Skip to main content

Advertisement

Log in

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

  • Original Article
  • Published:
Rheumatology International Aims and scope Submit manuscript

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.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

Abbreviations

ABI:

Applied biosystems

ACR:

American college of Rheumatology

ATP:

Adenosine triphosphate

BMI:

Body mass index

CI:

Confidence interval

CILP:

Cartilage intermediate layer protein

DNA:

Deoxyribonucleic acid

GDF5:

Growth differentiation factor 5

HR:

Hazard ratio

IL1RN:

Interleukin-1 receptor antagonist

JSW:

Joint space width

KL:

Kellgren and Lawrence

MRC:

Mitochondrial respiratory chain

mtDNA:

Mitochondrial deoxyribonucleic acid

OA:

Osteoarthritis

OAI:

Osteoarthritis initiative

OR:

Odds ratio

OXHPOS:

Oxidative phosphorylation system

PCR:

Polymerase chain reaction

RFLP:

Restriction fragment length polymorphism

ROS:

Reactive oxygen species

SBE:

Single base extension

SNP:

Single nucleotide polymorphism

SPSS:

Statistical package for the social sciences

References

  1. Felson DT, Zhang Y (1998) An update on the epidemiology of knee and hip osteoarthritis with a view to prevention. Arthritis Rheum 41(8):1343–1355

    Article  CAS  PubMed  Google Scholar 

  2. Valdes AM, Spector TD (2011) Genetic epidemiology of hip and knee osteoarthritis. Nat Rev Rheumatol 7(1):23–32

  3. Blanco FJ, Rego I, Ruiz-Romero C (2011) The role of mitochondria in osteoarthritis. Nat Rev Rheumatol 7(3):161–169

    Article  CAS  PubMed  Google Scholar 

  4. Maneiro E, Martin MA, de Andres MC et al (2003) Mitochondrial respiratory activity is altered in osteoarthritic human articular chondrocytes. Arthritis Rheum 48(3):700–708

    Article  CAS  PubMed  Google Scholar 

  5. Kim HA, Blanco FJ (2007) Cell death and apoptosis in osteoarthritic cartilage. Curr Drug Targets 8(2):333–345

    Article  CAS  PubMed  Google Scholar 

  6. Cillero-Pastor B, Carames B, Lires-Dean M, Vaamonde-Garcia C, Blanco FJ, Lopez-Armada MJ (2008) Mitochondrial dysfunction activates cyclooxygenase 2 expression in cultured normal human chondrocytes. Arthritis Rheum 58(8):2409–2419

    Article  CAS  PubMed  Google Scholar 

  7. Blanco FJ, Lopez-Armada MJ, Maneiro E (2004) Mitochondrial dysfunction in osteoarthritis. Mitochondrion 4(5–6):715–728

  8. Henrotin Y, Kurz B (2007) Antioxidant to treat osteoarthritis: dream or reality? Curr Drug Targets 8(2):347–357

    Article  CAS  PubMed  Google Scholar 

  9. Grishko VI, Ho R, Wilson GL, Pearsall AW (2009) Diminished mitochondrial DNA integrity and repair capacity in OA chondrocytes. Osteoarthritis Cartilage 17(1):107–113

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  10. Torroni A, Huoponen K, Francalacci P et al (1996) Classification of European mtDNAs from an analysis of three European populations. Genetics 144(4):1835–1850

    CAS  PubMed Central  PubMed  Google Scholar 

  11. Rego-Perez I, Fernandez-Moreno M, Fernandez-Lopez C, Arenas J, Blanco FJ (2008) Mitochondrial DNA haplogroups: role in the prevalence and severity of knee osteoarthritis. Arthritis Rheum 58(8):2387–2396

    Article  CAS  PubMed  Google Scholar 

  12. Rego I, Fernández-Moreno M, Fernández-López C et al (2010) Role of European mitochondrial DNA haplogroups in the prevalence of hip osteoarthritis in Galicia, Northern Spain. Ann Rheum Dis 69(1):210–213

    Article  CAS  PubMed  Google Scholar 

  13. Soto-Hermida A, Fernandez-Moreno M, Oreiro N, Fernandez-Lopez C, Rego-Perez I, Blanco FJ (2014) mtDNA haplogroups and osteoarthritis in different geographic populations. Mitochondrion 15:18–23

  14. Fang H, Liu X, Shen L et al (2014) Role of mtDNA haplogroups in the prevalence of knee osteoarthritis in a southern Chinese population. Int J Mol Sci 15(2):2646–2659

    Article  PubMed Central  PubMed  Google Scholar 

  15. Rego-Pérez I, Fernández-Moreno M, Deberg M et al (2010) Mitochondrial DNA haplogroups modulate the serum levels of biomarkers in patients with osteoarthritis. Ann Rheum Dis 69(5):910–917

    Article  PubMed  Google Scholar 

  16. Rego-Perez I, Fernandez-Moreno M, Deberg M et al (2011) Mitochondrial DNA haplogroups and serum levels of proteolytic enzymes in patients with osteoarthritis. Ann Rheum Dis 70(4):646–652

  17. Garnero P, Ayral X, Rousseau JC et al (2002) Uncoupling of type II collagen synthesis and degradation predicts progression of joint damage in patients with knee osteoarthritis. Arthritis Rheum 46(10):2613–2624

    Article  CAS  PubMed  Google Scholar 

  18. Valdes AM, Hart DJ, Jones KA et al (2004) Association study of candidate genes for the prevalence and progression of knee osteoarthritis. Arthritis Rheum 50(8):2497–2507

    Article  CAS  PubMed  Google Scholar 

  19. Kamarainen OP, Solovieva S, Vehmas T et al (2008) Common interleukin-6 promoter variants associate with the more severe forms of distal interphalangeal osteoarthritis. Arthritis Res Ther 10(1):R21

  20. Attur M, Wang HY, Kraus VB, et al (2010) Radiographic severity of knee osteoarthritis is conditional on interleukin 1 receptor antagonist gene variations. Ann Rheum Dis 69(5):856–861

  21. Altman R, Asch E, Bloch D et al (1986) Development of criteria for the classification and reporting of osteoarthritis. Classification of osteoarthritis of the knee. Diagnostic and Therapeutic Criteria Committee of the American Rheumatism Association. Arthritis Rheum 29(8):1039–1049

    Article  CAS  PubMed  Google Scholar 

  22. Zhang W, McWilliams DF, Ingham SL et al (2011) Nottingham knee osteoarthritis risk prediction models. Ann Rheum Dis 70(9):1599–1604

    Article  PubMed  Google Scholar 

  23. Vilím V, Olejárová M, Machácek S, Gatterová J, Kraus VB, Pavelka K (2002) Serum levels of cartilage oligomeric matrix protein (COMP) correlate with radiographic progression of knee osteoarthritis. Osteoarthritis Cartilage 10(9):707–713

    Article  PubMed  Google Scholar 

  24. Botha-Scheepers S, Riyazi N, Watt I et al (2009) Progression of hand osteoarthritis over 2 years: a clinical and radiological follow-up study. Ann Rheum Dis 68(8):1260–1264

    Article  CAS  PubMed  Google Scholar 

  25. Martínez-Redondo D, Marcuello A, Casajús JA et al (2010) Human mitochondrial haplogroup H: the highest VO2max consumer—is it a paradox? Mitochondrion 10(2):102–107

    Article  PubMed  Google Scholar 

  26. Gómez-Durán A, Pacheu-Grau D, López-Gallardo E et al (2010) Unmasking the causes of multifactorial disorders: OXPHOS differences between mitochondrial haplogroups. Hum Mol Genet 19(17):3343–3353

    Article  PubMed  Google Scholar 

  27. Mishmar D, Ruiz-Pesini E, Golik P et al (2003) Natural selection shaped regional mtDNA variation in humans. Proc Natl Acad Sci USA 100(1):171–176

  28. Kenney MC, Chwa M, Atilano SR et al (2013) Mitochondrial DNA variants mediate energy production and expression levels for CFH, C3 and EFEMP1 genes: implications for age-related macular degeneration. PLoS One 8(1):e54339

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  29. Ruiz-Pesini E, Lapeña AC, Díez-Sánchez C et al (2000) Human mtDNA haplogroups associated with high or reduced spermatozoa motility. Am J Hum Genet 67(3):682–696

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  30. Larsen S, Díez-Sánchez C, Rabøl R, Ara I, Dela F, Helge JW (2014) Increased intrinsic mitochondrial function in humans with mitochondrial haplogroup H. Biochim Biophys Acta 1837(2):226–231

    Article  CAS  PubMed  Google Scholar 

  31. Ruiz-Pesini E, Mishmar D, Brandon M, Procaccio V, Wallace DC (2004) Effects of purifying and adaptive selection on regional variation in human mtDNA. Science 303(5655):223–226

    Article  CAS  PubMed  Google Scholar 

  32. Wallace DC (1999) Mitochondrial diseases in man and mouse. Science 283(5407):1482–1488

    Article  CAS  PubMed  Google Scholar 

  33. Mueller EE, Brunner SM, Mayr JA, Stanger O, Sperl W, Kofler B (2012) Functional differences between mitochondrial haplogroup T and haplogroup H in HEK293 cybrid cells. PLoS One 7(12):e52367

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  34. Hudson G, Panoutsopoulou K, Wilson I et al (2013) No evidence of an association between mitochondrial DNA variants and osteoarthritis in 7393 cases and 5122 controls. Ann Rheum Dis 72(1):136–139

    Article  PubMed Central  PubMed  Google Scholar 

  35. Zeggini E, Panoutsopoulou K, Southam L et al (2012) Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study. Lancet 380(9844):815–823

    Article  PubMed  Google Scholar 

  36. Zhai G, Hart DJ, Kato BS, MacGregor A, Spector TD (2007) Genetic influence on the progression of radiographic knee osteoarthritis: a longitudinal twin study. Osteoarthritis Cartilage 15(2):222–225

  37. Kerkhof HJ, Doherty M, Arden NK et al (2011) Large-scale meta-analysis of interleukin-1 beta and interleukin-1 receptor antagonist polymorphisms on risk of radiographic hip and knee osteoarthritis and severity of knee osteoarthritis. Osteoarthritis Cartilage 19(3):265–271

  38. Miyamoto Y, Mabuchi A, Shi D et al (2007) A functional polymorphism in the 5′ UTR of GDF5 is associated with susceptibility to osteoarthritis. Nat Genet 39(4):529–533

    Article  CAS  PubMed  Google Scholar 

  39. Takahashi H, Nakajima M, Ozaki K, Tanaka T, Kamatani N, Ikegawa S (2010) Prediction model for knee osteoarthritis based on genetic and clinical information. Arthritis Res Ther 12(5):R187

  40. Valdes AM, Doherty M, Spector TD (2008) The additive effect of individual genes in predicting risk of knee osteoarthritis. Ann Rheum Dis 67(1):124–127

Download references

Acknowledgments

The authors express appreciation to Lourdes Sanjurjo and Maria Dolores Velo and to the Department of Orthopaedic Surgery from the CHU A Coruña. This study was supported by grants from Fundación Española de Reumatologia (programa GEN-SER) and from Fondo Investigación Sanitaria (CIBER- CB06/01/0040)-Spain, Fondo Investigacion Sanitaria-PI 12/329 Ministerio Ciencia en Innovacion PLE2009-0144, with participation of funds from FEDER (European Community). Ignacio Rego-perez was supported by Contrato Miguel Servet-Fondo Investigacion Sanitaria (CP12/03192).

Conflict of interest

The authors declare that they have no conflict interest.

Author information

Authors and Affiliations

Authors

Corresponding authors

Correspondence to Francisco J. Blanco or Ignacio Rego-Pérez.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Soto-Hermida, A., Fernández-Moreno, M., Pértega-Díaz, S. et al. Mitochondrial DNA haplogroups modulate the radiographic progression of Spanish patients with osteoarthritis. Rheumatol Int 35, 337–344 (2015). https://doi.org/10.1007/s00296-014-3104-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00296-014-3104-1

Keywords

Navigation