An Innovative Synbiotic Formulation Decreases Free Serum Indoxyl Sulfate, Small Intestine Permeability and Ameliorates Gastrointestinal Symptoms in a Randomized Pilot Trial in Stage IIIb-IV CKD Patients.
An Innovative Synbiotic Formulation Decreases Free Serum Indoxyl Sulfate, Small Intestine Permeability and Ameliorates Gastrointestinal Symptoms in a Randomized Pilot Trial in Stage IIIb-IV CKD Patients.
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创新的合成型配方可降低自由血清硫酸硫酸盐,小肠的渗透性,并在IIIB-IV期CKD患者的随机试验试验中减轻胃肠道症状。
DOI:
10.3390/toxins13050334
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发表时间:
2021-05-05
期刊:
影响因子:
4.2
通讯作者:
Gesualdo L
中科院分区:
文献类型:
--
作者:
Cosola C;Rocchetti MT;di Bari I;Acquaviva PM;Maranzano V;Corciulo S;Di Ciaula A;Di Palo DM;La Forgia FM;Fontana S;De Angelis M;Portincasa P;Gesualdo L
Proteolytic dysbiosis of the gut microbiota has been recognized as both a typical feature of chronic kidney disease (CKD) and a risk factor for its progression. Blood accumulation of gut-derived uremic toxins (UTs) like indoxyl sulfate (IS) and p-cresyl sulfate (PCS), intestinal permeability and constipation are typical features accompanying CKD progression and triggering chronic inflammation. In order to verify the efficacy of the innovative synbiotic formulation NATUREN G® in modulating the levels of circulating UTs, intestinal permeability and gastrointestinal symptoms, we set up a randomized, single-blind, placebo-controlled, pilot trial in stage IIIb-IV CKD patients and in healthy controls. Two-month administration of the synbiotic resulted in a decrease of free IS, as compared with the placebo-treated arm, only in the CKD group. The other UTs did not significantly change, although different trends in time (increase in the placebo arm and decrease in the synbiotic arm) were observed. Moreover, after supplementation, reduction of small intestinal permeability and amelioration of abdominal pain and constipation syndromes were observed only in the CKD group. The obtained results suggest the specificity of action of NATUREN G® in CKD and justify further validation in a wider study population.
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影响因子:
--
作者:
Chao G;Wang Y;Zhang S;Yang W;Ni Z;Zheng X
通讯作者:
Zheng X
DOI:
10.2215/cjn.05240515
发表时间:
2016-02-01
影响因子:
9.8
作者:
Rossi, Megan;Johnson, David W.;Campbell, Katrina L.
通讯作者:
Campbell, Katrina L.
DOI:
10.1152/ajprenal.00148.2013
发表时间:
2013-10-01
影响因子:
4.2
作者:
Lv, Lin-Li;Cao, Yu-Han;Liu, Bi-Cheng
通讯作者:
Liu, Bi-Cheng
影响因子:
2.5
作者:
SIMENHOFF, ML;SAUKKONEN, JJ;GORDON, SJ
通讯作者:
GORDON, SJ
影响因子:
1.9
作者:
Riordan, SM;McIver, CJ;Thomas, MC
通讯作者:
Thomas, MC