Regulatory polymorphism of CXCL10 rs1439490 in seronegative occult hepatitis C virus infection.
Regulatory polymorphism of CXCL10 rs1439490 in seronegative occult hepatitis C virus infection.
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CXCL10 rs1439490在血清阴性隐匿性丙型肝炎病毒感染中的调控多态性
DOI:
10.3748/wjg.v24.i20.2191
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发表时间:
2018-05-28
影响因子:
4.3
通讯作者:
Wang JB
中科院分区:
文献类型:
--
作者:
Wang X;Wang S;Liu ZH;Qi WQ;Zhang Q;Zhang YG;Sun DR;Xu Y;Wang HG;Li ZX;Cong XL;Zhao P;Zhou CY;Wang JB
To examine the relationship between the single nucleotide polymorphism CXCL10 rs1439490 and seronegative occult hepatitis C virus (HCV) infection (OCI). One hundred and three cases of seronegative OCI and 155 cases of seropositive chronic HCV infection (CHC) were diagnosed at five Liver Centers in Northeastern China, from 2012 to 2016. CXCL10 rs1439490, rs1440802, and IL-28B rs12979860 were analyzed by sequencing. Serum CXCL10 was measured by ELISA. Intrahepatic CXCL10 was determined by quantitative PCR and immunohistochemical semi-quantitative scoring. Liver necroinflammation and fibrosis were scored according to the METAVIR system. CXCL10 rs1439490 G/G was more prevalent in OCI patients (n = 93/103; 90.3%) than in CHC patients (n = 116/155; 74.8%; P = 0.008). OCI patients had lower serum CXCL10 levels than CHC patients (192.91 ± 46.50 pg/mL vs 354.78 ± 102.91 pg/mL, P < 0.0001). Of IL-28B rs12979860 C/C patients, OCI patients with rs1439490 G/G had lower serum and liver levels of CXCL10 and lower levels of liver necroinflammation and fibrosis than non-G/G patients. OCI patients had higher alanine aminotransferase normalization rates after Peg-interferon treatment than CHC patients (P < 0.05) and serum CXCL10 decreased significantly (P < 0.0001). Liver necroinflammation and fibrosis were alleviated in 8 OCI patients after treatment. Multivariate analysis indicated that rs1439490 G/G significantly influenced the occurrence of OCI in HCV infection (OR = 0.31, 95%CI: 0.15-0.66, P = 0.002). CXCL10 rs1439490 G/G is positively associated with OCI in HCV infection and antiviral outcome.
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影响因子:
6.4
作者:
Castillo, I;Pardo, M;Carreño, V
通讯作者:
Carreño, V
影响因子:
13.5
作者:
Bedossa, P;Poynard, T
通讯作者:
Poynard, T
影响因子:
29.4
作者:
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通讯作者:
He, Fuchu
影响因子:
12.7
作者:
Bokharaei-Salim, Farah;Keyvani, Hossein;Alizadeh, Amir Houshang Mohammad
通讯作者:
Alizadeh, Amir Houshang Mohammad
影响因子:
5.4
作者:
Bartolome, Javier;Manuel Lopez-Alcorocho, Juan;Carreno, Vicente
通讯作者:
Carreno, Vicente