IP Library Granted Patent US 8,586,317
Granted Patent B2
US 8,586,317 · App. 13/084,203 · Granted Nov 19, 2013

Methods of diagnosing hypophosphatemic disorders

Inventors: Michael Econs (Indianapolis, IN); Kenneth E. White (Carmel, IN); Tim Matthias Strom (Munich, DE); Thomas Meitinger (Munich, DE)
Assignees: Advanced Research & Technology Institute; Ludwig-Maximilians-Universitat Munchen Abeteilung Mediziniche Genetik
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Quick Facts
Patent No.
US 8,586,317
App. No.
13/084,203
Granted
Nov 19, 2013
Kind
B2
Abstract

The present invention relates to methods of diagnosing hypophosphatemic disorders.

Claims (8)

1. A method of diagnosing a hypophosphatemic disorder in a mammal, said method comprising (a) obtaining a biological sample from said mammal and (b) contacting said biological sample with a reagent that detects the level of fibroblast growth factor-23 (FGF23) polypeptide in said sample,

wherein the FGF23 polypeptide is a polypeptide selected from the group consisting of a polypeptide comprising the amino acid sequence of SEQ ID NO:2, a polypeptide comprising the amino acid sequence of SEQ ID NO:4, a polypeptide comprising an arginine-to-glutamine mutation at amino acid 176 (R176Q) relative to SEQ ID NO:2, a polypeptide comprising an arginine-to-glutamine mutation at amino acid 179 (R179Q) relative to SEQ ID NO:2, and a polypeptide comprising an arginine-to-tryptophan mutation at amino acid 179 (R179W) relative to SEQ ID NO:2,

wherein an elevated level of FGF23 polypeptide in said sample, relative to the level of FGF23 polypeptide in a sample obtained from a control mammal, is an indication that said mammal is afflicted with said hypophosphatemic disorder, thereby diagnosing said hypophosphatemic disorder in said mammal.

2. The method of claim 1 , wherein said mammal afflicted with said hypophosphatemic disorder is afflicted with one of the hypophosphatemic disorders selected from the group consisting of X-linked hereditary rickets (XLH), hereditary hypophosphatemic rickets (HHRH), hypophosphatemic bone disease (HBD), autosomal dominant hypophosphatemic rickets (ADHR), tumor induced osteomalacia, epidermal nevus syndrome, fibrous dysplasia, and nephrolithiasis.

3. The method of claim 1 , wherein said biological sample is selected from the group consisting of blood and urine.

4. The method of claim 1 , wherein said reagent is an FGF23 antibody.

5. The method of claim 1 , wherein said reagent is detectably labeled.

6. The method of claim 1 , wherein said reagent is detectably labeled with a label selected from the group consisting of a radioisotope, a bioluminescent compound, a chemiluminescent compound, a fluorescent compound, a metal chelate, and an enzyme.

Assignments (1)
CONFIRMATORY LICENSE Recorded May 26, 2011
From: INDIANA UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 026347/0158 →
Continuity (5)
Division 11983190 · Nov 7, 2007
Division 10379334 · Mar 4, 2003
Division 09901938 · Jul 10, 2001
Provisional Application 60219137 · Jul 19, 2000
Related Publication 20120064544A1 · Mar 15, 2012