Lack of association of severe preeclampsia with maternal and fetal mutant alleles for tumor necrosis factor alpha and lymphotoxin alpha genes and plasma tumor necrosis factor alpha levels

Citation
Jc. Livingston et al., Lack of association of severe preeclampsia with maternal and fetal mutant alleles for tumor necrosis factor alpha and lymphotoxin alpha genes and plasma tumor necrosis factor alpha levels, AM J OBST G, 184(6), 2001, pp. 1273-1277
Citations number
26
Categorie Soggetti
Reproductive Medicine","da verificare
Journal title
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY
ISSN journal
00029378 → ACNP
Volume
184
Issue
6
Year of publication
2001
Pages
1273 - 1277
Database
ISI
SICI code
0002-9378(200105)184:6<1273:LOAOSP>2.0.ZU;2-Z
Abstract
OBJECTIVE: The purpose of this study was to determine whether the increased frequency of mutant alleles of the gene for tumor necrosis factor alpha an d elevated maternal and fetal plasma levels of tumor necrosis factor a were associated with severe preeclampsia. STUDY DESIGN: We performed a prospective cross-sectional study involving 11 2 patients with severe preeclampsia matched for gestational age with 106 no rmotensive pregnant women. Deoxyribonucleic acid for restriction fragment l ength polymorphism analysis was extracted from maternal and fetal blood. Tw o mutations associated with the gene for tumor necrosis factor a were assay ed by polymerase chain reaction. Poly polymerase chain reaction products we re digested with the restriction enzyme Ncol and then fractionated by gel e lectrophoresis. Genotypic frequencies were calculated. Maternal and fetal p lasma tumor necrosis factor a levels were assayed by the dual monoclonal an tibody sandwich enzyme-linked immunosorbent assay technique. The chi (2) te st, the Fisher exact test, the Student t test, and the Mann-Whitney test we re performed to calculate statistical significance. RESULTS: The differences in the genotypic frequencies of the two loci were not significant in either maternal or fetal samples between control women a nd women with pregnancies complicated by severe preeclampsia. There was no statistical difference in median maternal plasma levels of tumor necrosis f actor ct between control subjects (0.0 pg/mL) and patients with severe pree clampsia (2.5 pg/mL; P=.36): Unexpectedly, fetal plasma tumor necrosis fact or cc levels were found to be significantly elevated in control women (18.4 pg/mL) relative to women with severe preeclampsia (9.1 pg/mL; P <.0001). CONCLUSION: Neither the genotypic frequencies for tumor necrosis factor <al pha> mutant alleles nor maternal tumor necrosis factor a plasma levels were increased in patients with severe preeclampsia. (Am J Obstet Gynecol 2001; 184:1273-7).