Means and methods for determining risk of type-1 diabetes by serum protein biomarkers

Patent metadata

Field	Value
Publication number	US-10877034-B2
Application number	US-201515319515-A
Country	US
Kind code	B2
Filing date	Jun 18, 2015
Priority date	Jun 18, 2014
Publication date	Dec 29, 2020
Grant date	Dec 29, 2020

Abstract

The present invention relates to methods for predicting a risk of a subject for Type 1 diabetes (T1D) on the basis of expression levels of protein markers in a sample obtained from the subject. The present invention also relates to in vitro kits for use in said methods.

First claim

The invention claimed is:

1. A method of determining an individual at risk of and/or progression towards Type 1 Diabetes (T1D), the method comprising:
a) determining a protein marker profile in a sample obtained from the individual, said profile comprising afamin (AFAM) and apolipoprotein C-IV (APOC4);
b) comparing the determined protein marker profile of APOC4 and AFAM of the individual with that of a corresponding control profile of APOC4 and AFAM in a control sample from a control individual or a pool of control individuals,
c) responsive to the comparison, determining the risk of and/or progression towards T1D in the individual, wherein a lower and a higher level of APOC4 and AFAM, respectively, in the sample obtained from the individual as compared to the levels of APOC4 and AFAM in the control sample indicates that the individual is at risk of and/or progression towards T1D, and
d) providing a treatment or dietary change to the individual to prevent T1D development.

2. The method according to claim 1 , wherein the individual is determined at risk of and/or progressing towards T1D prior to seroconversion in the individual.

3. The method according to claim 1 , wherein the individual has a Human Leukocyte Antigen-conferred (HLA-conferred) risk of T1D.

4. The method according to claim 1 , further comprising:
determining one or more protein markers selected from the group consisting of sex hormone-binding globulin (SHBG), adiponectin (ADIPO), thyroxine-binding globulin (THBG), apolipoprotein C-II (APOC2), insulin-like growth factor-binding protein 2 (IBP2), apolipoprotein C-I (APOC1), apolipoprotein C-III (APOC3), fetuin-B (FETUB), serum amyloid P-component (SAMP), clusterin (CLUS), C4b-binding protein alpha chain (C4BPA), C4b-BIRCH, binding protein beta chain (C4BPB), complement factor I (CFAI), inter-alpha-trypsin inhibitor heavy chain H4 (ITIH4), insulin-like growth factor-binding protein 3 (IBP3), Serum amyloid A4 protein (SAA4), complement component C8 alpha chain (CO8A), complement C1q subcomponent subunit B (C1QB), hyaluronan-binding protein 2 (HABP2), complement component C8 gamma chain (CO8G), transforming growth factor-beta-induced protein ig-h3 (BGH3), ectonucleotide pyrophosphatase/phosphodiesterase family member 2 (ENPP2), poliovirus receptor (PVR), vinculin (VINC), N-acetylmuramoyl-L-alanine amidase (PGRP2), contactin-1 (CNTN1), L-lactate dehydrogenase B chain 46 (LDHB), extracellular superoxide dismutase [Cu—Zn] (SODE), apolipoprotein A-IV (APOA4), neural cell adhesion and molecule 1 (NCAM1), and
comparing the determined one or more protein markers with that of corresponding control markers,
wherein a lower level of SHBG, ADIPO, THBG, APOC2, APOC1, APOC3, BGH3, ENPP2, PVR, VINC, PGRP2, CNTN1, LDHB, SODE, APOA4, NCAM1, or IBP2 in the sample obtained from the individual as compared to the levels in the control sample indicates that the individual is at risk of and/or progression towards T1D, and
wherein a higher level of FETUB, SAMP, CLUS, C4BPA, C4BPB, CFAI, ITIH4, IBP3, SAA4, CO8A, C1QB, HABP2, or CO8G in the sample obtained from the individual as compared to the levels in the control sample indicates that the individual is at risk of and/or progression towards T1D.

5. The method according to claim 1 , wherein said a)-c) steps are performed by a processor of a computing device.

6. The method according to claim 1 , wherein said sample is selected from the group consisting of a whole blood sample, a plasma sample, a serum sample, a sample comprising purified blood cells, a tissue sample, and a urine sample.

Assignees

• Turun Yliopisto

Inventors

• Moulder Robert
• Bhosale Santosh
• Goodlett David
• Lähdesmäki Harri
• Simell Olli
• Lahesmaa Riitta

Classifications

• G01N2800/50

  Determining the risk of developing a disease · CPC title

• G01N2333/775

  Apolipopeptides · CPC title

• G01N2560/00

  Chemical aspects of mass spectrometric analysis of biological material · CPC title

• G01N2800/042

  Disorders of carbohydrate metabolism, e.g. diabetes, glucose metabolism · CPC title

• G01N33/564 Primary

  for pre-existing immune complex or autoimmune disease {, i.e. systemic lupus erythematosus, rheumatoid arthritis, multiple sclerosis, rheumatoid factors or complement components C1-C9} · CPC title