Probiotic normalization of systemic inflammation in siblings of type 1 diabetes patients: an open-label pilot study.
Probiotic normalization of systemic inflammation in siblings of type 1 diabetes patients: an open-label pilot study.
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DOI:
10.1038/s41598-022-07203-6
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发表时间:
2022-02-28
影响因子:
4.6
通讯作者:
Hessner MJ
中科院分区:
文献类型:
--
作者:
Cabrera SM;Coren AT;Pant T;Ciecko AE;Jia S;Roethle MF;Simpson PM;Atkinson SN;Salzman NH;Chen YG;Hessner MJ
The incidence of type 1 diabetes (T1D) has increased, coinciding with lifestyle changes that have likely altered the gut microbiota. Dysbiosis, gut barrier dysfunction, and elevated systemic inflammation consistent with microbial antigen exposure, have been associated with T1D susceptibility and progression. A 6-week, single-arm, open-label pilot trial was conducted to investigate whether daily multi-strain probiotic supplementation could reduce this familial inflammation in 25 unaffected siblings of T1D patients. Probiotic supplementation was well-tolerated as reflected by high participant adherence and no adverse events. Community alpha and beta diversity were not altered between the pre- and post-supplement stool samplings. However, LEfSe analyses identified post-supplement enrichment of the family Lachnospiraceae, producers of the anti-inflammatory short chain fatty acid butyrate. Systemic inflammation was measured by plasma-induced transcription and quantified with a gene ontology-based composite inflammatory index (I.I.com). Post-supplement I.I.com was significantly reduced and pathway analysis predicted inhibition of numerous inflammatory mediators and activation of IL10RA. Subjects with the greatest post-supplement reduction in I.I.com exhibited significantly lower CD4+ CD45RO+ (memory):CD4+ CD45RA+ (naïve) T-cell ratios after supplementation. Post-supplement IL-12p40, IL-13, IL-15, IL-18, CCL2, and CCL24 plasma levels were significantly reduced, while post-supplement butyrate levels trended 1.4-fold higher. Probiotic supplementation may modify T1D susceptibility and progression and warrants further study.
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DOI:
10.1038/ismej.2012.8
发表时间:
2012-08
期刊:
The ISME journal
影响因子:
--
作者:
通讯作者:
--
影响因子:
5
作者:
Chen, Y-G;Mordes, J. P.;Blankenhorn, E. P.;Kashmiri, H.;Kaldunski, M. L.;Jia, S.;Geoffrey, R.;Wang, X.;Hessner, M. J.
通讯作者:
Hessner, M. J.
影响因子:
48
作者:
Callahan BJ;McMurdie PJ;Rosen MJ;Han AW;Johnson AJ;Holmes SP
通讯作者:
Holmes SP
影响因子:
7.7
作者:
Bonifacio E;Warncke K;Winkler C;Wallner M;Ziegler AG
通讯作者:
Ziegler AG
影响因子:
8.2
作者:
Cabrera SM;Chen YG;Hagopian WA;Hessner MJ
通讯作者:
Hessner MJ