Cited by 156Gut microbiota and healthPsoriasis: Treatment and PathogenesisDermatology and Skin Diseases

Gut–Skin Axis: Unravelling the Connection between the Gut Microbiome and Psoriasis

Open access
Thye, Angel Yun-Kuan, Bah, Yi-Rou, Law, Jodi Woan-Fei, Tan, Loh Teng-Hern, He, Ya-Wen, Wong, Sunny-Hei, Thurairajasingam, Sivakumar, Chan, Kok-Gan +2 more·2022·Biomedicines

Abstract

Evidence has shown that gut microbiome plays a role in modulating the development of diseases beyond the gastrointestinal tract, including skin disorders such as psoriasis. The gut–skin axis refers to the bidirectional relationship between the gut microbiome and skin health. This is regulated through several mechanisms such as inflammatory mediators and the immune system. Dysregulation of microbiota has been seen in numerous inflammatory skin conditions such as atopic dermatitis, rosacea, and psoriasis. Understanding how gut microbiome are involved in regulating skin health may lead to development of novel therapies for these skin disorders through microbiome modulation, in particularly psoriasis. In this review, we will compare the microbiota between psoriasis patients and healthy control, explain the concept of gut–skin axis and the effects of gut dysbiosis on skin physiology. We will also review the current evidence on modulating gut microbiome using probiotics in psoriasis.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.3390/biomedicines10051037

Cites

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • Probiotics have been investigated for their ability to alleviate irritable bowel syndrome (IBS) symptoms, and certain probiotic strains like Bifidobacterium infantis and Lactobacillus plantarum can reduce inflammation and restore gut barrier function in IBS patients.

    “Bloating, stomach discomfort, and constipation are all signs of irritable bowel syndrome (IBS), and probiotics have been investigated for their ability to alleviate these conditions. Inflammation can be reduced and gut barrier function can be restored in IBS patients by taking certain probiotic strains like Bifidobacterium infantis and Lactobacillus plantarum.”

    From Unveiling the therapeutic symphony of probiotics, prebiotics, and postbiotics in gut-immune harmony (2024) · cites this paper as [31]

    Split into 2 atoms — 0 confirmed, 1 partially supported, 0 disputed, 1 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.

    Experimental — accuracy not yet measured
  • The anti-inflammatory effects of postbiotics, especially short-chain fatty acids, are important in the regulation of inflammatory bowel disease (IBD) symptoms.

    “The anti-inflammatory effects of postbiotics, especially short-chain fatty acids, are important in the regulation of inflammatory bowel disease (IBD) symptoms.”

    From Unveiling the therapeutic symphony of probiotics, prebiotics, and postbiotics in gut-immune harmony (2024) · cites this paper as [31]

    Section 3 describes the anti-inflammatory properties of short-chain fatty acids and their role in gut immune regulation. Section 7 links a butyrate-producing bacterium to IBD, but notes conflicting findings; it does not establish that postbiotics regulate IBD symptoms. Page numbers are unavailable in our copy. (LLM, conf=0.86)

    Experimental — accuracy not yet measured
  • Evidence is mounting that probiotics and prebiotics may be useful in controlling autoimmune illnesses including rheumatoid arthritis and multiple sclerosis by altering the composition of the gut flora, affecting immunological dysregulation and potentially reducing autoimmune reactions.

    “Evidence is mounting that probiotics and prebiotics may be useful in controlling autoimmune illnesses including rheumatoid arthritis and multiple sclerosis by altering the composition of the gut flora. These bioactive compounds affect immunological dysregulation and might reduce autoimmune reactions.”

    From Unveiling the therapeutic symphony of probiotics, prebiotics, and postbiotics in gut-immune harmony (2024) · cites this paper as [31]

    Split into 2 atoms — 0 confirmed, 2 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.

    Experimental — accuracy not yet measured
  • Probiotics and prebiotics improve glucose metabolism and decrease inflammation in diabetes patients by altering the makeup and function of the gut microbiota.

    “Glycemic management and insulin sensitivity in people with type 2 diabetes have been studied as a possible benefit of probiotics and prebiotics. These bioactive compounds improve glucose metabolism and decrease inflammation in diabetes patients by altering the makeup and function of the gut microbiota.”

    From Unveiling the therapeutic symphony of probiotics, prebiotics, and postbiotics in gut-immune harmony (2024) · cites this paper as [31]

    The Treatment section says probiotics and prebiotics can reshape gut microbiota, and reports reduced inflammatory markers with probiotics in psoriasis subjects. It does not report improved glucose metabolism or reduced inflammation in diabetes patients; its Introduction mentions type 2 diabetes only as a psoriasis comorbidity. The claim extends findings from psoriasis to a different patient population and outcome. (LLM, conf=0.82)

    Experimental — accuracy not yet measured
  • Probiotics and prebiotics can mitigate allergy diseases including eczema and rhinitis by regulating the balance between Th1 and Th2 immune responses.

    “It has been investigated whether or not probiotics and prebiotics can mitigate allergy diseases including eczema and rhinitis. They are essential in the regulation of the balance between Th1 and Th2 immune responses, which are responsible for the development of allergic disorders.”

    From Unveiling the therapeutic symphony of probiotics, prebiotics, and postbiotics in gut-immune harmony (2024) · cites this paper as [31]

    The Treatment section reports that probiotics can modulate immune responses and that probiotics and prebiotics can reshape the gut microbiome. Its treatment findings concern psoriasis, however; the passages do not support mitigation of eczema or rhinitis through regulation of the Th1/Th2 balance. The Gut–Skin Axis section instead discusses Treg/Th17 balance in psoriasis. No page numbers were available in our copy. (LLM, conf=0.83)

    Experimental — accuracy not yet measured

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

The citation lists haven’t been fetched yet

References 194 · Cited by 156

Research works printed but not linked: 177

  1. [3]Barnas J.L. Ritchlin C.T. Etiology and pathogenesis of psoriatic arthritis Rheum. Dis. Clin. 2015 41 643 663 10.1016/j.rdc.2015.07.006 26476224 · DOI
  2. [4]Boehncke W.-H. Etiology and pathogenesis of psoriasis Rheum. Dis. Clin. 2015 41 665 675 10.1016/j.rdc.2015.07.013 26476225 · DOI · Paper page
  3. [5]Kulig P. Musiol S. Freiberger S.N. Schreiner B. Gyülveszi G. Russo G. Pantelyushin S. Kishihara K. Alessandrini F. Kündig T. IL-12 protects from psoriasiform skin inflammation Nat. Commun. 2016 7 1 14 10.1038/ncomms13466 27892456 PMC5133729 · DOI
  4. [6]Roberson E.D. Bowcock A.M. Psoriasis genetics: Breaking the barrier Trends Genet. 2010 26 415 423 10.1016/j.tig.2010.06.006 20692714 PMC2957827 · DOI
  5. [7]Sondermann W. Djeudeu Deudjui D. Körber A. Slomiany U. Brinker T. Erbel R. Moebus S. Psoriasis, cardiovascular risk factors and metabolic disorders: Sex-specific findings of a population-based study J. Eur. Acad. Dermatol. Venereol. 2020 34 779 786 10.1111/jdv.16029 31797464 · DOI
  6. [8]Meglio P.D. Villanova F. Nestle F.O. Psoriasis Cold Spring Harb. Perspect. Med. 2014 4 a015354 10.1101/cshperspect.a015354 25085957 PMC4109580 · DOI
  7. [9]Gupta R. Debbaneh M.G. Liao W. Genetic epidemiology of psoriasis Curr. Dermatol. Rep. 2014 3 61 78 10.1007/s13671-013-0066-6 25580373 PMC4285384 · DOI
  8. [10]Lee E.J. Do Han K. Han J.H. Lee J.H. Smoking and risk of psoriasis: A nationwide cohort study J. Am. Acad. Dermatol. 2017 77 573 575 10.1016/j.jaad.2017.04.015 28807112 · DOI
  9. [11]Jensen P. Skov L. Psoriasis and obesity Dermatology 2016 232 633 639 10.1159/000455840 28226326 · DOI
  10. [12]Barrea L. Nappi F. Di Somma C. Savanelli M.C. Falco A. Balato A. Balato N. Savastano S. Environmental risk factors in psoriasis: The point of view of the nutritionist Int. J. Environ. Res. Public Health 2016 13 743 10.3390/ijerph13070743 PMC4962284 27455297 · DOI
  11. [13]Fry L. Baker B.S. Triggering psoriasis: The role of infections and medications Clin. Dermatol. 2007 25 606 615 10.1016/j.clindermatol.2007.08.015 18021899 · DOI
  12. [14]Kamiya K. Kishimoto M. Sugai J. Komine M. Ohtsuki M. Risk Factors for the Development of Psoriasis Int. J. Mol. Sci. 2019 20 4347 10.3390/ijms20184347 31491865 PMC6769762 · DOI
  13. [15]Danielsen K. Olsen A. Wilsgaard T. Furberg A.S. Is the prevalence of psoriasis increasing? A 30-year follow-up of a population-based cohort Br. J. Dermatol. 2013 168 1303 1310 10.1111/bjd.12230 23374051 · DOI
  14. [16]Parisi R. Symmons D.P. Griffiths C.E. Ashcroft D.M. Global epidemiology of psoriasis: A systematic review of incidence and prevalence J. Invest. Dermatol. 2013 133 377 385 10.1038/jid.2012.339 23014338 · DOI
  15. [17]Rachakonda T.D. Schupp C.W. Armstrong A.W. Psoriasis prevalence among adults in the United States J. Am. Acad. Dermatol. 2014 70 512 516 10.1016/j.jaad.2013.11.013 24388724 · DOI
  16. [18]Jacobson C.C. Kumar S. Kimball A.B. Latitude and psoriasis prevalence J. Am. Acad. Dermatol. 2011 65 870 873 10.1016/j.jaad.2009.05.047 21920244 · DOI
  17. [19]Le S. Toussi A. Maverakis N. Marusina A.I. Barton V.R. Merleev A.A. Luxardi G. Raychaudhuri S.P. Maverakis E. The cutaneous and intestinal microbiome in psoriatic disease Clin. Immunol. 2020 108537 10.1016/j.clim.2020.108537 32679247 · DOI
  18. [20]Szántó M. Dózsa A. Antal D. Szabó K. Kemény L. Bai P. Targeting the gut-skin axis—Probiotics as new tools for skin disorder management? Exp. Dermatol. 2019 28 1210 1218 10.1111/exd.14016 31386766 · DOI · Paper page
  19. [22]Zheng D. Liwinski T. Elinav E. Interaction between microbiota and immunity in health and disease Cell Res. 2020 30 492 506 10.1038/s41422-020-0332-7 32433595 PMC7264227 · DOI · Paper page
  20. [23]Toor D. Wsson M.K. Kumar P. Karthikeyan G. Kaushik N.K. Goel C. Singh S. Kumar A. Prakash H. Dysbiosis disrupts gut immune homeostasis and promotes gastric diseases Int. J. Mol. Sci. 2019 20 2432 10.3390/ijms20102432 31100929 PMC6567003 · DOI
  21. [24]Nishida A. Inoue R. Inatomi O. Bamba S. Naito Y. Andoh A. Gut microbiota in the pathogenesis of inflammatory bowel disease Clin. J. Gastroenterol. 2018 11 1 10 10.1007/s12328-017-0813-5 29285689 · DOI
  22. [25]Korman N. Management of psoriasis as a systemic disease: What is the evidence? Br. J. Dermatol. 2020 182 840 848 10.1111/bjd.18245 31225638 PMC7187293 · DOI
  23. [26]Gerdes S. Mrowietz U. Boehncke W.-H. Komorbidität bei Psoriasis vulgaris Hautarzt. 2016 67 438 444 10.1007/s00105-016-3805-3 27221798 · DOI
  24. [27]Kim H.-N. Han K. Park Y.-G. Lee J.H. Metabolic syndrome is associated with an increased risk of psoriasis: A nationwide population-based study Metabolism 2019 99 19 24 10.1016/j.metabol.2019.07.001 31279740 · DOI
  25. [28]Gisondi P. Fostini A.C. Fossà I. Girolomoni G. Targher G. Psoriasis and the metabolic syndrome Clin. Dermatol. 2018 36 21 28 10.1016/j.clindermatol.2017.09.005 29241748 · DOI
  26. [29]Singh S. Young P. Armstrong A.W. Relationship between psoriasis and metabolic syndrome: A systematic review G. Ital. Dermatol. Venereol. 2016 151 663 677 27589483
  27. [30]Ramessur R. Gill D. The effect of statins on severity of psoriasis: A systematic review Indian J. Dermatol. Venereol. Leprol. 2017 83 10.4103/0378-6323.188655 27549870 · DOI
  28. [31]Ogdie A. Gelfand J. Clinical risk factors for the development of psoriatic arthritis among patients with psoriasis: A review of available evidence Curr. Rheumatol. Rep. 2015 17 1 7 10.1007/s11926-015-0540-1 PMC5278907 26290111 · DOI
  29. [32]Alinaghi F. Tekin H.G. Burisch J. Wu J.J. Thyssen J.P. Egeberg A. Global prevalence and bidirectional association between psoriasis and inflammatory bowel disease—a systematic review and meta-analysis J. Crohn’s Colitis 2020 14 351 360 10.1093/ecco-jcc/jjz152 31504363 · DOI
  30. [33]Komine M. Recent advances in psoriasis research; the clue to mysterious relation to gut microbiome Int. J. Mol. Sci. 2020 21 2582 10.3390/ijms21072582 32276410 PMC7177330 · DOI
  31. [34]O’Neill C.A. Monteleone G. McLaughlin J.T. Paus R. The gut-skin axis in health and disease: A paradigm with therapeutic implications Bioessays 2016 38 1167 1176 10.1002/bies.201600008 27554239 · DOI · Paper page
  32. [35]Levkovich T. Poutahidis T. Smillie C. Varian B.J. Ibrahim Y.M. Lakritz J.R. Alm E.J. Erdman S.E. Probiotic bacteria induce a ‘glow of health’ PLoS ONE 2013 8 e53867 10.1371/journal.pone.0053867 23342023 PMC3547054 · DOI
  33. [36]Ramírez-Boscá A. Navarro-López V. Martínez-Andrés A. Such J. Francés R. de la Parte J.H. Asín-Llorca M. Identification of bacterial DNA in the peripheral blood of patients with active psoriasis JAMA Dermatol. 2015 151 670 671 10.1001/jamadermatol.2014.5585 25760018 · DOI
  34. [37]Sacchetti L. Nardelli C. Gut microbiome investigation in celiac disease: From methods to its pathogenetic role Clin. Chem. Lab. Med. 2020 58 340 349 10.1515/cclm-2019-0657 31494628 · DOI
  35. [39]Abhishek S. Krishnan S.P. Epidermal differentiation complex: A review on its epigenetic regulation and potential drug targets Cell J. 2016 18 1 27054112 PMC4819378
  36. [40]Hsu D.K. Fung M.A. Chen H.-L. Role of skin and gut microbiota in the pathogenesis of psoriasis, an inflammatory skin disease Med. Microecol. 2020 4 100016 10.1016/j.medmic.2020.100016 · DOI
  37. [41]Weaver C.T. Elson C.O. Fouser L.A. Kolls J.K. The Th17 pathway and inflammatory diseases of the intestines, lungs, and skin Annu. Rev. Pathol.: Mech. Dis. 2013 8 477 512 10.1146/annurev-pathol-011110-130318 23157335 PMC3965671 · DOI · Paper page
  38. [42]Gaur M. Dobke M. Lunyak V.V. Mesenchymal stem cells from adipose tissue in clinical applications for dermatological indications and skin aging Int. J. Mol. Sci. 2017 18 208 10.3390/ijms18010208 PMC5297838 28117680 · DOI
  39. [43]Kobayashi T. Naik S. Nagao K. Choreographing immunity in the skin epithelial barrier Immunity 2019 50 552 565 10.1016/j.immuni.2019.02.023 30893586 PMC6455972 · DOI
  40. [44]Matejuk A. Skin immunity Arch. Immunol. Ther. Exp. (Warsz.) 2018 66 45 54 10.1007/s00005-017-0477-3 28623375 PMC5767194 · DOI
  41. [45]Yazdi A.S. Röcken M. Ghoreschi K. Cutaneous immunology: Basics and new concepts Semin. Immunopathol. 2016 38 3 10 26563284
  42. [46]Liang Y. Sarkar M.K. Tsoi L.C. Gudjonsson J.E. Psoriasis: A mixed autoimmune and autoinflammatory disease Curr. Opin. Immunol. 2017 49 1 8 10.1016/j.coi.2017.07.007 28738209 PMC5705427 · DOI
  43. [47]Blauvelt A. Chiricozzi A. The immunologic role of IL-17 in psoriasis and psoriatic arthritis pathogenesis Clin. Rev. Allergy Immunol. 2018 55 379 390 10.1007/s12016-018-8702-3 30109481 PMC6244934 · DOI
  44. [48]Wang A. Bai Y. Dendritic cells: The driver of psoriasis J. Dermatol 2020 47 104 113 10.1111/1346-8138.15184 31833093 · DOI
  45. [49]Albanesi C. Madonna S. Gisondi P. Girolomoni G. The interplay between keratinocytes and immune cells in the pathogenesis of psoriasis Front. Immunol. 2018 9 1549 10.3389/fimmu.2018.01549 30034395 PMC6043636 · DOI
  46. [50]Luger T. Loser K. Novel insights into the pathogenesis of psoriasis Clin. Immunol. 2017 186 43 45 10.1016/j.clim.2017.07.014 28736273 · DOI
  47. [51]Harden J.L. Krueger J.G. Bowcock A.M. The immunogenetics of psoriasis: A comprehensive review J. Autoimmun. 2015 64 66 73 10.1016/j.jaut.2015.07.008 26215033 PMC4628849 · DOI
  48. [52]Dainichi T. Kitoh A. Otsuka A. Nakajima S. Nomura T. Kaplan D.H. Kabashima K. The epithelial immune microenvironment (EIME) in atopic dermatitis and psoriasis Nat. Immunol. 2018 19 1286 1298 10.1038/s41590-018-0256-2 30446754 · DOI
  49. [53]Chimenti M.S. Perricone C. Novelli L. Caso F. Costa L. Bogdanos D. Conigliaro P. Triggianese P. Ciccacci C. Borgiani P. Interaction between microbiome and host genetics in psoriatic arthritis Autoimmun. Rev. 2018 17 276 283 10.1016/j.autrev.2018.01.002 29378263 · DOI
  50. [54]Chandra A. Ray A. Senapati S. Chatterjee R. Genetic and epigenetic basis of psoriasis pathogenesis Mol. Immunol. 2015 64 313 323 10.1016/j.molimm.2014.12.014 25594889 · DOI
  51. [55]Lowes M.A. Russell C.B. Martin D.A. Towne J.E. Krueger J.G. The IL-23/T17 pathogenic axis in psoriasis is amplified by keratinocyte responses Trends Immunol. 2013 34 174 181 10.1016/j.it.2012.11.005 23291100 PMC3721313 · DOI
  52. [56]Zeng B. Shi S. Ashworth G. Dong C. Liu J. Xing F. ILC3 function as a double-edged sword in inflammatory bowel diseases Cell Death Dis. 2019 10 1 12 10.1038/s41419-019-1540-2 30962426 PMC6453898 · DOI
  53. [57]Benhadou F. Mintoff D. Del Marmol V. Psoriasis: Keratinocytes or immune cells–which is the trigger? Dermatology 2019 235 91 100 10.1159/000495291 30566935 · DOI
  54. [58]Ellis S.R. Nguyen M. Vaughn A.R. Notay M. Burney W.A. Sandhu S. Sivamani R.K. The skin and gut microbiome and its role in common dermatologic conditions Microorganisms 2019 7 550 10.3390/microorganisms7110550 31717915 PMC6920876 · DOI
  55. [59]Power S.E. O’Toole P.W. Stanton C. Ross R.P. Fitzgerald G.F. Intestinal microbiota, diet and health Br. J. Nutr. 2014 111 387 402 10.1017/S0007114513002560 23931069 · DOI · Paper page
  56. [60]Ipci K. Altıntoprak N. Muluk N.B. Senturk M. Cingi C. The possible mechanisms of the human microbiome in allergic diseases Eur. Arch. Otorhinolaryngol. 2017 274 617 626 10.1007/s00405-016-4058-6 27115907 · DOI
  57. [61]Mowat A.M. Agace W.W. Regional specialization within the intestinal immune system Nat. Rev. Immunol. 2014 14 667 685 10.1038/nri3738 25234148 · DOI
  58. [62]Yatsunenko T. Rey F.E. Manary M.J. Trehan I. Dominguez-Bello M.G. Contreras M. Magris M. Hidalgo G. Baldassano R.N. Anokhin A.P. Human gut microbiome viewed across age and geography Nature 2012 486 222 227 10.1038/nature11053 22699611 PMC3376388 · DOI · Paper page
  59. [63]Bäckhed F. Roswall J. Peng Y. Feng Q. Jia H. Kovatcheva-Datchary P. Li Y. Xia Y. Xie H. Zhong H. Dynamics and stabilization of the human gut microbiome during the first year of life Cell Host Microbe 2015 17 690 703 10.1016/j.chom.2015.04.004 25974306 · DOI · Paper page
  60. [64]Li M. Wang M. Donovan S.M. Early development of the gut microbiome and immune-mediated childhood disorders Semin. Reprod. Med. 2014 32 74 86 24390924
  61. [65]Qin J. Li R. Raes J. Arumugam M. Burgdorf K.S. Manichanh C. Nielsen T. Pons N. Levenez F. Yamada T. A human gut microbial gene catalogue established by metagenomic sequencing Nature 2010 464 59 65 10.1038/nature08821 20203603 PMC3779803 · DOI · Paper page
  62. [66]McKenzie C. Tan J. Macia L. Mackay C.R. The nutrition-gut microbiome-physiology axis and allergic diseases Immunol. Rev. 2017 278 277 295 10.1111/imr.12556 28658542 · DOI
  63. [67]Mazidi M. Rezaie P. Kengne A.P. Mobarhan M.G. Ferns G.A. Gut microbiome and metabolic syndrome Diabetes Metab. Syndr. Clin. Res. Rev. 2016 10 S150 S157 10.1016/j.dsx.2016.01.024 26916014 · DOI
  64. [68]Lin S. Wang Z. Lam K.-L. Zeng S. Tan B.K. Hu J. Role of intestinal microecology in the regulation of energy metabolism by dietary polyphenols and their metabolites Food Nutr. Res. 2019 63 10.29219/fnr.v63.1518 30814920 PMC6385797 · DOI
  65. [69]Spencer S.P. Fragiadakis G.K. Sonnenburg J.L. Pursuing human-relevant gut microbiota-immune interactions Immunity 2019 51 225 239 10.1016/j.immuni.2019.08.002 31433970 PMC7205593 · DOI
  66. [70]Chelakkot C. Ghim J. Ryu S.H. Mechanisms regulating intestinal barrier integrity and its pathological implications Exp. Mol. Med. 2018 50 1 9 10.1038/s12276-018-0126-x PMC6095905 30115904 · DOI · Paper page
  67. [71]Lee J.K.-F. Hern Tan L.T. Ramadas A. Ab Mutalib N.-S. Lee L.-H. Exploring the Role of Gut Bacteria in Health and Disease in Preterm Neonates Int. J. Environ. Res. Public Health 2020 17 6963 10.3390/ijerph17196963 PMC7579082 32977611 · DOI
  68. [72]Boyle R.J. Lahtinen S.J. Tang M.L. Probiotics and skin Nutrition and Skin Springer Berlin/Heidelberg, Germany 2011 111 127
  69. [73]Kosiewicz M.M. Dryden G.W. Chhabra A. Alard P. Relationship between gut microbiota and development of T cell associated disease FEBS Lett. 2014 588 4195 4206 10.1016/j.febslet.2014.03.019 24681103 · DOI
  70. [74]Lee L.-H. Wong S.H. Chin S.-F. Singh V. Ab Mutalib N.-S. Editorial: Human Microbiome: Symbiosis to Pathogenesis Front. Microbiol. 2021 12 10.3389/fmicb.2021.605783 PMC7928290 33679632 · DOI
  71. [75]Lau A. Teng Hern T. Ab Mutalib N.-S. Wong S. Letchumanan V. Lee L.H. The chemistry of gut microbiome in health and diseases Prog. Microbes Mol. Biol. 2021 4 10.36877/pmmb.a0000175 · DOI
  72. [76]Shen T.-C.D. Diet and gut microbiota in health and disease Nestle Nutr. Inst. Workshop Ser. 2017 88 117 126 28346928
  73. [77]Vallianou N. Stratigou T. Christodoulatos G.S. Dalamaga M. Understanding the role of the gut microbiome and microbial metabolites in obesity and obesity-associated metabolic disorders: Current evidence and perspectives Curr. Obes. Rep. 2019 8 317 332 10.1007/s13679-019-00352-2 31175629 · DOI
  74. [78]Scher J.U. Littman D.R. Abramson S.B. Microbiome in inflammatory arthritis and human rheumatic diseases Arthritis Rheumatol. 2016 68 35 10.1002/art.39259 26331579 PMC4789258 · DOI
  75. [79]Stevens B.R. Roesch L. Thiago P. Russell J.T. Pepine C.J. Holbert R.C. Raizada M.K. Triplett E.W. Depression phenotype identified by using single nucleotide exact amplicon sequence variants of the human gut microbiome Mol. Psychiatry 2021 26 4277 4287 10.1038/s41380-020-0652-5 31988436 PMC11549940 · DOI
  76. [80]Kitai T. Tang W.W. Gut microbiota in cardiovascular disease and heart failure Clin. Sci. 2018 132 85 91 10.1042/CS20171090 PMC6413501 29326279 · DOI
  77. [81]Shah K.R. Boland C.R. Patel M. Thrash B. Menter A. Cutaneous manifestations of gastrointestinal disease: Part I J. Am. Acad. Dermatol. 2013 68 189.e1 189.e21 10.1016/j.jaad.2012.10.037 23317980 · DOI
  78. [82]Thrash B. Patel M. Shah K.R. Boland C.R. Menter A. Cutaneous manifestations of gastrointestinal disease: Part II J. Am. Acad. Dermatol. 2013 68 211.e1 211.e33 10.1016/j.jaad.2012.10.036 23317981 · DOI
  79. [83]Gloster H. Gebauer L. Mistur R. Cutaneous manifestations of gastrointestinal disease Absolute Dermatology Review Springer Cham, Switzerland 2016 171 179
  80. [84]Kim H.-J. Lee S.-H. Hong S.-J. Antibiotics-induced dysbiosis of intestinal microbiota aggravates atopic dermatitis in mice by altered short-chain fatty acids Allergy Asthma Immunol. Res. 2020 12 137 148 10.4168/aair.2020.12.1.137 31743970 PMC6875482 · DOI
  81. [85]Polkowska-Pruszyńska B. Gerkowicz A. Krasowska D. The gut microbiome alterations in allergic and inflammatory skin diseases–an update J. Eur. Acad. Dermatol. Venereol. 2020 34 455 464 10.1111/jdv.15951 31520544 · DOI
  82. [86]Purchiaroni F. Tortora A. Gabrielli M. Bertucci F. Gigante G. Ianiro G. Ojetti V. Scarpellini E. Gasbarrini A. The role of intestinal microbiota and the immune system Eur. Rev. Med. Pharmacol. Sci. 2013 17 323 333 23426535
  83. [87]Rajilić-Stojanović M. De Vos W.M. The first 1000 cultured species of the human gastrointestinal microbiota FEMS Microbiol. Rev. 2014 38 996 1047 10.1111/1574-6976.12075 24861948 PMC4262072 · DOI · Paper page
  84. [88]Sirisinha S. The potential impact of gut microbiota on your health: Current status and future challenges Asian Pac. J. Allergy Immunol. 2016 34 249 264 28042926
  85. [89]Huttenhower C. Gevers D. Knight R. Abubucker S. Badger J.H. Chinwalla A.T. Creasy H.H. Earl A.M. FitzGerald M.G. Fulton R.S. Structure, function and diversity of the healthy human microbiome Nature 2012 486 207 214 10.1038/nature11234 22699609 PMC3564958 · DOI · Paper page
  86. [90]Samuelson D.R. Welsh D.A. Shellito J.E. Regulation of lung immunity and host defense by the intestinal microbiota Front. Microbiol. 2015 6 1085 10.3389/fmicb.2015.01085 26500629 PMC4595839 · DOI
  87. [91]Dawson L.F. Donahue E.H. Cartman S.T. Barton R.H. Bundy J. McNerney R. Minton N.P. Wren B.W. The analysis of para-cresol production and tolerance in Clostridium difficile 027 and 012 strains BMC Microbiol. 2011 11 1 10 10.1186/1471-2180-11-86 21527013 PMC3102038 · DOI
  88. [92]Miyazaki K. Masuoka N. Kano M. Iizuka R. Bifidobacterium fermented milk and galacto-oligosaccharides lead to improved skin health by decreasing phenols production by gut microbiota Benef. Microbes 2014 5 121 128 10.3920/BM2012.0066 23685373 · DOI
  89. [93]Zákostelská Z. Málková J. Klimešová K. Rossmann P. Hornová M. Novosádová I. Stehlíková Z. Kostovčík M. Hudcovic T. Štepánková R. Intestinal microbiota promotes psoriasis-like skin inflammation by enhancing Th17 response PLoS One 2016 11 e0159539 10.1371/journal.pone.0159539 27434104 PMC4951142 · DOI
  90. [94]Stehlikova Z. Kostovcikova K. Kverka M. Rossmann P. Dvorak J. Novosadova I. Kostovcik M. Coufal S. Srutkova D. Prochazkova P. Crucial role of microbiota in experimental psoriasis revealed by a gnotobiotic mouse model Front. Microbiol. 2019 10 236 10.3389/fmicb.2019.00236 30846974 PMC6394148 · DOI
  91. [95]Suzuki K. Kawamoto S. Maruya M. Fagarasan S. GALT: Organization and dynamics leading to IgA synthesis Adv. Immunol. 2010 107 153 185 21034974
  92. [96]Adarsh M. Dogra S. Vaiphei K. Vaishnavi C. Sinha S. Sharma A. Evaluation of subclinical gut inflammation using faecal calprotectin levels and colonic mucosal biopsy in patients with psoriasis and psoriatic arthritis Br. J. Dermatol. 2019 181 401 402 10.1111/bjd.17745 30729502 · DOI
  93. [97]Sikora M. Chrabąszcz M. Maciejewski C. Zaremba M. Waśkiel A. Olszewska M. Rudnicka L. Intestinal barrier integrity in patients with plaque psoriasis J. Dermatol 2018 45 1468 1470 10.1111/1346-8138.14647 30222202 · DOI
  94. [98]Vlachos C. Gaitanis G. Katsanos K.H. Christodoulou D.K. Tsianos E. Bassukas I.D. Psoriasis and inflammatory bowel disease: Links and risks Psoriasis (Auckl) 2016 6 73 29387596 PMC5683131
  95. [99]Visser M.J. Kell D.B. Pretorius E. Bacterial dysbiosis and translocation in psoriasis vulgaris Front. Cell. Infect. Microbiol. 2019 9 7 10.3389/fcimb.2019.00007 30778377 PMC6369634 · DOI
  96. [100]Alesa D.I. Alshamrani H.M. Alzahrani Y.A. Alamssi D.N. Alzahrani N.S. Almohammadi M.E. The role of gut microbiome in the pathogenesis of psoriasis and the therapeutic effects of probiotics J. Family Med. Prim. Care 2019 8 3496 31803643 PMC6881942
  97. [101]Forbes J.D. Van Domselaar G. Bernstein C.N. The gut microbiota in immune-mediated inflammatory diseases Front. Microbiol. 2016 7 1081 10.3389/fmicb.2016.01081 27462309 PMC4939298 · DOI
  98. [102]Shapiro J. Cohen N.A. Shalev V. Uzan A. Koren O. Maharshak N. Psoriatic patients have a distinct structural and functional fecal microbiota compared with controls J. Dermatol 2019 46 595 603 10.1111/1346-8138.14933 31141234 · DOI
  99. [104]Vinolo M.A. Rodrigues H.G. Nachbar R.T. Curi R. Regulation of inflammation by short chain fatty acids Nutrients 2011 3 858 876 10.3390/nu3100858 22254083 PMC3257741 · DOI · Paper page
  100. [105]Plöger S. Stumpff F. Penner G.B. Schulzke J.D. Gäbel G. Martens H. Shen Z. Günzel D. Aschenbach J.R. Microbial butyrate and its role for barrier function in the gastrointestinal tract Ann. N. Y. Acad. Sci. 2012 1258 52 59 10.1111/j.1749-6632.2012.06553.x 22731715 · DOI
  101. [106]Lopez-Siles M. Khan T.M. Duncan S.H. Harmsen H.J. Garcia-Gil L.J. Flint H.J. Cultured representatives of two major phylogroups of human colonic Faecalibacterium prausnitzii can utilize pectin, uronic acids, and host-derived substrates for growth Appl. Environ. Microbiol. 2012 78 420 428 10.1128/AEM.06858-11 22101049 PMC3255724 · DOI · Paper page
  102. [107]Sitkin S. Pokrotnicks J. Clinical Potential of Anti-inflammatory Effects of Faecalibacterium prausnitzii and Butyrate in Inflammatory Bowel Disease Inflamm. Bowel Dis. 2019 25 e40 e41 10.1093/ibd/izy258 30085080 · DOI
  103. [108]Codoñer F.M. Ramírez-Bosca A. Climent E. Carrión-Gutierrez M. Guerrero M. Pérez-Orquín J.M. De La Parte J.H. Genovés S. Ramón D. Navarro-López V. Gut microbial composition in patients with psoriasis Sci. Rep. 2018 8 1 7 10.1038/s41598-018-22125-y 29491401 PMC5830498 · DOI
  104. [109]Staiano-Coico L. Khandke L. Krane J.F. Sharif S. Gottlieb A.B. Krueger J.G. Heim L. Rigas B. Higgins P.J. TGF-α and TGF-β expression during sodium-N-butyrate-induced differentiation of human keratinocytes: Evidence for subpopulation-specific up-regulation of TGF-β mRNA in suprabasal cells Exp. Cell Res. 1990 191 286 291 10.1016/0014-4827(90)90016-4 2257881 · DOI
  105. [111]Tan L. Zhao S. Zhu W. Wu L. Li J. Shen M. Lei L. Chen X. Peng C. The Akkermansia muciniphila is a gut microbiota signature in psoriasis Exp. Dermatol. 2018 27 144 149 10.1111/exd.13463 29130553 · DOI
  106. [112]Chen Y.J. Ho H.J. Tseng C.H. Lai Z.L. Shieh J.J. Wu C.Y. Intestinal microbiota profiling and predicted metabolic dysregulation in psoriasis patients Exp. Dermatol. 2018 27 1336 1343 10.1111/exd.13786 30238519 · DOI
  107. [113]Yeh N.-L. Hsu C.-Y. Tsai T.-F. Chiu H.-Y. Gut microbiome in psoriasis is perturbed differently during secukinumab and ustekinumab therapy and associated with response to treatment Clin. Drug Investig. 2019 39 1195 1203 10.1007/s40261-019-00849-7 31549347 · DOI
  108. [114]Scher J.U. Ubeda C. Artacho A. Attur M. Isaac S. Reddy S.M. Marmon S. Neimann A. Brusca S. Patel T. Decreased bacterial diversity characterizes the altered gut microbiota in patients with psoriatic arthritis, resembling dysbiosis in inflammatory bowel disease Arthritis Rheumatol. 2015 67 128 139 10.1002/art.38892 25319745 PMC4280348 · DOI
  109. [115]Hidalgo-Cantabrana C. Gomez J. Delgado S. Requena-López S. Queiro-Silva R. Margolles A. Coto E. Sanchez B. Coto-Segura P. Gut microbiota dysbiosis in a cohort of patients with psoriasis Br. J. Dermatol. 2019 181 1287 1295 10.1111/bjd.17931 30920647 · DOI · Paper page
  110. [116]Huang L. Gao R. Yu N. Zhu Y. Ding Y. Qin H. Dysbiosis of gut microbiota was closely associated with psoriasis Sci. China Life Sci. 2019 62 807 815 10.1007/s11427-018-9376-6 30264198 · DOI
  111. [117]Wagner B.D. Grunwald G.K. Zerbe G.O. Mikulich-Gilbertson S.K. Robertson C.E. Zemanick E.T. Harris J.K. On the use of diversity measures in longitudinal sequencing studies of microbial communities Front. Microbiol. 2018 9 1037 10.3389/fmicb.2018.01037 29872428 PMC5972327 · DOI
  112. [119]Calcinaro F. Dionisi S. Marinaro M. Candeloro P. Bonato V. Marzotti S. Corneli R. Ferretti E. Gulino A. Grasso F. Oral probiotic administration induces interleukin-10 production and prevents spontaneous autoimmune diabetes in the non-obese diabetic mouse Diabetologia 2005 48 1565 1575 10.1007/s00125-005-1831-2 15986236 · DOI
  113. [120]Lavasani S. Dzhambazov B. Nouri M. Fåk F. Buske S. Molin G. Thorlacius H. Alenfall J. Jeppsson B. Weström B. A novel probiotic mixture exerts a therapeutic effect on experimental autoimmune encephalomyelitis mediated by IL-10 producing regulatory T cells PLoS One 2010 5 e9009 10.1371/journal.pone.0009009 20126401 PMC2814855 · DOI
  114. [121]De Preter V. Machiels K. Joossens M. Arijs I. Matthys C. Vermeire S. Rutgeerts P. Verbeke K. Faecal metabolite profiling identifies medium-chain fatty acids as discriminating compounds in IBD Gut 2015 64 447 458 10.1136/gutjnl-2013-306423 24811995 · DOI
  115. [122]Kostic A.D. Xavier R.J. Gevers D. The microbiome in inflammatory bowel disease: Current status and the future ahead Gastroenterology 2014 146 1489 1499 10.1053/j.gastro.2014.02.009 24560869 PMC4034132 · DOI · Paper page
  116. [123]Scher J.U. The microbiome in psoriasis and psoriatic arthritis: Joints J. Rheumatol. Suppl. 2018 94 32 35 10.3899/jrheum.180134 29858351 · DOI
  117. [124]Eppinga H. Sperna Weiland C.J. Thio H.B. van der Woude C.J. Nijsten T.E. Peppelenbosch M.P. Konstantinov S.R. Similar depletion of protective Faecalibacterium prausnitzii in psoriasis and inflammatory bowel disease, but not in hidradenitis suppurativa J. Crohn’s Colitis 2016 10 1067 1075 10.1093/ecco-jcc/jjw070 26971052 · DOI
  118. [125]Cani P.D. de Vos W.M. Next-generation beneficial microbes: The case of Akkermansia muciniphila Front. Microbiol. 2017 8 1765 10.3389/fmicb.2017.01765 29018410 PMC5614963 · DOI · Paper page
  119. [127]Schneeberger M. Everard A. Gómez-Valadés A.G. Matamoros S. Ramírez S. Delzenne N.M. Gomis R. Claret M. Cani P.D. Akkermansia muciniphila inversely correlates with the onset of inflammation, altered adipose tissue metabolism and metabolic disorders during obesity in mice Sci. Rep. 2015 5 1 14 10.1038/srep16643 26563823 PMC4643218 · DOI · Paper page
  120. [129]Reunanen J. Kainulainen V. Huuskonen L. Ottman N. Belzer C. Huhtinen H. de Vos W.M. Satokari R. Akkermansia muciniphila adheres to enterocytes and strengthens the integrity of the epithelial cell layer Appl. Environ. Microbiol. 2015 81 3655 3662 10.1128/AEM.04050-14 25795669 PMC4421065 · DOI
  121. [130]Bian X. Wu W. Yang L. Lv L. Wang Q. Li Y. Ye J. Fang D. Wu J. Jiang X. Administration of Akkermansia muciniphila ameliorates dextran sulfate sodium-induced ulcerative colitis in mice Front. Microbiol. 2019 10 2259 10.3389/fmicb.2019.02259 31632373 PMC6779789 · DOI
  122. [131]Gaffen S.L. Jain R. Garg A.V. Cua D.J. The IL-23–IL-17 immune axis: From mechanisms to therapeutic testing Nat. Rev. Immunol. 2014 14 585 600 10.1038/nri3707 25145755 PMC4281037 · DOI · Paper page
  123. [132]Warren R. Menter A. Handbook of Psoriasis and Psoriatic Arthritis Springer Berlin/Heidelberg, Germany 2016
  124. [133]Salem I. Ramser A. Isham N. Ghannoum M.A. The gut microbiome as a major regulator of the gut-skin axis Front. Microbiol. 2018 9 1459 10.3389/fmicb.2018.01459 30042740 PMC6048199 · DOI · Paper page
  125. [134]Song C. Yang C. Meng S. Li M. Wang X. Zhu Y. Kong L. Lv W. Qiao H. Sun Y. Deciphering the mechanism of Fang-Ji-Di-Huang-Decoction in ameliorating psoriasis-like skin inflammation via the inhibition of IL-23/Th17 cell axis J. Ethnopharmacol. 2021 281 114571 10.1016/j.jep.2021.114571 34464701 · DOI
  126. [135]Yao X. Zhu Z. Manandhar U. Liao H. Yu T. Wang Y. Bian Y. Zhang B. Zhang X. Xie J. RNA-seq reveal RNA binding protein GNL3 as a key mediator in the development of psoriasis vulgaris by regulating the IL23/IL17 axis Life Sci. 2022 293 119902 10.1016/j.lfs.2021.119902 34487784 · DOI
  127. [136]Haugh I.M. Preston A.K. Kivelevitch D.N. Menter A.M. Risankizumab: An anti-IL-23 antibody for the treatment of psoriasis Drug Des. Devel. Ther. 2018 12 3879 10.2147/DDDT.S167149 PMC6237136 30518998 · DOI
  128. [137]Dong J. Goldenberg G. New biologics in psoriasis: An update on IL-23 and IL-17 inhibitors Cutis 2017 99 123 127 28319618
  129. [138]Kamata M. Tada Y. Safety of biologics in psoriasis J. Dermatol 2018 45 279 286 10.1111/1346-8138.14096 29226369 · DOI
  130. [139]Molinelli E. Campanati A. Brisigotti V. Offidani A. Biologic therapy in psoriasis (Part II): Efficacy and safety of new treatment targeting IL23/IL-17 pathways Curr. Pharm. Biotechnol. 2017 18 964 978 10.2174/1389201019666180103140643 29299984 · DOI
  131. [142]Chen Y.-H. Wu C.-S. Chao Y.-H. Lin C.-C. Tsai H.-Y. Li Y.-R. Chen Y.-Z. Tsai W.-H. Chen Y.-K. Lactobacillus pentosus GMNL-77 inhibits skin lesions in imiquimod-induced psoriasis-like mice J. Food Drug Anal. 2017 25 559 566 10.1016/j.jfda.2016.06.003 28911642 PMC9328808 · DOI
  132. [145]Gasbarrini G. Bonvicini F. Gramenzi A. Probiotics history J. Clin. Gastroenterol. 2016 50 S116 S119 10.1097/MCG.0000000000000697 27741152 · DOI
  133. [146]George Kerry R. Patra J.K. Gouda S. Park Y. Shin H.-S. Das G. Benefaction of probiotics for human health: A review J. Food Drug Anal. 2018 26 927 939 10.1016/j.jfda.2018.01.002 29976412 PMC9303019 · DOI · Paper page
  134. [147]Yamashiro Y. Probiotics to Prebiotics and Their Clinical Use Encyclopedia of Infection and Immunity Rezaei N. Elsevier Oxford, UK 2022 674 688
  135. [148]Hui M.L. Tan L.T. Letchumanan V. He Y.W. Fang C.M. Chan K.G. Law J.W. Lee L.H. The Extremophilic Actinobacteria: From Microbes to Medicine Antibiotics 2021 6 682 10.3390/antibiotics10060682 PMC8230038 34201133 · DOI
  136. [149]Tan L.T.-H. Chan K.-G. Lee L.-H. Goh B.-H. Streptomyces Bacteria as Potential Probiotics in Aquaculture Front. Microbiol. 2016 7 10.3389/fmicb.2016.00079 26903962 PMC4742533 · DOI
  137. [150]Law J. Letchumanan V. Teng Hern T. Ser H.L. Goh B.H. Lee L.H. The Rising of “Modern Actinobacteria” Era Prog. Microbes Mol. Biol. 2020 3 10.36877/pmmb.a0000064 · DOI
  138. [152]Benyacoub J. Bosco N. Blanchard C. Demont A. Philippe D. Castiel-Higounenc I. Guéniche A. Immune modulation property of Lactobacillus paracasei NCC2461 (ST11) strain and impact on skin defences Benef. Microbes 2014 5 129 136 10.3920/BM2013.0014 24322880 · DOI
  139. [153]Baba H. Masuyama A. Yoshimura C. Aoyama Y. Takano T. Ohki K. Oral intake of Lactobacillus helveticus-fermented milk whey decreased transepidermal water loss and prevented the onset of sodium dodecylsulfate-induced dermatitis in mice Biosci. Biotechnol. Biochem. 2010 74 18 23 10.1271/bbb.90370 20057148 · DOI
  140. [154]Gueniche A. Benyacoub J. Philippe D. Bastien P. Kusy N. Breton L. Blum S. Castiel-Higounenc I. Lactobacillus paracasei CNCM I-2116 (ST11) inhibits substance P-induced skin inflammation and accelerates skin barrier function recovery in vitro Eur. J. Dermatol. 2010 20 731 737 20965806
  141. [155]Philippe D. Stephanie B. Benyacoub J. Oral Lactobacillus paracasei improves skin barrier function recovery and reduces local skin inflammation Eur. J. Dermatol. 2011 21 279 280 10.1684/ejd.2010.1242 21489918 · DOI
  142. [157]Ogawa C. Inoue R. Yonejima Y. Hisa K. Yamamoto Y. Suzuki T. Supplemental Leuconostoc mesenteroides strain NTM048 attenuates imiquimod-induced psoriasis in mice J. Appl. Microbiol. 2021 131 3043 3055 10.1111/jam.15161 34028144 · DOI
  143. [158]Lu W. Deng Y. Fang Z. Zhai Q. Cui S. Zhao J. Chen W. Zhang H. Potential role of probiotics in ameliorating psoriasis by modulating gut microbiota in imiquimod-induced psoriasis-like mice Nutrients 2021 13 2010 10.3390/nu13062010 34207960 PMC8230682 · DOI
  144. [159]Deng Y.D. Fang Z.F. Cui S.M. Zhao J.X. Zhang H. Chen W. Lu W.W. Evaluation of probiotics for inhibiting hyperproliferation and inflammation relevant to psoriasis in vitro J. Funct. Foods 2021 81 10.1016/j.jff.2021.104433 · DOI
  145. [160]Thio H.B. The microbiome in psoriasis and psoriatic arthritis: The skin perspective J. Rheumatol. Suppl. 2018 94 30 31 10.3899/jrheum.180133 29858350 · DOI
  146. [161]Vijayashankar M. Raghunath N. Pustular psoriasis responding to probiotics–A new insight Our Dermatol. Online 2012 3 326 10.7241/ourd.20124.71 · DOI
  147. [162]Lin C. Zeng T. Deng Y. Yang W. Xiong J. Treatment of psoriasis vulgaris using Bacteroides fragilis BF839: A single-arm, open preliminary clinical study Shengwu Gongcheng Xuebao/Chin. J. Biotechnol. 2021 37 3828 3835 10.13345/j.cjb.210198 34841788 · DOI
  148. [163]Moludi J. Khedmatgozar H. Saiedi S. Razmi H. Alizadeh M. Ebrahimi B. Probiotic supplementation improves clinical outcomes and quality of life indicators in patients with plaque psoriasis: A randomized double-blind clinical trial Clin. Nutr. ESPEN 2021 46 33 39 10.1016/j.clnesp.2021.09.004 34857215 · DOI
  149. [164]Akbarzadeh A. Taheri M. Ebrahimi B. Alirezaei P. Doosti-Irani A. Soleimani M. Nouri F. Evaluation of Lactocare® Synbiotic Administration on the Serum Electrolytes and Trace Elements Levels in Psoriasis Patients: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial Study Biol. Trace Elem. Res. 2021 10.1007/s12011-021-03020-6 34845600 PMC8629602 · DOI
  150. [165]Navarro-López V. Martínez-Andrés A. Ramírez-Boscá A. Ruzafa-Costas B. Núñez-Delegido E. Carrión-Gutiérrez M.A. Prieto-Merino D. Codoñer-Cortés F. Ramón-Vidal D. Genovés-Martínez S. Efficacy and Safety of Oral Administration of a Mixture of Probiotic Strains in Patients with Psoriasis: A Randomized Controlled Clinical Trial Acta Derm. Venereol. 2019 99 1078 1084 10.2340/00015555-3305 31453631 · DOI
  151. [166]Davidovici B.B. Sattar N. Jörg P.C. Puig L. Emery P. Barker J.N. Van De Kerkhof P. Ståhle M. Nestle F.O. Girolomoni G. Psoriasis and systemic inflammatory diseases: Potential mechanistic links between skin disease and co-morbid conditions J. Invest. Dermatol. 2010 130 1785 1796 10.1038/jid.2010.103 20445552 · DOI
  152. [167]Dowlatshahi E. Van Der Voort E. Arends L. Nijsten T. Markers of systemic inflammation in psoriasis: A systematic review and meta-analysis Br. J. Dermatol. 2013 169 266 282 10.1111/bjd.12355 23550658 · DOI
  153. [168]Suárez-Farinas M. Li K. Fuentes-Duculan J. Hayden K. Brodmerkel C. Krueger J.G. Expanding the psoriasis disease profile: Interrogation of the skin and serum of patients with moderate-to-severe psoriasis J. Invest. Dermatol. 2012 132 2552 2564 10.1038/jid.2012.184 22763790 PMC3472561 · DOI
  154. [169]El Dib R. Periyasamy A.G. de Barros J.L. França C.G. Senefonte F.L. Vesentini G. Alves M.G.O. Rodrigues J.V.d.S. Gomaa H. Gomes Júnior J.R. Probiotics for the treatment of depression and anxiety: A systematic review and meta-analysis of randomized controlled trials Clin. Nutr. ESPEN 2021 45 75 90 10.1016/j.clnesp.2021.07.027 34620373 · DOI · Paper page
  155. [170]McFarland L.V. Karakan T. Karatas A. Strain-specific and outcome-specific efficacy of probiotics for the treatment of irritable bowel syndrome: A systematic review and meta-analysis EClinicalMedicine 2021 41 101154 10.1016/j.eclinm.2021.101154 34712929 PMC8529205 · DOI
  156. [171]Kano M. Masuoka N. Kaga C. Sugimoto S. Iizuka R. Manabe K. Sone T. Oeda K. Nonaka C. Miyazaki K. Consecutive intake of fermented milk containing Bifidobacterium breve strain Yakult and galacto-oligosaccharides benefits skin condition in healthy adult women Biosci. Microbiota Food Health 2013 32 33 39 10.12938/bmfh.32.33 24936360 PMC4034291 · DOI
  157. [173]Sabbagh F. Kim B.S. Recent advances in polymeric transdermal drug delivery systems J. Control. Release 2022 341 132 146 10.1016/j.jconrel.2021.11.025 34813879 · DOI
  158. [174]Crovesy L. Masterson D. Rosado E.L. Profile of the gut microbiota of adults with obesity: A systematic review Eur. J. Clin. Nutr. 2020 74 1251 1262 10.1038/s41430-020-0607-6 32231226 · DOI
  159. [175]Sobhonslidsuk A. Chanprasertyothin S. Pongrujikorn T. Kaewduang P. Promson K. Petraksa S. Ongphiphadhanakul B. The association of gut microbiota with nonalcoholic steatohepatitis in Thais Biomed Res. Int. 2018 2018 9340316 10.1155/2018/9340316 29682571 PMC5842744 · DOI
  160. [176]Yoshida N. Yamashita T. Hirata K.-i. Gut microbiome and cardiovascular diseases Diseases 2018 6 56 10.3390/diseases6030056 PMC6164700 29966270 · DOI
  161. [177]Moreno-Indias I. Sánchez-Alcoholado L. García-Fuentes E. Cardona F. Queipo-Ortuño M.I. Tinahones F.J. Insulin resistance is associated with specific gut microbiota in appendix samples from morbidly obese patients Am. J. Transl. Res 2016 8 5672 28078038 PMC5209518
  162. [178]Wang Z. Klipfell E. Bennett B.J. Koeth R. Levison B.S. DuGar B. Feldstein A.E. Britt E.B. Fu X. Chung Y.-M. Gut flora metabolism of phosphatidylcholine promotes cardiovascular disease Nature 2011 472 57 63 10.1038/nature09922 21475195 PMC3086762 · DOI · Paper page
  163. [180]Koeth R.A. Wang Z. Levison B.S. Buffa J.A. Org E. Sheehy B.T. Britt E.B. Fu X. Wu Y. Li L. Intestinal microbiota metabolism of L-carnitine, a nutrient in red meat, promotes atherosclerosis Nat. Med. 2013 19 576 585 10.1038/nm.3145 23563705 PMC3650111 · DOI · Paper page
  164. [181]Valguarnera E. Wardenburg J.B. Good gone bad: One toxin away from disease for Bacteroides fragilis J. Mol. Biol. 2020 432 765 785 10.1016/j.jmb.2019.12.003 31857085 · DOI
  165. [182]Guerreiro C.S. Calado Â. Sousa J. Fonseca J.E. Diet, microbiota, and gut permeability—the unknown triad in rheumatoid arthritis Front. Med. 2018 5 349 10.3389/fmed.2018.00349 30619860 PMC6302746 · DOI
  166. [183]Zhou C. Zhao H. Xiao X.-y. Guo R.-j. Wang Q. Chen H. Zhao L.-d. Zhang C.-C. Jiao Y.-H. Ju Y.-m. Metagenomic profiling of the pro-inflammatory gut microbiota in ankylosing spondylitis J. Autoimmun. 2020 107 102360 10.1016/j.jaut.2019.102360 31806420 · DOI
  167. [184]De Filippis F. Pasolli E. Tett A. Tarallo S. Naccarati A. De Angelis M. Neviani E. Cocolin L. Gobbetti M. Segata N. Distinct genetic and functional traits of human intestinal Prevotella copri strains are associated with different habitual diets Cell Host Microbe 2019 25 444 453.e443 10.1016/j.chom.2019.01.004 30799264 · DOI
  168. [185]Tett A. Huang K.D. Asnicar F. Fehlner-Peach H. Pasolli E. Karcher N. Armanini F. Manghi P. Bonham K. Zolfo M. The Prevotella copri complex comprises four distinct clades underrepresented in westernized populations Cell Host Microbe 2019 26 666 679.e667 10.1016/j.chom.2019.08.018 31607556 PMC6854460 · DOI · Paper page
  169. [186]Miquel S. Martin R. Rossi O. Bermúdez-Humarán L. Chatel J. Sokol H. Thomas M. Wells J. Langella P. Faecalibacterium prausnitzii and human intestinal health Curr. Opin. Microbiol. 2013 16 255 261 10.1016/j.mib.2013.06.003 23831042 · DOI
  170. [187]Stefia L.V. Lee J. Patel J. de Sousa S.R. Legrand J. Rodero M. Burman S. Linedale R. Morrison M. Khosrotehrani K. Secretome components from Faecalibacterium prausnitzii strains A2-165 and AHMP21 Modulate Cutaneous Wound Inflammation J. Invest. Dermatol. 2020 140 2312 2315.e2316 10.1016/j.jid.2020.02.027 32247858 · DOI
  171. [188]Hansen R. Russell R.K. Reiff C. Louis P. McIntosh F. Berry S.H. Mukhopadhya I. Bisset M.W. Barclay A.R. Bishop J. Microbiota of De-NovoPediatric IBD: Increased Faecalibacterium Prausnitziiand Reduced Bacterial Diversity in Crohn’s But Not in Ulcerative Colitis Am. J. Gastroenterol. 2012 107 1913 1922 10.1038/ajg.2012.335 23044767 · DOI
  172. [189]Zheng H. Liang H. Wang Y. Miao M. Shi T. Yang F. Liu E. Yuan W. Ji Z.-S. Li D.-K. Altered gut microbiota composition associated with eczema in infants PLoS One 2016 11 e0166026 10.1371/journal.pone.0166026 27812181 PMC5094743 · DOI
  173. [190]Everard A. Belzer C. Geurts L. Ouwerkerk J.P. Druart C. Bindels L.B. Guiot Y. Derrien M. Muccioli G.G. Delzenne N.M. Cross-talk between Akkermansia muciniphila and intestinal epithelium controls diet-induced obesity Proc. Natl. Acad. Sci. USA 2013 110 9066 9071 10.1073/pnas.1219451110 23671105 PMC3670398 · DOI · Paper page
  174. [191]Toya T. Corban M.T. Marrietta E. Horwath I.E. Lerman L.O. Murray J.A. Lerman A. Coronary artery disease is associated with an altered gut microbiome composition PLoS One 2020 15 e0227147 10.1371/journal.pone.0227147 31995569 PMC6988937 · DOI
  175. [192]Sikora M. Chrabąszcz M. Waśkiel-Burnat A. Rakowska A. Olszewska M. Rudnicka L. Claudin-3–a new intestinal integrity marker in patients with psoriasis: Association with disease severity J. Eur. Acad. Dermatol. Venereol. 2019 33 1907 1912 10.1111/jdv.15700 31120609 · DOI
  176. [193]Sikora M. Stec A. Chrabaszcz M. Waskiel-Burnat A. Zaremba M. Olszewska M. Rudnicka L. Intestinal fatty acid binding protein, a biomarker of intestinal barrier, is associated with severity of psoriasis J. Clin. Med. 2019 8 1021 10.3390/jcm8071021 PMC6678629 31336842 · DOI
  177. [194]Mottawea W. Butcher J. Li J. Abujamel T. Manoogian J. Mack D. Stintzi A. The mucosal–luminal interface: An ideal sample to study the mucosa-associated microbiota and the intestinal microbial biogeography Pediatr. Res. 2019 85 895 903 10.1038/s41390-019-0326-7 30758325 · DOI

Authors
Thye, A. Y.-K., Bah, Y.-R., Law, J. W.-F., Tan, L. T.-H., He, Y.-W., Wong, S.-H., Thurairajasingam, S., Chan, K.-G., Lee, L.-H., & Letchumanan, V.
Affiliations
  • Monash University Malaysia (MY)
  • Shanghai Jiao Tong University (CN)
  • Nanyang Technological University (SG)
  • Jiangsu University (CN)
Corresponding author
  • Chan, Kok-Gan
  • Lee, Learn-Han
Venue
Biomedicines
Publisher
MDPI AG
Published
2022-04-30
Volume
10
Issue
5
Pages
1037
ISSN
2227-9059 (ISSN-L)
OpenAlex
W4225113201
Cited by
156
References
194
Citations by year
2026: 32 · 2025: 43 · 2024: 46 · 2023: 29 · 2022: 6
FWCI
3.23
Type
journal article
Language
en
Open access
Locations
  • Biomedicines (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • Monash University Research Portal (Monash University) (submittedVersion, cc-by)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
  • DR-NTU (Nanyang Technological University) (submittedVersion, cc-by)
Funders
  • Jeffrey Cheah School of Medicine and Health Sciences Strategic Grant 2021 (STG-000051, BMRG2018-01, FP022-2018A)
  • External Industry Grant from Biomerge Sdn Bhd (STG-000051, BMRG2018-01, FP022-2018A)
  • University of Malaya Research Grant (STG-000051, BMRG2018-01, FP022-2018A)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
  • Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
  • Health Sciences › Medicine › Dermatology › Dermatology and Skin Diseases
Keywords
gut-skin axis, gut microbiota, psoriasis, gut dysbiosis, probiotics, inflammatory skin diseases, atopic dermatitis, rosacea, immune regulation, inflammatory mediators, microbiota-based therapy

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review