Why the study?
Numerous clinical and experimental studies have investigated resistin, but its role in the pathophysiology and its clinical utility as a biochemical marker in type 2 diabetes complications needed summarization.
Is resistin a reliable biochemical marker for the diagnosis or prognosis of macrovascular and microvascular complications in type 2 diabetes?
Is resistin a reliable biochemical marker for the diagnosis or prognosis of macrovascular and microvascular complications in type 2 diabetes?
While experimental models suggest resistin plays a role in T2D complications, current clinical evidence does not support its use as a diagnostic or prognostic biomarker.
Answers are grounded in this paper and cite their sources.
Resistin may flag vascular complication risk in diabetes; leaves open its causal role and therapeutic targeting.
Resistin is an adipokine produced in adipose tissue with pro-inflammatory properties, whose elevation has been associated with insulin resistance and diabetes. Over the past years, significant research has explored the pathophysiological mechanisms involving resistin, utilizing various in vitro and in vivo models. Additionally, numerous clinical studies have aimed to establish a correlation between resistin and the development and progression of macrovascular and microvascular complications in type 2 diabetes. This narrative review summarizes in vitro, in vivo, and human studies published in English since the discovery of resistin in 2001 to the present, examining the role of this adipokine in the pathophysiology of macrovascular and microvascular complications in in vivo and in vitro T2D models, as well as the clinical evidence supporting its use as a biochemical marker in patients with these conditions. The results exhibit considerable heterogeneity and appear to be dependent on the experimental model or population studied. While experimental evidence supports resistin's involvement at the cellular and molecular levels in the pathogenesis of these complications, current clinical evidence remains insufficient to justify its use as a biochemical marker for either diagnosis or prognosis. Therefore, further well-designed studies are required to elucidate resistin's potential role in the clinical setting.
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Reynoso-Roa et al. (2025) studied this question.
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