Evidence map›Paper›PMID 29261674›Full record

ArticlePloS one2017

Mitochondrial haplogroups in patients with rheumatoid arthritis: No association with disease and disease manifestations.

Pernille Hurup Duhn, Jacob Sode, Christian Munch Hagen, Michael Christiansen, Henning Locht

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Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Pernille Hurup DuhnDepartment of Rheumatology Frederiksberg Hospital, Nordre Fasanvej, Frederiksberg, Denmark.ORCID http://orcid.org/0000-0001-8729-0634
Jacob SodeDepartment of Rheumatology Frederiksberg Hospital, Nordre Fasanvej, Frederiksberg, Denmark.
Christian Munch HagenDepartment for Congenital Disorders, Statens Serum Institut, Artillerivej, Copenhagen S, Denmark.
Michael ChristiansenDepartment for Congenital Disorders, Statens Serum Institut, Artillerivej, Copenhagen S, Denmark.
Henning LochtDepartment of Rheumatology Frederiksberg Hospital, Nordre Fasanvej, Frederiksberg, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo describe the distribution of specific mitochondrial DNA (mtDNA) haplogroups (hgs) in a cohort of patients with rheumatoid arthritis (RA).

methodsTwo-hundred nineteen consecutive patients with RA had mtDNA isolated from their blood, sequenced and haplotyped. Patients were diagnosed according to the American College of Rheumatology (ACR)/European league against Rheumatism (EULAR) criteria. Demographic and clinical data were retrieved from the Danish nationwide database (DANBIO). Logistic regression analyses were performed to test for associations.

resultsOne-hundred eighty-four patients were eligible for analysis. Haplogroup frequencies were: H (n = 88; 47.8%), U (n = 37; 20.1%), T (n = 22; 12.0%), J (n = 16; 8.7%), K (n = 11; 5.9%), HV (n = 6; 3.3%) and V (n = 4; 2.2%). The distribution of individual hgs was identical to the background population. Radiographic erosions were significantly associated with hg clusters JT (OR = 2.37, 95% confidence interval (CI): 1.07-5.53, p = 0.038). Significantly fewer patients from hg cluster JT received biological treatment (OR = 0.17, 95% CI: 0.03-0.87, p = 0.038). Albeit, none of these associations were significant when corrected for multiple tests.

conclusionThere was no significant association between mtDNA hgs and presence of RA or disease manifestations. There was an, albeit insignificant, overrepresentation of patients with hg JT among patients with erosive disease; however, slightly fewer patients in the JT group were treated with biological drugs.

Indexed as

HaplotypesAdultAgedAged, 80 and overArthritis, RheumatoidDNA, MitochondrialFemaleHumansMaleMiddle AgedProspective StudiesDNA, Mitochondrial

Identifiers

PMID29261674
PMCPMC5737896

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