Key result
Adiponectin exerts anti-inflammatory and cardioprotective effects, but its circulating levels are paradoxically increased in advanced cardiovascular disease, complicating its use as a clinical biomarker.
This review elucidates the adiponectin paradox, highlighting that while adiponectin has cardioprotective and anti-inflammatory properties, its elevated circulating levels serve as a marker for advanced cardiovascular disease.
Adiponectin may counter CVD mechanisms via anti-inflammatory effects; leaves open therapeutic targeting pending clinical trials.
Adipose tissue (AT) has recently been identified as a dynamic endocrine organ secreting a wide range of adipokines. Adiponectin is one such hormone, exerting endocrine and paracrine effects on the cardiovascular system. At a cellular and molecular level, adiponectin has anti-inflammatory, antioxidant and anti-apoptotic roles, thereby mitigating key mechanisms underlying cardiovascular disease (CVD) pathogenesis. However, adiponectin expression in human AT as well as its circulating levels are increased in advanced CVD states, and it is actually considered by many as a 'rescue hormone'. Due to the complex mechanisms regulating adiponectin's biosynthesis in the human AT, measurement of its levels as a biomarker in CVD is highly controversial, given that adiponectin exerts protective effects on the cardiovascular system but at the same time its increased levels flag advanced CVD. In this review article, we present the involvement of adiponectin in CVD pathogenesis and we discuss its role as a clinical biomarker. LINKED ARTICLES: This article is part of a themed section on Targeting Inflammation to Reduce Cardiovascular Disease Risk. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v174.22/issuetoc and http://onlinelibrary.wiley.com/doi/10.1111/bcp.v82.4/issuetoc.
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Woodward et al. (2016) conducted a review in Cardiovascular disease. Adiponectin was evaluated. Adiponectin exerts anti-inflammatory and cardioprotective effects, but its circulating levels are paradoxically increased in advanced cardiovascular disease, complicating its use as a clinical biomarker.
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