- Research article
- Open Access
Polymorphic variation of hypoxia inducible factor-1 A (HIF1A) gene might contribute to the development of knee osteoarthritis: a pilot study
BMC Musculoskeletal Disorders volume 16, Article number: 218 (2015)
Osteoarthritis (OA) is a multifactorial degenerative condition of the whole joint with a complex pathogenesis whose development and progression is significantly mediated by interactions between the joint cartilage and articular tissues, particularly, proinflammatory mediators and oxidative stress, which results in cartilage deterioration and subchondral bone destruction. HIF-1 alpha regulates oxygen homeostasis in hypoxic tissues such as joint cartilage; efficiency of transcriptional activity of the HIF1A gene is strongly influenced by the presence of polymorphic variants. Given the loss of articular cartilage and with intention to restore damaged tissue, WISP-1 participates in the development of subchondral bone; further, its expression is highly increased in chondrocytes of OA patients. The aim of this study was to evaluate gene frequencies of HIF1A and WISP1 polymorphisms in Mexican patients suffering from knee OA.
We determined HIF1A rs11549465 (P582S), rs11549467 (A588T), and rs2057482 (C191T), and WISP1 rs2929970 (A2364G) polymorphisms in 70 Mexican patients with knee OA and compare them to those present in 66 ethnically matched healthy controls. Genotyping for these polymorphisms was performed by Real-Time PCR using TaqMan probes.
Gene frequencies exhibited a significant increase of the CC genotype of rs11549465 polymorphism in knee OA patients as compared with those present in controls (P = 0.003 OR = 5.7, 95 % CI = 1.7–21.6); CT genotype and T allele showed decreased frequency in the knee OA group vs. the controls (P = 0.003 OR = 0.2, CI = 0.05–0.6; and P = 0.004 OR = 0.2, CI = 0.05–0.65, respectively). Allele frequencies of the other polymorphic variants were similar in both patients and controls.
These results suggest that the presence of the rs11549465 SNP (HIF1A) plays a role protective in the loss of articular cartilage in our population, and offers the possibility to further study the molecular mechanisms within cartilage and subchondral bone.
Osteoarthritis (OA) is one of the most common rheumatic disorders; it is characterized by joint disease whose cause is not completely understood. OA has a complex pathogenesis due to the interaction of genetic, mechanical, biochemical, metabolic, endocrine, and environmental factors that result in cartilage breakdown and diverse changes in subchondral bone, which may lead to chronic pain, joint swelling, deformity and whole joint abnormalities resulting in disability [1–3]. This process entails the formation of bony outgrowths (osteophytes) and inflammation of the synovial membrane, thus triggering catabolic and proinflammatory mediators such as cytokines, prostaglandin E2, neuropeptides and nitric oxide [4–7]. Worldwide estimates indicate that 9.6 % of men and 18 % of women ≥ 60 years have symptomatic OA [8–11].
Through inflammatory mediators, biochemical injury and oxidative stress, viability of chondrocytes is compromised. Increased oxidative stress in articular cartilage has been the target of molecular research and therapeutic intervention [12–14]. Healthy articular cartilage is typically an avascular tissue, the oxygen tension ranges from 0.5 to 10 % . Therefore, in order to maintain oxygen homeostasis in chondrocytes and cartilage, hypoxia-inducible factor-1 alpha (HIF-1α) is necessary to survive extremely low oxygen tensions. [12, 15, 16]. Furthermore, this transcriptional factor also has a role in the regulation of glucose transport, anaerobic energy generation and matrix synthesis by articular chondrocytes. The active site of this protein is an oxygen-dependent degradation domain (ODDD) that functions as an oxygen sensor [17, 18].
In the presence of normal oxygen tension levels, HIF-1α is hydroxylated in a proline residue within ODDD; it subsequently binds to ubiquitin and is degraded in the proteasome [17–19]. However, under hypoxic conditions, hydroxylation is inhibited and HIF-1α accumulates in the cytoplasm, is phosphorylated and translocates to the nucleus in order to activate transcription of its target genes [18–22]. Some of these target genes include nitric oxide synthase 2 (NOS2), vascular endothelial growth factor (VEGF), erythropoietin (EPO), some glucose transporters (GLUT1, GLUT3), Insulin-like growth factor type 2 (IGF2), which potentially acts in order to maintain the chondroprotective functions challenged by the detrimental conditions occurring in the OA joint environment [16, 20–25]. This relationship among different genes renders the close relation of HIF-1α with several pathologies [26–31].
It have been described polymorphic variants within the HIF1A gene; for example, the rs11549465 (P582S), and rs11549467(A588T) single-nucleotide polymorphisms (SNPs) are located in exon 12, on 14th chromosome and influence the transcriptional activity of this gene to increase dramatically in comparison with the common isoform [32, 33].
Due to loss of articular cartilage and with the intention to restore damaged tissue, WNT inducible signaling pathway protein-1 (WISP-1) participates in the development of subchondral bone. This protein plays an important role in the formation, differentiation, growth, and maintenance of bone and articular cartilage. Active Wnt signaling contributes to osteophyte formation and might play an essential role in the anabolic pattern of joint remodeling observed in ankylosing spondylitis and OA . Furthermore, it has also been showed that in both OA patients and experimental models that there is an important increase in the Wnt signaling pathway and over expression of the WISP1 gene [35–38]. Likewise, it was discovered that variant rs2929970 (A2364G) of the WISP1 gene (located within of the 8th chromosome) is related with the development of spinal OA in postmenopausal women .
Because of the genetic variability of OA, the aim of this study was to analyze rs11549465, rs11549467 and rs2057482 SNPs of the HIF1A gene, and rs2929970 SNP of the WISP1 gene in Mexican patients with severe knee OA.
Patients and methods
This study meets all criteria contained in the Declaration of Helsinki and was approved by the Ethics and Research Committee of the Instituto Nacional de Rehabilitación (INR) (Ref. INR-18/13). All participants signed an informed consent letter that included questions regarding age, gender, weight, Body mass index (BMI), and birth origin. All participants were >40 years, and declared to be native to the central region of Mexico, and to have parents and grandparents born in the same geographical region.
A total of seventy patients diagnosed with primary knee OA, and sixty-six age-matched healthy controls without symptoms or signs of OA, other types of arthritis, or any joint diseases were recruited in this study. The diagnosis of knee OA was based on the criteria of the American College of Rheumatology , which included primary OA with any symptoms and radiographic signs of OA according to the Kellgren-Lawrence (K&L) scale (≥2 scale). The clinical examination and radiological assessment were performed by two independent examiners who were blinded to the clinical information. The control subjects were consecutively selected among individuals without a personal and family history of OA; asymptomatic healthy subjects sex and age matched were include as control group. Other etiologies causing knee diseases such as inflammatory arthritis (rheumatoid, polyarthritic or autoimmune disease), posttraumatic or post septic arthritis, skeletal dysplasia or developmental dysplasia were also excluded.
Peripheral blood samples were extracted by venipuncture from each study participant to obtain blood serum for the study of biochemical parameters, and EDTA tubes for isolating DNA.
Determination of biochemical parameters
After collection of blood samples, the serum was separated and maintained at −80 °C until use. For determination of glucose, total cholesterol, and uric acid levels in both study groups, we employed a commercial kit (Diagnostic Systems, Germany). Quantification was performed in by spectrophotometry (iMark™, BioRad).
Obtaining genomic DNA
Genomic DNA was extracted from 200 μL of whole blood with the commercial QIAamp® DNA Blood Mini Kit, QIAGEN (Hilden, Germany), following all of the supplier’s instructions. DNA concentration was determined by spectrophotometry (NanoDrop 2000, Thermo Scientific), and was of ~40 ng/μL.
Selection of HIF1A and WISP1 SNPs and Genotyping
Selection of SNP in HIF1A and WISP1 genes was conducted based on information from the dbSNP database (http://www.ncbi.nlm.nih.gov/projects/SNP/). Three polymorphisms were included for the HIF1A gene and one for the WISP1 gene in the genotyping tests (Table 1). Real-time PCR was performed in a total volume of 10 μL, that contained 40 ng DNA (1 μL), 1X TaqMan Universal PCR Master Mix (5 μL), TaqMan Probes 20X (0.5 μL), and water (3.5 μL). Thermal cycling conditions were as follows: 95 °C for 10 min, followed by 40 cycles at 92 °C for 15 s and at 60 °C for 1 min. The Rotor-Gene Q Real-time PCR System (QIAGEN, Hilden, Germany) was employed for data acquisition. Genotyping of the HIF1A and WISP1 polymorphisms were carried out using the 5′ exonuclease TaqMan Allelic Discrimination assay, which was performed utilizing minor groove binder probes fluorescently labeled with VIC or FAM and the protocol recommended by the supplier (Applied Biosystems, Foster City, CA, USA). Analysis for interpretation was performed with Rotor-Gene Q Series ver. 2.0.2 software.
The demographic and clinical data were presented as Mean ± SD and compared between groups by the Student’s t-test. Multivariate logistic regression was used to estimate odds ratios (ORs) and 95 % confidence intervals (CI) after adjustment for age, gender, BMI, glucose, total cholesterol, and uric acid, by using STATA ver. 12 software. The genotype and allelic frequencies were evaluated by Hardy-Weinberg equilibrium (HWE) and compared by the Chi-square test and Fisher’s exact test by using an online calculator tool (http://www.oege.org/software/hardy-weinberg.html). Allelic and gene frequencies of the HIF1A and WISP1 genes from both study groups were calculated by direct count. P values < 0.05 were considered statistically significant. For estimating risks, we employed OR with a 95 % CI. These calculations were performed using the EpiInfo statistical program (ver. 6, Centers for Disease Control and Prevention, Atlanta, GA, USA).
The demographical variables age, gender, weight, BMI, glucose, total cholesterol, and uric acid of our study populations are depicted in Table 2. Cases were older than controls (P < 0.00001, 55.8 ± 6.7 vs. 47.5 ± 6.6, respectively). The mean BMI of the OA group (29.8 ± 5.1) was significantly higher than the control group (26.9 ± 4.6) (P = 0.0007), similar with the previous studies that reported high BMI increased the risk of developing OA. None of the individuals belonging to the control group had a BMI characteristic of obesity.
Serum levels of glucose and total cholesterol in both groups were similar in patients and controls. Mean values uric acid, were lower in the group of patients with OA as compared to those present in the control group (P = 0.03, 5.48 ± 1.18 vs. 6.28 ± 2.2, respectively). According to radiological KL classification, 62 patients were grade 2 and eight were grade 4.
The HWE demonstrated no differences in the distribution of all polymorphisms studied in both groups (Table 3). Table 4 shows the gene and allele frequencies of the polymorphisms studied in patients in comparison with the control group. Only rs11549465 polymorphism of the HIF1A gene was found to be significantly associated with increased risk of OA. The OA group exhibited an increased frequency of the CC genotype and the C allele in comparison with the control group (P = 0.003, 94.2 vs. 74.2 %, OR = 5.7, 95 % CI = 1.7–21.6; and P = 0.004, 97.0 vs. 87.1 %, OR = 5.03, 95 % CI = 1.53–18.2, respectively). For the same polymorphism, CT genotype and the T allele frequencies were higher in the control group in comparison with the knee OA group (P = 0.003, 25.8 vs. 5.8 %, OR = 0.2, 95 % CI = 0.05–0.60; and P = 0.004, 12.9 vs. 3.0 %, OR = 0.2, 95 % CI = 0.05–0.65, respectively). Distribution of rs11549467 and rs2057482 polymorphisms of the HIF1A gene and the rs2929970 polymorphism of the WISP1 gene in both study groups were statistically nonsignificant.
After adjustment of age, gender, weight, BMI, glucose, total cholesterol, and uric acid, no statistically significant associations with OA were found. Additionally, we investigate the relationship between the radiological grade of OA and the rs11549465 polymorphism showing that the grade 2 maintains a relationship with the polymorphism (CC genotype: P = 0.009, OR = 5.0; C allele: P = 0.01, OR = 4.4; CT genotype: P = 0.009, OR = 0.2; T allele: P = 0.01, OR = 0.2); whereas the grade 4 did not showed any relationship (Additional file 1).
As is the case of other ethnic groups, OA is the most common human arthritis in Mexicans , its incidence is increasing due to the current pandemic of overweight and obesity in this ethnic group. Several risk factors have been described for the development, progression and severity of OA; however, at present it is not possible to explain interindividual variability in destruction of joint cartilage. We studied Mexican patients with knee OA, some SNP in HIF1A and WISP1 genes related with oxygen homeostasis in joint cartilage and bone development, and their relationship with biochemical parameters.
Our results show that the BMI in the patients with OA was higher with respect the healthy control group. This is in line with previous studies that reported how a higher BMI is a risk factor for developing knee OA, probably induced by the biomechanical joint stress .
Interestingly, our results showed a significant decreased level of uric acid in the OA patients with respect the healthy control. This is in line with the study of Mishra et al. , who attributed this phenomenon to the antioxidant properties of uric acid since they found an inverse correlation between uric acid and the presence of malondialdehyde (pro-oxidant agent). This induces to consider a possible link between the reduction of both the content and the antioxidant property of uric acid and the inflammatory process of OA.
Regarding the analysis of polymorphic variants of HIF1A, we found that the rs11549465 SNP located in the exon 12 within the HIF1A gene was associated in Mexican patients with knee OA. Our results show that the presence of the CC homozygous variant or C allele represent potential risk factors for development of knee OA; contrarily, we detected that the heterozygous variant of CT or T allele of the rs11549465 polymorphism of the HIF1A gene (in comparison with the homozygous carriers) play a protector role against the disease. This phenomenon may be explained by the fact that the presence of this polymorphism confers greater stability to the HIF-1α protein, as demonstrated by Tanimoto et al. . In their study it has been demonstrated that the substitution of proline by serine in the 582 (P582S) position enhances its transcriptional activity due to an alteration in the characteristics and properties of the binding sites with the target genes . This permit supposes a beneficial effect in maintaining cartilage homeostasis and therefore avoiding joint damage. A similar phenomenon was also obtained in other immunological disease such as type 2 diabetes mellitus .
Additionally, endochondral ossification process is triggered by the development of osteophytes. WISP-1 is an osteogenic factor and an osteoblast differentiation factor that has been studied in OA models, in which an increase in its expression was reported [32, 33]. WISP-1 is a member of the CCN family of connective tissue growth factors, which also includes WISP-2 and WISP-3. Members of the CCN family have been implicated in developmental processes such as chondrogenesis, osteogenesis, and angiogenesis. French et al.  could show that WISP-1 functions as osteogenesis potentiating factor promoting mesenchymal cell proliferation while repressing chondrocytic differentiation in vitro. This would suggest that the CCN family play a critical role in cartilage homeostasis. Urano et al.  analyzed the rs2929970 (A2364G) 3′UTR polymorphism in Japanese women with vertebral OA, demonstrating an increase in the GG genotype in the sub-group with end-plate sclerosis. This polymorphism is located in the 3′ untranslated region, within a region of splicing variation, and it may influence messenger RNA stability, translational efficiency or gene expression, and subsequently contribute to the risk of OA. Under the same context, and based on the frequency of polymorphism in our population, we decided use the same variant of the WISP1 gene in Mexican patients with knee OA, but in our study we did not find any association. Whatsoever, it is possible that the evaluated polymorphism, do not play a major role in the development of knee OA in our population, so interesting it would be to explore other polymorphic sites within the WISP1 gene. It will be important to replicate this study in distinct ethnic groups to better understand the mechanisms whereby gene interacts with environmental factors to develop OA.
We are aware that a larger cohort of patients is needed in order to strengthen the statistical power of results, and this aspect is the main limitation of our study. However we believe that our preliminary results could be of interest since that there are no papers focused in this topic, especially involving a population with particular genotype such as Mexican population, and could differ from that typically is reported in other populations. Further investigation involving large cohort of patients and different centers could support better these preliminary results.
In conclusion, our results suggest that the presence of the rs11549465 SNP (HIF1A) plays a role protective in the loss of articular cartilage in our population, and offers the possibility to further study the molecular mechanisms within cartilage and subchondral bone. Thus, HIF-1α would be a useful molecular tool for the development of new diagnostic markers, as well as of therapeutic target in OA.
Meulenbelt I. Osteoarthritis year 2011 in review: genetics. Osteoarthritis Cartilage. 2012;20:218–22.
Fernández M, Rego F, Blanco F. Genetics in osteoarthritis. Reumatol Clin. 2007;3 Suppl 3:S1 3-8.
Chapman K, Valdes AM. Genetic factors in OA pathogenesis. Bone. 2012;51:258–64.
Tawonsawatruk T, Changthong T, Pingsuthiwong S, Trachoo O, Saura T, Wajanavisit W. A genetic association study between growth differentiation factor (GDF5) polymorphism and knee osteoarthritis in Thai population. J Orthopaed Surg Res. 2011;6:2–5.
Shin M, Lee S, Kee S, Song S, Kweon S, Park D, et al. Genetic association analysis of GDF5 and ADAM12 for knee osteoarthritis. Joint Bone Spine. 2012;79:488–91.
Shi D, Zheng Q, Chen D, Zhu L, Qin A, Fan J, et al. Association of single-nucleotide polymorphism in HLA class II/III region with knee osteoarthritis. Osteoarthritis Cartilage. 2010;18:1454–7.
Meulenbelt I, Min J, Bos S, Riyazi N, Houwing J, Wijk H, et al. Identification of DIO2 as a new susceptibility locus for symptomatic osteoarthritis. Hum Mol Genet. 2008;17:1867–75.
Arden N, Nevitt M. Osteoarthritis: epidemiology. Best Pract Res Clin Rheumatol. 2006;20:3–25.
De Filippis L, Gulli S, Caliri A, Romano C, Munaó F, Trimarchi G, et al. Epidemiology and risk factors in osteoarthritis: literature review data from “OASIS” study. Reumatismo. 2004;56:169–84.
Peláez-Ballestas I, Sanin LH, Moreno-Montoya J, Alvarez-Nemegyei J, Burgos-Vargas R, Garza-Elizondo M, et al. Epidemiology of the Rheumatic Disease in Mexico. A Study of 5 regions based on the COPCORD Methodology. J Rheum Suppl. 2011;86:3–8.
Woolf AD, Pfleger B. Burden of major musculoskeletal conditions. Bull World Health Organ. 2003;81:646–56.
Ströbel S, Loparic M, Wendt D, Schenk A, Candrian C, Lindberg R, et al. Anabolic and catabolic responses of human articular chondrocytes to varying oxygen percentages. Arthritis Res Ther. 2010;12:R34.
Schipani E, Ryan HE, Didrickson S, Kobayashi T, Knight M, Johnson RS. Hypoxia in cartilage: HIF-1 alpha is essential for chondrocyte growth arrest and survival. Genes Dev. 2001;15:2865–76.
Gelse K, Pfander D, Obier S, Knaup KX, Wiesener M, Henning FF, et al. Role of hypoxia-inducible factor 1 alpha in the integrity of articular cartilage in murine knee joints. Arthritis Res Ther. 2008;10(5):R111.
Grimmer C, Pfander D, Swoboda B, Aingner T, Mueller L, Henning F, et al. Hypoxia-inducible factor 1alpha is involved in the prostaglandin metabolism of osteoarthritic cartilage through up-regulation of microsomal prostaglandin E synthase 1 in articular chondrocytes. Arthritis Rheum. 2007;56:4084–94.
Pfander D, Swoboda B, Cramer T. The role of HIF-1 alpha in maintaining cartilage homeostasis and during the pathogenesis of osteoarthritis. Arthritis Res Ther. 2006;8:104. Epub 2006 Jan 18.
Görlach A. Regulation of HIF-1 alpha at the transcriptional level. Curr Pharm Des. 2009;15:3844–52.
Semenza GL. HIF-1: mediator of physiological and pathophysiological responses to hypoxia. J Appl Physiol. 2000;88:1474–80.
Maxwell PH. Hypoxia-inducible factor as a physiological regulator. Exp Physiol. 2005;90:791–7.
Catrina SB, Okamoto K, Pereira T, Brismar K, Poellinger L. Hyperglycemia regulates hypoxia-inducible factor-1 alpha protein stability and function. Diabetes. 2004;53:3226–32.
Zhou J, Hara K, Inoue M, Hamada S, Yasuda H, Moriyama H, et al. Regulation of hypoxia-inducible factor 1 by glucose availability under hypoxic conditions. Kobe J Med Sci. 2008;53:283–96.
Tanimoto K, Yoshiga K, Eguchi H, Kaneyasu M, Ukon K, Kumazaki T, et al. Hypoxia-inducible factor-1a polymorphisms associated with enhanced transactivation capacity, implying clinical significance. Carcinogenesis. 2003;24:1779–83.
Yamada N, Horikawa Y, Oda N, Iizuka K, Shihara N, Kishi S, et al. Genetic variation in the hypoxia-inducible factor-1α gene is associated with type 2 diabetes in Japanese. J Clin Endocrinol Metab. 2005;90:5841–7.
Tzouvelekis A, Ntolios P, Karameris A, Koutsopoulos A, Boglou P, Koulelidis A, et al. Expression of hypoxia-inducible factor (HIF)-1a-vascular endothelial growth factor (VEGF)-inhibitory growth factor (ING)-4- axis in sarcoidosis patients. BMC Res Notes. 2012;5:654. doi:10.1186/1756-0500-5-654.
Sartori-Cintra AR, Mara CS, Argolo DL, Coimbra IB. Regulation of hypoxia-inducible factor-1α (HIF-1α) expression by interleukin-1β (IL-1 β), insulin-like growth factors I (IGF-I) and II (IGF-II) in human osteoarthritic chondrocytes. Clinics (Säo Paulo, Brazil). 2012;67:35–40.
Konac E, Dogan I, Onen HI, Yurdakul AS, Ozturk C, Varol A, et al. Genetic variations in the hypoxia-inducible factor-1alpha gene and lung cancer. Exp Biol Med. 2009;234:1109–16.
Li P, Cao Q, Shao PF, Cai HZ, Zhou H, Chen JW, et al. Genetic polymorphisms in HIF1A are associated with prostate cancer risk in a Chinese population. Asian J Androl. 2012;14:864–9.
Alidoosti M, Ghaedi M, Soleimani A, Bakhtiyari S, Rezvanfard M, Golkhu S, et al. Study on the role of environmental parameters and HIF-1A gene polymorphism in coronary collateral formation among patients with ischemic heart disease. Clin Biochem. 2010;44:1421–4.
Bahadori B, Uitz E, Mayer A, Harauer J, Dam K, Truschnig-Wilders M, et al. Polymorphisms of the hypoxia-inducible factor 1 gene and peripheral artery disease. Vasc Med. 2010;15:371–4.
Nagy G, Kovacs R, Kereszturi E, Somogyi A, Szekely A, Nemeth N, et al. Association of hipoxia inducible factor-1 alpha gene polymorphism with both type 1 and type 2 diabetes in a Caucasian (Hungarian) sample. BMC Med Genet. 2009;10:79. doi:10.1186/1471-2350-10-79.
Kolyada AY, Tighiouart H, Perianayagam MC, Liangos O, Madias NE, Jaber BL. A genetic variant of hypoxia-inducible factor-1 alpha is associated with adverse outcomes in acute kidney injury. Kidney Int. 2009;75:1322–9.
Sánchez EN, Nava S, Morán C, Romero JF, Cerbón MA. The two leading hypothesis regarding the molecular mechanisms and etiology of preeclampsia, and the Mexican experience in the world context. Rev Invest Clin. 2010;62:252–60.
Nava S, Sánchez E, Mendoza CA, Morán C, Romero JF, Cerbón MA. Polymorphisms in the hypoxia-inducible factor 1 alpha gene in Mexican patients with preeclampsia: a case-control study. BMC Res Notes. 2011;4:68.
Schett G, Zwerina J, David JP. The role of Wnt proteins in arthritis. Nat Clin Pract Rheumatol. 2008;4:473–80.
Blom A, Brockbank S, Lent P, Beuningen H, Geurts J, Takahashi N, et al. Involvement of the Wnt signaling pathway in experimental and human osteoarthritis. Arthritis Rheum. 2009;60:501–12.
Ono M, Inkson C, Kilts T, Young M. WISP-1/CCN4 Regulates by enhancing BMP-2 activity. J Bone Miner Res. 2011;26:193–208.
Leask A. Will o´ the wisp: CCN4 as a novel molecular target in osteoarthritis. J Cell Commun Signal. 2011;5:51–2.
van den Bosch MH, Blom AB, van Lent PL, van Beuningen HM, Blaney Davidson EN, van der Kraan PM, et al. Canonical Wnt signaling skews TGF-β signaling in chodrocytes towards signaling via ALK1 and Smad 1/5/8. Cell Signal. 2014;26:951–8.
Urano T, Narusawa K, Hosoi T, Ouchi Y, Nakamura T, Inoue S. Association of a single nucleotide polymorphism in the WISP1 gene with spinal osteoarthritis in postmenopausal Japanese women. J Bone Miner Metab. 2007;25:253–8.
Altman R, Asch E, Bloch D, Bole G, Borenstein D, Brandt K, et al. The American College of Rheumatology criteria for the classification and reporting of osteoarthritis of the knee. Arthritis Rheum. 1986;29:1039–49.
Oyeyemi AL. Body mass index, pain and function in individuals with knee osteoarthritis. Niger Med J. 2013;54:230–5.
Mishra R, Singh A, Chandra V, Negi M, Tripathy BC, Prakash J, et al. A comparative analysis of serological parameters and oxidative stress in osteoarthritis and rheumatoid arthritis. Rheumatol Int. 2012;32:2377–82.
Hong JM, Kim TH, Chae SC, Koo KH, Lee YJ, Park EK, et al. Association study of hypoxia inducible factor 1alpha (HIF1alpha) with osteonecrosis of femoral head in a Korean population. Osteoarthritis Cartilage. 2007;15:688–94.
French DM, Kaul RJ, D’Souza AL, Crowley CW, Bao M, Frantz GD, et al. WISP-1 is an osteoblastic regulator expressed during skeletal development and fracture repair. Am J Pathol. 2004;165:855–67.
The authors thank Daniel Medina for his assistance in preparing the manuscript.
The authors declare that they have no competing interests.
JFT and ALR participate in study coordination, responsibility for the integrity of the work, interpretation of data, drafted the manuscript, and gave final approval of the version of the paper to be published. CHD, REM, JCG, NGS, YZC, KMF and MSO, collected and interpretation of data, drafted the manuscript. ALM, GAMN and MG performed the statistical analysis, interpretation of data, and help to draft the manuscript. CP and JG help to draft and revise the manuscript, interpretation of data. All authors read and approved the final version of the manuscript.
About this article
Cite this article
Fernández-Torres, J., Hernández-Díaz, C., Espinosa-Morales, R. et al. Polymorphic variation of hypoxia inducible factor-1 A (HIF1A) gene might contribute to the development of knee osteoarthritis: a pilot study. BMC Musculoskelet Disord 16, 218 (2015). https://doi.org/10.1186/s12891-015-0678-z
- Uric Acid
- Articular Cartilage
- Subchondral Bone
- Rs11549465 Polymorphism
- HIF1A Gene