IP Library › Granted Patent US 11,016,107
Granted Patent B2
US 11,016,107 · App. 16/173,236 · Granted May 25, 2021

Method for diagnosing or monitoring kidney function or diagnosing kidney dysfunction

Inventor: Andreas Bergmann (Berlin, DE)
Assignee: SPHINGOTEC GMBH
G01N33/74G01N33/54366G01N33/6893G01N2333/70G01N2800/347G01N2800/52
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Quick Facts
Patent No.
US 11,016,107
App. No.
16/173,236
Granted
May 25, 2021
Kind
B2
Abstract

A method for (a) diagnosing or monitoring kidney function in subject or (b) diagnosing kidney dysfunction in a subject or (c) predicting or monitoring the risk of an adverse events in a diseased subject or (d) predicting or monitoring the success of a therapy or intervention comprising determining the level of Pro-Enkephalin (PENK) or fragments thereof of at least 5 amino acids in a bodily fluid obtained from said subject; and correlating said level of Pro-Enkephalin or fragments thereof with (a) kidney function in a subject or (b) kidney dysfunction in said subject or (c) enhanced risk of adverse events or (d) success of a therapy or intervention in a diseased subject.

Claims (28)

1. A method for diagnosing or monitoring kidney function in a subject comprising:

determining the level of Pro-Enkephalin or fragments thereof of at least 5 amino acids in a bodily fluid obtained from said subject; and

monitoring kidney function in a subject with a follow-up measurement of the level of Pro-Enkephalin or fragments thereof of at least 5 amino acids in a bodily fluid obtained from said subject,

wherein during said follow-up measurement, a relative change of Pro-Enkephalin or fragments thereof of at least 5 amino acids that is lowered, correlates with the improvement of the subject's kidney function, or

wherein during said follow-up measurement, a relative change of Pro-Enkephalin or fragment thereof of at least 5 amino acids that is increased, correlates with the worsening of the subject's kidney function, and

wherein said determination of Pro-Enkephalin or fragments thereof of at least 5 amino acids is performed more than once in one subject, and

wherein said Pro-Enkephalin or fragment thereof is SEQ ID No. 1, or SEQ ID No. 6 and

wherein an assay is used comprising two binders that bind to two different regions within the region of Pro-Enkephalin that is amino acid 133-140 (LKELLETG, SEQ ID NO. 13) and amino acid 152-159 (SDNEEEVS, SEQ ID No. 14) wherein each of said regions comprises at least 4 or 5 amino acids.

2. A method according to claim 1 , wherein each binder is an antibody, an antibody fragment or a non-Ig-Scaffold binding to Pro-Enkephalin or fragments thereof of at least 5 amino acids.

3. A method according to claim 1 , wherein each binder binds to a region within the amino acid sequence SEQ ID No. 1, or SEQ ID No. 6, and does not bind to enkephalin peptides [Met]enkephalin SEQ ID No: 3, or [Leu]enkephalin SEQ ID No: 4.

4. A method according to claim 1 , wherein the level of Pro-Enkephalin is measured with an immunoassay and each binder is an antibody, or an antibody fragment binding to Pro-Enkephalin or fragments thereof of at least 5 amino acids.

5. A method according to claim 1 , wherein an assay is used for determining the level of Pro-Enkephalin or fragments thereof of at least 5 amino acids and wherein the assay sensitivity of said assay is able to quantify the Pro-Enkephalin or Pro-Enkephalin fragments of healthy subjects and is <15 pmol/L.

6. A method according to claim 1 , wherein said bodily fluid is blood, serum, plasma, urine, cerebrospinal liquid (CSF), or saliva.

7. A method according to claim 1 , wherein additionally at least one clinical parameter is determined wherein said clinical parameter is BUN, NGAL, Creatinine Clearance, Creatinine or Apache Score.

8. A method according to claim 1 , wherein said monitoring is performed in order to evaluate the response of said subject to preventive and/or therapeutic measures taken.

9. A method according to claim 8 , in order to stratify said subjects into risk groups.

10. A method for diagnosing or monitoring kidney function in a subject comprising:

determining the level of Pro-Enkephalin or fragments thereof of at least 5 amino acids in a bodily fluid obtained from said subject; and

monitoring kidney function in a subject with a follow-up measurement of the level of Pro-Enkephalin or fragments thereof of at least 5 amino acids in a bodily fluid obtained from said subject,

wherein during said follow-up measurement, a relative change of Pro-Enkephalin or fragments thereof of at least 5 amino acids that is lowered correlates with the improvement of the subject's kidney function, or

wherein during said follow-up measurement, a relative change of Pro-Enkephalin or fragments thereof of at least 5 amino acids that is increased correlates with the worsening of the subject's kidney function, and

wherein said determination of Pro-Enkephalin or fragments thereof of at least 5 amino acids is performed more than once in one subject, and

wherein said Pro-Enkephalin or fragment thereof is SEQ ID No. 1, or SEQ ID No. 6

and

wherein additionally at least one clinical parameter is determined that is age, BUN, NGAL, Creatinine Clearance, Creatinine or Apache Score

and

wherein an assay is used comprising two binders that bind to two different regions within the region of Pro-Enkephalin that is amino acid 133-140 (LKELLETG, SEQ ID NO. 13) and amino acid 152-159 (SDNEEEVS, SEQ ID No. 14) wherein each of said regions comprises at least 4 or 5 amino acids.

11. A method according to claim 10 , wherein each binder binds to a region with sequence SEQ ID No. 6.

Priority Claims (2)
EP 12187051 · Oct 2, 2012 · regional
EP 13170327 · Jun 3, 2013 · regional
Continuity (3)
Continuation 15590571 · May 9, 2017
Continuation 14432957
Related Publication 20190049470A1 · Feb 14, 2019