Gut microbiome predictors of treatment response and recurrence in primary Clostridium difficile infection

S Khanna, E Montassier, B Schmidt… - Alimentary …, 2016 - Wiley Online Library
Alimentary pharmacology & therapeutics, 2016Wiley Online Library
Background Clostridium difficile infection (CDI) may not respond to initial therapy and
frequently recurs, but predictors of response and recurrence are inconsistent. The impact of
specific alterations in the gut microbiota determining treatment response and recurrence in
patients with CDI is unknown. Aim To assess microbial signatures as predictors of treatment
response and recurrence in CDI. Methods Pre‐treatment stool samples and clinical
metadata including outcomes were collected prospectively from patients with their first CDI …
Background
Clostridium difficile infection (CDI) may not respond to initial therapy and frequently recurs, but predictors of response and recurrence are inconsistent. The impact of specific alterations in the gut microbiota determining treatment response and recurrence in patients with CDI is unknown.
Aim
To assess microbial signatures as predictors of treatment response and recurrence in CDI.
Methods
Pre‐treatment stool samples and clinical metadata including outcomes were collected prospectively from patients with their first CDI episode. Next generation 16s rRNA sequencing using MiSeq Illumina platform was performed and changes in microbial community structure were correlated with CDI outcomes.
Results
Eighty‐eight patients (median age 52.7 years, 60.2% female) were included. Treatment failure occurred in 12.5% and recurrence after response in 28.5%. Patients who responded to treatment had an increase in Ruminococcaceae, Rikenellaceae, Clostridiaceae, Bacteroides, Faecalibacterium and Rothia compared to nonresponders. A risk‐index built from this panel of microbes differentiated responders (mean 0.07 ± 0.24) from nonresponders (0.52 ± 0.42; P = 0.0002). Receiver operating characteristic (ROC) curve demonstrated that risk‐index was a strong predictor of treatment response with an area under the curve (AUC) of 0.85. Among clinical parameters tested, only proton pump inhibitor use predicted recurrent CDI (OR 3.75, 95% CI 1.27–11.1, P = 0.01). Patients with recurrent CDI had statistically significant increases in Veillonella, Enterobacteriaceae, Streptococci, Parabacteroides and Lachnospiraceae compared to patients without recurrence and a risk index was able to predict recurrence (AUC = 0.78).
Conclusion
Gut microbiota signatures predict treatment response and recurrence potentially, allowing identification of patients with Clostridium difficile infection that may benefit from early institution of alternate therapies.
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