Evidence map›Paper›PMID 32964174›Full record

ArticleJournal of the Endocrine Society2020

Circulating Thyroid Hormone Profile in Response to a Triiodothyronine Challenge in Familial Longevity.

Ana Zutinic, Gerard J Blauw, Hanno Pijl, Bart E Ballieux, Rudi G J Westendorp, Ferdinand Roelfsema, Diana van Heemst

Open access · goldAbstract read
In one paragraph

Article in Journal of the Endocrine Society, 2020. 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
0.7field-weighted citation impact, top 27% 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, 5 citations in OpenAlex.

  1. Review
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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

7 authors at 3 institutions in 2 countries.

Ana ZutinicDepartment of Internal Medicine, Division of Gerontology and Geriatrics, Leiden University Medical Centre, Leiden, ZA, the Netherlands.ORCID 0000-0002-9224-7179
Gerard J BlauwDepartment of Internal Medicine, Division of Gerontology and Geriatrics, Leiden University Medical Centre, Leiden, ZA, the Netherlands.
Hanno PijlDepartment of Internal Medicine, Division of Endocrinology and Metabolic Diseases, Leiden University Medical Centre, Leiden, the Netherlands.ORCID 0000-0002-3076-1551
Bart E BallieuxDepartment of Clinical Chemistry and Laboratory Medicine, Leiden University Medical Centre, Leiden, the Netherlands.
Rudi G J WestendorpPublic Health and Centre for Healthy Aging, University of Copenhagen, Copenhagen, Denmark.
Ferdinand RoelfsemaDepartment of Internal Medicine, Division of Endocrinology and Metabolic Diseases, Leiden University Medical Centre, Leiden, the Netherlands.ORCID 0000-0001-6276-2834
Diana van HeemstDepartment of Internal Medicine, Division of Gerontology and Geriatrics, Leiden University Medical Centre, Leiden, ZA, the Netherlands.
Leiden University · NLLeiden University Medical Center · NLUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

contextFamilial longevity is associated with higher circulating levels of thyrotropin (TSH), in the absence of differences in circulating thyroid hormones, and a lower thyroid responsivity to TSH, as previously observed in the Leiden Longevity Study (LLS). Further mechanisms underlying these observations remain unknown.

objectiveWe hypothesized that members from long-lived families (offspring) have higher thyroid hormone turnover or less negative feedback effect on TSH secretion compared to controls.

methodsIn a case-control intervention study, 14 offspring and 13 similarly aged controls received 100 µg 3,5,3'-triiodothyronine (T3) orally. Their circulating T3, free T3 (fT3), and TSH levels were measured during 5 consecutive days. We compared profiles of circulating T3, fT3, and TSH between offspring and controls using general linear modeling (GLM) and calculated the percentage decline in TSH following T3 administration.

resultsCirculating T3 and fT3 levels increased to supraphysiologic values and normalized over the course of 5 days. There were no serious adverse events. T3 and fT3 concentration profiles over 5 days were similar between offspring and controls (T3 GLM

conclusionsMembers of long-lived families have neither higher T3 turnover nor diminished negative feedback of T3 on TSH secretion. The cause and biological role of elevated TSH levels in familial longevity remain to be elucidated.

Indexed as

3,5,3′-triiodothyroninelongevitynegative feedbackthyroidTSH

Identifiers

PMID32964174
PMCPMC7491925
OpenAlexW3081264603

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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.