Natriuretic peptides and placental-growth factor/soluble VEGF-receptor discriminate cardiac dysfunction related to heart disease from a placenta-associated cardiac dysfunction in pregnant woman
A technology of placental growth factor and dysfunction, applied in the direction of biomaterial analysis, analytical materials, biological testing, etc., can solve the problem that natriuretic peptide cannot prove the cause of cardiac dysfunction in pregnant women, distinguish cardiac dysfunction in pregnant women, and does not describe the cardiac function of pregnant women Obstacles and other issues
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[0163] A clinical study in the presence of placenta-related cardiac dysfunction or in the presence of heart disease-related cardiac dysfunction has been performed in a cohort of 55 pregnant women. Reference values for sFlt-1, PlGF and NT-proBNP were determined for pregnant women (N=55) classified as second trimester (N=9) and third trimester (N=46). The sFlt-1 and PlGF values of pregnant women with elevated NT-proBNP values (>125 pg / ml) are shown in Table 1.
[0164] Passed Elecsys NT-Ex-BNP TM The assay (Roche Diagnostics) analyzed maternal blood samples for NT-proBNP concentrations. The concentration of sFlt-1 has been analyzed by using the human soluble VEGF R1 / Flt-1 immunoassay "Quantikine" (Catalog No. DVR100B) from R&D Systems. Quantitative determination of human placental growth factor (PlGF) concentration was analyzed by using the human PlGF immunoassay "Quantikine" (Catalog No. DPG00) from R&D Systems.
[0165] Table 1: sFlt-1 and PlGF values in pregnant wo...
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