Key result
Circulating sgp130 shows inconsistent associations with cardiovascular outcomes despite preclinical trans-signaling benefits.
Why the study?
The role of soluble gp130 in IL-6 trans-signaling and its potential clinical application in preventing cardiovascular disease remains unclear due to inconsistent epidemiological data.
Does sgp130 treatment prevent cardiovascular disease?
Does sgp130 treatment prevent cardiovascular disease?
This review highlights the discrepancy between the preclinical benefits of IL-6 trans-signaling inhibition via sgp130 and the inconsistent epidemiological data regarding its role in cardiovascular disease prevention.
Inflammation plays a major role in the onset of cardiovascular disease (CVD). Interleukine-6 (IL-6) is a multifunctional cytokine involved both in the beneficial acute inflammatory response and in the detrimental chronic low-grade systemic inflammation. Large genetic human studies, using Mendelian randomization approaches, have clearly showed that IL-6 pathway is causally involved in the onset of myocardial infarction. At the same time, IL-6 pathway is divided into two arms: classic signaling (effective in hepatocytes and leukocytes) and trans-signaling (with ubiquitous activity). Trans-signaling is known to be inhibited by the circulating soluble glycoprotein 130 (sgp130). In animal and in vitro models, trans-signaling inhibition with sgp130 antibody clearly shows a beneficial effect on inflammatory disease and atherosclerosis. Conversely, epidemiological data report inconsistent results between sgp130 levels and CV risk factors as well as CV outcome. We have reviewed the literature to understand the role of sgp130 and to find the evidence in favor of or against a possible clinical application of sgp130 treatment in the prevention of cardiovascular disease.
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Morieri et al. (2017) conducted a review in Cardiovascular disease. Soluble gp130 (sgp130) was evaluated. Soluble gp130 levels show inconsistent associations with cardiovascular risk factors and outcomes in epidemiological studies, despite beneficial effects of trans-signaling inhibition in animal models.
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