Abstract
Purpose
Spexin, a novel 14-amino acid peptide, has multiple physiological functions. The purpose of this paper was to systematically evaluate the current literature on the role of Spexin neuropeptide in obesity and its related comorbidities, food intake and overall metabolic status in human, animal and in vitro studies.
Methods
Multiple databases, including PubMed, EMBASE, ProQuest, Scopus and Google Scholar were searched for English-language papers published since inception until December 2018, that investigated Spexin levels in relation to chronic metabolic diseases, overall metabolism control and feeding-related behaviors.The quality of the included observational studies was assessed by a version of the Newcastle Ottawa Scale (NOS) designed for non-randomized studies and SYRCLE’s assessment tool for animal models.
Results
Out of 224 records screened, search results led to a total of 24 related studies (12 human studies (ten cross-sectional studies, one cohort study, and one longitudinal study) and 12 studies in either animals or in vitro).Nine of the included cross-sectional studies and one Longitudinal study had moderate to good study quality, and one cross-sectional and one cohort study had high-quality (or low risk of bias).
Conclusion
It appears that Spexin has a positive impact on overall metabolic status. As a novel appetite-regulating peptide, Spexin can act as an anorexigenic factor. Information about Spexin is very limited, and well-designed randomized controlled clinical trials are warranted for replicating, validating, and extending the current findings.
PROSPERO registration number
CRD42018117198).
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Conceived and designed the systematic review: MB,AO.
Systematic literature search: ZF, MB.
Screened the titles and abstracts of the retrieved articles: VM,SP,EV.
Quality assessment and data extraction: MB,VM,AO.
Wrote the paper: All of authors.
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Behrooz, M., Vaghef-Mehrabany, E., Maleki, V. et al. Spexin status in relation to obesity and its related comorbidities: a systematic review. J Diabetes Metab Disord 19, 1943–1957 (2020). https://doi.org/10.1007/s40200-020-00636-8
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DOI: https://doi.org/10.1007/s40200-020-00636-8