Volume 29, Issue 7 pp. 1110-1115

Effects of probiotic therapy on portal pressure in patients with cirrhosis: a pilot study

Puneeta Tandon

Puneeta Tandon

Department of Medicine, University of Alberta, Edmonton, AB, Canada

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Karli Moncrief

Karli Moncrief

Department of Medicine, University of Alberta, Edmonton, AB, Canada

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Karen Madsen

Karen Madsen

Department of Medicine, University of Alberta, Edmonton, AB, Canada

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Marie C. Arrieta

Marie C. Arrieta

Department of Medicine, University of Alberta, Edmonton, AB, Canada

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Richard J. Owen

Richard J. Owen

Department of Radiology, University of Alberta, Edmonton, AB, Canada

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Vince G. Bain

Vince G. Bain

Department of Medicine, University of Alberta, Edmonton, AB, Canada

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Winnie W. Wong

Winnie W. Wong

Department of Medicine, University of Alberta, Edmonton, AB, Canada

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Mang M. Ma

Mang M. Ma

Department of Medicine, University of Alberta, Edmonton, AB, Canada

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First published: 02 July 2009
Citations: 56
Correspondence
Puneeta Tandon, Zeidler Ledcor Centre, University of Alberta, 130-University Campus, Edmonton, AB, T6G 2X8, Canada
Tel: +780 492 9845
Fax: +780 492 9873
e-mail: [email protected]

Abstract

Background: Recent literature has supported the role of bacterial translocation as a mediator of splanchnic vasodilatation and portal hypertension. The objective of this study was to determine whether the probiotic VSL#3 would reduce portal pressure in patients with cirrhosis.

Methods: Eight patients with compensated or very early decompensated cirrhosis and hepatic venous pressure gradient (HVPG) >10 mmHg, received 2 months of VSL#3 (3600 billion bacteria daily). The HVPG, intestinal permeability, endotoxin, tumour necrosis factor (TNF)-α, interleukin (IL)-6, IL-8, renin and aldosterone were measured at baseline and study end.

Results: There was no change in the HVPG or intestinal permeability from baseline to study end but there was a trend to reduction in plasma endotoxin (P=0.09), a mild but significant increase in serum TNF-α (P=0.02) and a significant reduction in plasma aldosterone (P=0.03).

Conclusions: Within the limitations of small sample size, there does not appear to be a benefit of probiotic therapy for portal pressure reduction in patients with compensated or early decompensated cirrhosis. The reductions in endotoxin and aldosterone suggest possible beneficial effects of probiotics for this patient population. The clinical significance of the small but unexpected increase in TNF-α is unclear. Future studies are planned in patients with decompensated cirrhosis.

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