- Research article
- Open Access
Vitamin D receptor gene polymorphisms and susceptibility of hand osteoarthritis in Finnish women
Arthritis Research & Therapy volume 8, Article number: R20 (2005)
We examined whether polymorphisms of the vitamin D receptor (VDR) gene was associated with individual risk of hand osteoarthritis (OA). Radiographs of both hands of 295 dentists and of 248 teachers were examined and classified for the presence of OA using reference images. The VDR ApaI and TaqI genotypes were determined by PCR-based methods. No association was observed between the VDR polymorphisms and the odds of overall hand OA. However, the carriers of the VDR t allele or At haplotype were at almost half the odds of symmetrical hand OA (odds ratio [OR] = 0.60, 95% confidence interval [CI] = 0.38–0.94 and OR = 0.59, 95% CI = 0.38–0.93, respectively) compared with the carriers of the T allele and of the non-At haplotype, respectively. Increased odds of this disease, on the contrary, was observed for women with two copies of the VDR a allele (OR = 1.93, 95% CI = 1.99–3.70) compared with women with the AA genotype. Conversely, the VDR a allele carriage was associated with a tendency of lowered odds of osteophyte (OR = 0.51, 95% CI = 0.25–1.03). When the genotype data were used to construct haplotypes, the VDR AaTt joint genotype appeared to pose a remarkably lower odds (OR = 0.26, 95% CI = 0.08–0.91) of osteophyte compared with the AAtt joint genotype. As a novel finding we observed a joint effect of a low calcium intake and VDR polymorphisms on symmetrical OA; the OR was 2.64 (95% CI = 1.29–5.40) for carriers of the aT haplotype with low daily calcium intake compared with non-carriers of the haplotype with high daily calcium intake. Our results suggest that VDR gene polymorphisms play a role in the etiology of symmetrical hand OA. Moreover, the association between the VDR gene and OA may be modified by calcium intake.
Osteoarthritis (OA) is the most frequent cause of musculoskeletal disability in developed countries. Two main subsets of the disease are recognized: monoarticular OA and polyarticular OA . Despite the fact that OA is the most common joint disease, its etiology remains unclear. Among the most commonly suspected risk factors are age , previous injury , and obesity [2, 4]. Current evidence suggests a genetic component to OA, with the heritability for hand OA and knee OA ranging from 39% to 65% [5, 6].
Some of the studies have proposed that genetic susceptibility may be more relevant to OA in women than to OA in men, and that the role of genes in the development and progression of OA may vary between joint groups .
Hand OA often aggregates with knee OA [5, 8, 9]. Epidemiologic studies have shown that women with radiographic changes in the knee or the hand have an increased bone mass after adjustment for age and other covariates as compared with those women without OA [10, 11]. Genetic factors affecting bone density may therefore play a role in the development of OA.
The vitamin D endocrine system, consisting of the steroid vitamin D, the vitamin D receptor (VDR) and the metabolizing enzymes, plays an important role in skeletal metabolism, OA, the immune response, and cancer . The VDR gene acts as an important regulator of calcium metabolism and bone cell function , and it was the first candidate gene to be studied in osteoporosis. Biological support for an association between the VDR genotype and OA comes from studies showing that serum levels of vitamin D are related to the progression of knee OA  and to incident changes of radiographic hip OA characterized by joint space narrowing .
It has been shown that common allelic variations in the VDR locus can be used to predict the bone turnover rate . The polymorphisms at the 3' end of the gene include two polymorphisms detectable with BsmI and ApaI restriction enzymes that are located in intron 8 and one polymorphism detectable with TaqI restriction enzyme located in exon 9, while a poly(A) microsatellite polymorphism is located in the 3' untranslated region of the gene. The ApaI, BsmI, and TaqI polymorphisms have been shown to be in strong linkage disequilibrium .
Keen and colleagues  examined the VDR TaqI polymorphism, associated with bone mineral density and osteoporosis, in relation to OA among postmenopausal English women. They found that women carrying one or two TaqI wild-type alleles (T) had an approximately threefold risk of OA in the knee joints compared with homozygotes for the variant allele (t). Uitterlinden and colleagues [18, 19], on the other hand, demonstrated that a VDR aT haplotype (the T allele together with variant a allele at the ApaI locus) was related to knee OA, especially in osteophyte formation among elderly Dutch men and women.
It can be expected that the same polymorphisms could be important for both knee OA and hand OA, although no association between the VDR genotypes and hand OA was found in Japanese women  and in American men and women . Various factors may have contributed to these apparently discordant results among studies, including the differences in the VDR genotypes distribution, the genetic environment and age structure of the studied population , and, more specifically, failure to take into account factors that modulate the effect of VDR gene on the risk of OA. Observations that the VDR genotypes are associated with intestinal calcium absorption [23, 24] and that calcium interacts with VDR gene polymorphisms in studies of bone density [25, 26] may suggest that the effect of VDR polymorphisms on the risk of OA may be modified by daily calcium intake.
The Finnish population is genetically relatively homogeneous and represents an isolated gene pool, the isolation being caused by linguistic and geographic factors. To our knowledge, the association between the VDR gene polymorphisms and OA has not been studied in the Finnish population. The aim of the present study was to examine whether the VDR polymorphisms, which were previously associated with knee OA, are also associated with the risk of hand OA in Finnish middle-aged women. In addition, we evaluated whether the calcium intake modifies the relationship between the VDR gene polymorphisms and hand OA.
Materials and methods
The potential study subjects were identified through the register of the Finnish Dental Association and the Finnish Teachers Trade Union. Four hundred and thirty six women aged 45–63 years were randomly selected from each occupational group using the place of residence as an inclusion criterion (Helsinki or its neighboring cities) for participation in a study concerning work-related factors and individual susceptibility in the etiology of hand OA. Of those who received the questionnaires in 2002, 295 (67.7%) dentists and 248 (56.9%) teachers participated in a clinical examination between October 2002 and March 2003. Participation in the study was voluntary and based on informed consent. The Hospital District of Helsinki and Uusimaa Ethics Committee for Research in Occupational Health and Safety approved the study proposal.
Hand radiography and image analysis
Both hands of the participants were radiographed. Kodak X-ray films were exposed with Siemens X-ray equipment (48 kV, 10 mA, focus film distance = 115 cm; Siemens, Munich, Germany). The analogue radiographs were evaluated by an experienced radiologist (TV) who was blinded to the occupation, age, and all health data of the subjects.
Each distal interphalangeal (DIP) joint, proximal interphalangeal (PIP) joint, thumb interphalangeal joint, and metacarpophalangeal (MCP) joint of both hands was graded separately, and was classified for the presence of OA using a modified Kellgren and Lawrence system . The classification criteria were: grade 0 = no OA, grade 1 = doubtful OA, grade 2 = mild OA, grade 3 = moderate OA, and grade 4 = severe OA . Osteophytes were separately classified as absent (grade 0), minimal or questionable (grade 1), or distinct (grade 2). Reference images were used. The description of reference images has been given elsewhere .
The reliability of the readings was estimated by measuring intraobserver and interobserver agreements, using the weighted Cohen's kappa coefficient with quadratic weights , for 46 randomly chosen subjects. For this estimation, a second reading was independently performed by TV and another experienced radiologist (KL). The inter-observer agreement for OA ranged from 0.67 to 0.85 for DIP joints, from 0.39 to 0.61 for PIP joints, and from 0.18 to 0.69 for MCP joints. The intraobserver agreement for OA ranged from 0.73 to 0.88 for DIP joints, from 0.67 to 0.92 for PIP joints, and from 0.59 to 1.0 for MCP joints. The readings of TV only were used in the subsequent statistical analyses.
If the subject had at least three finger joints with radiographic OA of grade 2–4, she was classified as having finger OA. Symmetrical OA was defined as a subcategory of OA in at least two symmetrical pairs of the joints (if two joints of the hand are affected, the same joints of the opposite hand are also affected). If the subject had at least two finger joints with distinct osteophyte (grade 2), she was classified as having finger osteophyte.
All DNA samples were extracted from lymphocytes by a DNA extraction kit (PUREGENE® DNA Purification Kit; Gentra Systems, Plymouth, MN, USA).
The VDR ApaI and TaqI genotypes were resolved by a PCR-based method employing primers described by Riggs and colleagues . Briefly, the PCR reactions were set up as follows: 50–100 ng template, 1 U DNA polymerase (Biotools; B&M Labs, SA, Madrid, Spain), 0.2 mM dNTPs, 0.5 μM each primer and 1.5 mM MgCl2 in the magnesium-free PCR buffer (Biotools; B&M Labs, SA). After initial denaturation of 2 min at 94°C, 28 cycles of 10 s at 94°C, 20 s at 60°C, and 30 s at 72°C were performed, followed by a 5 min final extension at 72°C. Aliquots of the PCR products were digested with Bsp120I (Fermentas) and TaqI (Fermentas) for ApaI and TaqI polymorphisms, respectively, and were electrophoresed on 3% agarose gel containing ethidium bromide. The final results were interpreted from pictures of the gels photographed under UV light; alleles lacking restriction sites for ApaI and TaqI were denoted as VDR A and T alleles, and alleles with the restriction sites as a and t, respectively.
Data regarding individual characteristics were collected by a self-administered questionnaire that included items on anthropometric measures, use of hormone therapy, dietary habits, and smoking history.
The use of hormone therapy was assessed by the questions 'Do you use hormonal medication? If yes, what is the name of medication?' and 'How long have you been using this hormonal medication?'
Queries about dietary habits on a daily average basis included coffee consumption (the number of cups), milk/sour milk consumption (the number of cups, one cup = 2 dl), yogurt consumption (the number of deciliters), and cheese consumption (the number of slices). Alcohol consumption was reported on a weekly average basis (number of portions, one portion = 12 cl for wine, 0.33 l for beer, and 4 cl for vodka or liquor).
Daily calcium intakes from particular dairy products were calculated from a knowledge of amounts of calcium per 100 g (1 dl) of each dairy product and amount of each product consumed per day. Subjects were asked about their daily intake of calcium from vitamin supplements. Daily calcium intake was determined by adding up the calcium level of the dairy products and the amount of calcium from vitamin supplements. For the analysis, daily calcium intake was compared with Finnish limit values  and was classified into low intake (<400 mg/day), adequate intake (400–800 mg/day), and high intake (>800 mg/day).
Weight was measured without shoes to the accuracy of 0.1 kg. The body mass index (BMI) (weight [kg] per height squared [m2]) was calculated based on self-reported height and the weight measured during the clinical examination session. The BMI was placed into tertiles for logistic regression analysis (low, <22.5 kg/m2; medium, 22.5–25.5 kg/m2; and high, >25.5 kg/m2).
Based on their smoking history, subjects were classified into never daily smokers or daily (current or previous) smokers.
Allele and genotype frequencies were compared between individuals with and without OA using Fisher's exact probability test or the chi-square test. Carriage rates for the alleles were calculated as the proportion of individuals with at least one copy of the allele. Each gene locus was also examined for an allele dosage effect, by comparing the numbers of individuals heterozygous and homozygous for the test allele among those with and without OA.
The VDR haplotypes were statistically reconstructed from population genotype data using the PHASE program with the Markov chain method for haplotype assignments .
A set of logistic regression analyses was performed to examine the association between the VDR genotypes and hand OA. To evaluate whether the association between the genotypes and OA is modified by daily calcium intake, the odds ratio (OR) of having OA was calculated as a function of daily calcium intake (low intake versus moderate or high intake), of the presence of a risk allele, and of their interaction. An absence of a risk allele and high or moderate daily calcium intake was used as reference group.
Crude and adjusted ORs and their 95% confidence intervals (CIs) were calculated using the SPSS statistical package (SPSS Inc., Chicago, IL, USA). The ORs were adjusted for the potential confounding factors of age, occupation, height, BMI, use of hormone therapy, daily calcium intake, and coffee and alcohol consumption. Since the crude and adjusted ORs did not differ significantly, only the adjusted ORs are shown.
The prevalence of the overall hand OA, symmetrical OA, and osteophytes among the female dentists and teachers aged 45–63 years were 29%, 21%, and 7%, respectively. The basic characteristics of the study subjects by their hand OA status (absence or presence of OA) are summarized in Table 1. Radiographic findings were more prevalent in the teachers, in the subjects who were older, and in more often users of hormone therapy.
The genotype and allele distributions of the VDR ApaI and TaqI loci did not deviate significantly from Hardy–Weinberg equilibrium, and the frequencies agreed with those previously observed in Finnish women .
Six of the possible nine joint genotypes were reconstructed by the PHASE program  from the ApaI and TaqI genotype data. Five of the genotypes (AaTt, AaTT, aaTT, AATt, and AAtt) were relatively common, exhibiting frequencies of 28.4%, 21.0%, 18.6%, 16.6%, and 11.8%, whereas the frequency for the AATT genotype was only 3.7%. The frequencies of the VDR aT, At and AT haplotypes were 43%, 34%, and 32%, respectively.
The age, height, BMI, occupation, use of hormone therapy, smoking history, coffee consumption, and alcohol drinking were similar in the VDR genotype groups, but the daily calcium intake was higher in the tt and Tt genotype groups compared with the TT genotype group (775 ± 382, 678 ± 380, and 647 ± 355 mg, respectively, P = 0.05). The proportion of ever-smokers was higher among the carriers of the aT haplotype compared with the non-carriers (24% versus 17%, P = 0.042).
No association was observed between individual VDR gene polymorphisms and the overall odds of hand OA. However, the VDR aa genotype posed an almost doubled odds of symmetrical hand OA (OR = 1.93, 95% CI = 1.00–3.70) compared with the AA genotype (Table 2). The women with at least one copy of the VDR t allele (Table 2) or carrying the At haplotype (Table 3) were at almost halved odds of this disease (OR = 0.60, 95% CI = 0.38–0.94 and OR = 0.59, 95% CI = 0.38–0.93, respectively) compared with the carriers of T allele and the non-At haplotype, respectively. On the other hand, the VDR a allele carriage was associated with a tendency (OR = 0.51, 95% CI = 0.25–1.03) to lowered odds of osteophyte.
The VDR AaTt joint genotype appeared to pose a remarkably lower odds of osteophyte (OR = 0.26, 95% CI = 0.08–0.91) compared with the AAtt joint genotype (Table 3).
The separate and joint effects of the VDR aT haplotype and a low calcium intake on the risk of hand OA are presented in Table 4. The presence of the aT haplotype alone was associated with an increased odds of symmetrical OA (OR = 1.58, 95% CI = 0.88–2.85) and with a decreased odds of osteophytes (OR = 0.39, 95% CI = 0.18–0.85). Similarly, there was no statistically significant association between a low calcium intake and OA among subjects without the aT haplotype. However, both factors (the aT haplotype and low calcium intake) acted synergistically to increase the odds of OA. We observed a joint effect of a low calcium intake and carriage of the VDR aT haplotype on symmetrical OA; the OR was 2.64 (95% CI = 1.29–5.40) for carriers of the aT haplotype with a low daily calcium intake compared with non-carriers of the haplotype with a moderate or high daily intake.
In agreement with previous observations  that the VDR a allele appeared to always be associated with the T allele, identical ORs for the VDR a allele carriage and the aT haplotype carriage were seen in the present study (Tables 2 and 3).
An age-dependent pattern for the presence of finger OA has been found among adult participants of the Tecumseh Community Health Study . Among individuals under the age of 44 years OA was observed almost exclusively in the DIP joints, whereas among older participants the PIP and MCP joints were affected. Several studies provided clear evidence for a polyarticular subset of hand OA in women [28, 35–37], with three major determinants of the pattern of polyarticular involvement being symmetry, clustering by row, and clustering by ray (in descending order of importance). While OA in a specific joint (monoarticular OA) may result from acute trauma  or from mechanical stress  to the joint, OA with multiple joint involvement (polyarticular OA) might be dominated by systemic factors to which all joints would be equally susceptible.
In the present study we aimed to examine more severe cases of OA, which are more likely to bear a genetic component. OA was therefore defined to be present if there was a radiograph reading of grade 2–4 in at least three joints of the fingers. OA was defined to be symmetrical if at least two symmetrical pairs of joints (the same joint in both hands) were affected.
Our findings suggest that there may indeed be a relationship between the VDR ApaI and TaqI polymorphisms and the risk of symmetrical hand OA in Finnish women. The VDR aa genotype, which has previously been associated with high bone mass , posed a nearly twofold increased odds of symmetrical hand OA as compared with the AA genotype associated with lower bone mass. In contrast, the odds of this disease was almost halved among those with the VDR t allele, which has previously been associated with a higher rate of bone turnover  and lower bone mass  compared with the T allele.
In our study, the association between the VDR aT haplotype and hand OA depended on the interaction with dietary calcium intake. A joint effect of a low calcium intake and carriage of the VDR aT haplotype on risk of symmetrical OA exceeded their additive effects, indicating that the VDR aT haplotype is a potential risk factor for OA among women with insufficient calcium intake. These relationships were independent of other risk factors such as age, occupation, BMI, use of hormone therapy, and smoking history.
Regulation of intracellular calcium plays a key role in hypertension, insulin resistance, and obesity . A protective effect of dietary calcium in preventing bone fragility and certain cancers has been reported . Several previous studies have recognized that the association between VDR alleles and bone mineral density may vary depending on the level of calcium intake [25, 26, 43–45], and there is evidence that calcium is able to enhance cartilage repair and stimulate collagen production . The VDR baT haplotype has been related to enhanced abnormality in the calcium regulation of the parathyroid hormone secretion from adenomatous parathyroid cells of primary human parathyroid tumor . However, no other study has evaluated the potential relation between calcium intake and VDR genotypes in OA etiology. Our finding, if confirmed, implies a considerable potential for a role of nutritional interventions for OA.
In the Framingham study  the growth of knee osteophytes was found to be associated with the vitamin D level. In the present study, women with the VDR AaTt joint genotype had the lowest odds and those with the AATT genotype the highest odds of hand osteophytes as compared with the AAtt genotype. The direction of these associations contrast the findings in the studies of osteophytes formation in the knee [17–19] and the lumbar spine , but agree with the findings related to the severity and presence of lumbar spine osteophytes .
The large amount of positive genetic association data in a number of diseases such as osteoporosis, OA, diabetes, and cancer  suggest functional consequences of VDR gene polymorphisms. The ApaI polymorphism is unlikely to have functional consequences, however, since it is located in intron 8 and is not affecting any splicing site or transcription factor binding site. Moreover, although the TaqI polymorphism is located in the coding sequence (exon 9) of the VDR gene, it has no effect to the encoded protein sequence . Nevertheless, supporting the modifying role of the VDR polymorphisms in the VDR functionality, lower VDR mRNA levels were found to be associated with homozygosity for the a and T alleles .
Our study has several limitations. The cross-sectional study design precluded the assessment of an effect of dietary calcium intake on the incidence or progression of OA. The relatively small number of subjects reduced the power of the study to detect differences. Another limitation arises from the fact that calcium intake was assessed based on a questionnaire, and thus the recall bias may affect the accuracy of information gathered. Finally, vitamin D intake was not assessed in our population.
Despite these limitations, the present findings are not anticipated to be caused by selection bias. First, selection on the genotype is unlikely since all study subjects were of homogeneous Finnish origin. Second, the prevalence of hand OA among the women analyzed in this study is similar to that seen in other studies [52–54]. Third, the VDR genotype frequencies in this population did not significantly deviate from the Hardy–Weinberg equilibrium and the genotype frequencies were similar to those previously observed in Finnish women . Neither could the associations be explained by other risk factors, since these potential confounders were controlled in all statistical analyses.
The lower level of interobserver agreement for radiographic findings was not surprising. Despite training and the use of reference images, each reader graded the radiographs according to his or her own inherent standard about what constituted a positive finding. The high intraobserver agreement suggests that the classification criteria applied here are highly reproducible. Because all radiographs were evaluated by one observer who was blind to subjects' genetic data, the high intraobserver repeatability implies that the comparison between subjects with different VDR genotypes was unbiased. The possibility of non-differential misclassification of osteoarthritis cannot be ruled out. Non-differential misclassification of a binary outcome usually produces bias toward the null.
It could be argued that at least some of the associations found in this study were spurious, considering multiple comparisons were performed. However, there are several arguments to support the consistency of these results rather than attributing them to chance. First, we hypothesized a priori that the interaction observed in this study would occur, based on the known biology of the VDR gene in regulation of calcium metabolism. Second, our sample was homogeneous in terms of age, gender, ethnicity, and genetic background. Third, haplotypes were constructed taking into account the knowledge that collective grouping of single nucleotide polymorphisms in haplotypes has a stronger association with the phenotype than individual polymorphisms. Finally, to minimize the number of analyses performed, the interaction hypothesis was tested with the risk haplotype only.
Although the possibility remains that the studied polymorphisms do not directly affect the individual susceptibility of hand OA, but are in linkage disequilibrium with an unknown nearby susceptibility locus, our results provide evidence of the involvement of the VDR polymorphism in the etiology of symmetrical hand OA. In addition, our findings suggest a detrimental effect of low dietary calcium intake on OA. The findings remain to be weighted in future studies. Further studies into mechanisms underlying the relationships between calcium and OA may improve the understanding of the obtained results.
= body mass index
= confidence interval
= distal interphalangeal
= polymerase chain reaction
= proximal interphalangeal
= odds ratio
= vitamin D receptor.
Kellgren JH, Moore R: Generalized osteoarthritis and Heberden's nodes. BMJ. 1952, 1: 181-187.
Felson DT, Lawrence RC, Dieppe PA, Hirsch R, Helmick CG, Jordan JM, Kington RS, Lane NE, Nevitt MC, Zhang Y, et al: Osteoarthritis: new insights. Part 1: the disease and its risk factors. Ann Intern Med. 2000, 133: 635-646.
Sharma L: Local factors in osteoarthritis. Curr Opin Rheumatol. 2001, 13: 441-446. 10.1097/00002281-200109000-00017.
Sowers M: Epidemiology of risk factors for osteoarthritis: systemic factors. Curr Opin Rheumatol. 2001, 13: 447-451. 10.1097/00002281-200109000-00018.
Spector TD, Cicuttini F, Baker J, Loughlin J, Hart D: Genetic influences on osteoarthritis in women: a twin study. BMJ. 1996, 312: 940-943.
Bijkerk C, Houwing-Duistermaat JJ, Valkenburg HA, Meulenbelt I, Hofman A, Breedveld FC, Pols HA, van Duijn CM, Slagboom PE: Heritabilities of radiologic osteoarthritis in peripheral joints and of disc degeneration of the spine. Arthritis Rheum. 1999, 42: 1729-1735. 10.1002/1529-0131(199908)42:8<1729::AID-ANR23>3.0.CO;2-H.
Loughlin J: Genome studies and linkage in primary osteoarthritis. Rheum Dis Clin North Am. 2002, 28: 95-109. 10.1016/S0889-857X(03)00071-1.
Hart DJ, Spector TD: Definition and epidemiology of osteoarthritis of the hand: a review. Osteoarthritis Cartilage. 2000, 8 Suppl A: S2-S7.
Englund M, Paradowski PT, Lohmander LS: Association of radiographic hand osteoarthritis with radiographic knee osteoarthritis after meniscectomy. Arthritis Rheum. 2004, 50: 469-475. 10.1002/art.20035.
Hart DJ, Mootoosamy I, Doyle DV, Spector TD: The relationship between osteoarthritis and osteoporosis in the general population: the Chingford Study. Ann Rheum Dis. 1994, 53: 158-162.
Sowers MF, Hochberg M, Crabbe JP, Muhich A, Crutchfield M, Updike S: Association of bone mineral density and sex hormone levels with osteoarthritis of the hand and knee in premenopausal women. Am J Epidemiol. 1996, 143: 38-47.
Haussler MR, Whitfield GK, Haussler CA, Hsieh JC, Thompson PD, Selznick SH, Dominguez CE, Jurutka PW: The nuclear vitamin D receptor: biological and molecular regulatory properties revealed. J Bone Miner Res. 1998, 13: 325-349. 10.1359/jbmr.19184.108.40.2065.
Uitterlinden AG, Fang Y, van Meurs JB, van Leeuwen H, Pols HA: Vitamin D receptor gene polymorphisms in relation to Vitamin D related disease states. J Steroid Biochem Mol Biol. 2004, 89–90: 187-193. 10.1016/j.jsbmb.2004.03.083.
McAlindon TE, Felson DT, Zhang Y, Hannan MT, Aliabadi P, Weissman B, Rush D, Wilson PW, Jacques P: Relation of dietary intake and serum levels of vitamin D to progression of osteoarthritis of the knee among participants in the Framingham Study. Ann Intern Med. 1996, 125: 353-359.
Lane NE, Gore LR, Cummings SR, Hochberg MC, Scott JC, Williams EN, Nevitt MC: Serum vitamin D levels and incident changes of radiographic hip osteoarthritis: a longitudinal study. Study of Osteoporotic Fractures Research Group. Arthritis Rheum. 1999, 42: 854-860. 10.1002/1529-0131(199905)42:5<854::AID-ANR3>3.0.CO;2-I.
Morrison NA, Qi JC, Tokita A, Kelly PJ, Crofts L, Nguyen TV, Sambrook PN, Eisman JA: Prediction of bone density from vitamin D receptor alleles. Nature. 1994, 367: 284-287. 10.1038/367284a0.
Keen RW, Hart DJ, Lanchbury JS, Spector TD: Association of early osteoarthritis of the knee with a Taq I polymorphism of the vitamin D receptor gene. Arthritis Rheum. 1997, 40: 1444-1449.
Uitterlinden AG, Burger H, Huang Q, Odding E, Duijn CM, Hofman A, Birkenhager JC, van Leeuwen JP, Pols HA: Vitamin D receptor genotype is associated with radiographic osteoarthritis at the knee. J Clin Invest. 1997, 100: 259-263.
Uitterlinden AG, Burger H, van Duijn CM, Huang Q, Hofman A, Birkenhager JC, van Leeuwen JP, Pols HA: Adjacent genes, for COL2A1 and the vitamin D receptor, are associated with separate features of radiographic osteoarthritis of the knee. Arthritis Rheum. 2000, 43: 1456-1464. 10.1002/1529-0131(200007)43:7<1456::AID-ANR7>3.0.CO;2-M.
Huang J, Ushiyama T, Inoue K, Kawasaki T, Hukuda S: Vitamin D receptor gene polymorphisms and osteoarthritis of the hand, hip, and knee: a case-control study in Japan. Rheumatology. 2000, 39: 79-84. 10.1093/rheumatology/39.1.79.
Baldwin CT, Cupples LA, Joost O, Demissie S, Chaisson C, Mcalindon T, Myers RH, Felson D: Absence of linkage or association for osteoarthritis with the vitamin D receptor/type II collagen locus: the Framingham Osteoarthritis Study. J Rheumatol. 2002, 29: 161-165.
Thakkinstian A, D'Este C, Attia J: Haplotype analysis of VDR gene polymorphisms: a meta-analysis. Osteoporos Int. 2004, 15: 729-734. 10.1007/s00198-004-1601-x.
Gennari L, Becherini L, Masi L, Gonnelli S, Cepollaro C, Martini S, Mansani R, Brandi ML: Vitamin D receptor genotypes and intestinal calcium absorption in postmenopausal women. Calcif Tissue Int. 1997, 61: 460-463. 10.1007/s002239900368.
Zmuda JM, Cauley JA, Danielson ME, Wolf RL, Ferrell RE: Vitamin D receptor gene polymorphisms, bone turnover, and rates of bone loss in older African-American women. J Bone Miner Res. 1997, 12: 1446-1452. 10.1359/jbmr.19220.127.116.116.
Krall EA, Parry P, Lichter JB, Dawson-Hughes B: Vitamin D receptor alleles and rates of bone loss: influences of years since menopause and calcium intake. J Bone Miner Res. 1995, 10: 978-984.
Kiel DP, Myers RH, Cupples LA, Kong XF, Zhu XH, Ordovas J, Schaefer EJ, Felson DT, Rush D, Wilson PW, et al: The BsmI vitamin D receptor restriction fragment length polymorphism (bb) influences the effect of calcium intake on bone mineral density. J Bone Miner Res. 1997, 12: 1049-1057. 10.1359/jbmr.1918.104.22.1689.
Kellgren JH, Lawrence JS: Radiologic assessment of osteoarthritis. Ann Rheum Dis. 1957, 16: 494-502.
Solovieva S, Vehmas T, Riihimäki H, Luoma K, Leino-Arjas P: Hand use and patterns of joint involvement in osteoarthritis. A comparison of female dentists and teachers. Rheumatology (Oxford). 2005, 44: 521-528. 10.1093/rheumatology/keh534.
Cohen J: Weighted kappa. Nominal scale agreement with provision for scaled disagreement or partial credit. Psychol Bull. 1968, 70: 213-220. 10.1037/h0026256.
Riggs BL, Nguyen TV, Melton LJ, Morrison NA, O'Fallon WM, Kelly PJ, Egan KS, Sambrook PN, Muhs JM, Eisman JA: The contribution of vitamin D receptor gene alleles to the determination of bone mineral density in normal and osteoporotic women. J Bone Miner Res. 1995, 10: 991-996.
National Nutrition Council: Finnish Nutrition Recommendations. Committee Report of the Ministry of Agriculture and Forestry 1998, 7. Helsinki. 1999
Stephens M, Smith NJ, Donnelly P: A new statistical method for haplotype reconstruction from population data. Am J Hum Genet. 2001, 68: 978-989. 10.1086/319501.
Sillanpää P, Hirvonen A, Kataja V, Eskelinen M, Kosma V-M, Uusitupa M, Vainio H, Mitrunen K: Vitamin D receptor gene polymorphism as an important modifier of positive family history related breast cancer risk. Pharmacogenetics. 2004, 14: 239-245. 10.1097/00008571-200404000-00003.
Butler WJ, Hawthorne VM, Mikkelsen WM, Carman WJ, Bouthillier DL, Lamphiear DE, Kazi IU: Prevalence of radiologically defined osteoarthritis in the finger and wrist joints of adult residents of Tecumseh, Michigan, 1962–65. J Clin Epidemiol. 1988, 41: 467-473. 10.1016/0895-4356(88)90048-0.
Egger P, Cooper C, Hart DJ, Doyle DV, Coggon D, Spector TD: Patterns of joint involvement in osteoarthritis of the hand: the Chingford Study. J Rheumatol. 1995, 22: 1509-1513.
Chaisson CE, Zhang Y, McAlindon TE, Hannan MT, Aliabadi P, Naimark A, Levy D, Felson DT: Radiographic hand osteoarthritis: incidence, pattern, and influence of pre-existing disease in a population based sample. J Rheumatol. 1997, 24: 1337-1343.
Niu J, Zhang Y, LaValley M, Chaisson CE, Aliabadi P, Felson DT: Symmetry and clustering of symptomatic hand osteoarthritis in elderly men and women: the Framingham Study. Rheumatology (Oxford). 2003, 42: 343-348. 10.1093/rheumatology/keg110.
Hadler NM, Gillings DB, Imbus HR, Levitin PM, Makuc D, Utsinger PD, Yount WJ, Slusser D, Moskovitz N: Hand structure and function in an industrial setting. Arthritis Rheum. 1978, 21: 210-220.
Sheehan D, Bennett T, Cashman K: The genetics of osteoporosis: vitamin D receptor gene polymorphisms and circulating osteocalcin in healthy Irish adults. Ir J Med Sci. 2001, 170: 54-57.
Duman BS, Tanakol R, Erensoy N, Ozturk M, Yilmazer S: Vitamin D receptor alleles, bone mineral density and turnover in postmenopausal osteoporotic and healthy women. Med Princ Pract. 2004, 13: 260-266. 10.1159/000079524.
Zemel MB: Calcium modulation of hypertension and obesity: mechanisms and implications. J Am Coll Nutr. 2001, 20 (5 Suppl): 428S-435S.
Barger-Lux MJ, Heaney RP: The role of calcium intake in preventing bone fragility, hypertension, and certain cancers. J Nutr. 1994, 124 (8 Suppl): 1406S-1411S.
Salamone LM, Glynn NW, Black DM, Ferrell RE, Palermo L, Epstein RS, Kuller LH, Cauley JA: Determinants of premenopausal bone mineral density: the interplay of genetic and lifestyle factors. J Bone Miner Res. 1996, 11: 1557-1565.
Rubin LA, Hawker GA, Peltekova VD, Fielding LJ, Ridout R, Cole DE: Determinants of peak bone mass: clinical and genetic analyses in a young female Canadian cohort. J Bone Miner Res. 1999, 14: 633-643. 10.1359/jbmr.1922.214.171.1243.
Brown MA, Haughton MA, Grant SF, Gunnell AS, Henderson NK, Eisman JA: Genetic control of bone density and turnover: role of the collagen 1alpha1, estrogen receptor, and vitamin D receptor genes. J Bone Miner Res. 2001, 16: 758-764. 10.1359/jbmr.2001.16.4.758.
Ghosh P, Smith M: Osteoarthritis, genetic and molecular mechanisms. Biogerontology. 2002, 3: 85-88. 10.1023/A:1015219716583.
Carling T, Ridefelt P, Hellman P, Rastad J, Åkerström G: Vitamin D receptor polymorphisms correlate to parathyroid cell function in primary hyperparathyroidism. J Clin Endocrinol Metab. 1997, 82: 1772-1775. 10.1210/jc.82.6.1772.
Videman T, Gibbons LE, Battié MC, Maravilla K, Vanninen E, Leppävuori J, Kaprio J, Peltonen L: The relative roles of intragenic polymorphisms of the vitamin d receptor gene in lumbar spine degeneration and bone density. Spine. 2001, 26: E7-E12. 10.1097/00007632-200102010-00003.
Jones G, White C, Sambrook P, Eisman J: Allelic variation in the vitamin D receptor, lifestyle factors and lumbar spinal degenerative disease. Ann Rheum Dis. 1998, 57: 94-99.
Zmuda JM, Cauley JA, Ferrell RE: Molecular epidemiology of vitamin D receptor gene variants. Epidemiol Rev. 2000, 22: 203-217.
Carling T, Rastad J, Åkerström G, Westin G: Vitamin D receptor (VDR) and parathyroid hormone messenger ribonucleic acid levels correspond to polymorphic VDR alleles in human parathyroid tumors. J Clin Endocrinol Metab. 1998, 83: 2255-2259. 10.1210/jc.83.7.2255.
van Saase JL, van Romunde LK, Cats A, Vandenbroucke JP, Valkenburg HA: Epidemiology of osteoarthritis: Zoetermeer survey. Comparison of radiological osteoarthritis in a Dutch population with that in 10 other populations. Ann Rheum Dis. 1989, 48: 271-280.
Sowers M, Lachance L, Hochberg M, Jamadar D: Radiographically defined osteoarthritis of the hand and knee in young and middle-aged African American and Caucasian women. Osteoarthritis Cartilage. 2000, 8: 69-77. 10.1053/joca.1999.0273.
Haara MM, Manninen P, Kröger H, Arokoski JP, Kärkkäinen A, Knekt P, Aromaa A, Heliövaara M: Osteoarthritis of finger joints in Finns aged 30 or over: prevalence, determinants, and association with mortality. Ann Rheum Dis. 2003, 62: 151-158. 10.1136/ard.62.2.151.
This work was financially supported by the Finnish Work Environment Fund.
The authors declare that they have no competing interests.
SS participated in the design of the study, performed the statistical analysis, and drafted the manuscript. AH and PS carried out the genotyping analysis. TV carried out the evaluation of hand radiographs. KL participated in the evaluation of reliability of radiographs' readings. HR conceived of the study and participated in its design. PLA conceived of the study and participated in its design and coordination. All authors read and approved the final manuscript.
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Solovieva, S., Hirvonen, A., Siivola, P. et al. Vitamin D receptor gene polymorphisms and susceptibility of hand osteoarthritis in Finnish women. Arthritis Res Ther 8, R20 (2005). https://doi.org/10.1186/ar1874
- Calcium Intake
- Daily Calcium Intake
- TaqI Polymorphism
- TaqI Genotype
- AATT Genotype