Key result
Plasma soluble CD36 levels were not associated with the presence of subclinical carotid atherosclerosis in subjects with type 1 diabetes, type 2 diabetes, or nondiabetic individuals.
Why the study?
The study aimed to determine the association of the fatty acid transporter plasma soluble CD36 (sCD36) with subclinical carotid atherosclerosis.
Is circulating soluble CD36 associated with subclinical carotid atherosclerosis in subjects with type 1 diabetes, type 2 diabetes, or without diabetes?
Cross-Sectional (n=1,023)
Is circulating soluble CD36 associated with subclinical carotid atherosclerosis in subjects with type 1 diabetes, type 2 diabetes, or without diabetes?
Circulating soluble CD36 is not a useful biomarker for subclinical carotid atherosclerosis in patients with or without diabetes.
May support sCD36 as SCA marker in diabetes; leaves open validation in prospective cohorts.
This study aimed to determine the association of fatty acid transporter plasma soluble cluster of differentiation 36 (sCD36) with subclinical carotid atherosclerosis (SCA). A cross-sectional study was conducted in 1023 subjects, 225 with type 1 diabetes (T1D), 276 with type 2 diabetes (T2D) and 522 who were nondiabetic. Carotid atherosclerotic plaque (CAP) presence was determined using B-mode carotid ultrasound imaging. sCD36 were analysed by ELISA, and CD36 surface receptor and mRNA expression were measured by flow cytometry and real-time PCR. Logistic regression models were used to evaluate sCD36 as a biomarker of SCA. Up to 376 (36.75%) participants had at least one CAP, 76 T1D, 164 T2D and 136 without diabetes, while the remaining 647 (63.25%) did not have any CAP. There were no differences in sCD36 between patients with and without CAP in T1D (p = 0.287) or T2D (p = 0.513). Although nondiabetic subjects with plaques had lower sCD36 levels than those without (p = 0.023), the multivariate models revealed no association of sCD36 with CAP in any of the three study groups. No differences were found in surface CD36 or CD36 mRNA expression between the patients with and without CAP. sCD36 is not associated with SCA in type 1 or type 2 diabetic or in nondiabetic subjects.
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Castelblanco et al. (2020) conducted a cross-sectional in Type 1 and Type 2 Diabetes Mellitus (n=1,023). Plasma soluble CD36 (sCD36) was evaluated on Presence of subclinical carotid atherosclerosis (carotid atherosclerotic plaque) (p=0.287 (T1D), 0.513 (T2D)). Plasma soluble CD36 levels were not associated with the presence of subclinical carotid atherosclerosis in subjects with type 1 diabetes, type 2 diabetes, or nondiabetic individuals.
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