V.M. Holers
University of Colorado Denver
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Featured researches published by V.M. Holers.
Obstetrics & Gynecology | 2011
Anne M. Lynch; Ronald S. Gibbs; Murphy; Patricia C. Giclas; Jane E. Salmon; V.M. Holers
OBJECTIVE: To estimate whether elevations of complement C3a early in pregnancy are predictive of the subsequent development of adverse pregnancy outcomes. METHODS: A plasma sample was obtained from each enrolled pregnant woman before 20 weeks of gestation. The cohort (n=1,002) was evaluated for the development of adverse pregnancy outcomes defined as hypertensive diseases of pregnancy (gestational hypertension or preeclampsia), preterm birth (before 37 weeks of gestation), premature rupture of the membranes, pregnancy loss (during the embryonic and fetal period), intrauterine growth restriction, and the composite outcome of any adverse outcome. RESULTS: One or more adverse pregnancy outcomes occurred in 211 (21%) of the cohort. The mean levels (ng/mL) of C3a in early pregnancy were significantly (P=<.001) higher among women with one or more adverse outcomes (858±435) compared with women with an uncomplicated pregnancy (741±407). Adjusted for parity and prepregnancy body mass index, women with levels of C3a in the upper quartile in early pregnancy were three times more likely to have an adverse outcome later in pregnancy compared with women in the lowest quartile (95% confidence interval, 1.8–4.8; P<.001). The link between early elevated C3a levels and adverse pregnancy outcomes was driven primarily by individual significant (P<.05) associations of C3a with hypertensive diseases of pregnancy, preterm birth, and premature rupture of the membranes. CONCLUSION: Elevated C3a as early as the first trimester of pregnancy is an independent predictive factor for adverse pregnancy outcomes, suggesting that complement-related inflammatory events in pregnancy contribute to the subsequent development of poor outcomes at later stages of pregnancy. LEVEL OF EVIDENCE: II
British Journal of Obstetrics and Gynaecology | 2010
Anne M. Lynch; James Murphy; Ronald S. Gibbs; Richard J. Levine; Pc Giclas; Jane E. Salmon; V.M. Holers
Please cite this paper as: Lynch A, Murphy J, Gibbs R, Levine R, Giclas P, Salmon J, Holers V. The interrelationship of complement‐activation fragments and angiogenesis‐related factors in early pregnancy and their association with pre‐eclampsia. BJOG 2010; 117:456–462.
Molecular Immunology | 2011
Nirmal K. Banda; Stephanie L. Hyatt; Magdalena J. Glogowska; Kazue Takahashi; T.J. Merkel; Gregory L. Stahl; B. Lu; Craig Gerard; Rick A. Wetsel; William P. Arend; V.M. Holers
Obstetric Anesthesia Digest | 2011
Anne M. Lynch; James Murphy; Ronald S. Gibbs; R.J. Levine; Patricia C. Giclas; Jane E. Salmon; V.M. Holers
Molecular Immunology | 2007
Iris Leinhase; Joshua M. Thurman; Denise Harhausen; Wade R. Smith; Oliver I. Schmidt; Wolfgang Ertel; V.M. Holers; P. F. Stahel
Molecular Immunology | 2013
William P. Arend; Gaurav Mehta; Alexandra H. Antonioli; M. Takahashi; Kazue Takahashi; Gregory L. Stahl; V.M. Holers; Nirmal K. Banda
Molecular Immunology | 2013
Bärbel Rohrer; Liudmila Kulik; Lynne M. Mitchell; Dennis E. Hourcade; Jonathan P. Hannan; Beth Coughlin; Alex Woodell; Matthew C. Pickering; V.M. Holers; Joshua M. Thurman
Molecular Immunology | 2013
M. Neher; C. Keene; M. Rich; S. Weckbach; A. Bolden; J. T. Losacco; V.M. Holers; Philip F. Stahel
Molecular Immunology | 2011
Anne M. Lynch; Robert H. Eckel; James Murphy; Ronald S. Gibbs; Nancy A. West; Patricia C. Giclas; Jane E. Salmon; V.M. Holers
Obstetric Anesthesia Digest | 2009
Anne M. Lynch; Ronald S. Gibbs; James Murphy; Tim Byers; Margaret C. Neville; Patricia C. Giclas; Jane E. Salmon; T. M. Van Hecke; V.M. Holers