Jin Ping, Shao Yong
Department of Obstetrics and Gynecology, First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
Zhonghua Fu Chan Ke Za Zhi. 2011 May;46(5):329-32.
To investigate the effect of Interleukin (IL)-18, IL-12 and tumor necrosis factor-α (TNF-α) in hepatic injury in intrahepatic cholestasis of pregnancy (ICP).
Sixty-two cases of ICP patients (ICP group), 30 cases of normal pregnant women (control group) and 30 cases of hepatitis B (HBV) women (hepatitis group) were recruited. Serum IL-18, IL-12 and TNF-α were examined by ELISA. Serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were examined by automatic biochemical analysis instrument.
(1) In hepatitis group, serum concentrations of IL-18, IL-12 and TNF-α were (256 ± 51) ng/L, (122 ± 96) ng/L and (207 ± 3) ng/L; serum levels of ALT and AST were (363 ± 174) U/L and (359 ± 237) U/L, respectively. In ICP group, serum concentrations of IL-18, IL-12 and TNF-α were (72 ± 32) ng/L, (42 ± 28) ng/L and (48 ± 14) ng/L; serum levels of ALT and AST were (201 ± 128) U/L and (132 ± 87) U/L, respectively.While in control group, serum concentrations of IL-18, IL-12 and TNF-α were (43 ± 13) ng/L, (10 ± 3) ng/L and (33 ± 9) ng/L; serum levels of ALT and AST were (13 ± 4) U/L and (15 ± 3) U/L, respectively. Serum IL-18, IL-12, TNF-α, ALT and AST levels in hepatitis group were significantly higher than those in ICP group and control group (P < 0.05). Serum IL-18, IL-12, TNF-α, ALT and AST levels in ICP group were significantly higher than those in control group(P < 0.05). (2) In severe ICP subgroup, serum concentrations of IL-18, IL-12 and TNF-α were (81 ± 32) ng/L, (50 ± 25) ng/L and (50 ± 14) ng/L; serum levels of ALT and AST were (269 ± 111) U/L and (181 ± 73) U/L. In mild ICP subgroup, serum concentrations of IL-18, IL-12 and TNF-α were (48 ± 18) ng/L, (17 ± 4) ng/L and (40 ± 10) ng/L; serum levels of ALT and AST were (87 ± 46) U/L and (50 ± 21) U/L, respectively. Serum IL-18, IL-12, TNF-α, ALT and AST levels in severe ICP subgroup were significantly higher than those in mild ICP subgroup and control group (P < 0.05). And serum ALT and AST levels in mild ICP subgroup were significantly higher than those in control group (P < 0.05). (3) There were 16 cases with preterm birth (50%, 16/32) and 10 cases with meconium-stained amniotic fluid (31%, 10/32) in severe ICP subgroup, significantly higher than those in mild ICP subgroup (P < 0.05), which contained 2 preterm births (7%, 2/30) and 1 meconium-stained amniotic fluid (3%, 1/30). While in control group, the numbers were 1 (3%, 1/30) and 1 (3%, 1/30), respectively. As for the cases of neonates whose 1 minute Apgar score were not more than 7, there were 2 cases, 1 case and 1 case in severe ICP subgroup, mild ICP subgroup and control group, respectively, which showed no significant difference (P > 0.05).
Serum IL-18, IL-12 and TNF-α may be involved in the process of hepatic injury of ICP.
探讨白细胞介素(IL)-18、IL-12及肿瘤坏死因子-α(TNF-α)在妊娠期肝内胆汁淤积症(ICP)肝损伤中的作用。
选取62例ICP患者(ICP组)、30例正常孕妇(对照组)及30例乙型肝炎(HBV)患者(肝炎组)。采用酶联免疫吸附测定(ELISA)法检测血清IL-18、IL-12及TNF-α水平。采用全自动生化分析仪检测血清丙氨酸氨基转移酶(ALT)及天冬氨酸氨基转移酶(AST)水平。
(1)肝炎组血清IL-18、IL-12及TNF-α浓度分别为(256±51)ng/L、(122±96)ng/L及(207±3)ng/L;血清ALT及AST水平分别为(363±174)U/L及(359±237)U/L。ICP组血清IL-18、IL-12及TNF-α浓度分别为(72±32)ng/L、(42±28)ng/L及(48±14)ng/L;血清ALT及AST水平分别为(201±128)U/L及(132±87)U/L。对照组血清IL-18、IL-12及TNF-α浓度分别为(43±13)ng/L、(10±3)ng/L及(33±9)ng/L;血清ALT及AST水平分别为(13±4)U/L及(15±3)U/L。肝炎组血清IL-18、IL-12、TNF-α、ALT及AST水平显著高于ICP组及对照组(P<0.05)。ICP组血清IL-18、IL-12、TNF-α、ALT及AST水平显著高于对照组(P<0.05)。(2)重度ICP亚组血清IL-18、IL-12及TNF-α浓度分别为(81±32)ng/L、(50±25)ng/L及(50±14)ng/L;血清ALT及AST水平分别为(269±111)U/L及(181±73)U/L。轻度ICP亚组血清IL-18、IL-12及TNF-α浓度分别为(48±18)ng/L、(17±4)ng/L及(40±10)ng/L;血清ALT及AST水平分别为(87±46)U/L及(50±21)U/L。重度ICP亚组血清IL-18、IL-12、TNF-α、ALT及AST水平显著高于轻度ICP亚组及对照组(P<0.05)。轻度ICP亚组血清ALT及AST水平显著高于对照组(P<0.05)。(3)重度ICP亚组有16例早产(占50%,16/32),10例羊水粪染(占31%,10/32),显著高于轻度ICP亚组(P<0.05),轻度ICP亚组有2例早产(占7%,2/30),1例羊水粪染(占3%,1/30)。对照组分别为1例(占3%,1/30)及1例(占3%,1/30)。1分钟Apgar评分≤7分的新生儿例数,重度ICP亚组、轻度ICP亚组及对照组分别为2例、1例及1例,差异无统计学意义(P>0.05)。
血清IL-18、IL-12及TNF-α可能参与ICP肝损伤过程。