IP Library Granted Patent US 9,857,382
Granted Patent B2
US 9,857,382 · App. 15/078,835 · Granted Jan 2, 2018

Assessing renal structural alterations and outcomes

Inventors: Sasantha J. Sangaralingham (Rochester, MN); John C. Burnett, Jr. (Rochester, MN); Alessandro Cataliotti (Rochester, MN); Denise M. Heublein (Altura, MN)
Assignee: Mayo Foundation for Medical Education and Research
G01N33/6893A61K38/2242A61K45/06C07K14/58G01N2333/58G01N2800/04G01N2800/042G01N2800/32G01N2800/324G01N2800/325G01N2800/347G01N2800/52G01N2800/56
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Quick Facts
Patent No.
US 9,857,382
App. No.
15/078,835
Granted
Jan 2, 2018
Kind
B2
Abstract

This document provides methods and materials involved in assessing renal structural alterations (e.g., renal fibrosis, glomerular basement thickening, mesangial matrix expansion, swollen podocytes, and foot processes effacement) as well as methods and materials involved in assessing outcomes. For example, methods and materials for using the level of urinary CNP (e.g., a urinary to plasma CNP ratio) to determine whether or not a mammal is developing renal structural alterations (e.g., renal fibrosis, glomerular basement thickening, mesangial matrix expansion, swollen podocytes, and foot processes effacement) as well as methods and materials for using the level of urinary CNP levels to identify patients having an increased likelihood of experiencing a poor outcome are provided.

Claims (9)

1. A method for treating a mammal having an increased risk of acute decompensated heart failure, wherein said method comprises:

(a) determining that said mammal has an elevated level of urinary NT-CNP-53,

(b) monitoring said mammal for the presence of a risk factor for said acute decompensated heart failure, and

(c) administering an ACE inhibitor, an angiotensin receptor blocker, an aldosterone antagonist, a statin, a native natriuretic peptide, or a designer natriuretic peptide to said mammal.

2. The method of claim 1 , wherein said mammal is a human.

3. The method of claim 1 , wherein said elevated level is greater than 36,000 pg of NT-CNP-53/day.

4. The method of claim 1 , wherein said elevated level is greater than 42,000 pg of NT-CNP-53/day.

5. The method of claim 1 , wherein said risk factor is selected from the group consisting of an age factor, hypertension, an elevated serum creatinine level, proteinuria, an elevated body mass index, an elevated cholesterol level, a smoking habit, and diabetes.

6. The method of claim 1 , wherein said method comprises administering said angiotensin receptor blocker to said mammal.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 22, 2016
From: SANGARALINGHAM, SASANTHA J.; BURNETT, JOHN C., JR.; CATALIOTTI, ALESSANDRO; HEUBLEIN, DENISE M.
To: MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH
Reel/Frame 039236/0569 →
CONFIRMATORY LICENSE Recorded Jun 27, 2016
From: MAYO CLINIC ROCHESTER
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 039167/0477 →
Continuity (3)
Continuation 14367185
Provisional Application 61580139 · Dec 23, 2011
Related Publication 20160252528A1 · Sep 1, 2016