Evidence map›Paper›PMID 29074892›Full record

Trial reportScientific reports2017

Effects of Supra-Physiological Levothyroxine Dosages on Liver Parameters, Lipids and Lipoproteins in Healthy Volunteers: A Randomized Controlled Crossover Study.

Barbara Sjouke, Laura P B Elbers, Bregje van Zaane, John J P Kastelein, G Kees Hovingh, Victor E A Gerdes

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.7field-weighted citation impact, top 26% 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

0 citing papers in PubMed, 4 citations in OpenAlex.

No citing paper in PubMed yet.

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

6 authors at 1 institution in 1 country.

Barbara SjoukeDepartment of Vascular Medicine, Academic Medical Center, PO box 22660, 1100 DD, Amsterdam, The Netherlands. b.sjouke@amc.nl.
Laura P B ElbersDepartment of Vascular Medicine, Academic Medical Center, PO box 22660, 1100 DD, Amsterdam, The Netherlands. l.p.elbers@amc.nl.
Bregje van ZaaneDepartment of Vascular Medicine, Academic Medical Center, PO box 22660, 1100 DD, Amsterdam, The Netherlands.
John J P KasteleinDepartment of Vascular Medicine, Academic Medical Center, PO box 22660, 1100 DD, Amsterdam, The Netherlands.
G Kees HovinghDepartment of Vascular Medicine, Academic Medical Center, PO box 22660, 1100 DD, Amsterdam, The Netherlands.
Victor E A GerdesDepartment of Vascular Medicine, Academic Medical Center, PO box 22660, 1100 DD, Amsterdam, The Netherlands.
Academic Medical Center · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Eprotirome, a liver specific thyroid hormone agonist, was shown to induce significant increases in markers of liver injury along with a modest decrease in atherogenic lipids and lipoproteins. To get more insight into whether these effects on liver parameters were compound specific or the effect of mimicking thyrotoxicosis, we studied the effects of supra-physiological levothyroxine dosages on liver parameters, lipids and lipoproteins. We used data of a single-blinded, randomized controlled crossover trial. Herein, healthy volunteers received levothyroxine or no medication for 14 days. Thyroid hormone excess did not induce clinically relevant changes in liver parameters, while significant reductions in total cholesterol, low-density lipoprotein-cholesterol as well as apolipoprotein-B levels were observed in the intervention periods compared with the control periods. Supra-physiological thyroid hormone levels did not induce clinically relevant increases in markers of liver injury after 2 weeks of exposure, while it reduced total cholesterol, low-density lipoprotein cholesterol and apolipoprotein B levels. This suggests that the effects of eprotirome on liver parameters in previous studies were either off-target and compound specific or due to drug-drug interaction at the level of the liver. The results of our study are relevant for the development of novel thyroid hormone agonists to reduce atherogenic lipoproteins.

Indexed as

AdultCross-Over StudiesDose-Response Relationship, DrugEnzymesFemaleHealthy VolunteersHumansLipidsLipoproteinsLiverMaleThyroxineTriiodothyronineEnzymesLipidsLipoproteinsThyroxineTriiodothyronine

Identifiers

PMID29074892
PMCPMC5658438
OpenAlexW2766544330

What OpenQuestion holds

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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.