Hospital for obstetric ultrasound as part of the antenatal investigation programme [14]. Two of the pregnant women were excluded (Figure 1), because they had a diagnosis of hypothyroidism and took levothyroxin replacement therapy at the time of enrollment. None of the remaining women had a history of thyroid disease verified by a doctor.

After providing informed consent, participants were asked to fill out a questionnaire including obstetric history, socio-demographics and smoking habits, and to list detailed information on any medication and intake of vitamin and/or mineral supplements. Information about dietary supplements was verified by interview; and at the time of enrollment, the women were asked to provide a spot urine sample. The time of sampling was between 8 am and 1 pm, except for two women who had sampled the urine at home the same day prior to inclusion into the study (at 6:00 a.m. and 7:10 a.m., respectively). The study protocol was approved by the local ethics committee.

Laboratory procedures

Urine samples were stored at –20 °C until measurement of urinary iodine concentration in runs during the time of study inclusion. Urinary iodine concentrations (µg/l) were determined by the cerium/arsenite method after alkaline ashing, as previously described [15]. The analytical sensitivity was 2 µg/l. The iodine laboratory was certified by the U.S. Centers for Disease Control and Prevention’s EQUIP Programme. Urinary creatinine concentrations (µmol/l) were measured immediately after urinary sampling on a Cobas 8,000 system. The equipment was calibrated according to the manufacturer’s instructions, and external standards were included.

Statistical analyses

Characteristics of the pregnant women according to intake of iodine containing supplements were compared using Fisher’s exact test, and predictors of iodine supplement intake were examined in multivariate logistic regression. Urinary iodine excretion was expressed as spot urine concentration (µg iodine/l), iodine/creatinine ratio (µg iodine/g creatinine) and estimated 24-h iodine excretion (µg iodine/24 h) calculated from the mean 24-h urinary creatinine excretion (1.09 g creatinine/24 h) previously measured in Danish pregnant women [11]. Urinary iodine concentrations showed a skewed distribution, and the results were expressed as medians with 25th and 75th percentiles. Non-parametric tests were used to compare urinary iodine excretion stratified by iodine supplement intake (Mann-Whitney test) and by gestational week (Kruskal-Wallis test). Statistical analyses were performed using Stata 11 (StataCorp, College Station, TX, USA), and a 5% level of significance was chosen.

Trial registration: not relevant.

RESULTS

Study population

A total of 245 women were included in the final study population (Figure 1), corresponding to 73.8% of the women invited to participate upon arrival at the Obstetric Department. The median age at the time of enrollment was 30.5 years (range 18.4-41.2 years), the median gestational age was week 20 (range week 10-37), and approximately half of the women were expecting their first child (Table 1).

Use of iodine-containing supplements

Nearly all of the pregnant women used dietary supplements (95.9%) at the time of enrollment, and 206 women (84.1%) reported a regular intake of iodine-containing supplements, whereas 39 women (15.9%) were taking either no vitamin and/or mineral supplements (n = 10) or vitamin and/or mineral supplements not containing iodine (n = 29).

The iodine containing supplements typically contained 175 µg iodine/day (81.1%); less often 150 µg iodine per day (17.0%); and a few women (1.9%) took iodine-containing supplements different from the recommended dose (87.5 and 375 µg iodine per day, respectively). The intake of the iodine supplement was often initiated during pregnancy (75.2%) at median gestational week 6 (range week 1-32), but some of the pregnant women had initiated iodine supplement intake in the year preceding the pregnancy (16.5%) at median 10 weeks before conception (range 2-52 weeks), or more than a year before conception (8.3%). Among iodine supplement users, 38 women reported intake of another iodine-containing supplement before their current supplement, and eight of the current non-users had stopped iodine supplement intake during the pregnancy before study inclusion.

Predictors of iodine supplement intake

In the univariate analyses, only maternal age significantly differed according to intake of iodine-containing supplements (Table 1). In the multivariate analyses including all variables listed in Table 1 as categoricals, lower maternal age (≤ 35 years, p = 0.001) and maternal education, i.e. qualifying for a profession (vocational or higher education versus primary/secondary school only, p = 0.039), were significant predictors of maternal intake of iodine-containing supplements. On the other hand, the total number of years of education did not significantly predict iodine supplement intake.

Urinary iodine excretion

The overall median urinary iodine concentration (Figure 2) was just within the recommended range for the non-pregnant state (100-199 µg/l), but below the recommended level during pregnancy (150-249 µg/l). The median urinary iodine concentration was higher in the group of pregnant women reporting an intake of iodine-containing supplements (Table 2) and below the lower recommended level for even the non-pregnant state in the group with no iodine supplement intake. The findings were similar when urinary iodine excretion was expressed as an iodine/creatinine ratio and estimated 24-h iodine excretion (Table 2). There was no significant difference in urinary iodine concentrations among iodine supplement users when stratified by gestational age; median urinary iodine week 10-15 (n = 73): 107 µg/l (25th-75th percentile: 66-197 µg/l), week 19-21 (n = 103): 102 µg/l (65-170 µg/l), week 28-37 (n = 23): 140 µg/l (91-252 µg/l), p = 0.06.

DISCUSSION

Principal findings

More than ten years after the introduction of mandatory iodine fortification of salt in Denmark, pregnant women living in an area previously characterized by moderate iodine deficiency had urinary iodine concentrations below the level recommended during pregnancy. As expected, pregnant women who took iodine-containing supplements had a higher median urinary iodine concentration than pregnant women with no intake of iodine supplements, and the median urinary iodine concentration was within the recommended level for the non-pregnant state in this group. The frequency of iodine supplement intake during pregnancy in Denmark had increased steeply compared with a previous study and was significantly predicted by maternal age and education. However, a subgroup of women still took no iodine supplements during pregnancy, and in this group the median urinary iodine concentration was considerably below the level recommended even for the non-pregnant state.

Iodine supplement use in Danish pregnant women

In a previous study [13] conducted in Denmark before the year 2000, nearly all pregnant women reported taking vitamin and/or mineral supplements (93.4%) when asked upon arrival for delivery, but only 36% reported an intake of iodine-containing supplements (150 µg iodine/day). Thus, the frequency of dietary supplement during pregnancy before the year 2000 was comparable to that observed in our study population (95.9%), but the use of iodine-containing supplements had increased considerably. The reasons for this increase are not completely clear. There are no current official recommendations on the intake of iodine-containing supplements during pregnancy in Denmark. Iodine supplement was obtained by intake of a multivitamin pill, and official recommendations on the intake of folic acid, vitamin D and iron during pregnancy do exist [14]. Thus, it seems likely that iodine supplement intake is incidental to other recommendations during pregnancy in Denmark. The gestational age of the women included in our study ranged 10-37 weeks. No previous study specifically addressed the use of iodine supplements in early pregnancy in Denmark.

Urinary iodine excretion in Danish pregnant women

Several of the previous studies on urinary iodine excretion in Danish pregnant women examined pregnant women living in Western Denmark, an area where moderate iodine deficiency was previously observed. In the studies by Pedersen et al [11, 12], the median urinary iodine concentration was low (approximately 50 and 40 µg/l in gestational weeks 17 and 37, respectively) and serum Tg was high in pregnant women with no intake of iodine-containing supplements. Furthermore, thyroid volume as well as TSH tended to increase during pregnancy. These changes were ameliorated by iodine supplement intake, and urinary iodine increased to 106 µg/l in late pregnancy after iodine supplement intake during the pregnancy [12], which was also shown in a study by Nohr et al [16].

Thus, our results indicate that the median urinary iodine concentration has increased in pregnant women with no iodine supplement intake, which corresponds to the general increase in the median urinary iodine concentration after the introduction of iodine fortification of salt in Denmark [9]. However, pregnant women with no intake of iodine-containing supplements still have urinary iodine concentrations substantially below the recommended level for pregnancy [4] and even below the recommended range for the non-pregnant state [4].

In the Danish population, the iodine fortification of salt increased urinary iodine to the lower threshold within the recommended range, but results from the DanThyr study (The Danish investigation on iodine intake and thyroid disease) [8] recently showed a modest decrease in urinary iodine concentration [10]. The present study confirms that the current level of iodization of salt in Denmark is insufficient, i.e. that it will not produce a urinary iodine concentration within the recommended range.

Strengths and limitations

Urinary iodine excretion is a recommended marker of recent iodine intake [4], and spot urine samples can be used in population studies [17]. The relatively large number of pregnant women included in our study increased the precision of the estimated iodine excretion [18]. However, the number of pregnant women in the stratified analyses was limited in some groups.

Our study only included women referred to Aalborg University Hospital, and we cannot exclude that differences in the use of dietary supplements during pregnancy may exist across Denmark. In a previous study performed in five Danish cities, the frequency of iodine supplement intake during pregnancy ranged from 21% to 50% when stratified by city [13]. The level of iodine in drinking water and urinary iodine excretion in the area investigated in our study was previously reported to correspond to the level observed in most parts of Western Denmark (i.e. west of the Great Belt) [6, 7].

We consecutively recruited healthy, pregnant women and the rate of participation was high. However, we cannot exclude some degree of selection bias.

CONCLUSION

Danish pregnant women living in an area previously characterized by moderate iodine deficiency still have urinary iodine concentrations below the recommended level for the pregnant state after the introduction of the mandatory iodine fortification of salt in Denmark. Pregnant women with no intake of iodine-containing supplements are at particular risk of insufficient iodine intake. Results indicate a need for more attention among healthcare professionals to ensure sufficient iodine status in Danish pregnant women. Intake of iodine-containing supplements during pregnancy in Denmark should be officially recommended, and our results may indicate a need for a modest increase in the level of iodine added to salt in Denmark.

Correspondence: Stine Linding Andersen, Endokrinologisk Afdeling, Aalborg Universitetshospital, Sdr. Skovvej 15, 9000 Aalborg, Denmark. E-mail: stine.a@rn.dk

Accepted: 22 April 2013

Conflicts of interest:Disclosure forms provided by the authors are available with the full text of this article at www.danmedj.dk

Referencer

  1. Delange F. The role of iodine in brain development. Proc Nutr Soc 2000;59:75-9.

  2. de Escobar GM, Obregon MJ, del Rey FE. Maternal thyroid hormones early in pregnancy and fetal brain development. Best Pract Res Clin Endocrinol Metab 2004;18:225-48.

  3. Yarrington C, Pearce EN. Iodine and pregnancy. J Thyroid Res 2011;2011:934104.

  4. WHO/UNICEF/ICCIDD. Assessment of iodine deficiency disorders and monitoring their elimination. A guide for programme managers. Geneva, Switzerland: World Health Organization, 2007:1-99.

  5. Laurberg P, Andersen S, Bjarnadottir RI et al. Evaluating iodine deficiency in pregnant women and young infants ‒ complex physiology with a risk of misinterpretation. Public Health Nutr 2007;10:1547-52.

  6. Pedersen KM, Nohr SB, Laurberg P. Iodine intake in Denmark. Ugeskr Læger 1997;159:2201-6.

  7. Pedersen KM, Laurberg P, Nohr S et al. Iodine in drinking water varies by more than 100-fold in Denmark. Importance for iodine content of infant formulas. Eur J Endocrinol 1999;140:400-3.

  8. Laurberg P, Jørgensen T, Ovesen L et al. Iodine fortification of salt and thyroid disease in Denmark. Ugeskr Læger 2011;173:3264-70.

  9. Rasmussen LB, Carle A, Jorgensen T et al. Iodine intake before and after mandatory iodization in Denmark: results from the Danish Investigation of Iodine Intake and Thyroid Diseases (DanThyr) study. Br J Nutr 2008;100:166-73.

  10. Bjergved L, Jorgensen T, Perrild H et al. Predictors of change in serum TSH after iodine fortification: an 11-year follow-up to the DanThyr study. J Clin Endocrinol Metab 2012;97:4022-9.

  11. Pedersen KM, Borlum KG, Knudsen PR et al. Urinary iodine excretion is low and serum thyroglobulin high in pregnant women in parts of Denmark. Acta Obstet Gynecol Scand 1988;67:413-6.

  12. Pedersen KM, Laurberg P, Iversen E et al. Amelioration of some pregnancy-associated variations in thyroid function by iodine supplementation. J Clin Endocrinol Metab 1993;77:1078-83.

  13. Nohr SB, Laurberg P, Borlum KG et al. Iodine deficiency in pregnancy in Denmark. Regional variations and frequency of individual iodine supplementation. Acta Obstet Gynecol Scand 1993;72:350-3.

  14. The Danish Health and Medicines Authority. Anbefalinger for svangreomsorgen. Copenhagen: Danish Health and Medicines Authority, 2009:84-5.

  15. Laurberg P. Thyroxine and 3,5,3‘-triiodothyronine content of thyroglobulin in thyroid needle aspirates in hyperthyroidism and hypothyroidism. J Clin Endocrinol Metab 1987;64:969-74.

  16. Nohr SB, Jorgensen A, Pedersen KM et al. Postpartum thyroid dysfunction in pregnant thyroid peroxidase antibody-positive women living in an area with mild to moderate iodine deficiency: is iodine supplementation safe? J Clin Endocrinol Metab 2000;85:3191-8.

  17. Vejbjerg P, Knudsen N, Perrild H et al. Estimation of iodine intake from various urinary iodine measurements in population studies. Thyroid 2009;19:1281-6.

  18. Andersen S, Karmisholt J, Pedersen KM et al. Reliability of studies of iodine intake and recommendations for number of samples in groups and in individuals. Br J Nutr 2008;99:813-8.