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Monocyte CD36 expression associates with atherosclerotic burden in diabetes mellitus
Jayanthi Chandran1, Neelam Wadhwa2, S V Madhu3
1Department of Pathology, University College of Medical Sciences & Guru Teg Bahadur Hospital, University of Delhi, Delhi 110095, India; Department of Pathology, Sri Manakula Vinayagar Medical College and Hospital, Puducherry, India(1).
Insights
Monocyte CD36 (mCD36) shows higher levels in type 2 diabetes patients, especially those with coronary artery disease. This biomarker effectively detects atherosclerosis and stratifies risk, even in individuals with normal ankle-brachial index.
Area of Science:
- Cardiovascular Research
- Diabetes Mellitus Research
- Biomarker Discovery
Background:
- Monocyte CD36 (mCD36) is implicated in oxidized low-density lipoprotein uptake and foam cell formation.
- mCD36 is explored as a potential non-invasive biomarker for atherosclerosis (ATH) in type 2 diabetes mellitus (DM).
Purpose of the Study:
- To evaluate the expression of mCD36 in patients with type 2 diabetes.
- To assess the correlation of mCD36 expression with atherosclerosis indicators like the ankle-brachial index (ABI) and coronary artery disease (CAD).
Main Methods:
- Flow cytometry was used to measure mCD36 expression.
- Participants included 70 type 2 DM patients (40 with CAD, 30 without) and 30 normoglycemic controls (NGCs).
- mCD36 levels were compared against ABI values and glycosylated hemoglobin (HbA1c).
Main Results:
- Type 2 DM patients exhibited significantly higher mCD36 levels than NGCs.
- Elevated mCD36 was observed in DM patients with CAD and poor glycemic control (HbA1c ≥ 7%).
- All 30 subjects with compromised ABI (≤0.9) had CAD and higher mCD36 indices; mCD36 levels increased progressively from NGCs to diabetics with and without CAD.
Conclusions:
- mCD36 plays a significant role in atherogenesis.
- mCD36 serves as a robust marker for ATH, correlating well with ABI.
- mCD36 can stratify ATH risk in individuals even with a normal ABI.
Background:
By virtue of its role in oxidized low-density lipoprotein uptake and foam cell transformation, monocyte CD36 (mCD36) is a potential non-invasive tool to detect atherosclerosis (ATH) in patients of type 2 diabetes mellitus (DM).
Methods:
Flowcytometric expression of mCD36 was evaluated with reference to ankle brachial index (ABI) in 70 patients of type 2 DM [40 with and 30 without coronary artery disease (CAD) respectively] and 30 age and gender matched normoglycemic controls (NGCs).
Results:
DM patients had significantly higher mCD36 indices than NGCs (p < 0.001). The mCD36 expression was significantly higher in DM persons with CAD and those with poor glycemia control (glycosylated haemoglobin, HbA1c ≥ 7%) than their respective counterparts (p < 0.001 for both). Thirty subjects had compromised ABI (≤0.9); all were DM persons with CAD. ABI compromised subjects had consistently higher mCD36 indices than all other sub-groups (p < 0.001 for all comparisons). Notably, within the ABI-uncompromised group, mCD36 indices differed significantly and showed progressive increase from NGCs to diabetics without and with CAD respectively.
Conclusions:
mCD36 plays an important role in atherogenesis. With reference to ABI, mCD36 performed robustly as a marker of ATH. Furthermore, it could stratify subjects within the 'ABI-uncompromised group' commensurate with their conventional clinico-pathological ATH risk predisposition.
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