PMID- 25182985 OWN - NLM STAT- MEDLINE DCOM- 20141222 LR - 20140903 IS - 1001-9391 (Print) IS - 1001-9391 (Linking) VI - 32 IP - 8 DP - 2014 Aug TI - [Relationship between genetic polymorphisms of matrix metalloproteinase-2 and -3 and susceptibility to silicosis]. PG - 573-7 AB - OBJECTIVE: To investigate the relationship between the genetic polymorphisms of matrix metalloproteinase-2 (MMP-2) (-735) and matrix metalloproteinase-3 (MMP-3) (-1171) and the susceptibility to silicosis. METHODS: A case-control study was conducted in 113 patients diagnosed with stage I silicosis (case group) and 115 dust-exposed workers without silicosis (control group); the two groups had the same sex, ethnic group, and type of dust and similar age and cumulative exposure time. Polymerase chain reaction-restriction fragment length polymorphism was used to determine the genotypes of MMP-2 (-735) and MMP-3 (-1171). RESULTS: No significant difference was observed in age, cumulative exposure time, or smoking rate between cases and controls (P > 0.05). The frequencies of genotypes C/C, C/T, and T/T at MMP-2 C-735T in the case group were 57.5% (65/113), 31.0% (35/113), and 11.5% (13/113), respectively, which were significantly different from those of the control group (69.6% (80/115), 26.9% (31/115), and 3.5% (4/115)), chi(2) = 6.542, P < 0.05). The frequencies of T allele in cases and controls were 27.0% and 17.0%, respectively, which were significantly different from each other chi(2) = 6.704, P < 0.05). Carriage of T allele at MMP-2 C-735T increased the risk of silicosis (OR = 1.811, 95% CI: 1.151-2.847). The frequencies of genotypes 6A/6A, 5A/6A, and 5A/5A at MMP-3 A-1171A were 67.2% (76/113), 24.8% (28/113), and 8.0% (9/113), respectively, in the case group, versus 59.1% (68/115), 37.4% (43/115), and 3.5% (4/115) in the control group (chi(2) = 5.519, P > 0.05). CONCLUSION: Genetic polymorphism at MMP-2 C-735T is significantly associated with the development of silicosis. Carriage of T allele increases the risk of silicosis among workers exposed to dust. No significant association was found between MMP-3 A-1171A polymorphism and silicosis in this study. FAU - Kou, Jie AU - Kou J AD - School of Public Health, Hebei United University, Tangshan, Hebei Province 063000, China. FAU - Fan, Xueyun AU - Fan X AD - School of Public Health, Hebei United University, Tangshan, Hebei Province 063000, China. E-mail: xueyun53@163.com. FAU - Shi, Yaxin AU - Shi Y AD - School of Public Health, Hebei United University, Tangshan, Hebei Province 063000, China. FAU - Wang, Xiaoyan AU - Wang X AD - School of Public Health, Hebei United University, Tangshan, Hebei Province 063000, China. FAU - Shen, Fuhai AU - Shen F AD - School of Public Health, Hebei United University, Tangshan, Hebei Province 063000, China. FAU - Jin, Yulan AU - Jin Y AD - School of Public Health, Hebei United University, Tangshan, Hebei Province 063000, China. E-mail: yulanjin225@qq.com. LA - chi PT - English Abstract PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - China TA - Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi JT - Zhonghua lao dong wei sheng zhi ye bing za zhi = Zhonghua laodong weisheng zhiyebing zazhi = Chinese journal of industrial hygiene and occupational diseases JID - 8410840 RN - EC 3.4.24.17 (MMP3 protein, human) RN - EC 3.4.24.17 (Matrix Metalloproteinase 3) RN - EC 3.4.24.24 (MMP2 protein, human) RN - EC 3.4.24.24 (Matrix Metalloproteinase 2) SB - IM MH - Adult MH - Aged MH - Aged, 80 and over MH - Case-Control Studies MH - Genetic Predisposition to Disease MH - Genotype MH - Humans MH - Matrix Metalloproteinase 2/*genetics MH - Matrix Metalloproteinase 3/*genetics MH - Middle Aged MH - *Polymorphism, Genetic MH - Silicosis/*genetics EDAT- 2014/09/04 06:00 MHDA- 2014/12/23 06:00 CRDT- 2014/09/04 06:00 PHST- 2014/09/04 06:00 [entrez] PHST- 2014/09/04 06:00 [pubmed] PHST- 2014/12/23 06:00 [medline] PST - ppublish SO - Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. 2014 Aug;32(8):573-7.