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Background: Congenital hypothyroidism (CH) is one of the most prevalent preventable cause of mental retardation and intellectual disability in newborns. Genetic and environmental factors have been related to congenital hypothyroidism. Hence, this study was conducted to illustrate the incidence and spatial distribution of the CH using the dataset from the national newborn CH screening information system during 2011-2020in counties affiliated to the Kohgiluyeh and Boyer Ahmad University of Medical Sciences.
Methods: This was a cross-sectional study. All newborns that were screened for CH in 3-5 days of age in the health centers of Yasuj University of Medical Sciences were enrolled the study since 2011-2020. Meteorological data including information on temperature, humidity, precipitation in a 10-year period (2011-2020) was taken from the Meteorological Organization. The required information layers include slope, slope direction, height, vegetation and political divisions of the province, were purchased from the organizations that made the layers. The data related to the incidence of congenital hypothyroidism was collected from the 10-year reports of the provincial health center. Addresses of patients were transferred to Arc GIS 10.5 software and entered in urban and rural points layer to prepare and draw disease distribution maps in the province's newborns. The influence of geographical factors on the occurrence of disease was done by SPSS 23 software using multivariate binary logistic regression. P-value < 0.05 was assumed as significant level.
Results: Out of 142,674 screened newborns for CH, 827 had positive screening, including 441 boys (53.3%) and 386 girls (46.7%). Total incidence per 1000 live birth was 5.79. Based on multivariate logistic regression, slope (sig = 0.0001, Exp(B) = 0.91, CI Exp(B) = 0.87-0.95), thin forest (sig = 0.001, Exp(B) = 0.2, CI Exp(B) = 0.07-0.53), water area (sig = 0.0001, Exp(B) = 8.91, CI Exp(B) = 3.35-23.69), were predicting factors of CH.
Conclusion: Given that, the incidence of CH in the Kohgiluyeh and Boyar Ahmad province is higher than the average of country (Iran), and the geographical factors of land slope and type of vegetation were related to it that cannot be changed, it is very important to carry out necessary nutritional interventions during pregnancy to prevent newborns from contracting this disease.
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http://dx.doi.org/10.1186/s12887-024-05292-y | DOI Listing |
Thyroid
September 2025
Department of Molecular Diagnostics, Department of Endocrinology, The Core Laboratory in Medical Center of Clinical Research, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
is a major cause of congenital hypothyroidism (CH) in Chinese patients, but clinical outcomes for those with biallelic mutations remain unclear. This study aimed to describe the clinical manifestations of CH due to defect. One hundred eighty-one patients with primary CH were recruited initially and were subjected to genetic screening.
View Article and Find Full Text PDFAnn Pediatr Endocrinol Metab
August 2025
Liaquat University of Medical and Health Sciences, Jamshoro, Pakistan.
Ann Pediatr Endocrinol Metab
August 2025
Pediatric Department, School of Medicine, University of Ioannina, Ioannina, Greece.
Eur J Endocrinol
September 2025
Department of Endocrinology and Internal Medicine, Aarhus University Hospital, Palle Juul-Jensens Boulevard 165, 8200 Aarhus N, Denmark.
Objective: Persistent symptoms and impaired quality of life(QoL) in hypothyroidism despite treatment with levothyroxine(LT4) receive increasing attention. We aimed at reviewing QoL in long-termly treated hypothyroidism.
Design: Systematic review and meta-analysis.
Biochemistry (Mosc)
August 2025
Endocrinology Research Center, Moscow, 117036, Russia.
Endocrine disorders represent a serious public health problem and frequently can be caused by genetic factors or their combination with environmental and lifestyle factors. Assessment of relevant genetic factors is important to estimate the risk of endocrine pathologies in an individual before their manifestation. Identification of genetic variations in proteins of the major histocompatibility complex is important with regard to the autoimmune nature of many endocrine pathologies, including type 1 diabetes.
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