Negative associations for fasting blood glucose, cholesterol and triglyceride levels with the development of giant cell arteritis
- PMID: 32240313
- PMCID: PMC7590417
- DOI: 10.1093/rheumatology/keaa080
Negative associations for fasting blood glucose, cholesterol and triglyceride levels with the development of giant cell arteritis
Abstract
Objectives: To investigate metabolic features that may predispose to GCA in a nested case-control study.
Methods: Individuals who developed GCA after inclusion in a population-based health survey (the Malmö Preventive Medicine Project; N = 33 346) were identified and validated through a structured review of medical records. Four controls for every validated case were selected from the database.
Results: A total of 76 cases with a confirmed incident diagnosis of GCA (61% female, 65% biopsy positive, mean age at diagnosis 70 years) were identified. The median time from screening to diagnosis was 20.7 years (range 3.0-32.1). Cases had significantly lower fasting blood glucose (FBG) at baseline screening compared with controls [mean 4.7 vs 5.1 mmol/l (S.d. overall 1.5), odds ratio (OR) 0.35 per mmol/l (95% CI 0.17, 0.71)] and the association remained significant when adjusted for smoking [OR 0.33 per mmol/l (95% CI 0.16, 0.68)]. Current smokers had a reduced risk of GCA [OR 0.35 (95% CI 0.18, 0.70)]. Both cholesterol [mean 5.6 vs 6.0 mmol/l (S.d. overall 1.0)] and triglyceride levels [median 1.0 vs 1.2 mmol/l (S.d. overall 0.8)] were lower among the cases at baseline screening, with significant negative associations with subsequent GCA in crude and smoking-adjusted models [OR 0.62 per mmol/l (95% CI 0.43, 0.90) for cholesterol; 0.46 per mmol/l (95% CI 0.27, 0.81) for triglycerides].
Conclusion: Development of GCA was associated with lower FBG and lower cholesterol and triglyceride levels at baseline, all adjusted for current smoking, suggesting that metabolic features predispose to GCA.
Keywords: epidemiology; giant cell arteritis; lipids.
© The Author(s) 2020. Published by Oxford University Press on behalf of the British Society for Rheumatology.
Comment in
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Comment on: Negative associations for fasting blood glucose, cholesterol and triglyceride levels with the development of giant cell arteritis.Rheumatology (Oxford). 2021 Jul 1;60(7):e258-e259. doi: 10.1093/rheumatology/keab132. Rheumatology (Oxford). 2021. PMID: 33560409 No abstract available.
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Comment on: Negative associations for fasting blood glucose, cholesterol and triglyceride levels with the development of giant cell arteritis: reply.Rheumatology (Oxford). 2021 Jul 1;60(7):e262-e263. doi: 10.1093/rheumatology/keab143. Rheumatology (Oxford). 2021. PMID: 33576780 Free PMC article. No abstract available.
References
-
- Salvarani C, Crowson CS, O’Fallon WM, Hunder GG, Gabriel SE. Reappraisal of the epidemiology of giant cell arteritis in Olmsted County, Minnesota, over a fifty-year period. Arthritis Rheum 2004;51:264–8. - PubMed
-
- Petursdottir V, Johansson H, Nordborg E, Nordborg C. The epidemiology of biopsy-positive giant cell arteritis: special reference to cyclic fluctuations. Rheumatology (Oxford) 1999;38:1208–12. - PubMed
-
- Mohammad AJ, Nilsson J-Å, Jacobsson LT, Merkel PA, Turesson C. Incidence and mortality rates of biopsy-proven giant cell arteritis in southern Sweden. Ann Rheum Dis 2015;74:993–7. - PubMed
-
- Tomasson G, Bjornsson J, Zhang Y, Gudnason V, Merkel PA. Cardiovascular risk factors and incident giant cell arteritis: a population-based cohort study. Scand J Rheumatol 2019;48:213–7. - PubMed
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