Loading…

The lack of long-range negative correlations in glucose dynamics is associated with worse glucose control in patients with diabetes mellitus

Abstract Glucose dynamics measured in ambulatory settings are fluid in nature and exhibit substantial complexity. We recently showed that a long-range negative correlation of glucose dynamics, which is considered to reflect blood glucose controllability over a substantial period, is absent in patien...

Full description

Saved in:
Bibliographic Details
Published in:Metabolism, clinical and experimental clinical and experimental, 2012-07, Vol.61 (7), p.1041-1050
Main Authors: Ogata, Hitomi, Tokuyama, Kumpei, Nagasaka, Shoichiro, Tsuchita, Takeshi, Kusaka, Ikuyo, Ishibashi, Shun, Suzuki, Hiroaki, Yamada, Nobuhiro, Hamano, Kumiko, Kiyono, Ken, Struzik, Zbigniew R, Yamamoto, Yoshiharu
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Abstract Glucose dynamics measured in ambulatory settings are fluid in nature and exhibit substantial complexity. We recently showed that a long-range negative correlation of glucose dynamics, which is considered to reflect blood glucose controllability over a substantial period, is absent in patients with diabetes mellitus. This was demonstrated using detrended fluctuation analysis (DFA), a modified random-walk analysis method for the detection of long-range correlations. In the present study, we further assessed the relationships between the established clinical indices of glycemic or insulinogenic control of hemoglobin A1c (HbA1c ), glycated albumin (GA), 1,5-anhydroglucitol, and urine C-peptide immunoreactivity and the recently proposed DFA-based indices obtained from continuous glucose monitoring in 104 Japanese diabetic patients. Significant correlations between the following parameters were observed: (1) HbA1c and the long-range scaling exponent α2 ( r = 0.236, P < .05), (2) GA and α2 ( r = 0.254, P < .05), (3) GA and the short-range scaling exponent α1 ( r = 0.233, P < .05), and (4) urine C-peptide immunoreactivity and the mean glucose fluctuations ( r = −0.294, P < .01). Therefore, we concluded that increases in the long-range DFA scaling exponent, which are indicative of the lack of a long-range negative correlation in glucose dynamics, reflected abnormalities in average glycemic control as clinically determined using HbA1c and GA parameters.
ISSN:0026-0495
1532-8600
DOI:10.1016/j.metabol.2011.12.007