Analysis reveals insulin resistance impacts mitochondrial function in platelets of older adults, suggesting links to diabetes and cardiovascular disorders.
Impaired glucose tolerance (IGT) and insulin resistance, including prediabetes and diabetes, increases risk of developing age-related disorders, such as cardiovascular disorders, kidney disorders, and Alzheimer’s disease (AD). We analyzed mitochondrial bioenergetics of platelets collected from 208 adults, 55 years and older, with IGT and insulin resistance and without (normoglycemic, NG). Platelets from IGT participants exhibited unique mitochondrial bioenergetic profiles exemplified by higher mitochondrial respiration compared to NG. IGT platelets exhibited higher glucose-dependent maximal (Max) and spare respiratory (SRC) capacities, and higher fatty acid oxidation (FAO)-dependent maximal coupled (MaxOXPHOS) and uncoupled (MaxETS) respiration, compared to NG. Correlating mitochondrial bioenergetics from all 208 participants with measures of glucose tolerance (oral glucose tolerance test values measured 120 mins after glucose administration (OGTT_120), and oral glucose tolerance test area under the curve (OGTT_AUC)), and historical glucose measures (hemoglobin A1 (HbA1c)) revealed significant positive associations. Most associations were unaltered with age, sex, and BMI adjustments. Examining NG and IGT participants separately, we found platelet respiration and HbA1c exhibited positive association in NG participants. Significant positive associations emerged between platelet SRC, FAO, FAO+CI (oxygen flux due to fatty acid oxidation + complex I activities) and HbA1c. No significant associations were observed in the IGT group. Given the utilization of blood based mitochondrial bioenergetic profiling strategies in clinical research, this work provides new insights into the clinical features of insulin resistance that can impact platelet mitochondrial bioenergetics.
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Mahapatra et al. (2025) studied this question.
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