Evidence map›Paper›PMID 36499571›Full record

ArticleInternational journal of molecular sciences2022

Atrial Fibrillation with Heart Failure in a Case with Resistance to Thyroid Hormone Due to a Rare Thyroid Hormone Receptor β Gene Mutation.

Huei-Pin Lai, Mei-Hsiu Chen

Open access · goldAbstract readCase Reports
In one paragraph

Article in International journal of molecular sciences, 2022. 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
0.4field-weighted citation impact, top 34% 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, 3 citations in OpenAlex.

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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

2 authors at 2 institutions in 1 country.

Huei-Pin LaiDivision of Endocrinology, Department of Internal Medicine, Far Eastern Memorial Hospital, New Taipei City 220, Taiwan.
Mei-Hsiu ChenDivision of Endocrinology, Department of Internal Medicine, Far Eastern Memorial Hospital, New Taipei City 220, Taiwan.ORCID 0000-0002-6007-5560
Far Eastern Memorial Hospital · TWMing Chuan University · TW

Funding

Far Eastern Memorial Hospital FEMH-2022-C-013
6 · The paper itself

Abstract

Resistance to thyroid hormone (RTH) is a rare disease typically associated with elevated levels of thyroid hormones and non-suppressed thyroid stimulating hormones. The most common cause of RTH is thyroid hormone receptor β (THRβ) gene mutation. Most individuals with RTH are considered clinical euthyroid. We report a family with a rare heterozygous point mutation, c.959G>T, (p.R320L) of the THRβ gene. The proband developed atrial fibrillation and life-threatening heart failure with pulmonary edema, which was quite different from previously reported THRβ gene mutations. Considering the rareness of RTH and the heterogeneity of its phenotypes, our report allows for a better understanding of the manifestation and management of patients with RTH and THRβ gene mutation.

Indexed as

Atrial FibrillationHeart FailureThyroid Hormone Resistance SyndromeHumansMutationThyroid Hormone Receptors betaThyroid HormonesThyroid Hormone Receptors betaThyroid Hormonesresistance to thyroid hormonethyroid hormone receptor β gene mutation

Identifiers

PMID36499571
PMCPMC9739295
OpenAlexW4310716578

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.