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KMID : 1200020110350020149
Diabetes & Metabolism Journal
2011 Volume.35 No. 2 p.149 ~ p.158
Changes in Adenosine Deaminase Activity in Patients with Type 2 Diabetes Mellitus and Effect of DPP-4 Inhibitor Treatment on ADA Activity
Lee Jae-Geun

Kang Dong-Gu
Yu Jung-Re
Kim Young-Ree
Kim Jin-Soek
Koh Gwan-Pyo
Lee Dae-Ho
Abstract
Background: Dipeptidyl peptidase 4 (DPP-4, also known as CD26) binds with adenosine deaminase (ADA) to activate T lymphocytes. Here, we investigated whether ADA activity is specifically affected by treatment with DPP-4 inhibitor (DPP4I) compared with other anti-diabetic agents.

Methods: Fasting ADA activity, in addition to various metabolic and biochemical parameters, were measured in 262 type 2 diabetes mellitus (T2DM) patients taking various anti-diabetic agents and in 46 non-diabetic control subjects.

Results: ADA activity was increased in T2DM patients compared with that in non-diabetic control subjects (mean¡¾standard error, 23.1¡¾0.6 U/L vs. 18.6¡¾0.8 U/L; P<0.05). ADA activity was correlated with fasting plasma glucose (r=0.258, P<0.05), HbA1c (r=0.208, P<0.05), aspartate aminotransferase (r=0.325, P<0.05), and alanine aminotransferase (r=0.248, P<0.05). Compared with the well-controlled T2DM patients (HbA1c<7%), the poorly controlled group (HbA1c>9%) showed significantly increased ADA activity (21.1¡¾0.8 U/L vs. 25.4¡¾1.6 U/L; P<0.05). The effect of DPP4I on ADA activity in T2DM patients did not differ from those of other oral anti-diabetic agents or insulin. T2DM patients on metformin monotherapy showed a lower ADA activity (20.9¡¾1.0 U/L vs. 28.1¡¾2.8 U/L; P<0.05) compared with that of those on sulfonylurea monotherapy.

Conclusion: Our results show that ADA activity is increased in T2DM patients compared to that in non-diabetic patients, is positively correlated with blood glucose level, and that DPP4I has no additional specific effect on ADA activity, except for a glycemic control- or HbA1c-dependent effect.
KEYWORD
Adenosine deaminase, Diabetes mellitus, type 2, Dipeptidyl peptidase
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