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Mitochondrial DNA haplogroups modulate the radiographic progression of Spanish patients with osteoarthritis.

Abstract：

:Not all patients with osteoarthritis (OA) show the same disease progression, as some of them remain relatively stable over time, while others progress to severe structural deterioration of the joint. In this sense, the main goal of both genetic and protein biomarkers in OA is to predict not only the risk of OA at an earlier stage of the disease but also which OA patients are more likely to progress to severe disease. Taking into account the incidence of the mitochondria and the mtDNA haplogroups in the pathogenesis of OA, the main objective of this work was to evaluate the incidence of the mtDNA haplogroups in the radiographic progression of the OA disease in a well-characterized follow-up cohort of Spanish patients. DNA from 281 OA patients from Hospital Universitario A Coruña was isolated to determine the European mtDNA haplogroups. Knee or hip radiographs from all affected joints were obtained at two time points with at least 36 months apart. Radiographs were evaluated using the Kellgren/Lawrence (K/L) scale; radiographic OA progression was defined as any radiographic worsening of the K/L joint score. Statistical analyses included Kaplan-Meier survival curves and Cox regression models. Patients belonging to the cluster TJ showed a slower radiographic OA progression than patients in the cluster KU (p = 0.036). Moreover, patients carrying the most common mtDNA haplogroup H are more apt to require total joint replacement surgery than non-H patients (p = 0.049). The inherited mitochondrial variants influence the radiographic progression of OA and could be considered among the genetic variants taken into account when the radiographic progression of OA is analyzed.

journal_name

Rheumatol Int

journal_title

Rheumatology international

authors

Soto-Hermida A,Fernández-Moreno M,Pértega-Díaz S,Oreiro N,Fernández-López C,Blanco FJ,Rego-Pérez I

doi

10.1007/s00296-014-3104-1

subject

Has Abstract

pub_date

2015-02-01 00:00:00

pages

337-44

issue

2

eissn

0172-8172

issn

1437-160X

journal_volume

35

pub_type

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