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Iodine status of pregnant women in a population changing from high to lower fish and milk consumption

Published online by Cambridge University Press:  22 May 2012

Ingibjorg Gunnarsdottir*
Affiliation:
Unit for Nutrition Research, University of Iceland and Landspitali-University Hospital, Reykjavik, Iceland Faculty of Food Science and Nutrition, University of Iceland, Eiriksgata 29, 101 Reykjavik, Iceland
Anita G Gustavsdottir
Affiliation:
Unit for Nutrition Research, University of Iceland and Landspitali-University Hospital, Reykjavik, Iceland
Laufey Steingrimsdottir
Affiliation:
Unit for Nutrition Research, University of Iceland and Landspitali-University Hospital, Reykjavik, Iceland Faculty of Food Science and Nutrition, University of Iceland, Eiriksgata 29, 101 Reykjavik, Iceland
Amund Maage
Affiliation:
National Institute of Nutrition and Seafood Reasearch (NIFES), Bergen, Norway
Ari J Johannesson
Affiliation:
Department of Endocrinology and Metabolism, Landspitali-University Hospital, Reykjavik, Iceland
Inga Thorsdottir
Affiliation:
Unit for Nutrition Research, University of Iceland and Landspitali-University Hospital, Reykjavik, Iceland Faculty of Food Science and Nutrition, University of Iceland, Eiriksgata 29, 101 Reykjavik, Iceland
*
*Corresponding author: Email [email protected]
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Abstract

Objectives

Pregnancy is one of the most critical periods for iodine deficiency. The aim of the present study was to assess the iodine status and dietary intake of pregnant women in a population changing from high to lower consumption of milk and fish.

Design

Cross-sectional observational study. Urine samples were collected for measuring urinary iodine concentration (UIC) and creatinine, and blood samples for measuring serum thyroid-stimulating hormone (TSH). Frequency of consumption of selected food and beverages was obtained through a semi-quantitative validated FFQ. The difference in the distribution of UIC, ratio of iodine to creatinine (I:Cr) and TSH between groups following recommendations on fish and dairy product intake or not (fish ≥2 times/week as a main meal, diary products ≥2 portions/d) was assessed.

Setting

Primary Health Care of the Capital Area, Reykjavik, Iceland.

Subjects

Randomly selected pregnant women (19–43 years old, n 162).

Results

The median UIC was 180 μg/l, I:Cr 173 μg/g and TSH 1·5 mmol/l. Women who did not consume fish ≥2 times/week and also did not consume dairy products in line with the recommended intake level of ≥2 portions/d had median UIC of 160 μg/l (I:Cr 149 μg/g) compared with 220 μg/l (I:Cr 190 μg/g) in the group following both the recommendations for fish and those for dairy products. Use of dietary supplements in the two groups was similar.

Conclusions

Iodine status in the population studied was within the optimal range (150–249 μg/d) defined by the WHO.

Type
Nutrition and health
Copyright
Copyright © The Authors 2012

Iodine deficiency is considered one of the most common nutritional disorders in the world and the world's largest single cause of preventable brain damage(Reference Delange, Benoist and Pretell1Reference Zimmerman3). All European countries except Iceland have experienced this health and socio-economic threat to a greater or lesser extent(4). The Icelandic population has in the past been known for its high iodine status, based on studies from 1939, 1988 and 1998(Reference Sigurjonsson5Reference Laurberg, Pedersen and Hreidarsson7). The good iodine status observed in these studies was suggested to be due to high fish consumption and abundant milk, both important dietary sources of iodine(Reference Reykdal, Thorlacius and Audunsson8Reference Haldimann, Alt and Blanc10). Dietary surveys in Iceland have shown that fish and milk consumption has decreased considerably during recent decades, with possible consequences for the iodine status of the population(Reference Steingrimsdottir, Thorgeirsdottir and Olafsdottir11, Reference Thorgeirsdottir, Valgeirsdottir and Gunnarsdottir12). Furthermore, the iodine content of milk and dairy products has decreased during the last decades(Reference Sigurdsson and Franzson6, Reference Reykdal, Thorlacius and Audunsson8, 13, Reference Reykdal, Hilmarsson and Auðunsson14). Iodized table salt is widely available in Europe, but not in Iceland.

The aim of the present study was to assess the iodine status and dietary intake of pregnant women in a population changing from high to lower consumption of milk and fish. Iodine status has not been assessed previously among pregnant women in Iceland but WHO urges governments to monitor the iodine status of vulnerable groups, including pregnant women(15).

Materials and methods

Sample

The data were collected between November 2007 and February 2009 at the Primary Health Care of the Capital Area, at four different clinics in the capital area providing prenatal care. All pregnant women who met the inclusion criteria were invited to participate in the study. The inclusion criteria were that the woman was able to understand Icelandic, lived in the capital area and was in her second or third trimester of pregnancy. The health-care clinics were selected based on location, aimed to represent the population of pregnant women in the capital area. Five per cent of the original sample (n 320) did not fulfil the participation criteria, 15 % could not be reached by telephone and 3 % had already given birth when contacted, had a miscarriage or had moved abroad, leaving 245 women. Of these 245 women, fifty-three declined participation and thirty did not show up at the clinic, leaving 162 women. The main reason for not participating was lack of time or lack of interest. The study was approved by The National Bioethics Committee (VSNb2007040006) and The Icelandic Data Protection Commission (2007040320). Written consent was obtained from the participants.

Determination of iodine status

Urine spot samples were collected for determination of iodine and creatinine. Samples were collected in vials between 09.00 and 15.00 hours. The samples used for measurement of urinary iodine concentration (UIC) were kept frozen at −80°C at Landspitali-University Hospital in Reykjavik, Iceland, until all samples had been collected. The samples were then sent by courier in dry ice packages to the National Institute of Nutrition and Seafood Research (NIFES) in Bergen, Norway. An Agilent quadrupole inductively coupled plasma–mass spectrometer ICP-MS 7500c (Yokogawa Analytical System Inc., Tokyo, Japan) was used as an iodine-specific detector for urinary determination. Optimization and operating conditions of the instrument are described elsewhere(Reference Dahl, Johansson and Julshamn9, Reference Julshamn, Dahl and Eckhoff16, Reference Dahl, Opsahl and Meltzer17). The uncertainty in the method is based on both use of a control chart (reproducibility) and by participation in round robins (correctness) and set at ±15 %. Data were collected using the Agilent Chemstation ICP-MS chromatographic software(Reference Dahl, Johansson and Julshamn9, Reference Julshamn, Dahl and Eckhoff16, Reference Dahl, Opsahl and Meltzer17). Certified reference material (Seronorm™ Trace Elements; Nycomed, Oslo, Norway) of iodine in human urine was included in each analytical series of twenty-five samples in order to control for the systematic errors of the analytical method.

Creatinine was measured with the VITROS CREA Slide method, using the VITROS CREA Slides and the VITROS Chemistry Products Calibrator Kit 1 (National Institute of Standards and Technology, Gaithersburg, MD, USA) on a VITROS Chemistry System. The VITROS CREA Slide is a multilayered analytical element, coated on a polyester support. Measurements were carried out at the Department of Clinical Biochemistry, Landspitali-University Hospital in Reykjavik, Iceland.

A blood sample was collected to measure serum thyroid-stimulating hormone (TSH). TSH was measured by electrochemiluminescence immunoasssy, using the MODULAR ANALYTICS E170 platform from Roche (Indianapolis, IN, USA), at the Department of Clinical Biochemistry, Landspitali-University Hospital in Reykjavik, Iceland.

According to WHO guidelines, median UIC in pregnant women should range between 150 and 249 μg/l(18). The use of the ratio μg iodine/g creatinine (I:Cr) is not recommended by WHO. However, it has been used in the past for adjusting dilution in spot samples. As urinary creatinine was analysed in the present study we decided to present our data as both median UIC (μg/l) and I:Cr (μg/g).

FFQ

Information on the average frequency of consumption of selected foods and beverages was obtained through a semi-quantitative validated FFQ, filled in during a personal interview by a trained research person. The participants chose from eleven possible responses that ranged from ‘never’ to ‘≥5 times per day’(Reference Thorsdottir, Gunnarsdottir and Steingrimsdottir19, Reference Olafsdottir, Thorsdottir and Gunnarsdottir20). The FFQ provides information on the consumption of 130 different food items and use of dietary supplements, designed to reflect food intake over the previous 3 months. According to previous national dietary surveys in Iceland, fish, milk and cheese are found to contribute more than 75 % of the total iodine in the diet(Reference Steingrimsdottir, Thorgeirsdottir and Olafsdottir11, Reference Thorgeirsdottir, Valgeirsdottir and Gunnarsdottir12). According to regulations from year 2007 (The Icelandic Food and Veterinary Authority), manufacturers of food and companies importing food should report use of any vitamin- and mineral-supplemented food, including iodized salt. In the case of iodized salt, no products have been reported to the authorities.

We assessed iodine status in groups according to adherence to public recommendations on fish and dairy product consumption(21, 22). Expectant mothers are advised, as are everyone else, to eat fish at least twice weekly. They are encouraged to enjoy common types of fish found in the waters surrounding Iceland, such as haddock, cod, flounder, catfish, monkfish (anglerfish), trout and salmon, as often as possible(22). Consumption of large predatory fish and toothed whales are discouraged due to possible contamination. Two glasses, bowls or cans of milk or dairy products daily are recommended for adults.

The FFQ was not designed to provide detailed information on iodine content of dietary supplements, and the participants were unable to provide us with brand names of the supplements. Two out of eleven dietary supplements listed in the FFQ might contain iodine (multivitamin and mineral supplements). Out of sixty-two multivitamin and mineral supplements on the Icelandic market, twenty-three contain iodine (information from The Icelandic Food and Veterinary Authority). The average iodine content per tablet/portion is 119 μg. The number of participants using supplements that might contain iodine is reported.

Anthropometric measures and lifestyle questioning

Participants’ weight was measured using a digital weighing scale (model 708; Seca, Hamburg, Germany) to the nearest 100 g with light clothing and without shoes. Standing height was measured using a stadiometer (model 708; Seca) to the nearest 1 mm. Participants were asked for their pre-pregnancy weight which was used to calculate BMI (kg/m2). Pre-pregnancy underweight was defined as BMI < 18·50 kg/m2, normal weight as BMI = 18·50–24·99 kg/m2, overweight as BMI ≥ 25·00–29·99 kg/m2 and obesity as BMI ≥ 30·00 kg/m2. Participants were also asked about their smoking habits and parity. Participants’ characteristics are given in Table 1.

Table 1 Characteristics of the participants: pregnant women aged 19–43 years (n 162), Reykjavik, Iceland, November 2007 to February 2009

Data analysis

Analysis was carried out using the IBM SPSS Statistics 20·0 statistical software package (IBM, Armonk, NY, USA). The results are presented as mean, standard deviation, median, 20th and 80th percentile. The difference in the distribution of UIC, I:Cr and serum TSH between groups following recommendations on fish and dairy product intake or not (fish ≥2 times/week as a main meal; milk and cheese ≥2 portions/d) was assessed using the non-parametric Mann–Whitney U test. The level of significance was taken as P < 0·05.

Results

Table 2 shows the iodine status of the population studied. Iodine status was not associated with smoking, parity or pre-pregnancy weight.

Table 2 Mean (sd), median, 20th and 80th percentiles of urinary iodine concentration (UIC), ratio of iodine to creatinine (I:Cr) and serum thyroid-stimulating hormone (TSH)Footnote * among the study participants: pregnant women aged 19–43 years (n 162), Reykjavik, Iceland, November 2007 to February 2009

* Analysis of urinary creatinine was missing for four women and thirty refused to have their blood drawn for analysis of TSH.

The average frequency of fish consumption was 1·6 times/week. Fish was consumed at least twice weekly by 54 % of the participants, while 25 % recorded consumption as less than once weekly. Haddock was recorded as the most commonly consumed fish species by 83 % of the participants. The average frequency of milk and dairy product consumption (including cheese) was 2·3 portions/d. About 60 % of participants reached the recommended intake of two portions daily. Use of dietary supplements that might have contained iodine was recorded by 66 % of the participants, of whom 52 % recorded daily use.

Median UIC, I:Cr and serum TSH was assessed in groups according to adherence to recommendations on fish and dairy intake (Table 3). Serum TSH was of borderline significance higher in those who consumed fish as a main meal less <2 times/week compared with those consuming fish in line with the recommendations (P = 0·082). In those who consumed milk or other dairy products in line with recommendations, I:Cr was significantly higher (P = 0·001) while UIC was of borderline significance higher (P = 0·074) compared with those who consumed <2 portions/d. Women who did not consume fish ≥2 times/week as a main meal and also did not consume dairy products in line with the recommended intake level of ≥2 portions/d had median UIC of 160 μg/l (I:Cr 149 μg/g) compared with 220 μg/l (I:Cr 190 μg/g) in the group following both the recommendations for fish and those for dairy products.

Table 3 Median urinary iodine concentration (UIC), ratio of iodine to creatinine (I:Cr) and serum thyroid-stimulating hormone (TSH) according to adherence to recommendations on fish and dairy intakeFootnote * among the study participants: pregnant women aged 19–43 years (n 162), Reykjavik, Iceland, November 2007 to February 2009

* According to the Icelandic food-based dietary guidelines(21) and guidelines to pregnant women(22). Fish as a main meal is recommended at least twice weekly. Consumption of two portions of milk or other dairy products daily is recommended (one portion equals 250 ml milk or 25 g cheese).

Number and percentage of women recording daily use of dietary supplements that might contain iodine.

Discussion

The results from the present study show that the iodine status of Icelandic pregnant women is in accordance with recommendations from WHO(15, 18). For many decades Iceland has been known for its high iodine status(Reference Sigurjonsson5Reference Laurberg, Pedersen and Hreidarsson7, Reference Sigurjonsson23). With the sharp decreases in milk and fish intakes during past decades, worries about iodine status in the population have increased(Reference Steingrimsdottir, Thorgeirsdottir and Olafsdottir11, Reference Thorgeirsdottir, Valgeirsdottir and Gunnarsdottir12, Reference Gunnarsdottir, Gunnarsdottir and Steingrimsdottir24).

Intake of dairy products and fish has frequently been reported to be related to iodine status(Reference Brantsæter, Haugen and Julshamn25Reference Girelli, Coin and Mian27). Although the scientific background for recommending consumption of fish at least twice weekly as a main meal and two portions of milk or other dairy products daily is rather related to cardiovascular risk and bone health, respectively(21), the present study suggests that adherence to these recommendations should be emphasized with iodine status in mind, at least in the population studied. Iodized salt is not available on the Icelandic market, only vitamin D and folic acid are recommended as dietary supplements during pregnancy, and iodine status has not yet received any special attention in prenatal care. It might be speculated that without dietary supplements the group consuming neither fish at least twice weekly nor two portions of milk or other dairy products daily might fall below the optimal range defined by WHO(15, 18). The UIC in that group was 160 μg/l (I:Cr 149 μg/g), while 58 % recorded use of dietary supplements that might have contained iodine.

The main limitation of the present study is the lack of information on the iodine content of dietary supplements. However, the percentage of women taking supplements that might contain iodine was similar between the groups assessed in the present study (Table 3). It might also be considered a limitation to the present study that UIC was measured in a spot sample and not by 24 h urine collection. The reason for choosing spot samples was mainly related to participation rate, as the greater burden of collecting 24 h urine samples might result in lower participation. Still, spot samples have been used successfully to assess iodine status in large population studies like the National Health and Nutrition Examination Survey (NHANES)(Reference Hollowell, Staehling and Hannon28) and the method is recommended by the WHO(18).

Conclusions

The iodine status of pregnant women in Iceland was found to be within the optimal range defined by the WHO despite sharp decreases in milk and fish intakes during past decades. Pregnant women in the population studied who consumed neither fish nor dairy products in line with recommendations, and at the same time did not use dietary supplements containing iodine, might be at risk of suboptimal iodine status.

Acknowledgements

This work was supported by RANNIS – the Icelandic Centre for Research (grant number 070423021, 2007). There are no conflicts of interest that could be perceived as prejudicing the impartiality of the research reported. I.G., I.T., A.J.J., A.M. and L.S. contributed to the design of the study. A.G.G. and I.G. contributed to the data collection and analysis of the data. A.M. analysed iodine concentration in urine. I.G. and A.G.G. wrote the first draft of the paper. All authors contributed to interpretation of the results and writing the final version of the paper. The authors thank Holmfridur Thorgeirsdottir, Gudrun Kristin Sigurgeirsdottir and Bryndis Elfa Gunnarsdottir for their assistance in data collection. They also thank the staff at the Primary Health Care of the Capital Area and Department of Clinical Biochemistry, Landspitali-University Hospital for their assistance; The Icelandic Food and Veterinary Authority for valuable information regarding iodine in dietary supplements and iodized salt on the Icelandic market; and last but not least all the women who participated in the study.

References

1.Delange, F, Benoist, B, Pretell, Eet al. (2001) Iodine deficiency in the world: where do we stand at the turn of the century? Thyroid 11, 437447.CrossRefGoogle ScholarPubMed
2.Delange, F (2007) Iodine requirements during pregnancy, lactation and the neonatal period and indicators of optimal iodine nutrition. Public Health Nutr 10, 15711580.CrossRefGoogle ScholarPubMed
3.Zimmerman, MB (2009) Iodine deficiency in pregnancy and the effects of maternal iodine supplementation on the offspring: a review. Am J Clin Nutr 89, issue 2, 668S672S.CrossRefGoogle Scholar
4.World Health Organization/UNICEF (2001) Iodine Deficiency in Europe: A Continuing Public Health Problem. Geneva: WHO.Google Scholar
5.Sigurjonsson, J (1940) Studies on the human thyroid in Iceland. Doctoral Dissertation, University of Iceland.Google Scholar
6.Sigurdsson, G & Franzson, L (1998) Urine excretion of iodine in an Icelandic population. Laeknabladid 74, 179181 (in Icelandic).Google Scholar
7.Laurberg, P, Pedersen, KM, Hreidarsson, Aet al. (1998) Iodine intake and the pattern of thyroid disorders: a comparative epidemiological study of thyroid abnormalities in the elderly in Iceland and in Jutland, Denmark. J Clin Endocrinol Metab 83, 765769.CrossRefGoogle ScholarPubMed
8.Reykdal, O, Thorlacius, A, Audunsson, GAet al. (2000) Selenium, iodine, fluorine, iron, copper, zinc, manganese, cadmium, mercury and lead in agricultural produce. Agricultural Mimeograph 204, 736 (in Icelandic).Google Scholar
9.Dahl, L, Johansson, L, Julshamn, Ket al. (2004) The iodine content of Norwegian foods and diets. Public Health Nutr 7, 569576.CrossRefGoogle ScholarPubMed
10.Haldimann, M, Alt, A, Blanc, Aet al. (2005) Iodine content of food groups. J Food Compost Anal 18, 461471.CrossRefGoogle Scholar
11.Steingrimsdottir, L, Thorgeirsdottir, H & Olafsdottir, AS (2003) The Icelandic National Nutrition Survey 2002. Reykjavik: Public Health Institute of Iceland.Google Scholar
12.Thorgeirsdottir, H, Valgeirsdottir, H, Gunnarsdottir, Iet al. (2011) The Icelandic National Nutrition Survey 2010–2011. Reykjavik: Directorate of Health, Icelandic Food and Veterinary Authority and Unit for Nutrition Research.Google Scholar
13.ISGEM (2009) Icelandic Database on Food Composition. Reykjavik: MATIS – Icelandic Food Research.Google Scholar
14.Reykdal, O, Hilmarsson, OTh & Auðunsson, GA (2007) Iodine in agricultural produce. Agriculture Conference 4, 516518 (in Icelandic).Google Scholar
15.World Health Organization/UNICEF (2007) Reaching Optimal Iodine Nutrition in Pregnant and Lactating Women and Young Children. Joint Statement of the World Health Organization and the United Nations Children's Fund. Geneva: WHO.Google Scholar
16.Julshamn, K, Dahl, L & Eckhoff, K (2001) Determination of iodine in seafood by inductively coupled plasma/mass spectrometry. J AOAC Int 84, 19761983.CrossRefGoogle ScholarPubMed
17.Dahl, L, Opsahl, JA, Meltzer, HMet al. (2003) Iodine concentration in Norwegian milk and dairy products. Br J Nutr 90, 679685.CrossRefGoogle ScholarPubMed
18.World Health Organization/UNICEF/International Council for the Control of Iodine Deficiency Disorders (2008) Assessment of the Iodine Deficiency Disorders and Monitoring Their Elimination. A Guide for Program Managers. Geneva: WHO.Google Scholar
19.Thorsdottir, I, Gunnarsdottir, I & Steingrimsdottir, L (2004) Validity of a food frequency questionnaire to assess dietary intake of adults. Laeknabladid 90, 3741 (in Icelandic).Google Scholar
20.Olafsdottir, AS, Thorsdottir, I, Gunnarsdottir, Iet al. (2006) Comparison of women's diet assessed by FFQs and 24-hour recalls with and without underreporters: associations with biomarkers. Ann Nutr Metab 50, 450460.CrossRefGoogle ScholarPubMed
21.Public Health Institute of Iceland (2006) Nutrition Recommendations and Food Based Recommendations for Adults and Children above 2-years. Reykjavik: Public Health Institute of Iceland (in Icelandic).Google Scholar
22.Public Health Institute of Iceland (2007) Diet and pregnancy. Information for women of child-bearing age. http://www2.lydheilsustod.is/media/manneldi/utgefid/baklingur_-_Matur_og_medganga-_enska.pdf (accessed February 2012).Google Scholar
23.Sigurjonsson, J (1940) Survey of diet and health in Iceland. Doctoral Dissertation, University of Iceland.Google Scholar
24.Gunnarsdottir, I, Gunnarsdottir, BE, Steingrimsdottir, Let al. (2010) Iodine status of adolescent girls in a population changing from high to lower fish consumption. Eur J Clin Nutr 64, 958964.CrossRefGoogle Scholar
25.Brantsæter, AL, Haugen, M, Julshamn, Ket al. (2009) Evaluation of urinary iodine excretion as a biomarker for intake of milk and dairy products in pregnant women in the Norwegian Mother and Child Cohort Study (MoBa). Eur J Clin Nutr 63, 347354.CrossRefGoogle ScholarPubMed
26.Rasmussen, LB, Ovesen, L, Bülow, Iet al. (2002) Dietary iodine intake and urinary iodine excretion in a Danish population: effect of geography, supplements and food choice. Br J Nutr 87, 6169.CrossRefGoogle Scholar
27.Girelli, ME, Coin, P, Mian, Cet al. (2004) Milk represents an important source of iodine in schoolchildren of the Veneto region, Italy. J Endocrinol Invest 27, 709713.CrossRefGoogle ScholarPubMed
28.Hollowell, JG, Staehling, NW, Hannon, WHet al. (1998) Iodine nutrition in the United States. Trends and public health implications: iodine excretion data from National Health and Nutrition Examination Surveys I and III (1971–1974 and 1988–1994). J Clin Endocrinol Metab 83, 34013408.Google Scholar
Figure 0

Table 1 Characteristics of the participants: pregnant women aged 19–43 years (n 162), Reykjavik, Iceland, November 2007 to February 2009

Figure 1

Table 2 Mean (sd), median, 20th and 80th percentiles of urinary iodine concentration (UIC), ratio of iodine to creatinine (I:Cr) and serum thyroid-stimulating hormone (TSH)* among the study participants: pregnant women aged 19–43 years (n 162), Reykjavik, Iceland, November 2007 to February 2009

Figure 2

Table 3 Median urinary iodine concentration (UIC), ratio of iodine to creatinine (I:Cr) and serum thyroid-stimulating hormone (TSH) according to adherence to recommendations on fish and dairy intake* among the study participants: pregnant women aged 19–43 years (n 162), Reykjavik, Iceland, November 2007 to February 2009