Increased high-density lipoprotein-3 binding to leukocytes following weight loss and improved glycemic control in type 2 diabetic patients
This study evaluates the effect on high-density lipoprotein (HDL) binding activity in cultured granulocytes before and after metabolic control of non—insulin-dependent diabetes mellitus ([NIDDM] type 2 diabetes) patients. In 20 type 2 diabetic patients, diabetic control was accomplished by administr...
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Published in | Metabolism, clinical and experimental Vol. 49; no. 6; pp. 692 - 697 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
New York, NY
Elsevier Inc
01.06.2000
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | This study evaluates the effect on high-density lipoprotein (HDL) binding activity in cultured granulocytes before and after metabolic control of non—insulin-dependent diabetes mellitus ([NIDDM] type 2 diabetes) patients. In 20 type 2 diabetic patients, diabetic control was accomplished by administration of oral antidiabetic agents and dietary restrictions. Adequate metabolic control was reflected by a decrease in the fasting glucose, glycosylated hemoglobin (HbA
1c), mean insulin, and body mass index (BMI). After control of the diabetes, the mean HDL
3 cholesterol was increased from 0.918 ± 0.05 to 1.008 ± 0.05 mmol/L (
P < .05) and apolipoprotein Al (apo Al) was increased from 103 ± 5.8 to 115 ± 5.1 mg/dL (
P < .01). The HDL
3 maximum specific binding was higher after versus before diabetic control, 77 ± 6 versus 122 ± 8 ng/mg cell protein (
P < .01). This increase was related to an increase in maximum binding ([B
max
] from 4.97 × 10
−10 to 8.3 × 10
−10 mol/L,
P < .001), and no significant changes were observed in the
K
d
(from 1.47 × 10
−7
v 2.04 × 10
−7 mol/L). These results suggest that the metabolic control of type 2 diabetes increases HDL
3 binding activity. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0026-0495 1532-8600 |
DOI: | 10.1053/meta.2000.6248 |