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Fracture incidence in Graves' disease : A population-based study

Khamisi, Selwan ; Udumyan, Ruzan ; Sjölin, Gabriel ; Calissendorff, Jan ; Filipsson Nyström, Helena ; Holmberg, Mats ; Hallengren, Bengt LU ; Lantz, Mikael LU ; Planck, Tereza LU and Wallin, Göran , et al. (2023) In Thyroid : official journal of the American Thyroid Association 33(11). p.1349-1357
Abstract

Background Population-based studies have indicated an increase in bone turnover in hyperthyroidism with a subsequent decrease in bone mineral density and an increased risk of fractures, especially in postmenopausal women. However, heterogeneity between studies prevents a definitive conclusion. Graves' disease (GD) is an autoimmune disease, and it is the most common cause of hyperthyroidism. The aim of this study was to investigate fracture risk in patients with GD. Methods A total of 2134 patients with incident GD and 21261 age, sex- and county-matched controls were included 16-18 years after diagnosis in a retrospective cohort study. Drug and patient national registries in Sweden were used to assess the risk of developing skeletal... (More)

Background Population-based studies have indicated an increase in bone turnover in hyperthyroidism with a subsequent decrease in bone mineral density and an increased risk of fractures, especially in postmenopausal women. However, heterogeneity between studies prevents a definitive conclusion. Graves' disease (GD) is an autoimmune disease, and it is the most common cause of hyperthyroidism. The aim of this study was to investigate fracture risk in patients with GD. Methods A total of 2134 patients with incident GD and 21261 age, sex- and county-matched controls were included 16-18 years after diagnosis in a retrospective cohort study. Drug and patient national registries in Sweden were used to assess the risk of developing skeletal complications. Up to ten age, sex- and county-matched controls per patient were selected from databases from The National Board of Health and Welfare and Statistics Sweden. Cox proportional hazards models were fitted to estimate hazard ratios (HR) and 95% confidence intervals. Results There were no significant differences in fracture rates between GD and controls but after adjustment for co-morbidities, the data showed higher vertebral fracture rates in male GD patients aged >52 years compared to male controls, HR=2.83 (1.05-7.64). The rates of osteoporosis treatments as well as treatment with corticosteroids were higher in patients with GD. However, HR for the association between GD and fractures remained largely unchanged after adjustment for osteoporosis treatments and treatments with corticosteroids. Conclusions There were no significant differences in total fracture rate between GD and the general population. However, men older than 52 years had a higher vertebral fracture rate. This study also shows that patients with treated GD receive more osteoporosis treatments compared to the general population.

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organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Thyroid : official journal of the American Thyroid Association
volume
33
issue
11
pages
1349 - 1357
publisher
Mary Ann Liebert, Inc.
external identifiers
  • pmid:37725590
  • scopus:85175449682
ISSN
1557-9077
DOI
10.1089/thy.2023.0162
language
English
LU publication?
yes
id
36af9e36-7412-4919-b094-fb37aa6caaa1
date added to LUP
2023-09-26 11:39:57
date last changed
2024-12-13 13:32:20
@article{36af9e36-7412-4919-b094-fb37aa6caaa1,
  abstract     = {{<p>Background Population-based studies have indicated an increase in bone turnover in hyperthyroidism with a subsequent decrease in bone mineral density and an increased risk of fractures, especially in postmenopausal women. However, heterogeneity between studies prevents a definitive conclusion. Graves' disease (GD) is an autoimmune disease, and it is the most common cause of hyperthyroidism. The aim of this study was to investigate fracture risk in patients with GD. Methods A total of 2134 patients with incident GD and 21261 age, sex- and county-matched controls were included 16-18 years after diagnosis in a retrospective cohort study. Drug and patient national registries in Sweden were used to assess the risk of developing skeletal complications. Up to ten age, sex- and county-matched controls per patient were selected from databases from The National Board of Health and Welfare and Statistics Sweden. Cox proportional hazards models were fitted to estimate hazard ratios (HR) and 95% confidence intervals. Results There were no significant differences in fracture rates between GD and controls but after adjustment for co-morbidities, the data showed higher vertebral fracture rates in male GD patients aged &gt;52 years compared to male controls, HR=2.83 (1.05-7.64). The rates of osteoporosis treatments as well as treatment with corticosteroids were higher in patients with GD. However, HR for the association between GD and fractures remained largely unchanged after adjustment for osteoporosis treatments and treatments with corticosteroids. Conclusions There were no significant differences in total fracture rate between GD and the general population. However, men older than 52 years had a higher vertebral fracture rate. This study also shows that patients with treated GD receive more osteoporosis treatments compared to the general population.</p>}},
  author       = {{Khamisi, Selwan and Udumyan, Ruzan and Sjölin, Gabriel and Calissendorff, Jan and Filipsson Nyström, Helena and Holmberg, Mats and Hallengren, Bengt and Lantz, Mikael and Planck, Tereza and Wallin, Göran and Ljunggren, Östen}},
  issn         = {{1557-9077}},
  language     = {{eng}},
  month        = {{09}},
  number       = {{11}},
  pages        = {{1349--1357}},
  publisher    = {{Mary Ann Liebert, Inc.}},
  series       = {{Thyroid : official journal of the American Thyroid Association}},
  title        = {{Fracture incidence in Graves' disease : A population-based study}},
  url          = {{http://dx.doi.org/10.1089/thy.2023.0162}},
  doi          = {{10.1089/thy.2023.0162}},
  volume       = {{33}},
  year         = {{2023}},
}