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The Journal of Clinical Endocrinology & Metabolism Vol. 82, No. 10 3430-3433
Copyright © 1997 by The Endocrine Society


Original Studies

Prevalence of Goiter and Urinary Iodine Excretion Levels in Children Around Chernobyl1

Kiyoto Ashizawa, Yoshisada Shibata, Shunichi Yamashita, Hiroyuki Namba, Masaharu Hoshi, Naokata Yokoyama, Motomori Izumi and Shigenobu Nagataki

The First Department of Internal Medicine (K.A., N.Y., M.I., S.N.), and Department of Preventive Medicine, Atomic Disease Institute (S.Y., H.N.), Nagasaki University School of Medicine, Nagasaki 852, Japan; Department of Epidemiology, Radiation Effects Research Foundation (Y.S.), Nagasaki 850, Japan; and International Radiation Information Center, Research Institute for Radiation Biology and Medicine, Hiroshima University (M.H.), 1–2-3 Kasumi, Minami-ku, Hiroshima 734, Japan

Address all correspondence and requests for reprints to: Kiyoto Ashizawa, The First Department of Internal Medicine, Nagasaki University School of Medicine, Sakamoto 1–7-1, Nagasaki 852, Japan.


    Abstract
 Top
 Abstract
 Introduction
 Subjects and Methods
 Results
 Discussion
 References
 
The prevalence of goiter among children living in areas affected by the Chernobyl accident was investigated by analysis of data on approximately 120,000 children examined at five medical diagnostic centers in Belarus, Russia, and the Ukraine. Examinations of thyroid gland were conducted with an arch-automatic ultrasonographic instrument at the five centers under the same protocol. The diagnosis of goiter was established when the thyroid volume exceeded a limit calculated from age, height, and body weight of a child. A considerable variation by region was noted in the prevalence of goiter. Highest in the Kiev region, the prevalence in the five regions was 54% in Kiev, 38% in the Zhitomir regions of the Ukraine, 18% in Gomel, 22% in the Mogilev regions of Belarus, and 41% in the Bryansk region of Russia. Urinary iodine content was measured in approximately 5700 children, and an endemic iodine deficient zone was confirmed in the Bryansk, Kiev, and Zhitomir regions. A significant negative correlation was observed between the prevalence of goiter and the median level of urinary iodine content (Spearman’s rank correlation coefficient was -0.35, P = 0.025).


    Introduction
 Top
 Abstract
 Introduction
 Subjects and Methods
 Results
 Discussion
 References
 
THE INCREASE in thyroid diseases and hematological disorders, especially thyroid cancer and leukemia, has been a worldwide concern since the Chernobyl accident. Indeed, a dramatic increase in childhood thyroid cancer has been reported in Belarus, Russia, and the Ukraine (1, 2, 3, 4, 5, 6, 7), and iodine prophylaxis has also become an important issue (8).

The affected areas around Chernobyl have been recognized as iodine- deficient areas, but the prevalence of goiter was not clear (9). It is therefore necessary to estimate the prevalence of goiter in these areas as accurately as possible to elucidate the effects of the Chernobyl accident on the thyroid gland.

Precise measurement of thyroid volume and an objective criterion for goiter are prerequisites for the accurate estimation of the prevalence of goiter. We therefore implemented an automatic arch-scanning ultrasonographic instrument with image recording function for the thyroid examinations, and established a formula to calculate the standard thyroid volume for each child from his or her demographic and anthropometric data.

Part of the Chernobyl Sasakawa Health and Medical Cooperation Project, the present study was launched 5 yr after the accident to provide health screening services for children in the affected areas who were age 0–10 yr at the time of the accident (10, 11). The project has three major health screening components: 1) measurement of whole body 137Cs; 2) detection of abnormalities in the thyroid gland; and 3) detection of hematological abnormalities. The examination of children has been conducted by five cooperative centers: Gomel Specialized Medical Dispensary in the Gomel region and Mogilev Regional Medical Diagnostic Center in the Mogilev region, Belarus; Klincy City Children’s Hospital in the Bryansk region, Russia; Kiev Regional Hospital No. 2 in the Kiev region, and Korosten Inter-Area Medical Diagnostic Center in the Zhitomir region, Ukraine. The same equipment, reagents, and protocol were used in all centers.


    Subjects and Methods
 Top
 Abstract
 Introduction
 Subjects and Methods
 Results
 Discussion
 References
 
Subjects

The subjects were 119,178 children (57,529 boys and 61,649 girls) born between April 26, 1976 and April 26, 1986 and examined from May 15, 1991 to April 30, 1996 at the five cooperative centers in Gomel, Mogilev, Bryansk, Kiev, and Zhitomir. A breakdown of the subjects is shown in Table 1Go.


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Table 1. Number of children in five regions examined and who were diagnosed with goiter from May 1991 to April 1996

 
Thyroid examinations

Examination of the thyroid gland was performed with an automatic arch-scanning ultrasonographic instrument (Aloka-SSD 520, Aloka Co., Tokyo, Japan), with a 7.5-MHz annular array transducer 25 mm in diameter. Children are examined in a supine position with their neck hyperextended. The transducer transverses 140 mm over the neck in a waterbath. Images of 11 cross-sections of the thyroid gland are recorded at 5-mm intervals on an optic disk, then the total volume is calculated by computerized digitizer (12).

Serum-free thyroxine (FT4) and TSH levels were measured with an Amerlite hormone analyzer (Amersham, Bunkyo-ku, Tokyo, Japan) using commercial assay kits, and the immunometric technique based on enhanced luminescence was used in a non-RIA system. Titers of antimicrosome antibody and antithyroglobulin antibody were determined by the reaction of indirect hemagglutination using commercial assay kits (Fujirebio, Tokyo).

Determination of iodine and creatinine content in the urine was carried out with an Auto Analyzer II system (Bran+Luebbe, Nordersted, Germany). This system is sensitive enough to detect 0.1 µg/dL of urinary iodine in a urine sample of 500 µL (13). The urinary iodine level was measured in 5710 children selected by the five cooperative centers. Each child was asked to collect a single sample of urine and to bring it to the center. The collected samples were frozen at -20 C and kept until assay at the Mogilev and Kiev centers.

Criterion for goiter

The criterion for goiter is a thyroid volume exceeding the volume calculated by the following formula:

where age is the age of the child in years at the time of the examination, height is the height of the child in centimeters, and body weight is the weight of the child in kilograms. The formula was derived by a statistical technique of model selection and linear regression on the basis of demographic and anthropometric data of 386 boys and 415 girls who were examined at the Mogilev Regional Medical Diagnostic center and who: 1) were age 5–15 yr at the time of examination; 2) were living in areas that are not iodine deficient (urinary iodine level being over 10 µg/dL), and where 137Cs contamination level is <1 Ci/km2; 3) had a whole body 137Cs count <50 Bq/kg; 4) had levels of TSH and FT4 within normal ranges, i.e. 0.24 <= TSH <= 2.90 mU/L and 10.0 <= FT4 <= 25.0 pmol/L); 5) had neither antimicrosome antibody nor antithyroglobulin antibody; and 6) had no thyroid abnormalities as revealed by ultrasonography, e.g. position, structure, echogenity, or presence of nodules and cysts (14).


    Results
 Top
 Abstract
 Introduction
 Subjects and Methods
 Results
 Discussion
 References
 
Thyroid volume

The median of thyroid volume of children examined at the five centers is shown in Fig. 1Go. Figure 1Go, A and B show that the thyroid volume of boys and girls was higher in the Bryansk and Kiev regions than in the other three regions through almost all age groups. A tendency of increase in thyroid volume with age was shown among boys and girls, but in girls the increase seemed to cease at age 14–16 yr (Fig. 1BGo).



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Figure 1. Median of thyroid volume by age and region in boys (A) and girls (B) age 0–10 yr at time of Chernobyl accident.

 
Prevalence of goiter

Goiter was diagnosed in 42,470 (35.6%) of the 119,178 children. A breakdown of the children with goiter is shown in Table 1Go. The prevalence of goiter in the Bryansk, Kiev, and Zhitomir regions was more than two times higher than that in the Gomel and Mogilev regions. A closer examination of the prevalence of goiter by district in the five regions (data not shown) indicated the highest prevalence in almost all districts of the Kiev region, and a relatively high prevalence in the Bryansk and Zhitomir regions. In contrast, a relatively low prevalence of goiter was observed in several districts around Gomel City in the Gomel region, where a high incidence of cancer has been noted (15).

Urinary iodine concentration

The region-specific distribution of urinary iodine excretion level measured in the 5710 selected children is depicted by box-and-whisker plots in Fig. 2Go. The median level of urinary iodine contents was as low as 7.0 µg/dL in Bryansk, 8.5 µg/dL in Kiev, 3.9 µg/dL in Zhitomir, 16.9 µg/dL in Gomel, and 17.7 µg/dL in Mogilev, Belarus. We classified these 5710 children into groups by place of residence and calculated the prevalence of goiter and the median level of urinary iodine excretion in each group excluding those with <10 children. As a result, there were 40 groups consisting of 5652 children, and a significant negative correlation was observed (Spearman’s rank correlation coefficient = -0.35, P = 0.025) between the prevalence of goiter and the median level of urinary iodine excretion (Fig. 3Go).



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Figure 2. Box-and-whisker plots of urinary iodine excretion by region. Bottom and top ends of box and bar inside box correspond to 25th, 75th, and 50th sample percentiles, respectively. • and {odot} represent extreme values, called outside and far out, respectively.

 


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Figure 3. Prevalence of goiter and median of urinary iodine excretion in children age 0–10 yr at time of accident. Calculation of prevalence and median was based on measurements of 5652 children living in 40 different places in five regions.

 

    Discussion
 Top
 Abstract
 Introduction
 Subjects and Methods
 Results
 Discussion
 References
 
The traditional diagnosis of goiter is based on palpation and World Health Organization (WHO) classification (16), but palpation is subjective and less reliable in children than in adults, and recent developments in ultrasound technology have facilitated the accurate measurement of thyroid volume. However, the measurements of thyroid volume in 30 Japanese adults (data not shown) indicated that the conventional method for estimation of thyroid volume in each lobe by the formula of width x length x thickness x 0.52 on the basis of the ellipsoid model was prone to underestimation of thyroid volume. The method used in the present study estimated the thyroid volume accurately, showing a correlation of 0.99 between the estimated volume and actual volume of surgical thyroid gland specimens (12).

The formula we used for calculation of standard thyroid volume was based on a model describing the variation in individual thyroid volume as a function of several covariates such as age, height, and body weight. The sex was also considered as a possible covariate, but the data indicated that the contribution of sex to the variation in thyroid volume was negligible after adjustment for the other three covariates. The contribution of iodine level was also negligible after the adjustment mentioned above. Similar covariates have been used to derive the standard thyroid volume (17, 18). However, the relationship between the thyroid volume and covariates was considered separately for each covariate. Modeling the thyroid volume as a function of multiple covariates can lead to a reasonable standard thyroid volume even with a relatively small sample.

Still, the formula for calculation of standard thyroid volume is not universal, and a different formula should be used for each population. For example, the thyroid volume of Japanese adults showed a dependency on sex, age at the time of examination, and body weight, but not on height (19). However, the statistical line leading to the present formula is deemed to be universal.

In the present study, the prevalence of goiter showed no association with whole body 137Cs count nor with 137Cs contamination level in the place of current residence and the place of residence at the time of the accident (data not shown). On the other hand, a significant negative correlation was indicated between the prevalence of goiter and urinary excretion level.

The lowest prevalence of goiter was observed in the Gomel region, where the highest incidence of childhood cancer has been reported (15), and the highest prevalence of goiter was observed in the Kiev region, where the incidence of childhood cancer is relatively low. These findings may be related to the fact that the present study was based on examinations of children commenced 5 yr after the accident. Because a significant change in iodine nutrition status may have occurred after the accident, the present study indicates the necessity for studies focusing on the iodine nutrition status before and after the accident in the area around Chernobyl.


    Acknowledgments
 
We are grateful to the staff members at Gomel Specialized Medical Dispensary, Mogilev Regional Medical Diagnostic Center, Klincy City Children’s Hospital, Kiev Regional Hospital No. 2, and Korosten Inter-Area Medical Diagnostic Center for their hard work in the examination of children.


    Footnotes
 
1 This work was supported by Sasakawa Memorial Health Foundation, Tokyo, Japan. Back

Received January 21, 1997.

Revised May 20, 1997.

Accepted June 19, 1997.


    References
 Top
 Abstract
 Introduction
 Subjects and Methods
 Results
 Discussion
 References
 

  1. Kazakov VS, Demidchik EP, Astakhova LN. 1992 Thyroid cancer after Chernobyl. Nature. 39:21.
  2. Demidchik EP, Drobyshevskaya IM, Cherstvoy ED, et al. 1996 Thyroid cancer in children in Belarus. In: Karaoglou A, Desmet G, Kelly GN, Menzel HG, eds. The radiological consequences of the Chernobyl accident. Luxembourg: ECSC-EC-EAEC; 677–682.
  3. Tronko N, Bogdanova T, Komissarenko I, et al. 1996 Thyroid gland in children and adolescents in Ukraine after the Chernobyl accident (1986–1995). In: Karaoglou A, Desmet G, Kelly GN, Menzel HG, eds. The radiological consequences of the Chernobyl accident. Luxembourg: ECSC-EC-EAEC; 683–690.
  4. Likhtarev IA, Sobolev BG, Kairo IA, et al. 1995 Thyroid cancer in the Ukraine. Nature. 375:365.[Medline]
  5. Tsyb AF, Parshkov EM, Shakhtarin VV, Stepanenko VF, Skvortsov VF, Chebotareva IV. 1996 Thyroid cancer in children and adolescents of Bryansk and Kaluga regions. In: Karaoglou A, Desmet G, Kelly GN, Menzel HG, eds. The radiological consequences of the Chernobyl accident. Luxembourg: ECSC-EC-EAEC; 691–697.
  6. Williams ED, Pacini F, Pinchera A. 1995 Thyroid cancer following Chernobyl. J Endocrinol Invest. 18:144–146.[Medline]
  7. Yamashita S, Nagataki S. 1995 Chernobyl and thyroid. Thyroid. 5:153–154.[Medline]
  8. Nauman J, Wolff J. 1993 Iodide prophylaxis in Poland after the Chernobyl reactor accident: benefits and risks. Am J Med. 94:524–532.[CrossRef][Medline]
  9. Gerasimov G. 1993 Update on IDD in the former USSR. IDD Newsletter. 9:43–48.
  10. Nagataki S, Ashizawa K. 1995 Screening for thyroid cancer in children. In: Karaoglou A, Desmet G, Kelly GN, Menzel HG, eds. The radiological consequences of the Chernobyl accident. Luxembourg: ECSC-EC-EAEC; 749–754.
  11. Yamashita S, Ito M, Namba H, et al. 1996 Screening for childhood thyroid diseases around Chernobyl. In: Nagataki S, Yamashita S, eds. Nagasaki Symposium, Radiation and Human Health: Proposal from Nagasaki. International Congress Series No. 1103. Amsterdam: Elsevier; 103–116.
  12. Yokoyama N, Nagayama Y, Kakezono F, et al. 1986 Determination of the volume of the thyroid gland by a high resolutional ultrasonic scanner. J Nucl Med. 27:1475–1479.[Abstract/Free Full Text]
  13. Tsuda K, Namba H, Nomura T, et al. 1995 Automated assay for urinary iodine with ultraviolet irradiation. Clin Chem. 41:581–585.[Abstract/Free Full Text]
  14. Shibata Y. 1993 Determination of standard thyroid volume in children. In: Yamashita S, Fujimura K, Hoshi M, Shibata Y, eds. A report on the 1993 Chernobyl Sasakawa Project Workshop. Tokyo: Sasakawa Memorial Health Foundation; 100–101.
  15. Williams ED, Becker D, Dimidchik EP, Nagataki S, Pinchera A, Tronko ND. 1996 Effects on the thyroid in populations exposed to radiation as a result of the Chernobyl accident. In: Delves D, Demir M, eds. One decade after Chernobyl. Vienna: STI/PUB/1001; 207–230.
  16. Perez C, Scrimshaw NS, Munoz JA. 1960 Technique of endemic goiter surveys. WHO Monograph Series 44: Endemic goiter. Geneva: WHO; 369–383.
  17. Delange F, Benker G, Caron Ph, et al. 1997 Thyroid volume and urinary iodine in European schoolchildren: standardization of values for assessment of iodine deficiency. Eur J Endocrinol. 136:180–187.[Abstract/Free Full Text]
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  19. Nagataki S, Shibata Y, Inoue S, Yokoyama N, Izumi M, Shimaoka K. 1994 Thyroid diseases among atomic bomb survivors in Nagasaki. JAMA. 272:364–370.[Abstract/Free Full Text]




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