Evidence map›Paper›PMID 37758506›Full record

ArticleThe Journal of clinical endocrinology and metabolism2024

Autoimmune Disease in Turner Syndrome in Sweden: An up to 25 Years' Controlled Follow-up Study.

Sabine Naessén, Malin Eliasson, Kerstin Berntorp, Margareta Kitlinski, Penelope Trimpou, Emily Amundson, Sofia Thunström, Bertil Ekman, Jeanette Wahlberg, Anders Karlsson and 5 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 3 pooled it
2.8field-weighted citation impact, top 9% 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

3 citing papers in PubMed, 3 syntheses or guidelines pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Turner Syndrome and the Thyroid Function-A Systematic and Critical Review.International journal of molecular sciences · 2024
    Pooled it
  3. Guideline
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

15 authors at 8 institutions in 1 country.

Sabine NaessénDepartment of Women's and Children's Health, Karolinska Institutet, 171 77 Stockholm, Sweden.ORCID 0000-0001-9245-6205
Malin EliassonPrimary Health Care, 442 34 Kungälv, Sweden.
Kerstin BerntorpGenomics, Diabetes and Endocrinology Research Unit, Department of Clinical Sciences Malmö, Lund University, 222 42 Malmö, Sweden.ORCID 0000-0002-5557-5085
Margareta KitlinskiDepartment of Reproductive Medicine, Skåne University Hospital, 214 28 Malmö, Sweden.
Penelope TrimpouSection of Endocrinology, Sahlgrenska University Hospital, 413 45 Gothenburg, Sweden.ORCID 0000-0003-2288-628X
Emily AmundsonDepartment of Internal Medicine and Clinical Nutrition, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, 413 45 Gothenburg, Sweden.ORCID 0000-0002-2639-8980
Sofia ThunströmDepartment of Internal Medicine and Clinical Nutrition, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, 413 45 Gothenburg, Sweden.
Bertil EkmanDepartment of Endocrinology, Linköping University Hospital, 581 85 Linköping, Sweden.ORCID 0000-0001-8732-7361
Jeanette WahlbergDepartment of Medicine, Örebro University Hospital, 701 85 Örebro, Sweden.ORCID 0000-0003-4061-6830
Anders KarlssonDepartment of Medical Sciences, Uppsala University, Uppsala University Hospital, 751 85 Uppsala, Sweden.
Magnus IsakssonDepartment of Medical Sciences, Uppsala University, Uppsala University Hospital, 751 85 Uppsala, Sweden.
Ingrid BergströmDepartment of Clinical Science, Intervention and Technology, Karolinska Institutet, 171 77 Solna, Sweden.ORCID 0000-0002-4900-2686
Carina LevelindDepartment of Women's and Children's Health, Karolinska Institutet, 171 77 Stockholm, Sweden.
Inger BrymanDepartment of Obstetrics and Gynecology, Institute of Clinical Sciences, Sahlgrenska Academy at the University of Gothenburg, 413 45 Gothenburg, Sweden.
Kerstin Landin-WilhelmsenSection of Endocrinology, Sahlgrenska University Hospital, 413 45 Gothenburg, Sweden.ORCID 0000-0003-1998-5105
Sahlgrenska University Hospital · SEKarolinska Institutet · SEUppsala University Hospital · SELinköping University Hospital · SEMalmö University · SEÖrebro University · SESkåne University Hospital · SEUniversity of Gothenburg · SE

Funding

ALF-agreement Dnr ALFGBG-682061county councilsSwedish governmentThe Faculty of Medicine at University of GothenburgThe National Board of Health and Welfare Dnr 1471:806The Swedish Heart and Lung Foundation
6 · The paper itself

Abstract

contextTurner syndrome (TS) is the most common chromosomal aberration in women; it is the result of structural or numeric abnormalities in the X chromosome. Autoimmune hypothyroidism has been recognized as one of the more prominent disorders associated with TS.

objectiveThis work aimed to study the prevalence of autoimmune diseases in TS.

methodsA cross-sectional, longitudinal, 25-year follow-up study was conducted of patients from adult Turner centers at the University Hospitals, Sweden. During 1994 to 2020, a total of 503 women aged 16 to 71 years with TS were evaluated consecutively every fifth year according to national guidelines. A random population sample of women, n = 401, aged 25 to 44 years, from the World Health Organization Monitoring of Trends and Determinants for Cardiovascular Disease (MONICA) project served as controls. Serum thyrotropin, free thyroxine, vitamin B12, antithyroid peroxidase (anti-TPO), and antitransglutaminase antibodies were measured.

resultsMean follow-up time (years) was 16 ± 7 for patients and 13 ± 1 for controls. From study start, the prevalence increased in TS for hypothyroidism 40% to 58%, vitamin B12 deficiency 5% to 12%, celiac disease 4% to 7%, positive anti-TPO 26% to 41%, and antitransglutaminase antibodies 6% to 8% (P < .0001 vs controls). Type 1 diabetes and Addison disease were rare. The only interrelationship was between hypothyroidism and vitamin B12 deficiency, both in TS and controls. No association between autoimmune disease and karyotype, antecedent growth hormone treatment, or ongoing estrogen hormone replacement, was seen in TS.

conclusionIn women with TS up to older than 80 years, more than half developed hypothyroidism, mainly autoimmune, during follow-up. Awareness of vitamin B12 deficiency and celiac disease throughout life is also recommended in women with TS.

Indexed as

Addison DiseaseCeliac DiseaseHypothyroidismTurner SyndromeVitamin B 12 DeficiencyAdultAntibodiesCross-Sectional StudiesFemaleFollow-Up StudiesHumansSwedenAntibodiesautoimmunityceliac diseasehypothyroidismTurner syndromevitamin B12 deficiency

Identifiers

PMID37758506
PMCPMC10795927
OpenAlexW4387113236

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.