Immunoglobulin free light chains: an inflammatory biomarker of diabetes.


Journal

Inflammation research : official journal of the European Histamine Research Society ... [et al.]
ISSN: 1420-908X
Titre abrégé: Inflamm Res
Pays: Switzerland
ID NLM: 9508160

Informations de publication

Date de publication:
Aug 2020
Historique:
received: 26 04 2020
accepted: 08 05 2020
revised: 06 05 2020
pubmed: 20 5 2020
medline: 9 6 2021
entrez: 20 5 2020
Statut: ppublish

Résumé

Inflammation is increasingly understood as playing an important role in type 2 diabetes mellitus (T2D) development. A critical mechanism of the inflammatory cascade in developing T2D is nuclear factor-kappa B (NF-kB) activation. As immunoglobulin free light chains (FLC) could be a biomarker of activation of NF-kB, we measured FLC in patients with T2D. The age range of the 77 patients with T2D and the 75 healthy control participants were 45-87 years (median 60) and 25-72 years (median 51), respectively. Serum FLC kappa and lambda were assayed by a competitive-inhibition multiplex Luminex assay. The concentration of circulating FLC the kappa/lambda ratio was lower in patients with T2D than in healthy volunteers. The area under the receiver operating curve (ROC-AUC) of the FLC kappa/lambda ratio showed the largest ROC-AUC compared with other FLC variables and hemoglobin A1c (HbA1c). The diagnostic performance for distinguishing between T2D and healthy control was a sensitivity of 0.96 and a specificity of 1. The odds ratio was 0.000018. These results suggest that FLC kappa/lambda may be more specific and sensitive for the diagnosis of T2D than HbA1c, and thus represents a potentially promising biomarker of inflammation.

Identifiants

pubmed: 32424470
doi: 10.1007/s00011-020-01357-7
pii: 10.1007/s00011-020-01357-7
doi:

Substances chimiques

Biomarkers 0
Immunoglobulin Light Chains 0
NF-kappa B 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

715-718

Commentaires et corrections

Type : ErratumIn

Auteurs

Akira Matsumori (A)

Clinical Research Center, Kyoto Medical Center, 1-1 Fukakusa Mukaihata-cho, Fushimi-ku, Kyoto, 612-8555, Japan. amat@kuhp.kyoto-u.ac.jp.

Toshio Shimada (T)

Clinical Research Center, Shizuoka General Hospital, Shizuoka, Japan.

Miho Shimada (M)

VCL Laboratory, Osaka, Japan.

Mark T Drayson (MT)

The University of Birmingham, Birmingham, UK.

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Classifications MeSH