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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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Cytokine gene polymorphisms in periodontal disease: a meta-analysis of 53 studies including 4178 cases and 4590 controls

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Συγγραφέας
Nikolopoulos, G. K.; Dimou, N. L.; Hamodrakas, S. J.; Bagos, P. G.
Ημερομηνία
2008
DOI
10.1111/j.1600-051X.2008.01298.x
Λέξη-κλειδί
cytokine
periodontities
polymorphism
meta-analysis
TUMOR-NECROSIS-FACTOR
GENERALIZED AGGRESSIVE PERIODONTITIS
SINGLE-NUCLEOTIDE POLYMORPHISMS
FACTOR-ALPHA GENE
GINGIVAL CREVICULAR
FLUID
EARLY-ONSET PERIODONTITIS
ADULT PERIODONTITIS
INTERLEUKIN-1
POLYMORPHISMS
PROMOTER REGION
IL-6 GENE
Dentistry, Oral Surgery & Medicine
Εμφάνιση Μεταδεδομένων
Επιτομή
Aim: We conducted a systematic review and a meta-analysis, in order to investigate the potential association of cytokine gene polymorphisms with either aggressive or chronic periodontal disease. Material and Methods: A comprehensive literature search was performed. We retrieved a total of 53 studies summarizing information about 4178 cases and 4590 controls. Six polymorphisms were included in our meta-analysis which are the following: IL-1A G[4845]T, IL-1A C[-889]T, IL-1B C[3953/4]T, IL-1B T[-511]C, IL-6 G[-174]C and TNFA G[-308]A. Random effect methods were used for the analysis. We calculated the specific odds ratios along with their 95% confidence intervals to compare the distribution of alleles and genotypes between cases and controls. Results and Conclusions: Using random effect methods we found statistically significant association of IL-1A C[-889]T and IL-1B C[3953/4]T polymorphisms with chronic periodontal disease without any evidence of publication bias or significant statistical heterogeneity. A weak positive association was also found concerning IL-1B T[-511]C and chronic periodontal disease. No association was found for all the cytokines examined as far as the aggressive form of the disease is concerned. Future studies may contribute to the investigation of the potential multigenetic predisposition of the disease and reinforce our findings.
URI
http://hdl.handle.net/11615/31397
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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