US2015293129A1PendingUtilityA1

Detection and treatment of pregnancy complications

Assignee: UNIV BROWNPriority: Nov 1, 2012Filed: Oct 28, 2013Published: Oct 15, 2015
Est. expiryNov 1, 2032(~6.3 yrs left)· nominal 20-yr term from priority
G01N 2400/10G01N 33/689G01N 33/76A61K 38/24G01N 2800/368G01N 2440/38
54
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Claims

Abstract

Disclosed herein is a method of of identifying and/or addressing incipient preeclampsia in a patient-subject by the steps of by the steps of (a) performing a bioassay to determine the level of at least one sialyl Lewis antigen in a said patient- subject at about 25 weeks of pregnancy or earlier; (b) performing a bioassay to determine the level of at least one sialyl Lewis antigen in a pregnant non-preeclampsia one or more subjects at about 30 weeks of pregnancy or later, wherein said at least one sialyl Lewis antigen assay is for a sialyl Lewis antigen assayed in step (a) is and if more than one subject is assayed, averaging said results; and (c) managing said patient-subject for preeclampsia, if said level of at least one sialyl Lewis antigen of step (a) is at or greater than about 20% above the level of such silalyl Lewis antigen assayed in step (b).

Claims

exact text as granted — not AI-modified
1 . A method of identifying and/or addressing incipient preeclampsia in a patient-subject by the steps of by the steps of
 (a) performing a bioassay to determine the level of at least one sialyl Lewis antigen in a said patient-subject at about 25 weeks of pregnancy or earlier;   (b) performing a bioassay to determine the level of at least one sialyl Lewis antigen in a pregnant non-preeclampsia one or more subjects at about 30 weeks of pregnancy or later, wherein said at least one sialyl Lewis antigen assay is for a sialyl Lewis antigen assayed in step (a) is and if more than one subject is assayed, averaging said results; and   (c) managing said patient-subject for preeclampsia, if said level of at least one sialyl Lewis antigen of step (a) is at or greater than about 20% above the level of such silalyl Lewis antigen assayed in step (b).   
     
     
         2 . The method of  claim 1  wherein step (a) is performed at about 20 weeks of pregnancy or earlier. 
     
     
         3 . The method of  claim 2  wherein step (a) is performed at about 10 weeks of pregnancy or earlier. 
     
     
         4 . A method of identifying and/or addressing incipient preeclampsia in a patient-subject by the steps of by the steps of
 (a) performing a bioassay to determine the level of least two or more sialyl Lewis antigens in a said patient-subject at about 25 weeks of pregnancy or earlier;   (b) performing a bioassay to determine the level of at least two or more sialyl Lewis antigens of step(a) in a pregnant non-preeclampsia one or more subjects at about 30 weeks of pregnancy or later, wherein said at least two or more sialyl Lewis antigens is for a sialyl Lewis antigen assayed in step (a) is and if more than one subject is assayed, averaging said results as to each antigen separately;   (c) managing said patient-subject for preeclampsia, if the sum level of at two or more sialyl Lewis antigens of step (a) is at or greater than about 30% above the level of the sum level of silalyl Lewis antigens assayed in step (b).   
     
     
         5 . The method of step  4  wherein three sialyl Lewis antigens are the subject of the bioassay of step (a) and step (b) wherein step (c) comprises managing said patient-subject for preeclampsia, if the sum level of said three sialyl Lewis antigens of step
 (a) is at or greater than about 50% above the level of the sum level of the sum of the silalyl Lewis antigens levels assayed in step (b). 
 
     
     
         6 . A method of determining incipient preeclampsia at  20  weeks of pregnancy or earlier by the steps of
 (a) performing a bioassay to determine the level of at least one sialyl Lewis antigen in a female subject with a diagnosis of preeclampsia about 30 weeks of pregnancy or later, said result being a first comparator; 
 (b) performing a bioassay to determine the level of said at least one sialyl Lewis antigen of stem (a) in a pregnant non-preeclampsia subject at about 30 weeks of pregnancy or later said result being a second comparator;, 
 (c) performing a bioassay to determine the level of sialyl Lewis antigen in a subject being tested for incipient preeclampsia; and, 
 (d) managing said patient-subject for preeclampsia, if, upon comparing the level of sialyl Lewis antigens of (c) with said first and second comparators, wherein a sialyl Lewis antigen of level closer to the level of (a) than (b) is predictive of incipient preeclampsia.

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