Cargando…

Congenital hypothyroidism in India: A systematic review and meta-analysis of prevalence, screen positivity rates, and etiology

BACKGROUND: Congenital hypothyroidism (CH) is the leading cause of preventable mental retardation, which is currently not universally screened in India. Knowledge of the country-specific prevalence of the disease can guide in establishing a universal screening program. METHODS: We performed a system...

Descripción completa

Detalles Bibliográficos
Autores principales: Anne, Rajendra Prasad, Rahiman, Emine A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10305877/
https://www.ncbi.nlm.nih.gov/pubmed/37383660
http://dx.doi.org/10.1016/j.lansea.2022.100040
_version_ 1785065826363113472
author Anne, Rajendra Prasad
Rahiman, Emine A.
author_facet Anne, Rajendra Prasad
Rahiman, Emine A.
author_sort Anne, Rajendra Prasad
collection PubMed
description BACKGROUND: Congenital hypothyroidism (CH) is the leading cause of preventable mental retardation, which is currently not universally screened in India. Knowledge of the country-specific prevalence of the disease can guide in establishing a universal screening program. METHODS: We performed a systematic review and meta-analysis to assess the prevalence, screen positivity rates, compliance to recall and etiology of CH in India. The databases of PubMed, Embase, Google scholar and IMSEAR were searched on 1(st) October 2021. All observational studies reporting at least one of the outcomes of interest were included. Two reviewers independently extracted the data and appraised the quality of studies using the Joanna Briggs tool for prevalence studies. Estimates were pooled using a random-effects model with double arcsine transformation (MetaXL software). PROSPERO database registration number was CRD42021277523. FINDINGS: Of the 2 073 unique articles retrieved, 70 studies were eligible for inclusion. The prevalence of CH (per 1 000 neonates screened) was 0·97 (95% confidence intervals/CI: 0·9, 1·04) in non-endemic areas (54 studies and 819 559 neonates), 79 (95% CI: 72, 86) in endemic areas (3 studies, 5 060 neonates), 50 (95% CI: 31, 72) in neonates born to mothers with thyroid disorders, and 14 (95% CI: 8, 22) in preterm neonates. At thyroid stimulation hormone cut-off of 20 mIU/L, the screen positivity rates were 5·6% (95% CI: 5·4%, 5·9%) for cord blood samples and 0·19% (95% CI: 0·18%, 0·2%) for postnatal sample. About 70% (95% CI: 70, 71) of screen positive neonates were retested with diagnostic tests. Among neonates with permanent hypothyroidism, thyroid dysgenesis 56·6% (95% CI: 50·9%, 62·2%) was more common than dyshormonogenesis 38·7% (95% CI: 33·2%, 44·3%). INTERPRETATION: The prevalence of congenital hypothyroidism in India is higher than global estimates. Screen positivity rate was higher for cord blood screening when compared to postnatal screening. Compliance with confirmatory testing was higher for cord blood screening. FUNDING: The study was not funded by any source.
format Online
Article
Text
id pubmed-10305877
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-103058772023-06-28 Congenital hypothyroidism in India: A systematic review and meta-analysis of prevalence, screen positivity rates, and etiology Anne, Rajendra Prasad Rahiman, Emine A. Lancet Reg Health Southeast Asia Articles BACKGROUND: Congenital hypothyroidism (CH) is the leading cause of preventable mental retardation, which is currently not universally screened in India. Knowledge of the country-specific prevalence of the disease can guide in establishing a universal screening program. METHODS: We performed a systematic review and meta-analysis to assess the prevalence, screen positivity rates, compliance to recall and etiology of CH in India. The databases of PubMed, Embase, Google scholar and IMSEAR were searched on 1(st) October 2021. All observational studies reporting at least one of the outcomes of interest were included. Two reviewers independently extracted the data and appraised the quality of studies using the Joanna Briggs tool for prevalence studies. Estimates were pooled using a random-effects model with double arcsine transformation (MetaXL software). PROSPERO database registration number was CRD42021277523. FINDINGS: Of the 2 073 unique articles retrieved, 70 studies were eligible for inclusion. The prevalence of CH (per 1 000 neonates screened) was 0·97 (95% confidence intervals/CI: 0·9, 1·04) in non-endemic areas (54 studies and 819 559 neonates), 79 (95% CI: 72, 86) in endemic areas (3 studies, 5 060 neonates), 50 (95% CI: 31, 72) in neonates born to mothers with thyroid disorders, and 14 (95% CI: 8, 22) in preterm neonates. At thyroid stimulation hormone cut-off of 20 mIU/L, the screen positivity rates were 5·6% (95% CI: 5·4%, 5·9%) for cord blood samples and 0·19% (95% CI: 0·18%, 0·2%) for postnatal sample. About 70% (95% CI: 70, 71) of screen positive neonates were retested with diagnostic tests. Among neonates with permanent hypothyroidism, thyroid dysgenesis 56·6% (95% CI: 50·9%, 62·2%) was more common than dyshormonogenesis 38·7% (95% CI: 33·2%, 44·3%). INTERPRETATION: The prevalence of congenital hypothyroidism in India is higher than global estimates. Screen positivity rate was higher for cord blood screening when compared to postnatal screening. Compliance with confirmatory testing was higher for cord blood screening. FUNDING: The study was not funded by any source. Elsevier 2022-07-14 /pmc/articles/PMC10305877/ /pubmed/37383660 http://dx.doi.org/10.1016/j.lansea.2022.100040 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Articles
Anne, Rajendra Prasad
Rahiman, Emine A.
Congenital hypothyroidism in India: A systematic review and meta-analysis of prevalence, screen positivity rates, and etiology
title Congenital hypothyroidism in India: A systematic review and meta-analysis of prevalence, screen positivity rates, and etiology
title_full Congenital hypothyroidism in India: A systematic review and meta-analysis of prevalence, screen positivity rates, and etiology
title_fullStr Congenital hypothyroidism in India: A systematic review and meta-analysis of prevalence, screen positivity rates, and etiology
title_full_unstemmed Congenital hypothyroidism in India: A systematic review and meta-analysis of prevalence, screen positivity rates, and etiology
title_short Congenital hypothyroidism in India: A systematic review and meta-analysis of prevalence, screen positivity rates, and etiology
title_sort congenital hypothyroidism in india: a systematic review and meta-analysis of prevalence, screen positivity rates, and etiology
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10305877/
https://www.ncbi.nlm.nih.gov/pubmed/37383660
http://dx.doi.org/10.1016/j.lansea.2022.100040
work_keys_str_mv AT annerajendraprasad congenitalhypothyroidisminindiaasystematicreviewandmetaanalysisofprevalencescreenpositivityratesandetiology
AT rahimaneminea congenitalhypothyroidisminindiaasystematicreviewandmetaanalysisofprevalencescreenpositivityratesandetiology