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Published on: January 23, 2018
Peripheral blood mitochondrial DNA content is related to insulin sensitivity in offspring of type 2 diabetic patients
1Department of Biomedical Sciences, Korean National Institute Health, Seoul.
Insights
Peripheral blood mitochondrial DNA (mtDNA) content was lower in offspring of type 2 diabetic patients and correlated with insulin sensitivity, suggesting it may be a hereditary factor for type 2 diabetes.
Area of Science:
- Genetics
- Metabolic Diseases
- Molecular Biology
Background:
- Type 2 diabetes (T2D) has a significant hereditary component.
- Insulin resistance is a key factor in the development of T2D.
- Mitochondrial dysfunction is implicated in metabolic disorders.
Purpose of the Study:
- To investigate if peripheral blood mitochondrial DNA (mtDNA) content is reduced in offspring of T2D patients.
- To determine the association between pb-mtDNA content and insulin resistance in this cohort.
Main Methods:
- Stratified, randomized sampling of 82 offspring of T2D patients and 52 controls from Korea.
- Measurement of pb-mtDNA content using real-time polymerase chain reaction.
- Correlation analysis between pb-mtDNA levels and insulin sensitivity parameters.
Main Results:
- pb-mtDNA content showed a trend towards lower levels in T2D offspring (P=0.051).
- Significantly lower pb-mtDNA was observed in offspring with normal or impaired glucose tolerance (P<0.05).
- In offspring with normal/impaired glucose tolerance, pb-mtDNA content correlated with insulin sensitivity (r=0.253, P<0.05) and predicted it.
Conclusions:
- Quantitative mtDNA status may be a hereditary factor linked to T2D.
- pb-mtDNA levels could serve as a potential indicator for insulin sensitivity.
Objective:
To investigate whether the peripheral blood mtDNA (pb-mtDNA) content is decreased and linked to insulin resistance in the offspring of type 2 diabetic patients.
Research Design And Methods:
A total of 82 offspring of type 2 diabetic patients and 52 age-, sex-, and BMI-matched normal subjects from the Mokdong, Korea, population were selected for this study by stratified, randomized sampling. Of the offspring of diabetic patients, 52 had normal glucose tolerance (NGT), 21 had impaired glucose tolerance (IGT), and 9 had newly diagnosed type 2 diabetes. The pb-mtDNA content was measured by real-time polymerase chain reaction with a mitochondria-specific fluorescent probe, normalized by a nuclear DNA, 285 rRNA gene. The associations between pb-mtDNA content and several parameters of insulin resistance were studied.
Results:
The pb-mtDNA contents tended to be lower in the 82 offspring of type 2 diabetic patients (1,084.7 +/- 62.6 vs. 1,304.0 +/- 99.2 in the offspring and control subjects, respectively, P = 0.051) and was significantly lower in the combined NGT and IGT offspring group (NGT+IGT, 1,068.0 +/- 67.8, P < 0.05) than in the control subjects. In NGT+IGT offspring, the pb-mtDNA content was significantly correlated with logarithmically transformed insulin sensitivity (r = 0.253, P < 0.05) and was the main predictor of insulin sensitivity.
Conclusions:
Quantitative mtDNA status might be a hereditary factor associated with type 2 diabetes and could serve as an indicator for insulin sensitivity.
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