Objective To evaluate the influence of the mitochondrial DNA (mtDNA) haplogroups in the risk of incident knee osteoarthritis (OA) and to explain the functional consequences of this association to identify potential diagnostic biomarkers and therapeutic targets.
Methods Two prospective cohorts contributed participants. The osteoarthritis initiative (OAI) included 2579 subjects of the incidence subcohort, and the cohort hip and cohort knee (CHECK) included 635, both with 8-year follow-up. The analysis included the association of mtDNA haplogroups with the rate of incident knee OA in subjects from both cohorts followed by a subsequent meta-analysis. Transmitochondrial cybrids harbouring haplogroup J or H were constructed to detect differences between them in relation to physiological features including specific mitochondrial metabolic parameters, reactive oxygen species production, oxidative stress and apoptosis.
Results Compared with H, the haplogroup J associates with decreased risk of incident knee OA in subjects from OAI (HR=0.680; 95% CI 0.470 to 0.968; p<0.05) and CHECK (HR=0.728; 95% CI 0.469 to 0.998; p<0.05). The subsequent meta-analysis including 3214 cases showed that the haplogroup J associates with a lower risk of incident knee OA (HR=0.702; 95% CI 0.541 to 0.912; p=0.008). J cybrids show a lower free radical production, higher cell survival under oxidative stress conditions, lower grade of apoptosis as well as lower expression of the mitochondrially related pro-apoptotic gene BCL2 binding component 3 (BBC3). In addition, J cybrids also show a lower mitochondrial respiration and glycolysis leading to decreased ATP production.
Conclusions The physiological effects of the haplogroup J are beneficial to have a lower rate of incident knee OA over time. Potential drugs to treat OA could focus on emulating the mitochondrial behaviour of this haplogroup.
- Knee Osteoarthritis
- Gene Polymorphism
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Osteoarthritis (OA) is a chronic progressive disorder involving movable joints characterised by cell stress and extracellular matrix degradation initiated by micro-injury and macro-injury that activates maladaptive repair responses including pro-inflammatory pathways of innate immunity. The disease manifests first as a molecular derangement (abnormal tissue metabolism) followed by anatomical and/or physiological derangements (characterised by cartilage degradation, bone remodelling, osteophyte formation, joint inflammation and loss of normal joint function) that can culminate in illness.1
OA is the most common form of arthritis, occurring in 10%–20% of the population aged over 50 years, and it is estimated that the population with OA will double in the next 30 years.2 Thus, the identification of risk factors that accelerate disease progression is critical since these factors could become potential targets for disease modification.3 To achieve this objective, the use of well-characterised study cohorts to identify prognostic factors that predict the course of OA, as well as to identify markers for the (early) diagnosis and course of joint damage, becomes imperative. In this sense, both osteoarthritis initiative (OAI) and cohort hip and cohort knee (CHECK) stand out.
OA is a heterogeneous disease in which a combination of modifiable (ie, body mass index (BMI), joint injury) and non-modifiable factors (ie, age, gender, genetics) interact. Thus, the pathogenesis of OA is still unclear; however, it is widely accepted that genetics plays a main role in the prevalence and progression of this disease;4 even prediction tools for knee OA based on genetic and clinical information have been developed.5 ,6 Besides, during the last years, increasing evidence points to the implication of the mitochondria and the mitochondrial DNA (mtDNA) haplogroups in the pathogenesis of the disease.2 ,7 ,8
The mtDNA haplogroups are the result of maternally inherited mutations in the mtDNA acquired throughout the human history and shaped by the climate selection when humans migrated into colder climates.9 ,10 Each of the mtDNA haplogroups harbours specific single nucleotide polymorphisms (SNPs) that influence the behaviour of the mitochondria11 and interact with the nuclear genome,12 influencing our health today.10 Some of these genetic variants have been associated with degenerative disorders,13 metabolic alterations14 or even increased longevity in humans.15
Regarding OA, several studies also reported the association of specific haplogroups with a lower prevalence of the disease,16–19 while others did not.20 Moreover, recent studies showed significant associations of specific haplogroups with a lower rate of radiographic progression and cartilage loss over time in different study cohorts worldwide such as the OAI21 and one Spanish cohort.22
In an attempt to ascertain the correlation of mtDNA haplogroups and the rate of incident knee OA, in this work we performed a replication study and meta-analysis of two individual studies involving subjects from CHECK and OAI cohorts. In addition, functional studies using transmitochondrial cybrids were performed to ascertain the cellular mechanisms underlying the association of mtDNA variants with the pathogenesis of the disease.
Incident knee OA study in subjects from the OAI and CHECK cohorts
The description of CHECK and OAI cohorts is included in the online supplementary methods section. For this study, we included longitudinal data, in terms of Kellgren and Lawrence (KL) grade, of 2579 participants of the incidence subcohort of the OAI and 635 CHECK participants that met the eligibility criteria for an incident knee OA study monitored at predefined intervals for a period of 8 years.
Incident knee OA criteria
The incidence of radiographic knee OA was defined on joint level (knees separately) following the appropriate proposed criteria for each of the two cohorts. In OAI subjects, we followed the definition of incident knee OA proposed by Felson et al23 consisted in a new-onset KL grade ≥2 from baseline to follow-up. In CHECK subjects, we followed the proposed definition of incident knee OA for this cohort24 ,25 consisted in a new-onset KL grade ≥1 from baseline to follow-up in accordance with the very early stage OA in CHECK subjects.
All the statistical analyses were performed using IBM-SPSS software V.19 (IBM, Armonk, New York, USA) and R software V.3.1.2 (The R Foundation for Statistical Computing). All comparisons were two-sided, with p<0.05 defined as statistically significant.
To avoid potential biases associated with the use of standard survival analysis in this context, interval-censored data analysis methods were used (see supplementary methods section). The multivariate analysis was performed by comparisons between haplogroups considering the most common haplogroup H as the reference group. Since there was no interest in all possible pairwise comparisons, no additional adjusting for multiple comparisons was done.
In this work, we performed a meta-analysis of incident knee OA including data from CHECK and OAI. Following the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) guidelines, we conducted a previous computerised search strategy to find other possible relevant studies to include in the meta-analysis (see supplementary methods).
The random-effects model described by DerSimonian and Laird26 was used to calculate a summary statistic and its 95% CI. Adjusted HRs were used as the effect size measure for the association between mtDNA haplogroups and OA incidence. Meta-analysis results were presented on a forest plot graph. To explore heterogeneity, the I2 index was computed. Meta-analysis was carried out using the R software programme (V.3.2.2), using the meta-package. A two-tailed p value <0.05 was considered to be significant. Meta-analysis was planned to be performed on k=2 studies, with an estimated statistical power of 91.9% to detect as statistically significant an HR ≤0.5 associated with each haplogroup, with a p=0.05 two-tailed significance level.
We only selected studies that met the following inclusion criteria: (i) evaluating the association between mtDNA haplogroups and the rate of incident OA over time; (ii) with sufficient data provided to calculate HRs with their corresponding 95% CI. On the contrary, those studies analysing the correlation between mtDNA haplogroups and the prevalence or risk of OA as well as those studies analysing other mtDNA mutations with incidence were excluded.
Functional studies using transmitochondrial cybrids
An extended version of the methodology described herein is available in the online supplementary methods.
Cybrid cultures and culture conditions
The human osteosarcoma cell line 143B.TK− Rho-0 was used to generate the transmitochondrial cybrids by fusing them with platelets from healthy donors carrying the haplogroups J or H following the protocol described by Chomyn,27 such that we finally obtained two types of cybrids: cybrids harbouring haplogroup J and cybrids harbouring haplogroup H.
Flux assay measurements
Extracellular acidification rate (ECAR) (largely result of glycolysis) and oxygen consumption rate (OCR) (indicator of mitochondrial respiration) was determined by direct measurement in a SeaHorse XFp extracellular flux analyser instrument (Seahorse Bioscience, Agilent Technologies) following manufacturer's instructions.
Mitochondrial reactive oxygen species production assay
Mitochondrial peroxide and peroxynitrite were evaluated with dihydrorhodamine 123 (Sigma) and mitochondrial superoxide anion production was assessed with MitoSox Red (Thermo Fisher Scientific).
Oxidative stress response assay: viability assay
After incubation of cells with 300 µM H2O2, the cell viability was measured using CellTiter 96 Aqueous Assay (Promega) following manufacturer's recommendations.
Cells were cultured in presence of staurosporine at 0.2 µM during 2 hours to induce apoptosis and were subsequently washed and resuspended in 1X Annexin-binding buffer; then 5 μL of the Annexin V-fluorescein isothiocyanate and 5 μL of propidium iodide (ImmunoStep) were added to each 100 μL of cell suspension.
In addition, the basal expression of the mitochondrial apoptotic-related genes B-cell CLL/lymphoma 2-like 13 (BCL2L13) and BCL2 binding component 3 (BBC3) in H and J cybrids was also quantified.
Results were expressed as the mean of three independent experiments (mean±SD) using two cybrids (two J cybrids and two H cybrids) from two individuals (two different J individuals and two different H individuals) and two clones from each cybrid. Statistically significant differences between the two groups were determined with t-test; p values <0.05 were considered to be significant.
mtDNA haplogroups and incident knee OA in subjects of the OAI cohort
No significant differences were detected in the distribution of age, BMI, Western Ontario and McMaster Universities Arthritis Index (WOMAC) and contralateral OA at baseline among patients with different haplogroups; however, a significantly different gender distribution was identified, both being haplogroups H and J that showed an increased percentage of females than the rest of haplogroups (table 1).
Cumulative probability of incident knee OA at 8 years was 25.1%. Subjects with the haplogroup J showed the lowest rate of incident knee OA over time, 20.1% (adjusted HR=0.680; 95% CI 0.470 to 0.968; p<0.05). In addition, males had a decreased risk too (adjusted HR=0.590; 95% CI 0.491 to 0.712; p<0.05), meanwhile BMI (adjusted HR=1.066; 95% CI 1.047 to 1.085; p<0.05), total WOMAC (adjusted HR=1.018; 95% CI 1.010 to 1.026;p<0.05) and contralateral knee OA (adjusted HR=1.593; 95% CI 1.328 to 1.900; p<0.05) at baseline were risk factors for a higher risk of incident knee OA (table 2).
mtDNA haplogroups and incident knee OA in subjects of CHECK cohort
No significant differences were detected in the distribution of age, gender, BMI, WOMAC and contralateral OA at baseline among patients with different haplogroups (table 1).
Global cumulative probability of incident knee OA at 8 years was 89.7%. The cumulative knee OA incidence was significantly lower in carriers of the haplogroup J, with 82.1% (adjusted HR=0.728; 95% CI 0.469 to 0.998; p<0.05). In addition, the model also showed that total WOMAC (adjusted HR=1.006; 95% CI 1.001 to 1.012; p<0.05) and contralateral knee OA (adjusted HR=1.313; 95% CI 1.087 to 1.576; p<0.05) at baseline were risk factors to develop incident knee OA (table 2).
The search process identified a total of seven non-duplicated articles and no unpublished article16 ,18 ,22 ,28–31 (see online supplementary table S1). However, after reading the titles and abstracts none of these seven articles was subsequently selected for meta-analysis because they did not follow the inclusion criteria; namely, they did not evaluate the association between mtDNA haplogroups and the rate of incident knee OA over time but analysed the association between these mtDNA variants, or any other mtDNA mutations, and the prevalence of OA in cross-sectional studies. In conclusion, only the two association studies performed herein were selected for subsequent meta-analysis reaching a total of 3214 subjects (2579 patients from the OAI and 635 patients from CHECK) (table 3).
List of evaluated articles to potentially include in the meta-analysis
No between-study heterogeneity was detected for the haplogroup J (I2=0%; p=0.798), however, the random-effects model was evenly used. Both studies showed a similar contribution or relative weight (W), being slightly higher in the OAI study (52.2%) compared with CHECK (47.8%). The results showed that haplogroup J significantly reduces the risk of incident knee OA (combined HR=0.702; 95% CI 0.541 to 0.912; p=0.008) (figure 1).
Functional study using transmitochondrial cybrids
Establishment of basal conditions
At 25 passages, the mtDNA copy number between H and J cybrids acquired the steady state levels (data not shown), meanwhile at 48 hours the doubling time (DT) showed no significant differences between H and J cybrids (data not shown). Based on these setting, all the experiments were performed starting from 25 passages and after 48 hours of cell culture.
Mitochondrial respiration and glycolytic capacity
To measure real-time glycolytic and mitochondrial respiration rates, cybrids were placed in an extracellular flux analyser (Seahorse Biosciences). The analyser measures ECAR and OCR in a transient microchamber, representing glycolysis and mitochondrial respiration, respectively. Glycolysis rate in H and J cybrids were 87.98±11.4 and 69.45±4.69 mpH/min, respectively, indicating a 21.06% decrease in J cybrids (p=0.0004); glycolytic capacity rates in H and J cybrids were 116.3±12.76 and 91.69±6.48 mph/min, respectively, indicating a 21.16% decrease in J cybrids (p<0.0001) (figure 2A). Similarly, mitochondrial basal respiration rate was significantly lower in J cybrids (96.58±60.01 pmol/min) compared with H cybrids (209.08±55.7 pmol/min, p=0.007); as a result, H cybrids showed an increased ATP production (149.95±23.29 vs 65.94±25.72 pmol/min in J cybrids; p<0.0001) (figure 2B).
Mitochondrial reactive oxygen species production and oxidative stress response
Cybrids carrying the haplogroup H had a significantly higher production of peroxide and peroxynitrite than cybrids carrying the haplogroup J (52.51±11.34 vs 41.26±7.48; p<0.05) (figure 2C). Moreover, the analysis of mitochondrial anion superoxide revealed the same significant trend by which H cybrids showed higher levels than J cybrids (8.58±3.0 vs 4.25±0.9; p<0.05) (figure 2D).
In relation to oxidative stress response, the results showed that the percentage of survival cells in presence of H2O2 in H cybrids was significantly lower than in J cybrids (29.63±3.3 vs 56.45±7.36; p<0.05) (figure 2E).
Analysis of apoptosis
The analysis of apoptosis assessed in basal conditions revealed no significant differences between H and J cybrids (3.69±2 and 4.17±1.1, respectively; p>0.05) (data not shown). However, after incubation with staurosporine, cybrids carrying the haplogroup H showed a significantly increased number of apoptotic cells in comparison with J cybrids (7.35±3.78 vs 4.69±1.68; p<0.05) (figure 2F).
Further analysis of the pro-apoptotic gene BBC3 and the anti-apoptotic gene BCL2L13 showed a significantly increased expression of BBC3 in H cybrids compared with J cybrids (3.3-fold; p<0.05). On the contrary, no significant differences were detected in the expression of BCL2L13 (figure 2G).
Here, we report the first replication study followed by a meta-analysis addressing the association between mtDNA haplogroups and the risk of incident knee OA over time using new haplogroup data from two well-characterised cohorts of patients; a previous meta-analysis involving the study of the mtDNA haplogroups consisted in the analysis of their association with the prevalence of the disease.28 In addition, we provide data supporting the possible explanation for these associations using transmitochondrial cybrids.
We assessed, for the first time, the influence of the mtDNA haplogroups in the rate of incident knee OA in subjects of the incidence subcohort of the OAI followed by a replication study in patients from CHECK. Despite OAI and CHECK are geographically different cohorts, the frequency distribution of the mtDNA haplogroups was very similar between both cohorts (χ2 test; p=0.924, data not shown), ruling out a potential confusion due to ethnic origin. Compared with the incidence subgroup of the OAI, CHECK participants experienced an increased radiographic change at follow-up (89.7% vs 25.1%) mainly because of the different incident knee OA criteria and mean age at baseline between both cohorts, as previously described.32 Although both cohorts focus on the early phase of OA, the CHECK cohort represents participants in an even earlier state of the disease33 and the incident knee OA criteria slightly differs from the proposed by Felson et al23 in subjects of the OAI. Notwithstanding, the results obtained reveal that subjects with haplogroup J show a lower rate of incident knee OA in both cohorts.
To date, different associations involving the haplogroup J have been described in the context of OA. Subjects carrying this haplogroup have a lower prevalence of knee and/or hip OA,16 ,17 ,19 ,28 besides this mtDNA variant also associates with lower serum levels of catabolic type II collagen biomarkers34 and metalloproteinases (MMPs)35 and has been correlated with higher telomere length and lower nitric oxide production in articular chondrocytes.36 However, a work by Hudson et al found no evidence of associations between mtDNA variants and the risk of OA.20 Although the study by Hudson et al is a prevalence study, and not an incident knee OA analysis as is the case of the study presented herein, some points could clarify this; control samples used in their study are population-based controls with symptomatic information and without radiographic data. Up to 50% of patients without joint symptoms may have radiographic changes related to OA,37 therefore, the selection of adequate healthy controls is crucial to draw consistent conclusions in case-control studies; this point could be one of the causes by which one study performed by the arcOGEN consortium also failed to replicate previous associations at genome-wide significance level (p≤5.0×10−8), such as GDF5, chromosome 7q22 or MCF2L gene polymorphisms.38 Finally, as postulated by these authors, the relative contribution of speciﬁc mtDNA variants could vary in different ethnic groups by means of homoplasy and/or geographic differences in the finer details of subhaplogroup structures of mtDNA.20
The results of the meta-analysis indicate that the associations are robust and reveal a strong association with the haplogroup J. The haplogroup J is characterised by a set of uncoupling mitochondrial polymorphisms,9 ,10 preferentially non-synonymous SNPs,39 acquired during its evolutionary history. These aspects make this haplogroup to be biochemically different from other mitochondrial variants, specially the haplogroup H.40 ,41
Increasing evidence suggests that low-grade chronic inflammation in the joint promotes OA progression, and changes in cellular bioenergy metabolism can reprogramme inflammatory response, leading to the disturbance of cellular energy balance and increase cell stress.42 This evidence implies that mitochondria, as the regulators of cell metabolism, as well as the mtDNA haplogroups, as one of the main modulators of cellular bioenergetics,43 are involved in the development of OA as previously proposed.2 ,44 Nevertheless, in an attempt to find out the possible cellular mechanisms underlying the associations described herein, we performed a functional study of the mtDNA haplogroups using transmitochondrial cybrids.
Transmitochondrial cybrids are cell lines consisting of mitochondria from different sources in a defined and uniform nuclear background. They constitute an interesting model and allow the study of the real role of different mtDNA polymorphisms under identical nuclei, and they also provide a window into early stages of disease pathogenesis, which is not available from pathological specimens. Because of that, these cell models have been proposed and widely used to explore the contribution of mitochondrial dysfunction and mtDNA mutations to the pathogenesis of human diseases, such as Parkinson or cancer.45 ,46 Through the use of this cellular model, recent studies showed that J variant associates with decreased expression of specific genes related to inflammatory response, complement and apoptosis when compared with the haplogroup H.12 The functional analysis described herein included specific metabolic measurements using an extracellular flux analyser as well as specific aspects proposed to be related to OA, such as mitochondrial reactive oxygen species (ROS) production, oxidative stress and apoptosis.7 ,44 ,47 The results obtained reveal that cells harbouring the haplogroup J show a physiological behaviour that seems to be protective against the development of OA.
This physiological behaviour includes a significantly lower production of mitochondrial superoxide anion and peroxynitrite, as well as a higher ability to cope with oxidative stress. It has been demonstrated that mitochondria-derived ROS and nitrogen radicals lead to an upregulation of MMPs44 as well as an overproduction of pro-inflammatory cytokines,48 cellular damage or, in some cases, apoptosis. Interestingly, cybrids harbouring the haplogroup J show a significant lower rate of apoptosis under stress conditions, and a lower expression of the pro-apoptotic gene BBC3, which induces apoptosis through mitochondrial dysfunction.
From a metabolic point of view, haplogroups H and J have a different behaviour too. H cybrids show higher mitochondrial respiration rate and glycolytic capacity, which is reflected in an increased ATP generation compared with cybrids carrying the haplogroup J. The haplogroup H presents the highest levels of conserved amino acids,9 which could determine its Oxidative Phosphorylation System (OXPHOS) coupling efficiency and ATP production41; however, this high efficiency would be accompanied by an increased ROS generation and a higher oxygen consumption, as demonstrated herein and proposed elsewhere.10 ,41
In recent years, several studies supported a key role of the mitochondria in the pathogenesis of OA and the study of this organelle in the context of this disease attracted much attention.2 ,49 ,50 The mechanisms underlying, at least in part, the association described herein are related to different functional consequences characteristic of specific mitochondrial polymorphisms; thus, ROS production (both peroxynitrite and superoxide anion), oxidative stress and apoptosis are downregulated in cells harbouring mitochondrial polymorphisms characteristic of the mtDNA haplogroup J.
Although a direct functional link between haplogroups and cartilage biology has not been made in this study, a recent work in conplastic mice (mice with constant nuclear background but different mtDNA variants) shows that mtDNA haplotype profoundly influences in health longevity through mitochondrial proteostasis and ROS generation, insulin signalling, obesity, telomere shortening or mitochondrial dysfunction.51 Because most of these aspects are also involved in OA pathogenesis, a functional link between mtDNA variation and cartilage biology could really exist.
Despite only two studies were combined, the results of the meta-analysis are consistent enough to support a real association of haplogroup J with a lower risk of incident knee OA. Furthermore, data from both cohorts were analysed in a similar way, and effect size measures were adjusted for baseline characteristics in order to minimise residual confounding. Both OAI and CHECK are well-characterised cohorts, constructed with rigorous methodology in which patients are evaluated by objective methods in spaced visits. This should contribute to minimise information biases and strengthen the conclusions of this study.
In summary, the results of this work have a special clinical relevance. On the one hand, they claim that polymorphisms of the mtDNA haplogroup J alter metabolism and cell physiology predisposing the cell to a less favourable environment to develop incident OA, which allows the design of potential drugs that emulate the physiological effects related to this haplogroup, as well as the consideration of the mtDNA haplogroups as candidate diagnostic biomarkers in OA; among these therapeutic strategies, potential drugs that modulate the activity of the mitochondrial respiratory chain in a similar way to that of the haplogroup J, or even the development of a cellular therapy using cells with mitochondria harbouring the haplogroup J, could be interesting. On the other hand, the results obtained permit to select patients with OA not harbouring the haplogroup J (ie, haplogroup H) as ideal candidates for clinical trials because they are more likely to suffer a higher rate of incident knee OA.
The OAI is a public-private partnership comprising five contracts (N01-AR-2-2258; N01-AR-2-2259; N01-AR-2-2260; N01-AR-2-2261; N01-AR-2-2262) funded by the National Institutes of Health (NIH), a branch of the Department of Health and Human Services, and conducted by the OAI Study Investigators. Private funding partners include Pfizer; Novartis Pharmaceuticals; Merck Research Laboratories and GlaxoSmithKline. Private sector funding for the OAI is managed by the Foundation for the NIH. This manuscript was prepared using an OAI public use data set and does not necessarily reflect the opinions or views of the OAI investigators, the NIH or the private funding partners. CHECK cohort study is funded by the Dutch Arthritis Association. It is led by a steering committee comprising 16 members with expertise in different fields of OA. It is chaired by Professor J W J Bijlsma and coordinated by J Wesseling. The following institutions are involved: Erasmus Medical Center Rotterdam; Kennemer Gasthuis Haarlem; Leiden University Medical Center; Maastricht University Medical Center; Martini Hospital Groningen/Allied Health Care Center for Rheumatology and Rehabilitation Groningen; Medical Spectrum Twente Enschede/Ziekenhuisgroep Twente Almelo; Reade, formerly Jan van Breemen Institute/VU Medical Center Amsterdam; St Maartens-kliniek Nijmegen; University Medical Center Utrecht and Wilhelmina Hospital Assen. We would like to thank the participants, principal investigators, co-investigators and staff of CHECK.
Handling editor Tore K Kvien
FJB and IR-P contributed equally.
Twitter Follow Ignacio Rego-Perez at @nacho_rego
Contributors FJB and IR-P contributed equally in the design and coordination of the study; both conceived the study, participated in its design and helped to draft the final version of the manuscript; MF-M carried out the cybrid experiments and helped to draft the manuscript and data interpretation; AS-H carried out the experimental procedures of mitochondrial haplogroup assignment; MEV-M, EC-P, SR and TH-G helped to carry out the cybrids cell culture, the subsequent experimental procedures and the haplogroup assignment; SP supervised the statistical procedures; NO-V and CF-L helped the understanding of the clinical and radiological variables included in the different OAI and CHECK datasets; RG provided the necessary infrastructure for the development of the transmitochondrial cybrids. All the authors approved the final version of the manuscript.
Funding This study was supported by grants from Fondo de Investigación Sanitaria CIBERCB06/01/0040-Spain, RETIC-RIER-RD12/0009/0018 and PI14/01254, integrated in the National Plan for Scientific Program, Development and Technological Innovation 2013–2016 and funded by the ISCIII-General Subdirection of Assessment and Promotion of Research-European Regional Development Fund (FEDER) ‘A way of making Europe’. IRP is supported by Contrato Miguel Servet-Fondo de Investigación Sanitaria (CP12/03192).
Competing interests None declared.
Patient consent Obtained.
Ethics approval National Institutes of Health and Dutch Arthritis Association.
Provenance and peer review Not commissioned; externally peer reviewed.
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