Evidence map›Paper›PMID 31592447›Full record

ArticleEndocrinology, diabetes & metabolism2019

Liver enzyme profile and progression in association with thyroid autoimmunity in Graves' disease.

Albert Hsieh, Stephen Adelstein, Susan V McLennan, Paul F Williams, Elizabeth L Chua, Stephen M Twigg

Abstract read
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Article in Endocrinology, diabetes & metabolism, 2019. 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
–field-weighted citation impact
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

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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.

  1. Article
  2. Article
  3. Article
  4. Liver Dysfunction in a Patient with Graves' Disease.Journal of clinical medicine · 2024
    Review
  5. Review
  6. Article
  7. Article
  8. Article
  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

6 authors.

Albert HsiehDepartment of Endocrinology Royal Prince Alfred Hospital Camperdown New South Wales Australia.ORCID https://orcid.org/0000-0003-4855-0581
Stephen AdelsteinDepartment of Clinical Immunology Royal Prince Alfred Hospital Camperdown New South Wales Australia.
Susan V McLennanDepartment of Endocrinology Royal Prince Alfred Hospital Camperdown New South Wales Australia.
Paul F WilliamsDepartment of Endocrinology Royal Prince Alfred Hospital Camperdown New South Wales Australia.
Elizabeth L ChuaDepartment of Endocrinology Royal Prince Alfred Hospital Camperdown New South Wales Australia.
Stephen M TwiggDepartment of Endocrinology Royal Prince Alfred Hospital Camperdown New South Wales Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the associations of Graves' disease (GD) severity, autoimmunity and longitudinal liver enzyme changes with time in a cohort with well-characterized GD.

designRetrospective cohort study. PATIENTS: Patients diagnosed with Graves' disease, treated at Royal Prince Alfred Hospital Sydney, Adult Thyroid Clinic from 2000 to 2012 inclusive. MEASUREMENTS: Inclusion criteria were patients with a complete set of TSH, FT4, FT3, liver enzymes and TSH receptor antibody (TRAb) results prior to commencement of thionamide therapy.

resultsOf the 146 patients who had complete results, 69 (47%) had at least one abnormal liver enzyme. Gamma glutamyltransferase (GGT) was most frequently abnormal (74%), followed by alanine aminotransferase (ALT) (57%), alkaline phosphatase (ALP) (39%) and then aspartate aminotransferase (AST) (29%). Subsequent to thyroid function normalization, 78% of the liver enzymes were normalized, 10% were persistently abnormal and 12% were lost to follow-up. Circulating TRAb, FT3 and FT4 results were categorized into mild, moderate and severe elevations. At univariate regression analyses, TRAb, FT3 and FT4 levels were each significantly associated with abnormal liver enzyme profile. Multivariate regression including TRAB, FT3 and FT4 as independent variables demonstrated FT3 and FT4 were more strongly associated with abnormal liver profile than TRAb. However, the initial FT3 and FT4 levels were not associated with abnormal liver profile in the subgroup with persistently abnormal liver profile.

conclusionGraves' disease is commonly associated with abnormal liver enzymes, and most commonly with abnormal levels of GGT, and that an abnormal liver enzyme profile is more directly linked to the degree of thyrotoxicosis than levels of TRAB.

Indexed as

Graves' diseaseliver enzymethyroid hormonethyrotoxicosisTSH receptor antibody

Identifiers

PMID31592447
PMCPMC6775470

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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.