Why the study?
The CTRP family plays a crucial role in metabolic disorders, but the association of CTRP1 and CTRP5 levels with obesity parameters and cIMT required evaluation.
Circulating levels of CTRP5 and the CTRP1/CTRP5 ratio are significant predictors of carotid intima-media thickness, suggesting a potential role for these adipokines in atherosclerosis and cardiometabolic risk in type 2 diabetes.
May inform risk stratification in T2D; leaves open causal roles and clinical utility pending prospective validation.
Background There is growing evidence that C1qTNF-related protein (CTRP) family has crucial role in physiology and pathophysiology of metabolic disorders such as Type 2 Diabetes (T2D) and obesity. We sought to identify the association of CTRP1 and CTRP5 circulating levels with various obesity parameters such as visceral adipose tissue (VAT) thickness, visceral adiposity index (VAI) and with carotid intima-media thickness (cIMT) in patients with T2D and healthy subjects. Methods This case- control study recruited 42 T2D patients and 42 healthy adults (all men). cIMT and VAT thickness measurement were performed using an Accuvix XQ ultrasound. Circulating CTRP1 and CTRP5 concentrations were measured by enzyme-linked immunosorbent assay (ELISA). Results CTRP-1 and CTRP1/CTRP5 ratio were markedly higher in patients with T2D compared to controls (p < 0001 and p < 0004 respectively). Interestingly, binominal logistic regression revealed that higher circulating level of CTRP1 was associated with presence of T2D (odds ratio [OR]: 13203.554 [95% CI: 65.186-2674407.708]; P=.000). When considering the study population as a whole, CTRP1 circulating levels were correlated with WHR, VAT and HOMA-IR. In addition, we observed that the ratio of CTRP1 to CTRP5 plasma levels (β = 0.648, P=0.005) and CTRP5 circulating levels (β = 0.4 44, P=0.049) are significant predictors for cIMT value. Conclusions Our results indicated that CTRP1 and CTRP5 concentrations were correlated with atherosclerosis in human subjects and these adipokines might have a causal role for cardiometabolic risk in type 2 diabetes disease
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Majidi et al. (2020) studied this question.
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