Investigating the incidence rate and geographical distribution of congenital hypothyroidism among neonates in Isfahan province using geographic information system (GIS) between 2002 and 2015
Abstract
Background
Congenital hypothyroidism (CH) is one of the main causes of mental retardation in neonates. The disease is associated with genetic, climatic and environmental factors. Accordingly, the present study was conducted to determine the incidence rate and correlation of geographic factors with CH in Isfahan province in order to explain the role of climatic factors in the incidence of disease in this province.
Methods
This cross-sectional study was conducted to determine the incidence rate and geographical distribution of CH in neonates born in the Isfahan province from the beginning of 2002 to the end of 2015. To estimate the geographic distribution, the ArcGIS software (version 10.3) was used and to investigate the relationship between geographical factors and CH, the Poisson regression test and dispersion diagrams were used. Data analysis was done using the SPSS16 software.
Results
According to the results of the screening of 1,006,404 neonates born in Isfahan, the mean incidence rate of CH in all infants was 2.3, and that in male and female infants was 2.39 and 2.2 per 1000 live births, respectively. There was a statistically significant correlation between the city of residence (p = 0.01), climatic conditions (p = 0.044), annual precipitation (p = 0.027), sunlight (p = 0.01) and CH. However, there was no significant relationship between the mean altitude above sea level (p = 0.6), land use (p = 0.4) and relative humidity (p = 0.24).
Conclusions
Based on the findings of this study, the incidence rate of CH in Isfahan province was higher than the average of the country. Moreover, among the geographical factors, climatic conditions, annual precipitation and sunlight were associated with CH.
Acknowledgments
We are grateful to the Deputy Health Minister of Isfahan Medical Sciences University, Kashan University of Medical Sciences and also thank the Deputy of Research and Technical information of Ilam University of Medical Sciences for their scientific support. This study is the result of a research project code 968055/142 at Ilam University of Medical Sciences.
Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.
Research funding: None declared.
Employment or leadership: None declared.
Honorarium: None declared.
Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.
References
1. Nili S, Ghotbi N. The incidence of congenital hypothyroidism in newborns in Kurdistan Province. Q. Paiesh 2010;10:15–20.Search in Google Scholar
2. Eftekhari N, Asadikaram G, Khaksari M, Salari Z, Ebrahimzadeh M. The prevalence rate of congenital hypothyroidism in Kerman/Iran in 2005–2007. J Kerman Univ Med Sci 2008;15:243–50.10.1016/S0020-7292(09)60616-0Search in Google Scholar
3. Namakin K, Sedighi E, Sharifzadeh G, Zardast M. Prevalence of congenital hypothyroidism In South Khorasan province (2006–2010). J Birjand Univ Med Sci 2012;19:191–9.Search in Google Scholar
4. Dorreh F, Chaijan PY, Javaheri J, Eshrati B, Amiri Z. Evaluation of 6 years performance of screening program of congenital hypothyroidism in Markazi province (2006–2012). Arak Med Univ J 2013;16:40–7.Search in Google Scholar
5. Medda E, Olivieri A, Stazi MA, Grandolfo ME, Fazzini C, et al. Risk factors for congenital hypothyroidism: results of a population case-control study (1997–2003). Eur J Endocrinol 2005;153:765–73.10.1530/eje.1.02048Search in Google Scholar PubMed
6. Barry Y, Bonaldi C, Goulet V, Coutant R, Leger J. Increased incidence of congenital hypothyroidism in France from 1982 to 2012: a nationwide multicenter analysis. Ann Epidemiol 2016;26:100–5.10.1016/j.annepidem.2015.11.005Search in Google Scholar PubMed
7. Mitrovic K, Vukovic R, Milenkovic T, Todorovic S, Radivojcevic J. Changes in the incidence and etiology of congenital hypothyroidism detected during 30 years of a screening program in central Serbia. Eur J Pediatr 2016;175:253–9.10.1007/s00431-015-2630-5Search in Google Scholar PubMed
8. Denga K, Hea C, Zhu J, Liang J, Li X, et al. Incidence of congenital hypothyroidism in China: data from the national newborn screening program, 2013–2015. J Pediatr Endocrinol Metab 2018;31:601–8.10.1515/jpem-2017-0361Search in Google Scholar PubMed
9. Osooli M, Haghdoost A, Yarahmadi S, Foruzanfar M, Dini M, et al. Spatial distribution of congenital hypothyroidism in Iran using geographic information system. Iran J Epidemiol 2009;5:1–8.Search in Google Scholar
10. Khanjani N, Ahmadzadeh A, Bakhtiari B, Madadizadeh F. The role of season and climate in the incidence of congenital hypothyroidism in Kerman province, Southeastern Iran. J Pediatr Endocrinol Metab 2017;30:149–57.10.1289/isee.2016.3157Search in Google Scholar
11. Mehran L, Yarahmadi S, Khalili D, Nazeri P, Delshad H, et al. The impact of iodine status on the recall rate of the screening program for congenital hypothyroidism: findings from two national studies in Iran. Nutrients 2017;9:1–10.10.3390/nu9111194Search in Google Scholar PubMed PubMed Central
12. Huang C, Jap TA. Systematic review of genetic studies of thyroid disorders in Taiwan. J Chin Med Assoc 2015;78:145–53.10.1016/j.jcma.2014.09.010Search in Google Scholar PubMed
13. Nicholas A, Serra E, Cangul H, Al-Yaarubi S, Ullah I. Investigating the genetic architecture of gland-in-situ congenital hypothyroidism by comprehensive screening of eight known causative genes. Endocrine Abstracts2015;38:55–9.10.1530/endoabs.38.OC5.5Search in Google Scholar
14. Rezaeian S, Moghimbeigi A, Esmailnasab N. Gender differences in risk factors of congenital hypothyroidism: an interaction hypothesis examination. Int J Endocrinol Metab 2014;12. Doi: 10.5812/ijem.13946.Search in Google Scholar PubMed PubMed Central
15. Szinnai G. Clinical genetics of congenital hypothyroidism. Endocr Dev 2014;26:60–78.10.1159/000363156Search in Google Scholar PubMed
16. Moghadam FJ, SayehMiri K, Shahbaziyan HB, Asadollahi K. Investigation of risk factors associated to congenital hypothyroidism in Mahshahr city between 1389–1395 and presentation of apreventive model. J Adv Pharm Educ Res 2019;9.Search in Google Scholar
17. Miyai K, Inaoka K, Miyagi T. Further studies on episodic occurrence of congenital dysgenetic hypothyroidism in Osaka, Japan. Endocr J 2005;52:599–603.10.1507/endocrj.52.599Search in Google Scholar PubMed
18. Hashemipour M, Amini M, Kelishadi R, Hovsepian S, Haghighi S. Seasonal variation in the incidence of congenital hypothyroidism in Isfahan, Iran. Saudi Med J 2007;28:1582–6.Search in Google Scholar
19. Aminzadeh M, Chomeili B, Riahi K, Dehdashtian M, Cheraghian B. Effect of temperature changes on the occurrence of congenital hypothyroidism. J Med Screen 2010;17:121–4.10.1258/jms.2010.010026Search in Google Scholar PubMed
20. Daliri S, Asadollahi K, Karimi A, Ehsanzadeh A, Rezaei N. Investigation of the incidence rate and geographical distribution of congenital hypothyroidism in the newborns in Ilam Province by using geographic information system (GIS) between 2006 and 2016. SJKU 2019;24:98–111.10.29252/sjku.24.1.98Search in Google Scholar
21. Mehrnejat N, Yazdanpanah H, Nobari RF, Hashemipour M, Maracy M, et al. Spatial analysis of neonatal congenital hypothyroidism and nitrate as an environmental pollutant in Isfahan Province during 2010–2013. Int J Prev Med 2015;6:1–6.Search in Google Scholar
22. Daliri S, Asadollahi K, Rahimi N, Sayehmiri K. Incidence of glucose-6-phosphate dehydrogenase deficiency in malariaprone regions of Fars province. Tehran Univ Med J 2017;75:669–74.Search in Google Scholar
23. Ashtari F, Karimi A, Delpisheh A, Meamar R, Sayehmiri K, et al. Estimated incidence rate of multiple sclerosis and its relationship with geographical factors in Isfahan Province between the years 2001 and 2014. Int J Prev Med 2018;9:103–8.10.4103/ijpvm.IJPVM_317_16Search in Google Scholar PubMed PubMed Central
24. Karimi A, Delpisheh A, Ashtari F, Sayehmiri K, Meamar R. The relationship between the amount of radiation, relative humidity, and temperature with the risk of multiple sclerosis in Isfahan province, Iran, during the years 2001–2014. J Isfahan Med School 2017;35:434–439.Search in Google Scholar
25. Veisani Y, Sayehmiri K, Rezaeian S, Delpisheh A. Congenital Hypothyroidism Screening Program in Iran; a Systematic Review and Meta analysis. Iran J Pediatr 2014;24:665–72.Search in Google Scholar
26. Beheshti Z, Rezaei R, Alipour A, Kosarian M, Saatsaz S. A 7-year study on the prevalence of congenital hypothyroidism in northern Iran. Electronic Physician 2018;10:6689–96.10.19082/6689Search in Google Scholar PubMed PubMed Central
27. Nili S, Ghotbi N. The rate of congenital hypothyroidism in newborns born in Kurdistan province. Q J Monit 2010;10:15–20.Search in Google Scholar
28. Karamizadeh Z, Saneifard H, Amirhakimi G, Karamifar H, Alavi M. Evaluation of congenital hypothyroidism in Fars province, Iran. Iran J Pediatr 2012;22:107–112.Search in Google Scholar
29. Shojaeefar H, YazdanPanah A, Vahdat S. Neonatal hypothyroidism and its related factors in infants born inYazd Province during the years 2013 to 2014. Toloo-e-behdasht 2017;15:135–44.Search in Google Scholar
30. Ordookhani A, Pearce E, Mirmiran P, Azizi F, Braverman LE. The effect of type of delivery and povidone-iodine application at delivery on cord dried-blood-specimen thyrotropin level and the rate of hyperthyrotropinemia in mature and normal-birthweight neonates residing in an iodine-replete area: report of Tehran Province, 1998–2005. Thyroid 2007;17:1097–102.10.1089/thy.2007.0058Search in Google Scholar PubMed
31. Hashemipour M, Hovsepian S, Kelishadi R, Iranpour R, Hadian R, et al. Permanent and transient congenital hypothyroidism in Isfahan–Iran. J Med Screen 2009;16:11–6.10.1258/jms.2009.008090Search in Google Scholar PubMed
32. Dalili S, Rezvany SM, Dadashi A, Medghalchi A, Mohammadi H, et al. Congenital hypothyroidism: a review of the risk factors. Acta Med Iran 2012;50:735–9.Search in Google Scholar
33. Ghasemi M, Hashemipour M, Hovsepian S, Heiydari K, Sajadi A, et al. Prevalence of transient congenital hypothyroidism in central part of Iran. J Res Med Sci 2013;18:699–703.Search in Google Scholar
34. Azizi F, Sheikholeslam R, Hedayati M, Mirmiran P, Malekafzali H, et al. Sustainable control of iodine deficiency in Iran: beneficial results of the implementation of the mandatory law on salt iodization. J Endocrinol Invest 2002;25:409–13.10.1007/BF03344029Search in Google Scholar PubMed
35. Hashemipoor M, Amini M, Gheisari A, Sharifei S, Iranpour R, et al. Comparison of urinary iodine excretion in neonates and their mothers in Isfahan, Iran. Endocr Pract 2002;8:347–50.10.4158/EP.8.5.347Search in Google Scholar PubMed
36. Hashemipour M, Ghasemi M, Hovsepian S, Heiydari K, Sajadi A, et al. Etiology of congenital hypothyroidism in Isfahan: does it different? Adv Biomed Res 2014;3:1–10.10.4103/2277-9175.124658Search in Google Scholar PubMed PubMed Central
37. Ordooei M, Rabie A, Soleimanizad R, Mirjalili F. Prevalence of permanent congenital hypothyroidism in children in Yazd, Central Iran. Iran J Public Health 2013;42:1016–20.Search in Google Scholar
38. Vandevijvere S, Coucke W, Vanderpas J, Trumpff C, Fauvart M, et al. Neonatal thyroid-stimulating hormone concentrations in Belgium: a useful indicator for detecting mild iodine deficiency? PLoS One 2012;7. Available at: https://doi.org/10.1371/journal.pone.0047770.10.1371/journal.pone.0047770Search in Google Scholar PubMed PubMed Central
39. Delshad H. History of the Iodine Deficiency in the World and Iran. Iran J Endocrinol Metab 2008;9:439–53.Search in Google Scholar
©2020 Walter de Gruyter GmbH, Berlin/Boston
Articles in the same Issue
- Frontmatter
- Editorial
- Inborn errors of metabolism
- Reviews
- Nutrition and medical support during pregnancy and lactation in women with inborn errors of intermediary metabolism disorders (IEMDs)
- The association between prenatal exposure to organochlorine compounds and neonatal thyroid hormone levels: a systematic review
- Original Articles
- Investigating the incidence rate and geographical distribution of congenital hypothyroidism among neonates in Isfahan province using geographic information system (GIS) between 2002 and 2015
- Analysis of five cases of hypermethioninemia diagnosed by neonatal screening
- What is the evidence for beneficial effects of growth hormone treatment beyond height in short children born small for gestational age? A review of published literature
- Machine learning-based prediction of response to growth hormone treatment in Turner syndrome: the LG Growth Study
- Pathogenic/likely pathogenic variants in the SHOX, GHR and IGFALS genes among Indian children with idiopathic short stature
- Celiac disease in Saudi children with isolated short stature: is it rare or are we not screening rigorously enough?
- The beneficial effect of psychological support on mothers with PKU children who suffer from social discrimination and damage of quality of life
- Long-term effects of GnRH agonist treatment on body mass index in girls with idiopathic central precocious puberty
- Sudden sex hormone withdrawal and the effects on body composition in late pubertal adolescents with gender dysphoria
- The alteration of IGF-1 levels and relationship between IGF-1 levels and growth velocity during GnRH analogue therapy
- BMI relationship to the onset of puberty: assessment of growth parameters and sexual maturity changes in Egyptian children and adolescents of both sexes
- The effects of a 12-week jump rope exercise program on body composition, insulin sensitivity, and academic self-efficacy in obese adolescent girls
- Onset of pituitary hormone deficiencies in optic nerve hypoplasia: a temporal trend analysis of 32 children at Mayo Clinic
- Dietary practices in methylmalonic acidaemia: a European survey
- Case Reports
- Clinical findings in five Turkish patients with citrin deficiency and identification of a novel mutation on SLC25A13
- A rare case of primary coenzyme Q10 deficiency due to COQ9 mutation
- Sinusitis, an under-reported adverse effect in children treated with radioactive iodine therapy and review of the current literature
- Acknowledgment
Articles in the same Issue
- Frontmatter
- Editorial
- Inborn errors of metabolism
- Reviews
- Nutrition and medical support during pregnancy and lactation in women with inborn errors of intermediary metabolism disorders (IEMDs)
- The association between prenatal exposure to organochlorine compounds and neonatal thyroid hormone levels: a systematic review
- Original Articles
- Investigating the incidence rate and geographical distribution of congenital hypothyroidism among neonates in Isfahan province using geographic information system (GIS) between 2002 and 2015
- Analysis of five cases of hypermethioninemia diagnosed by neonatal screening
- What is the evidence for beneficial effects of growth hormone treatment beyond height in short children born small for gestational age? A review of published literature
- Machine learning-based prediction of response to growth hormone treatment in Turner syndrome: the LG Growth Study
- Pathogenic/likely pathogenic variants in the SHOX, GHR and IGFALS genes among Indian children with idiopathic short stature
- Celiac disease in Saudi children with isolated short stature: is it rare or are we not screening rigorously enough?
- The beneficial effect of psychological support on mothers with PKU children who suffer from social discrimination and damage of quality of life
- Long-term effects of GnRH agonist treatment on body mass index in girls with idiopathic central precocious puberty
- Sudden sex hormone withdrawal and the effects on body composition in late pubertal adolescents with gender dysphoria
- The alteration of IGF-1 levels and relationship between IGF-1 levels and growth velocity during GnRH analogue therapy
- BMI relationship to the onset of puberty: assessment of growth parameters and sexual maturity changes in Egyptian children and adolescents of both sexes
- The effects of a 12-week jump rope exercise program on body composition, insulin sensitivity, and academic self-efficacy in obese adolescent girls
- Onset of pituitary hormone deficiencies in optic nerve hypoplasia: a temporal trend analysis of 32 children at Mayo Clinic
- Dietary practices in methylmalonic acidaemia: a European survey
- Case Reports
- Clinical findings in five Turkish patients with citrin deficiency and identification of a novel mutation on SLC25A13
- A rare case of primary coenzyme Q10 deficiency due to COQ9 mutation
- Sinusitis, an under-reported adverse effect in children treated with radioactive iodine therapy and review of the current literature
- Acknowledgment