Gut–Brain–Skin Axis in Psoriasis: A Review
Dermatology and Therapy, ISSN: 2190-9172, Vol: 11, Issue: 1, Page: 25-38
2021
- 54Citations
- 118Captures
- 3Mentions
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations54
- Citation Indexes54
- 54
- Captures118
- Readers118
- 118
- Mentions3
- News Mentions2
- News2
- Blog Mentions1
- Blog1
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November 19, 2020
Today, in this (late) Digest: a set of reviews about the role of microbiota in neurodegeneration, psoriasis and stroke; different studies about the microbiome genital/urinary
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Metagenomics Analysis of Altered Gut Microbiome in Psoriasis and the Mediation Analysis: A Case-Control Study
Introduction Psoriasis is a common immune-related inflammatory skin disease that affects over 100 million people worldwide.1,2 It is of great significance to explore the risk
Review Description
Introduction: Psoriasis is a common skin disease, with chronic inflammation and a complex etiology. It has long been recognized that chronic skin conditions and mental health disorders are often co-morbid. Thus, the concept of the gut–brain–skin axis emphasized in mental health disorders may also regulate the health of skin. Results: The gut microbiota has been found to be the bridge between the immune system and nervous system. By leveraging clinical cases and animal models of psoriasis, an important communication pathway has been identified along the gut–brain–skin axis that is associated with the modulation of neurotransmitters from the microbiota. Furthermore, mammalian neurotransmitters, including dopamine, serotonin, or γ-aminobutyric acid (GABA), can be produced and/or consumed by several types of bacteria. Other studies suggest that manipulating these neurotransmitters by bacteria may have an effect on host physiology, and the levels of neurotransmitter can be altered by microbiota-based interventions. Conclusions: Nonetheless, it is unknown whether or not the manipulation of neurotransmitter levels by bacteria can affect the occurrence and development of psoriasis. Notably, preliminary experiments found that oral consumption of probiotics improves the clinical symptoms in patients with psoriasis, perhaps correlated with the gut microbiome-mediated crosstalk between the immune system and the nervous system by secreting neurotransmitters in psoriasis. In this review, the communication along the gut–brain–skin axis is discussed.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85096215275&origin=inward; http://dx.doi.org/10.1007/s13555-020-00466-9; http://www.ncbi.nlm.nih.gov/pubmed/33206326; http://link.springer.com/10.1007/s13555-020-00466-9; https://dx.doi.org/10.1007/s13555-020-00466-9; https://link.springer.com/article/10.1007/s13555-020-00466-9
Springer Science and Business Media LLC
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