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Prevalence of Transient Congenital Hypothyroidism in Central Part of Iran



Ghasemi M1, 2 ; Hashemipour M3 ; Hovsepian S2 ; Heiydari K4 ; Sajadi A4 ; Hadian R4 ; Mansourian M5 ; Mirshahzadeh N3
Authors
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Authors Affiliations
  1. 1. Department of Pediatrics, Isfahan, Iran
  2. 2. Child Growth and Development Research Center, Isfahan, Iran
  3. 3. Department of Pediatric Endocrinology, Isfahan Endocrine and Metabolism Research Center, Isfahan, Iran
  4. 4. Isfahan Health Center, Isfahan, Iran
  5. 5. Department of Biostatistics and Epidemiology, Health School, Isfahan University of Medical Sciences, Isfahan, Iran

Source: Journal of Research in Medical Sciences Published:2013

Abstract

Background: Congenital hypothyroidism (CH) considered a common endocrine disorder in Iran. We report the epidemiologic findings of CH screening program in Isfahan, seven years after its development, regarding the prevalence of transient CH (TCH) and its screening properties comparing with permanent CH (PCH). Materials and Methods: In this cross-sectional study, children with primary diagnosis of CH were studied. Considering screening and follow-up lab data and the decision of pediatric endocrinologists, the final diagnosis of TCH was determined. Results: A total of 464,648 neonates were screened. Te coverage percent of the CH screening and recall rate was 98.9 and 2.1%, respectively. Out of which, 1,990 neonates were diagnosed with primary CH. TCH was diagnosed in 1,580 neonates. Te prevalence of TCH was 1 in 294 live births. 79.4% of patients with primary CH had TCH. Mean of screening (54.7 ± 59.0 in PCH vs 21.8 ± 28.9 in TCH), recall (56.5 ± 58.8 in PCH vs 36.6 ± 45.0 in TCH), and thyroid stimulating hormone (TSH) and mean of TSH before (2.0 ± 2.9 in PCH vs 1.6 ± 1.6 in TCH) and after (37.7 ± 29.5 in PCH vs 4.3 ± 1.9 in TCH) discontinuing treatment at 3 years of age was significantly higher in PCH than TCH (P < 0.0000). Conclusion: Te higher rate of CH in Isfahan is mainly due to the transient form of the disease. Further studies for evaluating the role of other environmental, autoimmune and/or genetic factors in the path physiology of the disease is warranted.
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