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Prevalence and comorbidity of relapsing polychondritis

Authors Ludvigsson J, van Vollenhoven R

Received 1 September 2016

Accepted for publication 2 September 2016

Published 30 September 2016 Volume 2016:8 Pages 361—362

DOI https://doi.org/10.2147/CLEP.S121272

Checked for plagiarism Yes

Editor who approved publication: Professor Henrik Toft Sørensen


Jonas F Ludvigsson,1–4 Ronald van Vollenhoven5

1
Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, 2Department of Pediatrics, Örebro University Hospital, Örebro, Sweden; 3Division of Epidemiology and Public Health, School of Medicine, University of Nottingham, Nottingham, UK; 4Department of Medicine, Celiac Disease Center, Columbia University College of Physicians and Surgeons, New York, NY, USA; 5Department of Rheumatology, Amsterdam Rheumatology & Immunology Center, Amsterdam, the Netherlands

Relapsing polychondritis (RP) is by no means an unknown disease, and already 30 years ago Michet et al1 had presented results from a single-center study of 112 patients with RP. In contrast to the earlier study,1 the study by Horvath et al2 published in Clinical Epidemiology allows some interesting revelations.

Disclosure

The authors are researchers and this editorial represents their own personal views and not necessarily those of their employers. The authors report no other conflicts of interest in this work.

References

1.

Michet CJ Jr, McKenna CH, Luthra HS, O’Fallon WM. Relapsing polychondritis. Survival and predictive role of early disease manifestations. Ann Intern Med. 1986;104(1):74–78.

2.

Horvath A, Pall N, Molnar K, et al. A nationwide study of the epidemiology of relapsing polychondritis. Clin Epidemiol. 2016;8:211–230.

3.

Kent PD, Michet CJ Jr, Luthra HS. Relapsing polychondritis. Curr Opin Rheumatol. 2004;16(1):56–61.

4.

Ludvigsson JF, Otterblad-Olausson P, Pettersson BU, Ekbom A. The Swedish personal identity number: possibilities and pitfalls in healthcare and medical research. Eur J Epidemiol. 2009;24(11):659–667.

5.

Pociot F, Lernmark A. Genetic risk factors for type 1 diabetes. Lancet. 2016;387(10035):2331–2339.

6.

Smigoc Schweiger D, Mendez A, Kunilo Jamnik S, et al. High-risk genotypes HLA-DR3-DQ2/DR3-DQ2 and DR3-DQ2/DR4-DQ8 in co-occurrence of type 1 diabetes and celiac disease. Autoimmunity. 2016;49(4):240–247.

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