Skills (19)
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Research experience
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Jun 2008–
presentResearch: Cholesterol Metabolism in fetal development
Collaboration of the University Aachen and BernSwitzerland · Bern -
Jun 2006–
presentTeaching: Medical Education in Obstetrics and Gynecology
Rheinisch-Westfälische Technische Hochschule Aachen · O&GGermany · Aachen -
Jun 2006–
presentResearch: Proteom Profiling in Gestation Related Diseases
Collaboration University Aachen and Rostock · Proteom center RostockGermany · Rostock
Education
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Apr 2012–
Apr 2013Inselspital, Universitätsspital Bern
Cholesterol efflux and lipid metabolisms in IUGR fetus · post DocSwitzerland · Bern -
Jun 2008–
Nov 2012Rheinisch-Westfälische Technische Hochschule Aachen
Lipid profiling in preeclampsia and IUGRGermany · Aachen -
Jun 2006–
Nov 2012Rheinisch-Westfälische Technische Hochschule Aachen
Serum proteom pattern generation in preeclampsia and IUGRGermany · Aachen -
Nov 2001–
Jun 2006Rheinisch-Westfälische Technische Hochschule Aachen
cytoskeletal changes in placental development and preeclampsia · MD (Dr. med.)Germany · Aachen
Awards & achievements
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May 2012Award: Vortragspreis 15. Kongress der DGPGM
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Apr 2012Grant: Rotations-Stipendium of the medical faculty RWTH Aachen
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May 2011Award: Vortragspreis 14. Deutsche Gestose Kongress
Other
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LanguagesGerman, English, French
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Scientific MembershipsISSHP, DGGG, NWGGG, AG Gestose
Questions and Answers (2) View all
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Answer added in Immunology Techniques5 Do you know a good quality control test for the biological activity of native human ApoE derived from serum?By Elwira Kaminska · St George's, University of LondonUlrich Pecks · Rheinisch-Westfälische Technische Hochschule AachenSend me an aliquot. I could do a cholesterol efflux and look whether or not it works as acceptor. Cholesterol efflux to apoE is mediated by ABCA1 at t... [more]Send me an aliquot. I could do a cholesterol efflux and look whether or not it works as acceptor. Cholesterol efflux to apoE is mediated by ABCA1 at the cell membrane.Following
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Answer added in Immunology Techniques5 Do you know a good quality control test for the biological activity of native human ApoE derived from serum?By Elwira Kaminska · St George's, University of LondonUlrich Pecks · Rheinisch-Westfälische Technische Hochschule Aachendepends on the function of apoE you want to assess...depends on the function of apoE you want to assess...Following
Publications (14) View all
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Article: Angiogenic factors and acute-phase proteins in serum samples of preeclampsia and HELLP patients: a matched-pair analysis.
Toralf Reimer, Henrike Rohrmann, Johannes Stubert, Ulrich Pecks, Michael O Glocker, Dagmar-Ulrike Richter, Bernd Gerber[show abstract] [hide abstract]
ABSTRACT: Objectives: To investigate the serum level distribution of angiogenic markers (PlGF, endoglin, sFlt-1) and acute-phase proteins (SAA, CRP) in patients with HELLP syndrome or preeclampsia (PE) including matched controls. Methods: The matching procedure revealed 46 controls for 23 HELLP cases, and 81 controls for 42 preeclamptic patients. Maternal serum concentrations were determined by immunoassays. Results: SAA and CRP levels were significantly higher in HELLP patients compared with controls. This finding was not observed in preeclamptic subgroup. Pro-angiogenic PlGF is significantly lower in PE and HELLP syndrome. Anti-angiogenic endoglin is significantly higher in PE and HELLP syndrome. The sFlt-1 analysis supports the anti-angiogenic shift in HELLP and preeclamptic patients, but with smaller differences between subgroups. The SAA/PlGF ratio showed the highest ROC value of all tested parameters in discrimination between HELLP and HELLP controls. Conclusions: These findings support the concept that patients with HELLP syndrome have both an anti-angiogenic state and a pronounced inflammatory response, while patients with PE are characterized only by an anti-angiogenic shift.The journal of maternal-fetal & neonatal medicine: the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 10/2012; · 1.36 Impact Factor -
Article: [Determination of maternal and foetal serum lipid profile and placental oxidised low density lipoprotein accumulation in preeclampsia and normotensive pregnancies].
[show abstract] [hide abstract]
ABSTRACT: Oxidised low density lipoproteins (oxLDL) are key players in the development of atherosclerotic cardiovascular diseases. Since there are similarities between the pathogenesis of preeclampsia and atherosclerosis we hypothesised an increased accumulation of oxLDL at the materno-foetal and foeto-foetal interface within the placental tissue of preeclamptic women compared to women with normotensive pregnancies (controls). Moreover, we analysed maternal and foetal serum lipid parameters.oxLDL was determined by immunohistochemistry in placental paraffin sections of 14 women suffering from preeclampsia (30th-39th week of gestation) and compared to 28 preterm and term deliveries (25th-40th week of gestation). 10 high power fields were chosen randomly by the newCAST software and oxLDL expression was analysed via standardised methods by 2 independent and blinded investigators. Maternal and foetal triglycerides, total cholesterol, LDL cholesterol and HDL cholesterol were measured. Statistical examination was carried out by the Mann-Whitney test.oxLDL was found in villous trophoblast and placental endothelium. No significant differences were observed in expression intensity between preeclampsia and controls. Maternal and foetal triglyceride levels were significantly increased in preeclampsia compared to controls (pre-eclampsia mothers: 293 [SD 87.4] mg/dL, con-trols: 214 [SD 89.4] mg/dL, p=0.0097; preeclampsia foetuses: 26 [SD 16.6] mg/dL, controls: 18 [SD 10.4] mg/dL, p=0.0463). No significant differences in other lipid concentrations were found.We could not confirm our initial hypothesis of an increased oxLDL accumulation in placental tissue of preeclampsia. However, preeclampsia is a condition of dyslipidaemia affecting both maternal and foetal serum with implications for development and programming of cardiovascular diseases in later life.Zeitschrift für Geburtshilfe und Neonatologie 10/2012; 216(5):220-5. -
Article: A proteome signature for intrauterine growth restriction derived from multifactorial analysis of mass spectrometry-based cord blood serum profiling.
Manja Wölter, Claudia Röwer, Cornelia Koy, Toralf Reimer, Werner Rath, Ulrich Pecks, Michael O Glocker[show abstract] [hide abstract]
ABSTRACT: Intrauterine growth restriction (IUGR) is defined as a condition in which the fetus does not reach its genetically given growth potential, resulting in low birth weight. IUGR is an important cause of perinatal morbidity and mortality, thus contributing substantially to medically indicated preterm birth in order to prevent fetal death. We subjected umbilical cord blood serum samples either belonging to the IUGR group (n = 15) or to the control group (n = 15) to fractionation by affinity chromatography using a bead system with hydrophobic interaction capabilities. So prepared protein mixtures were analyzed by MALDI-TOF mass spectrometric profiling. The six best differentiating ion signals at m/z 8205, m/z 8766, m/z 13 945, m/z 15 129, m/z 15 308, and m/z 16 001 were collectively assigned as IUGR proteome signature. Separation confidence of our IUGR proteome signature reached a sensitivity of 0.87 and a specificity of 0.93. Assignment of ion signals in the mass spectra to specific proteins was substantiated by SDS-PAGE in conjunction with peptide mass fingerprint analysis of cord blood serum proteins. One constituent of this proteome signature, apolipoprotein C-III(0) , a derivative lacking glycosylation, has been found more abundant in the IUGR cord blood serum samples, irrespective of gestational age. Hence, we suggest apolipoprotein C-III(0) as potential key-marker of the here proposed IUGR proteome signature, as it is a very low-density lipoprotein (VLDL) and high-density lipoprotein (HDL) member and as such involved in triglyceride metabolism that itself is discussed as being of importance in IUGR pathogenesis. Our results indicate that subtle alterations in protein glycosylation need to be considered for improving our understanding of the pathomechanisms in IUGR.Electrophoresis 07/2012; 33(12):1881-93. · 3.30 Impact Factor -
Article: Anti-oxidized Low-Density Lipoprotein (oxLDL) Antibody Levels are not Related to Increasing Circulating oxLDL Concentrations During the Course of Pregnancy.
[show abstract] [hide abstract]
ABSTRACT: To address the question of whether the high levels of oxidative modified low-density lipoproteins (oxLDL) in pregnancy are opposed by an appropriate humoral autoimmune response providing anti-oxLDL autoantibodies in maternal serum of healthy women throughout gestation. Blood was taken from 33 patients at four different time points from early to late gestation and post-partum. OxLDL and anti-oxLDL concentrations were measured by enzyme-linked immunosorbent assays. ANOVA was used for statistical evaluations followed by post hoc test with Bonferoni adjustment. Oxidized Low Density Lipoprotein concentrations increased while anti-oxLDL levels decreased significantly from early to late gestation. OxLDL was strongly positively correlated with LDL concentration and mildly negatively associated with anti-oxLDL levels. Estimating the status of oxidation by calculating oxLDL/LDL ratio revealed decreasing values with ongoing pregnancy. Multivariate analysis showed that anti-oxLDL levels were dependent on gestational age but neither on oxLDL levels nor on the oxLDL/LDL ratio. The results indicate that normal pregnancy is a well-balanced state of oxidative and anti-oxidative processes. However, we could not confirm a dependence of anti-oxLDL autoantibodies on oxLDL concentration. Whether or not the humoral immune system is involved in oxidative defence remains to be elucidated.American Journal Of Reproductive Immunology 05/2012; 68(4):345-52. · 2.17 Impact Factor -
Article: San Antonio Breast Cancer Symposium 2010
D.O. Bauerschlag, U. Pecks, N. MaassDer Gynäkologe 05/2012; 44(6):476-477.