Evidence map›Paper›PMID 32635414›Full record

ArticleJournal of clinical medicine2020

Familial Dysalbuminemic Hyperthyroxinemia: An Underdiagnosed Entity.

Xavier Dieu, Nathalie Bouzamondo, Claire Briet, Frédéric Illouz, Valérie Moal, Florence Boux de Casson, Natacha Bouhours-Nouet, Pascal Reynier, Régis Coutant, Patrice Rodien and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

9 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Effect of the Fetal THRB Genotype on the Placenta.The Journal of clinical endocrinology and metabolism · 2023
    Article
  6. Review
  7. Article
  8. Hormone Immunoassay Interference: A 2021 Update.Annals of laboratory medicine · 2022
    Review
  9. 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

11 authors at 2 institutions in 1 country.

Xavier DieuLaboratoire de Biochimie et Biologie Moléculaire, CHU Angers, 4 rue Larrey, CEDEX 9, 49933 Angers, France.ORCID 0000-0003-2287-7252
Nathalie BouzamondoLaboratoire de Biochimie et Biologie Moléculaire, CHU Angers, 4 rue Larrey, CEDEX 9, 49933 Angers, France.
Claire BrietUMR CNRS 6015-INSERM U1083, 3 rue Roger Amsler, 49100 Angers, France.
Frédéric IllouzCentre de référence des maladies rares de la thyroïde et des récepteurs hormonaux, CHU Angers, 4 rue Larrey, CEDEX 9,49933 Angers, France.
Valérie MoalLaboratoire de Biochimie et Biologie Moléculaire, CHU Angers, 4 rue Larrey, CEDEX 9, 49933 Angers, France.
Florence Boux de CassonLaboratoire de Biochimie et Biologie Moléculaire, CHU Angers, 4 rue Larrey, CEDEX 9, 49933 Angers, France.
Natacha Bouhours-NouetCentre de référence des maladies rares de la thyroïde et des récepteurs hormonaux, CHU Angers, 4 rue Larrey, CEDEX 9,49933 Angers, France.
Pascal ReynierLaboratoire de Biochimie et Biologie Moléculaire, CHU Angers, 4 rue Larrey, CEDEX 9, 49933 Angers, France.ORCID 0000-0003-0802-4608
Régis CoutantCentre de référence des maladies rares de la thyroïde et des récepteurs hormonaux, CHU Angers, 4 rue Larrey, CEDEX 9,49933 Angers, France.
Patrice RodienUMR CNRS 6015-INSERM U1083, 3 rue Roger Amsler, 49100 Angers, France.
Delphine Mirebeau-PrunierLaboratoire de Biochimie et Biologie Moléculaire, CHU Angers, 4 rue Larrey, CEDEX 9, 49933 Angers, France.
Centre Hospitalier Universitaire d'Angers · FRCentre National de la Recherche Scientifique · FR

Funding

ANR THYROMUT
6 · The paper itself

Abstract

Resistance to thyroid hormone (RTH) is a syndrome characterized by impaired sensitivity of tissues to thyroid hormone (TH). The alteration of TH-binding proteins, such as in Familial Dysalbuminemic Hyperthyroxinemia (FDH), can mimic the abnormal serum thyroid tests typical of RTH. We aimed to characterize a population referred to our center with suspected RTH and estimate the proportion of patients with FDH. For 303 different families, we collected clinical and hormonal data and sequenced the thyroid hormone receptor β gene (

Indexed as

albuminfamilial dysalbuminemic hyperthyroxinemiaimmunoassay interferenceresistance to thyroid hormoneTHRB

Identifiers

PMID32635414
PMCPMC7408830
OpenAlexW3040675348

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.