Serum soluble Fas in the syndrome of hemolysis, elevated liver enzymes, and low platelets

被引:10
作者
Harirah, H
Donia, SE
Hsu, CD
机构
[1] Univ Texas, Med Branch, Dept Obstet & Gynecol, Div Maternal Fetal Med, Galveston, TX 77555 USA
[2] Univ Nebraska, Ctr Med, Omaha, NE 68182 USA
关键词
D O I
10.1016/S0029-7844(01)01415-6
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
OBJECTIVE: To assess whether serum levels of soluble Fas and soluble Fas ligand are altered in the syndrome of hemolysis, elevated liver enzymes, and low platelets (HELLP) METHODS: Serum samples from 22 pregnant women diag nosed with HELLP syndrome were compared with sera from 37 healthy women with noncomplicated. singleton pregnancies. Serum levels of soluble Fas and soluble Fas ligands were determined by enzyme immunoassay. Student A chi (2), Pearson's correlation coefficient, and multiple regression tests were used for statistical analyses. RESULTS: Both soluble Fas and soluble Fas ligand were detected in the sera of normal pregnancies as well as in those with HELLP syndrome. The mean serum level of soluble Fas was significantly higher in women with HELLP syndrome than in healthy gravidas (10.75 +/- 0.93 versus 5.81 :+/- 0.37 U/mL, P < .001). However, there was no significant difference in mean serum soluble Fas ligand levels of the two group, (0.60 +/- 0.06 compared with 0.50 +/- 0.22 ng/mL, P = .23). In women with HELLP syndrome, there were no significant correlations between serum levels of soluble Fas or soluble Fas ligand with liver transaminases (aspartate and alanine aminotransferase) and platelet count. CONCLUSION: Serum levels of soluble Fas, but not soluble Fas ligand, are significantly higher in women with HELLP syndrome than healthy gravidas. ne source of elevated serum levels of soluble Fas in HELLP syndrome remains to be determined. (C) 2001 by the American College of Obstetricians and Gynecologists.
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页码:295 / 298
页数:4
相关论文
共 17 条
[1]  
*AM COLL OBST GYN, 1996, ACOG ED TECHN B, V219
[2]   Expression of the apoptosis-inducing Fas ligand (FasL) in human first and third trimester placenta and choriocarcinoma cells [J].
Bamberger, AM ;
Schulte, HM ;
Thuneke, I ;
Erdmann, I ;
Bamberger, CM ;
Asa, SL .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (09) :3173-3175
[3]   HEPATIC HISTOPATHOLOGIC CONDITION DOES NOT CORRELATE WITH LABORATORY ABNORMALITIES IN HELLP SYNDROME (HEMOLYSIS, ELEVATED LIVER-ENZYMES, AND LOW PLATELET COUNT) [J].
BARTON, JR ;
RIELY, CA ;
ADAMEC, TA ;
SHANKLIN, DR ;
KHOURY, AD ;
SIBAI, BM .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1992, 167 (06) :1538-1543
[4]   Immunologic dissonance: A continuing evolution in our understanding of the systemic inflammatory response syndrome (SIRS) and the multiple organ dysfunction syndrome (MODS) [J].
Bone, RC .
ANNALS OF INTERNAL MEDICINE, 1996, 125 (08) :680-687
[5]   PROTECTION FROM FAS-MEDIATED APOPTOSIS BY A SOLUBLE FORM OF THE FAS MOLECULE [J].
CHENG, JH ;
ZHOU, T ;
LIU, CD ;
SHAPIRO, JP ;
BRAUER, MJ ;
KIEFER, MC ;
BARR, PJ ;
MOUNTZ, JD .
SCIENCE, 1994, 263 (5154) :1759-1762
[6]  
DADELSZEN PV, 1999, AM J OBSTET GYNECOL, V181, P408
[7]  
Hammer A, 1999, AM J REPROD IMMUNOL, V41, P41
[8]  
HIRAMATSU N, 1994, HEPATOLOGY, V19, P1354, DOI 10.1002/hep.1840190606
[9]  
Hori Y, 1999, AM J HEMATOL, V61, P21
[10]   THE POLYPEPTIDE ENCODED BY THE CDNA FOR HUMAN CELL-SURFACE ANTIGEN FAS CAN MEDIATE APOPTOSIS [J].
ITOH, N ;
YONEHARA, S ;
ISHII, A ;
YONEHARA, M ;
MIZUSHIMA, S ;
SAMESHIMA, M ;
HASE, A ;
SETO, Y ;
NAGATA, S .
CELL, 1991, 66 (02) :233-243