Study summary · research use only
Circulating follistatin in relation to energy metabolism
Plain-language summary
Paraphrased from the published abstract below — not a verdict on whether anything works.
This narrative review discusses circulating follistatin in relation to energy metabolism in human subjects, based on evidence that the liver contributes significantly to circulating follistatin levels and that circulating follistatin is regulated by the glucagon-to-insulin ratio. The review states these findings challenge the previous view that circulating follistatin mainly reflects spill-over from local para/autocrine actions in various tissues, and instead suggest follistatin is a liver-derived protein regulated by the glucagon-to-insulin ratio, implying a relationship to energy metabolism. The authors state that conditions associated with elevated circulating follistatin share a metabolic profile of decreased insulin sensitivity and/or elevated glucagon levels.
Abstract
Recently, substantial evidence has emerged that the liver contributes significantly to the circulating levels of follistatin and that circulating follistatin is tightly regulated by the glucagon-to-insulin ratio. Both observations are based on investigations of healthy subjects. These novel findings challenge the present view of circulating follistatin in human physiology, being that circulating follistatin is a result of spill-over from para/autocrine actions in various tissues and cells. Follistatin as a liver-derived protein under the regulation of glucagon-to-insulin ratio suggests a relation to energy metabolism. In this narrative review, we attempt to reconcile the existing findings on circulating follistatin with the novel concept that circulating follistatin is a liver-derived molecule regulated by the glucagon-to-insulin ratio. The picture emerging is that conditions associated with elevated levels of circulating follistatin have a metabolic denominator with decreased insulin sensitivity and/or hyperglucagoneimia.
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