Evidence map›Paper›PMID 31215165›Full record

ArticleMolecular genetics & genomic medicine2019

A 10-year prevalence of congenital hypothyroidism in Khorramabad (Urban Western Iran).

Nadereh Taee, Mojgan Faraji Goodarzi, Mohammad Safdari, Amir Bajelan

Open access · goldAbstract read
In one paragraph

Article in Molecular genetics & genomic medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 25% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Prevalence of transient congenital hypothyroidism among neonates.Annals of medicine and surgery (2012) · 2021
    Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Nadereh TaeeDepartment of Pediatrics, Faculty of Medicine, Lorestan University of Medical Sciences, Khorramabad, Iran.ORCID 0000-0002-6046-6342
Mojgan Faraji GoodarziDepartment of Pediatrics, Faculty of Medicine, Lorestan University of Medical Sciences, Khorramabad, Iran.ORCID 0000-0002-7494-2557
Mohammad SafdariStudent Research Committee, Lorestan University of Medical Sciences, Khorramabad, Iran.
Amir BajelanStudent Research Committee, Lorestan University of Medical Sciences, Khorramabad, Iran.
Lorestan University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCongenital hypothyroidism in infants is the cause of mental retardation in children, it can be detected in patient and treated at a relatively cheap rate, preventing patient retard. This study aimed to determine the prevalence of congenital hypothyroidism among Khorramabad children.

methodsIn the present study, we identified all patients who had received levothyroxine prescriptions during the study period (2007-2017). Using this as a congenital hypothyroidism surrogate marker, we considered the congenital hypothyroidism prevalence in children above 3 years.

resultsOf 574 patients who had received levothyroxine during the neonatal period up to 3 years, the results of one-variable logistic regression analysis showed that the chance of temporary disease in children with small thyroid ultrasonography was 62% less, than for those without problems, and this difference was significant. The chance of temporary disease in children who had other cases was 87% less than those without problems, and this difference was statistically significant.

conclusionThe overall prevalence of congenital hypothyroidism in young patients up to 3 years is 0.143%, these values are at least twice those of previous estimates. This proposes an elevation in autoimmune thyroid disease, which is similitude to the rising prevalence of diabetes type 1, which possibly indicates a rising incidence of autoimmunity in youth.

Indexed as

ChildChild, PreschoolCongenital HypothyroidismDrug PrescriptionsFemaleHumansInfantInfant, NewbornIranMaleNeonatal ScreeningPrevalenceThyroid GlandThyrotropinThyroxineUltrasonographyThyrotropinThyroxineautoimmunitycongenital hypothyroidismtemporary disease

Identifiers

PMID31215165
PMCPMC6687863
OpenAlexW2953154547

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.