TY - JOUR
T1 - Increased plasma levels of ED1+ cellular fibronectin precede the clinical signs of preeclampsia
AU - Lockwood, Charles J.
AU - Peters, John H.
N1 - Funding Information:
From tlu Department of Obstetrics and Gynecology, Tufts U mversi(~ School of MedIcine: and the Department of Immunology, Research Institute of Scripps Climc, and Pulmonary Division. Department of Medicine, University of California, San DIego, School of M ed-icine.b Supported by United States Public Health Sen.nce grant Nos. GM-08172, HL-23584 (Umversity of Californza. San DIego. Spe-cialized Center for Research), GM-37696. and HL-28235. This is publicatIOn IMM-5528 from the Department of Immunology. Research Institute of Scripps Clinic. ReceIVed for publication June 1, 1989; revised August 31, 1989; accepted September 13, 1989. Reprint requests: C. J. Lockwood, MD. Department of Obstetrics. Gynecology, and Reproductive Sciences. DiVISion of Maternal-Fetal MedIcine, Mount Sinal MedIcal Center, One Gmtave Levy Place, New York, NY 10029-6574. 611116657
PY - 1990/2
Y1 - 1990/2
N2 - To evaluate alterations in fibronectin homeostasis in preeclampsia we measured the plasma concentrations of fibronectin bearing an extra type III domain in 33 preeclamptic and 36 control patients at varying gestational ages. This fibronectin variant is concentrated in the endothelium of blood vessels and has been shown to be released at sites of vascular injury. In addition, total circulating fibronectin levels, composed primarily of hepatic-derived fibronectin lacking the extra type III domain, were also determined. Significant elevations in the average circulating concentrations of fibronectin with an extra type III domain (5.5 μg/ml [95% confidence interval, 4.7,6.2] versus 3.2 μg/ml [95% confidence interval, 2.9,3.5]; p = 0.0001) as well as total fibronectin (387 μg/ml [95% confidence interval, 357,417] versus 327 μg/ml [95% confidence interval, 305,348]; p = 0.036) were observed in preeclamptic versus control patients. Significant elevations in fibronectin levels with an extra type III domain occurred in the first trimester before clinical evidence of preeclampsia. In addition, multivariate logistic regression demonstrated a 5.4-fold increase in the risk of preeclampsia with each 1 μg/ml elevation in concentration of fibronectin with an extra type III domain. These findings lend support to the hypothesis that endothelial-vascular injury is a primary event in the genesis of preeclampsia.
AB - To evaluate alterations in fibronectin homeostasis in preeclampsia we measured the plasma concentrations of fibronectin bearing an extra type III domain in 33 preeclamptic and 36 control patients at varying gestational ages. This fibronectin variant is concentrated in the endothelium of blood vessels and has been shown to be released at sites of vascular injury. In addition, total circulating fibronectin levels, composed primarily of hepatic-derived fibronectin lacking the extra type III domain, were also determined. Significant elevations in the average circulating concentrations of fibronectin with an extra type III domain (5.5 μg/ml [95% confidence interval, 4.7,6.2] versus 3.2 μg/ml [95% confidence interval, 2.9,3.5]; p = 0.0001) as well as total fibronectin (387 μg/ml [95% confidence interval, 357,417] versus 327 μg/ml [95% confidence interval, 305,348]; p = 0.036) were observed in preeclamptic versus control patients. Significant elevations in fibronectin levels with an extra type III domain occurred in the first trimester before clinical evidence of preeclampsia. In addition, multivariate logistic regression demonstrated a 5.4-fold increase in the risk of preeclampsia with each 1 μg/ml elevation in concentration of fibronectin with an extra type III domain. These findings lend support to the hypothesis that endothelial-vascular injury is a primary event in the genesis of preeclampsia.
KW - Cellular and plasma fibronectin
KW - endothelial and vascular injury
KW - preeclampsia
UR - https://www.scopus.com/pages/publications/0025125877
U2 - 10.1016/0002-9378(90)90385-K
DO - 10.1016/0002-9378(90)90385-K
M3 - Article
C2 - 2309814
AN - SCOPUS:0025125877
SN - 0002-9378
VL - 162
SP - 358
EP - 362
JO - American Journal of Obstetrics and Gynecology
JF - American Journal of Obstetrics and Gynecology
IS - 2
ER -