Skip to search boxSkip to navigationSkip to main content

Serum insulin-like growth factor binding protein 6 (IGFBP6) is increased in patients with type 1 diabetes and its complications

*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
Peer-review

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Insulin-like growth factor binding proteins (IGFBPs) are associated with insulin resistance and accelerated micro-and macro-vascular complications of diabetes. We investigated the relationship between serum levels of IGFBP6 in type-1 diabetes (T1D) patients and diabetic complications. In this study, IGFBP6 was measured in the sera from 697 T1D patients and 681 healthy controls using a Luminex assay. Mean serum levels of IGFBP6 were higher in T1D patients than controls matched for sex and age (119.7 vs 130.6 ng/ml, p < 10-4). Subject age, sex and duration of disease have a significant impact on serum IGFBP6 levels in both T1D patients and healthy controls. Patients with complications have significantly higher mean serum IGFBP6 than patients without any complication (p = 3.5×10-6). More importantly, conditional logistic regression analysis suggested that T1D patients are more likely to have very high levels of serum IGFBP6 (in the 4th quartile) (OR = 1.7) than healthy controls. Furthermore, T1D patients with various complications are more likely to have very high levels of serum IGFBP6 (in the 4th quartile) than patients without any complication (OR = 1.7-22.9). These results indicate the clinical importance of measuring IGFBP6 to the better management of T1D patients.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 229-237 (9 pages)

Journal (Volume, Issue Number)

International Journal of Clinical and Experimental Medicine (Volume 5, Issue 3)

Publication milestones

  • Published - 06/30/2012

Publication status

Published - 06/30/2012

ISSN

1940-5901

Publication IDs

  • Scopus: 84864313055
  • ORCID: /0000-0001-9597-4374/work/54990707
  • ORCID: /0000-0003-0385-3829/work/121881138

Publication metrics

Metrics

Fractional count
4
Fractional count
0.50
Fractional count
4
Fractional count
0.50
Fractional count
4
Fractional count
1
Scopus
citations
SciVal
FWCI
0.32
SciVal
Author count
8
SciVal
citations
9
SciVal
Paper percentile
63

PlumX

Citation count
19
Captures
29

Funding Details

FunderFunding number
NICHD
R01HD037800