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The Journal of Maternal-Fetal & Neonatal Medicine Volume 22, 2009 - Issue 8
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Original Article

Maternal anti-protein Z antibodies in pregnancies complicated by pre-eclampsia, SGA and fetal death

Offer Erez Perinatology Research Branch, NICHD/NIH/DHHS, Bethesda, Maryland, and, Detroit, Michigan, USA; Department of Obstetrics and Gynecology, Wayne State University, Detroit, Michigan, USA
,
Roberto Romero Perinatology Research Branch, NICHD/NIH/DHHS, Bethesda, Maryland, and, Detroit, Michigan, USA; Department of Obstetrics and Gynecology, Wayne State University, Detroit, Michigan, USA; Center for Molecular Medicine and Genetics, Wayne State University, Detroit, Michigan, USACorrespondence[email protected]
, MD,
Edi Vaisbuch Perinatology Research Branch, NICHD/NIH/DHHS, Bethesda, Maryland, and, Detroit, Michigan, USA; Department of Obstetrics and Gynecology, Wayne State University, Detroit, Michigan, USA
,
Shali Mazaki-Tovi Perinatology Research Branch, NICHD/NIH/DHHS, Bethesda, Maryland, and, Detroit, Michigan, USA; Department of Obstetrics and Gynecology, Wayne State University, Detroit, Michigan, USA
,
Juan Pedro Kusanovic Perinatology Research Branch, NICHD/NIH/DHHS, Bethesda, Maryland, and, Detroit, Michigan, USA; Department of Obstetrics and Gynecology, Wayne State University, Detroit, Michigan, USA
,
Tinnakorn Chaiworapongsa Perinatology Research Branch, NICHD/NIH/DHHS, Bethesda, Maryland, and, Detroit, Michigan, USA; Department of Obstetrics and Gynecology, Wayne State University, Detroit, Michigan, USA
,
Nandor Gabor Than Perinatology Research Branch, NICHD/NIH/DHHS, Bethesda, Maryland, and, Detroit, Michigan, USA
,
Francesca Gotsch Perinatology Research Branch, NICHD/NIH/DHHS, Bethesda, Maryland, and, Detroit, Michigan, USA
,
Chong Jai Kim Perinatology Research Branch, NICHD/NIH/DHHS, Bethesda, Maryland, and, Detroit, Michigan, USA; Department of Pathology, Wayne State University, Detroit, Michigan, USA
,
Pooja Mittal Perinatology Research Branch, NICHD/NIH/DHHS, Bethesda, Maryland, and, Detroit, Michigan, USA; Department of Obstetrics and Gynecology, Wayne State University, Detroit, Michigan, USA
,
Samuel Edwin Perinatology Research Branch, NICHD/NIH/DHHS, Bethesda, Maryland, and, Detroit, Michigan, USA
,
Percy Pacora Perinatology Research Branch, NICHD/NIH/DHHS, Bethesda, Maryland, and, Detroit, Michigan, USA
,
Sun Kwon Kim Perinatology Research Branch, NICHD/NIH/DHHS, Bethesda, Maryland, and, Detroit, Michigan, USA
,
Lami Yeo Perinatology Research Branch, NICHD/NIH/DHHS, Bethesda, Maryland, and, Detroit, Michigan, USA; Department of Obstetrics and Gynecology, Wayne State University, Detroit, Michigan, USA
,
Moshe Mazor Department of Obstetrics and Gynecology, Soroka University Medical Center, Ben Gurion University of the Negev, Beer Sheva, Israel
&
Sonia S. Hassan Perinatology Research Branch, NICHD/NIH/DHHS, Bethesda, Maryland, and, Detroit, Michigan, USA; Department of Obstetrics and Gynecology, Wayne State University, Detroit, Michigan, USA
 show all
Pages 662-671 | Received 26 Oct 2008, Accepted 20 Jan 2008, Published online: 19 Aug 2009

Figures & data

Table I.  Demographic and clinical characteristics of the study population.

Table II.  Maternal plasma concentration of anti-protein Z antibodies.

Figure 1. Maternal plasma concentrations of anti-protein Z anti-bodies in non-pregnant and pregnant women.

Figure 1. Maternal plasma concentrations of anti-protein Z anti-bodies in non-pregnant and pregnant women.

Figure 2. The association between maternal plasma anti-protein Z IgM antibodies and gestational age at blood collection.

Figure 2. The association between maternal plasma anti-protein Z IgM antibodies and gestational age at blood collection.

Figure 3. Maternal plasma concentrations of anti-protein Z antibodies in normal and complicated pregnancies.

Figure 3. Maternal plasma concentrations of anti-protein Z antibodies in normal and complicated pregnancies.

Table III.  Comparison of IgG anti-protein Z antibodies percentiles between the study groups.

Table IV.  Comparison of IgM anti-protein Z antibodies percentiles between the study groups.

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Related Research Data

Late-onset preeclampsia is associated with an imbalance of angiogenic and anti-angiogenic factors in patients with and without placental lesions consistent with maternal underperfusion
Source: Informa UK Limited
Full-length human placental sFlt-1-e15a isoform induces distinct maternal phenotypes of preeclampsia in mice.
Source: Public Library of Science (PLoS)
Placental Lesions Associated With Maternal Underperfusion Are More Frequent in Early-Onset Than in Late-Onset Preeclampsia
Source: Ovid Technologies (Wolters Kluwer Health)
Protein Z polymorphisms associated with vaso-occlusive crisis in young sickle cell disease patients
Source: Springer Science and Business Media LLC

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