Altered intestinal microbiota in patients with chronic pancreatitis: implications in diabetes and metabolic abnormalities

被引:89
|
作者
Jandhyala, Sai Manasa [1 ]
Madhulika, A. [2 ]
Deepika, G. [3 ]
Rao, G. Venkat [4 ]
Reddy, D. Nageshwar
Subramanyam, Chivukula [1 ]
Sasikala, Mitnala [1 ]
Talukdar, Rupjyoti [1 ,5 ]
机构
[1] Asian Hlth Care Found, Div Basic Sci, Hyderabad, Andhra Pradesh, India
[2] Asian Inst Gastroenterol, Dept Clin Nutr, Hyderabad, Andhra Pradesh, India
[3] Asian Inst Gastroenterol, Dept Biochem, Hyderabad, Andhra Pradesh, India
[4] Asian Inst Gastroenterol, Dept Surg Gastroenterol, Hyderabad, Andhra Pradesh, India
[5] Asian Inst Gastroenterol, Dept Med Gastroenterol, Hyderabad, Andhra Pradesh, India
来源
SCIENTIFIC REPORTS | 2017年 / 7卷
关键词
RESOURCE;
D O I
10.1038/srep43640
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Intestinal dysbiosis and its functional implications in chronic pancreatitis (CP) have not been elaborately studied. We evaluated the taxonomic and functional alterations in intestinal microbiota in 30 well-characterised patients with CP (16 without, 14 with diabetes) and 10 healthy controls. The patients with CP and diabetes had significantly longer disease duration and greater degree of malnutrition. There was increase in plasma endotoxin concentrations from controls to CP non-diabetics to CP diabetics. We observed significant differences in richness and alpha diversity between the groups. We also observed increase in the Firmicutes: Bacteroidetes ratio in CP patients without and with diabetes. There was reduction in abundance of Faecalibacterium prausnitzii and Ruminococcus bromii from controls to CP non-diabetics to CP diabetics. On the other hand, there was increase in LPS (endotoxin) synthetic pathways (KEGG orthology) in the groups. Faecalibacterium prausnitzii abundance correlated negatively with plasma endotoxin and glycemic status; while plasma endotoxin correlated positively with blood glucose and negatively with plasma insulin. Our results have important implications for future studies exploring mechanistic insights on secondary diabetes in CP.
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页数:10
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