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Vitamin D reseptör geni fokI polimorfizminin temporomandibular eklem dejenerasyonu ile ilişkisi

Yıl 2019, Cilt: 12 Sayı: 1, 72 - 79, 28.04.2019
https://doi.org/10.26559/mersinsbd.423103

Öz

Amaç: Temporomandibular Eklem
Düzensizliği (TME-İD) ve eklem osteoartritine (TME-OA) yatkınlık genetik
varyasyonlarla ilişkili olabilir. Vitamin D Reseptörü (VDR) gen polimorfizmleri buna adaydırlar.
Bu çaşmanın
amacı, VDR FokI polimorfizminin
temporomandibular
e
klem dejenerasyonu ile ilişkili olup olmadığını
cinsiyete göre değerlendirmekti. Yöntem: 58 osteoartritik
TME-İD hasta (32.07.±8.1) ve kontrol olarak 71 TMED olmayan birey
(28.28±5.95)
çaşmaya dahil edildi. Kan örneklerinden
DNA izolasyonu standart proteinaz
K/fenol-kloroform
metodu ile yapıldı. VDR geni FokI polimorfizmi, polimeraz zincir reaksiyonunu (PZR) takiben restriksiyon
fragment uzunluk
polimorfizmi
(RFLP) ntemi
ile
araştırıldı. Bulgular:
FokI genotip
dağımları
(rs2228570,  C>T) grupla arasında istatistiksel olarak
farklı idi
(p=0.026, χ²=7.2). Heterozigot Ff genotipi, FF genotipine re istatistiksel olarak farklı idi (OR=0.43, %95 GA:0.2-0.92, p=0.028). TME-İD’li kadınlarda heterozigot Ff
genotipi FF genotipine göre
farklılık sınırında idi (OR=0.43, %95 CI:0.16-1.10, p=0.07). Yine TME-İD’li kadınlarda ff genotipi
ile
FF genotipi arasında fark olmamasına rağmen (%95 GA: 0.29-26.03, p=0.37) risk faktörü 2.77 kat fazla idi. TME-İD/kontrol grubu ve kadın kontrollerde de F ve f alellerinin dağılımları farklı değildi. Sonuç: FokI polimorfizminin
TME-İD/TMEOA gelişmesi üzerinde önemli bir etkisi olduğu düşünülebilir. ff
genotipi, TME-İD hastalarında ve TME-İD’li kadınlarda temporomandibular eklem
dejenerasyonu ile ilgili olabilir.

Kaynakça

  • 1. Barclay P, Hollender LG, Maravilla KR, Truelove EL. Comparison of clinical and magnetic resonance imaging diagnosis in patients with disk displacement in the temporomandibular joint. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 1999; 88: 37-43.
  • 2. Sangani D, Suzuki A, VonVille H, Hixson JE, Iwata J. Gene Mutations Associated with temporomandibular Joint Disorders: A Systematic Review. OAlib 2015; 2(6): 1583.
  • 3. Tanaka E, Detamore MS, Mercuri LG. Degenerative disorders of the temporomandibular joint: etiology, diagnosis, and treatment. J Dent Res 2008; 87: 296–307.
  • 4. Stegenga B, de Bont LG, Boering G. Classification of temporomandibular joint osteoarthrosis and internal derangement. 2.Specific diagnostic criteria. Cranio 1992; 10: 107–116.
  • 5.de Leeuw R, Boering G, Stegenga B, de Bont LG (1995) Radiographic signs of temporomandibular joint osteoarthrosis and internal derangement 30 years after nonsurgical treatment. Oral Surg Oral Med Oral Pathol Radiol Endod 79:382–392.
  • 6. Le Resche L. Epidemiology of temporomandibular disorders: Implications for the investigation of etiologic factors. Crit Rev Oral Biol Med 1997; 8: 291-305.
  • 7. Colombini A, Cauci S, Lombardi G, Lanteri P, Croiset S, Brayda-Bruno M, Banfi G. Relationship between vitamin D receptor gene (VDR) polymorphisms, vitamin D status, osteoarthritis andintervertebral disc degeneration. J Steroid Biochem Mol Biol 2013; 138: 24-40.
  • 8. Bonato LL, Quinelato V, Borojevic R, Vieira AR, Modesto A, Granjeiro JM, Tesch R, Casado PL. Haplotypes ofthe RANK and OPG genes are associated with chronic arthralgia in individuals with and without temporomandibuler disorders. Int J Oral Maxillofac Surg 2017; 46(9): 1121-1129.
  • 9. Pike JW, Meyer MB. The vitamin D receptor: new paradigms for the regulation of gene expression by 1,25-dihydroxyvitamin D3. Rheum Dis Clin North Am 2012; 38(1): 13-27.
  • 10. Zilahi E, Chen JQ, Papp G, Szántó A, Zeher M. Lack of association of vitamin D receptor gene polymorphisms/haplotypes in Sjögren's syndrome. Clin Rheumatol 2015; 34(2): 247-53.
  • 11. Bid HK, Mishra DK, Mittal RD. Vitamin-D receptor (VDR) gene (Fok-I, Taq-I and Apa-I) polymorphisms in healthy individuals from north Indian population. Asian Pac J Cancer Prev 2005; 6(2): 147-52.
  • 12. Uitterlinden AG, Fang Y, Van Meurs JB, Pols HA, Van Leeuwen JP. Genetics and biology of vitamin D receptor polymorphisms. Gene 2004; 338: 143–156.
  • 13.Morrison NA, Yeoman R, Kelly PJ, et al. Contribution of trans-acting factor aleles to normal physiological variability: vitamin D receptor gene polymorphism and circulating osteocalcin. Proc Natl Acad Sci USA 1992; 89: 6665-9.
  • 14.Fang Y, van Meurs JB, Bergink AP, Hofman A, van Duijn CM, van Leeuwen JP, Pols HA, Uitterlinden AG. Cdx-2 polymorphism in the promoter region of the human vitamin D receptor gene determines susceptibility to fracture in the elderly. J Bone Miner Res 2003; 18: 1632– 1641.
  • 15. Baker AR, McDonnell DP, Hughes M, Crisp TM, Mangelsdorf DJ, Haussler MR, Pike JW, Shine J, O’Malley BW. Cloning and expression of full-length cDNA encoding human vitamin D receptor. Proc Natl Acad Sci USA 1988; 85: 3294–3298.
  • 16.Gross C, Eccleshall TR, Malloy PJ, Villa ML, Marcus R, Feldman D. The presence of a polymorphism at the translation initiation site of the vitamin D receptor gene is associated with low bone mineral density in postmenopausal Mexican-American women. J Bone Miner Res 1996; 11: 1850– 1855.
  • 17. Arai H, Miyamoto K, Taketani Y, Yamamoto H, Iemori Y, Morita K, Tonai T, Nishisho T, Mori S, Takeda E. A vitamin D receptor gene polymorphism in the translation initiation codon: effect on protein activity and relation to bone mineral density in Japanese women. J Bone Miner Res 1997; 12: 915–921.
  • 18.Chen L, Zhao S, Niu F, Bi GB. Association between vitamin D receptor gene polymorphisms and intervertebral disc degeneration: A meta-analysis. J Orthop Sci 2017; 2: 184-189.
  • 19. Valdes AM, Oene MV, Hart DJ, Surdulescu GL, Loughlin J, Doherty M, Spector TD. Reproducible genetic associations between candidate genes and clinical knee osteoarthritis in men and women. Arthritis Rheum. 2006; 54: 533–539.
  • 20. Muraki S, Dennison E, Jameson K, Boucher BJ, Akune T, Yoshimura N, Judge A, Arden NK, Javaid K, Cooper C. Association of vitamin D status withknee pain and radiographic knee osteoarthritis. Osteoarthritis Cartilage 2011; 19: 1301–1306.
  • 21. Uitterlinden AG, Fang Y, Van Meurs JB, Pols HA, Van Leeuwen JP. Genetics and biology of vitamin D receptor polymorphisms. Gene 2004; 338: 143–156.
  • 22. Yilmaz AD, Yazicioğlu D, Tuzuner Oncul MA, Ereş G, Sayan NB Association of Matrilin-3 Gene Polymorphism with temporomandibular Joint Internal Derangement. Genet Test Mol Biomarkers 2016; 20(10): 563-568.
  • 23. Sambrook J, Fritschi EF, Maniatis T. Molecular cloning: A laboratory manual.Cold Spring Harbor Laboratory Press 1989. New York
  • 24. Preacher KJ Calculation for the chi-square test: an interactive calculation tool for chi-square tests of goodness of fit and independence-computer software. 2001 Available at www.quantspy.org
  • 25.Altman DG Practical statistics for medical research. London: Chapman and Hall; 1991.
  • 26. Zhao J, Yang M, Shao J, Bai Y, Li M. Association Between VDR FokI Polymorphism and Intervertebral Disk Degeneration. Genomics Proteomics Bioinformatics 2015; 13(6): 371-6.
  • 27.Zhu ZH, Jin XZ, Zhang W, Chen M, Ye DQ, Zhai Y, Dong FL, Shen CL, Ding C. Associations between vitamin D receptor gene polymorphisms and osteoarthritis: an updatedmeta-analysis. Rheumatology 2014; 53(6): 998-1008.
  • 28. Corvol MT, Dumontier MF, Tsagris L, Lang F, Bourguignon J. Cartilage and vitamin D in vitro. Ann Endocrinol 1981; 142:482e7.
  • 29.Garfinkel RJ, Dilisio MF, Agrawal DK (2017) Vitamin D and Its Effects on Articular Cartilage and Osteoarthritis. Orthop J Sports Med 5(6):2325967117711376.

The relation between Vitamin D receptor gene fokI polymorphism and degeneration of the temporomandibular joint

Yıl 2019, Cilt: 12 Sayı: 1, 72 - 79, 28.04.2019
https://doi.org/10.26559/mersinsbd.423103

Öz

Objective: Predisposition to temporomandibular joint
internal
derangement (TMJ-ID) and osteoarthritis
of the joint
(TMJOA)
might be related to genetic variations.
Vitamin D receptor (VDR) gene
polymorphisms
are the candidates for
association with the disorder. The aim of
this study was to evaluate
whether VDR
FokI polymorphism is associated
with the degeneration of the temporomandibular joint
by
gender

Methods: The study included 58 unrelated TMJ-ID patients
(32.07
±8.1) and 71 healthy controls (28.28 ±5.95) without TMJ-ID. DNA extraction
was achieved by standard
proteinase
K/phenol-chloroform
method
from the blood samples.
 VDR gene FokI polymorphism was investigated
by a polymerase
chain reaction
(PCR) based restriction
fragment length polymorphism
(RFLP) assay.
Results: The genotype distributions
of FokI (rs2228570, C>T) showed statistically
significant results (p=0.026,
χ²=7.2). Ff
heterozygote genotype was statistically different as compared to FF genotype (OR=0.43, 95% CI: 0.2-0.92,
p=0.028).
Heterozygote
Ff genotype
was different
comparing to the FF
genotype in TMJ-ID women (OR=0.43, 95% CI: 0.16-1.10,
p=0.07).
Although the difference between ff and FF genotype

were not different, ff genotype was a 2.77 fold
risk factor
(95% CI:0.29-26.03,  p=0.37).
The distributions of F and f alleles were not different between the groups of
overall TMJ-ID vs. controls and women TMJ-ID vs. controls. Conclusion: The results of this study suggested that FokI polymorphism might
present susceptibility to TMJ-ID/TMJOA. ff genotype might
be associated
with the degeneration of temporomandibular joint in TMJ-ID patients and TMJ-ID women.

Kaynakça

  • 1. Barclay P, Hollender LG, Maravilla KR, Truelove EL. Comparison of clinical and magnetic resonance imaging diagnosis in patients with disk displacement in the temporomandibular joint. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 1999; 88: 37-43.
  • 2. Sangani D, Suzuki A, VonVille H, Hixson JE, Iwata J. Gene Mutations Associated with temporomandibular Joint Disorders: A Systematic Review. OAlib 2015; 2(6): 1583.
  • 3. Tanaka E, Detamore MS, Mercuri LG. Degenerative disorders of the temporomandibular joint: etiology, diagnosis, and treatment. J Dent Res 2008; 87: 296–307.
  • 4. Stegenga B, de Bont LG, Boering G. Classification of temporomandibular joint osteoarthrosis and internal derangement. 2.Specific diagnostic criteria. Cranio 1992; 10: 107–116.
  • 5.de Leeuw R, Boering G, Stegenga B, de Bont LG (1995) Radiographic signs of temporomandibular joint osteoarthrosis and internal derangement 30 years after nonsurgical treatment. Oral Surg Oral Med Oral Pathol Radiol Endod 79:382–392.
  • 6. Le Resche L. Epidemiology of temporomandibular disorders: Implications for the investigation of etiologic factors. Crit Rev Oral Biol Med 1997; 8: 291-305.
  • 7. Colombini A, Cauci S, Lombardi G, Lanteri P, Croiset S, Brayda-Bruno M, Banfi G. Relationship between vitamin D receptor gene (VDR) polymorphisms, vitamin D status, osteoarthritis andintervertebral disc degeneration. J Steroid Biochem Mol Biol 2013; 138: 24-40.
  • 8. Bonato LL, Quinelato V, Borojevic R, Vieira AR, Modesto A, Granjeiro JM, Tesch R, Casado PL. Haplotypes ofthe RANK and OPG genes are associated with chronic arthralgia in individuals with and without temporomandibuler disorders. Int J Oral Maxillofac Surg 2017; 46(9): 1121-1129.
  • 9. Pike JW, Meyer MB. The vitamin D receptor: new paradigms for the regulation of gene expression by 1,25-dihydroxyvitamin D3. Rheum Dis Clin North Am 2012; 38(1): 13-27.
  • 10. Zilahi E, Chen JQ, Papp G, Szántó A, Zeher M. Lack of association of vitamin D receptor gene polymorphisms/haplotypes in Sjögren's syndrome. Clin Rheumatol 2015; 34(2): 247-53.
  • 11. Bid HK, Mishra DK, Mittal RD. Vitamin-D receptor (VDR) gene (Fok-I, Taq-I and Apa-I) polymorphisms in healthy individuals from north Indian population. Asian Pac J Cancer Prev 2005; 6(2): 147-52.
  • 12. Uitterlinden AG, Fang Y, Van Meurs JB, Pols HA, Van Leeuwen JP. Genetics and biology of vitamin D receptor polymorphisms. Gene 2004; 338: 143–156.
  • 13.Morrison NA, Yeoman R, Kelly PJ, et al. Contribution of trans-acting factor aleles to normal physiological variability: vitamin D receptor gene polymorphism and circulating osteocalcin. Proc Natl Acad Sci USA 1992; 89: 6665-9.
  • 14.Fang Y, van Meurs JB, Bergink AP, Hofman A, van Duijn CM, van Leeuwen JP, Pols HA, Uitterlinden AG. Cdx-2 polymorphism in the promoter region of the human vitamin D receptor gene determines susceptibility to fracture in the elderly. J Bone Miner Res 2003; 18: 1632– 1641.
  • 15. Baker AR, McDonnell DP, Hughes M, Crisp TM, Mangelsdorf DJ, Haussler MR, Pike JW, Shine J, O’Malley BW. Cloning and expression of full-length cDNA encoding human vitamin D receptor. Proc Natl Acad Sci USA 1988; 85: 3294–3298.
  • 16.Gross C, Eccleshall TR, Malloy PJ, Villa ML, Marcus R, Feldman D. The presence of a polymorphism at the translation initiation site of the vitamin D receptor gene is associated with low bone mineral density in postmenopausal Mexican-American women. J Bone Miner Res 1996; 11: 1850– 1855.
  • 17. Arai H, Miyamoto K, Taketani Y, Yamamoto H, Iemori Y, Morita K, Tonai T, Nishisho T, Mori S, Takeda E. A vitamin D receptor gene polymorphism in the translation initiation codon: effect on protein activity and relation to bone mineral density in Japanese women. J Bone Miner Res 1997; 12: 915–921.
  • 18.Chen L, Zhao S, Niu F, Bi GB. Association between vitamin D receptor gene polymorphisms and intervertebral disc degeneration: A meta-analysis. J Orthop Sci 2017; 2: 184-189.
  • 19. Valdes AM, Oene MV, Hart DJ, Surdulescu GL, Loughlin J, Doherty M, Spector TD. Reproducible genetic associations between candidate genes and clinical knee osteoarthritis in men and women. Arthritis Rheum. 2006; 54: 533–539.
  • 20. Muraki S, Dennison E, Jameson K, Boucher BJ, Akune T, Yoshimura N, Judge A, Arden NK, Javaid K, Cooper C. Association of vitamin D status withknee pain and radiographic knee osteoarthritis. Osteoarthritis Cartilage 2011; 19: 1301–1306.
  • 21. Uitterlinden AG, Fang Y, Van Meurs JB, Pols HA, Van Leeuwen JP. Genetics and biology of vitamin D receptor polymorphisms. Gene 2004; 338: 143–156.
  • 22. Yilmaz AD, Yazicioğlu D, Tuzuner Oncul MA, Ereş G, Sayan NB Association of Matrilin-3 Gene Polymorphism with temporomandibular Joint Internal Derangement. Genet Test Mol Biomarkers 2016; 20(10): 563-568.
  • 23. Sambrook J, Fritschi EF, Maniatis T. Molecular cloning: A laboratory manual.Cold Spring Harbor Laboratory Press 1989. New York
  • 24. Preacher KJ Calculation for the chi-square test: an interactive calculation tool for chi-square tests of goodness of fit and independence-computer software. 2001 Available at www.quantspy.org
  • 25.Altman DG Practical statistics for medical research. London: Chapman and Hall; 1991.
  • 26. Zhao J, Yang M, Shao J, Bai Y, Li M. Association Between VDR FokI Polymorphism and Intervertebral Disk Degeneration. Genomics Proteomics Bioinformatics 2015; 13(6): 371-6.
  • 27.Zhu ZH, Jin XZ, Zhang W, Chen M, Ye DQ, Zhai Y, Dong FL, Shen CL, Ding C. Associations between vitamin D receptor gene polymorphisms and osteoarthritis: an updatedmeta-analysis. Rheumatology 2014; 53(6): 998-1008.
  • 28. Corvol MT, Dumontier MF, Tsagris L, Lang F, Bourguignon J. Cartilage and vitamin D in vitro. Ann Endocrinol 1981; 142:482e7.
  • 29.Garfinkel RJ, Dilisio MF, Agrawal DK (2017) Vitamin D and Its Effects on Articular Cartilage and Osteoarthritis. Orthop J Sports Med 5(6):2325967117711376.
Toplam 29 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Konular Sağlık Kurumları Yönetimi
Bölüm Araştırma Makalesi
Yazarlar

Ayça Dilara Yılmaz 0000-0002-8111-2594

Yayımlanma Tarihi 28 Nisan 2019
Gönderilme Tarihi 12 Mayıs 2018
Kabul Tarihi 23 Kasım 2018
Yayımlandığı Sayı Yıl 2019 Cilt: 12 Sayı: 1

Kaynak Göster

APA Yılmaz, A. D. (2019). Vitamin D reseptör geni fokI polimorfizminin temporomandibular eklem dejenerasyonu ile ilişkisi. Mersin Üniversitesi Sağlık Bilimleri Dergisi, 12(1), 72-79. https://doi.org/10.26559/mersinsbd.423103
AMA Yılmaz AD. Vitamin D reseptör geni fokI polimorfizminin temporomandibular eklem dejenerasyonu ile ilişkisi. Mersin Univ Saglık Bilim Derg. Nisan 2019;12(1):72-79. doi:10.26559/mersinsbd.423103
Chicago Yılmaz, Ayça Dilara. “Vitamin D reseptör Geni FokI Polimorfizminin Temporomandibular Eklem Dejenerasyonu Ile ilişkisi”. Mersin Üniversitesi Sağlık Bilimleri Dergisi 12, sy. 1 (Nisan 2019): 72-79. https://doi.org/10.26559/mersinsbd.423103.
EndNote Yılmaz AD (01 Nisan 2019) Vitamin D reseptör geni fokI polimorfizminin temporomandibular eklem dejenerasyonu ile ilişkisi. Mersin Üniversitesi Sağlık Bilimleri Dergisi 12 1 72–79.
IEEE A. D. Yılmaz, “Vitamin D reseptör geni fokI polimorfizminin temporomandibular eklem dejenerasyonu ile ilişkisi”, Mersin Univ Saglık Bilim Derg, c. 12, sy. 1, ss. 72–79, 2019, doi: 10.26559/mersinsbd.423103.
ISNAD Yılmaz, Ayça Dilara. “Vitamin D reseptör Geni FokI Polimorfizminin Temporomandibular Eklem Dejenerasyonu Ile ilişkisi”. Mersin Üniversitesi Sağlık Bilimleri Dergisi 12/1 (Nisan 2019), 72-79. https://doi.org/10.26559/mersinsbd.423103.
JAMA Yılmaz AD. Vitamin D reseptör geni fokI polimorfizminin temporomandibular eklem dejenerasyonu ile ilişkisi. Mersin Univ Saglık Bilim Derg. 2019;12:72–79.
MLA Yılmaz, Ayça Dilara. “Vitamin D reseptör Geni FokI Polimorfizminin Temporomandibular Eklem Dejenerasyonu Ile ilişkisi”. Mersin Üniversitesi Sağlık Bilimleri Dergisi, c. 12, sy. 1, 2019, ss. 72-79, doi:10.26559/mersinsbd.423103.
Vancouver Yılmaz AD. Vitamin D reseptör geni fokI polimorfizminin temporomandibular eklem dejenerasyonu ile ilişkisi. Mersin Univ Saglık Bilim Derg. 2019;12(1):72-9.

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