Kits and methods for prediction and treatment of preeclampsia
Biomarkers tests which can be used to predict a positive or negative risk of preeclampsia are described. More specifically, a panel of biomarkers including MMP-7 and gpIIbIIIa, described. The test is useful to predict preeclampsia when a biological sample is obtained between the 16 th and 22 nd week of pregnancy. Prediction later in pregnancy can be achieved by a combination of Siglec-6, Activin A, ALCAM, and/or FCN2.
1. A method consisting of:
obtaining a plasma or serum sample derived from a pregnant human subject in the 22 nd to 28 th week of gestation; and
contacting the sample with at least two binding ligands in one or more wells, wherein at least one binding ligand binds biomarker Sialic acid-binding Ig-like lectin 6 (Siglec-6) and at least one binding ligand binds biomarker Activin A.
2. The method of claim 1 , wherein the contacting comprises loading samples into the one or more wells coated with Siglec-6 binding ligands; and the one or more wells coated with Activin A binding ligands.
3. A method consisting of:
obtaining a first plasma or serum sample derived from a pregnant human subject in the 22 nd to 28 th week of gestation;
contacting the first sample with at least two binding ligands, at least one of which binds biomarker Sialic acid-binding Ig-like lectin 6 (Siglec-6) and at least one of which binds biomarker Activin A;
obtaining a second plasma or serum sample derived from the pregnant human subject in the 28 th to 32 nd week of gestation; and
contacting the second sample with one or more binding ligands in one or more wells that bind a biomarker, the one or more binding ligands selected from
at least one ligand that binds biomarker Siglec-6,
at least one ligand that binds biomarker CD166 antigen (ALCAM), and
at least one ligand that binds biomarker Ficolin-2 (FCN2).
4. The method of claim 3 , wherein the
one or more wells are coated with at least one of Siglec-6 binding ligands,
ALCAM binding ligands, and
FCN2 binding ligands.
5. A method consisting of:
assaying a serum or plasma sample obtained from a pregnant human subject in the 22 nd to 28 th week of gestation for expression level of biomarker proteins Sialic acid-binding Ig-like lectin 6 (Siglec-6) and Activin A:
wherein the assaying comprises loading samples into one or more wells coated with binding ligands.
6. The method of claim 5 wherein at least one of the one or more wells coated with binding ligands is coated with
Siglec-6 binding ligands, and at least one of the one or more wells coated with binding ligands is coated with Activin A binding ligands.
7. A method consisting of:
assaying a first serum or plasma sample obtained from a pregnant human subject in the 22 nd to 28 th week of gestation for expression level of biomarker proteins Sialic acid-binding lg-like lectin 6 (Siglec-6) and Activin A;
assaying a second serum or plasma sample obtained from the pregnant human subject in the 28 th to 32 nd week of gestation for expression level of biomarker proteins Siglec-6, CD166 antigen (ALCAM), and Ficolin-2 (FCN2);
wherein the assaying of the second serum comprises loading the second sample into one or more wells coated with binding ligands.
8. The method of claim 7 wherein:
the
one or more wells are coated with binding ligands selected from: Siglec-6 binding ligands,
ALCAM binding ligands, and
FCN2 binding ligands.