IP Library › Granted Patent US 9,250,251
Granted Patent B2
US 9,250,251 · App. 13/259,883 · Granted Feb 2, 2016

Methods for determining maternal health risks

Inventors: Kypros Nicolaides (London, GB); Tarja Ahola (Turku, FI)
Assignee: WALLAC OY
G01N33/74G01N2333/475G01N2800/368
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,250,251
App. No.
13/259,883
Granted
Feb 2, 2016
Kind
B2
Abstract

The present description relates to a method for determining the risk of a pregnant woman developing a hypertensive disorder, more specifically gestational hyper-tension or late onset preeclampsia. The present description provides methods useful for determining risk that a pregnant individual will develop a hypertensive disorder or condition of pregnancy, such as gestational hypertension, early preeclampsia, late preeclampsia and related disorders. Several useful combinations of biochemical markers and related clinical population studies are described herein. Additionally, it is proposed herein that certain sets of biochemical markers can be used to determine risk of multiple hypertensive disorders in a single screen. The biochemical markers are PlGF, Activin A and optionally P-Selectin.

Claims (7)

1. Method for determining the risk of late onset preeclampsia in a pregnant individual, comprising:

detecting the levels of biochemical markers placental growth factor (PlGF), Activin A and P-selectin in at least one blood sample from the pregnant individual; and

determining the increased risk of late onset preeclampsia if any of (i) to (iii) occur;

(i) when the level of PlGF in the blood sample obtained from the individual is decreased relative to the level of PlGF in a control sample,

(ii) when the level of Actin A in a sample obtained from the individual is increased relative to the level of Actin A in a control sample, and

(iii) when the level of P-selectin in a sample obtained from the individual is increased relative to the level of P-selectin in a control sample.

2. The method according to claim 1 , wherein sample is collected within first trimester.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 11, 2012
From: NICOLAIDES, KYPROS; AHOLA, TARJA
To: WALLAC OY
Reel/Frame 029109/0354 →
Continuity (2)
Provisional Application 61171955 · Apr 23, 2009
Related Publication 20120135427A1 · May 31, 2012