Proton Pump Inhibitor-Induced Gut Dysbiosis Increases Mortality Rates for Patients with Clostridioides difficile Infection
ABSTRACT Clostridioides difficile infection (CDI) is associated with high mortality rates among patients with chronic illnesses. We aimed to identify avoidable risk factors to reduce the mortality rate in CDI patients. A total of 306 patients with diarrhea and clinical suspicion of CDI were enrolled...
| Published in: | Microbiology Spectrum |
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| Main Authors: | , , , , , , , , |
| Format: | Article |
| Language: | English |
| Published: |
American Society for Microbiology
2022-08-01
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| Subjects: | |
| Online Access: | https://journals.asm.org/doi/10.1128/spectrum.00486-22 |
| _version_ | 1851917273871155200 |
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| author | Cheng-Yu Lin Hao-Tsai Cheng Chia-Jung Kuo Yun-Shien Lee Chang-Mu Sung Micah Keidan Krishna Rao John Y. Kao Sen-Yung Hsieh |
| author_facet | Cheng-Yu Lin Hao-Tsai Cheng Chia-Jung Kuo Yun-Shien Lee Chang-Mu Sung Micah Keidan Krishna Rao John Y. Kao Sen-Yung Hsieh |
| author_sort | Cheng-Yu Lin |
| collection | DOAJ |
| container_title | Microbiology Spectrum |
| description | ABSTRACT Clostridioides difficile infection (CDI) is associated with high mortality rates among patients with chronic illnesses. We aimed to identify avoidable risk factors to reduce the mortality rate in CDI patients. A total of 306 patients with diarrhea and clinical suspicion of CDI were enrolled, and fecal samples were gathered from 145 patients. CDI was diagnosed by fecal positivity for the C. difficile tcdB gene. Risk factors associated with death within 180 days were identified using Cox regression analysis. The fecal microbiota was determined through bacterial 16S rRNA gene sequencing. Of the patients with diarrhea, 240 (mean age, 69.1 years) were positive for CDI, and 91 died within 180 days. Multivariate analysis revealed that male sex, high Charlson Comorbidity Index and McCabe scores, high serum C-reactive protein levels, low hematocrit levels, low absolute eosinophil counts, high neutrophil/lymphocyte ratios, and daily use of proton pump inhibitors (PPIs) were independent risk factors for overall mortality. Cumulative analyses confirmed the association of duration-dependent PPI use with a high mortality rate. Fecal microbiota analyses showed associations of decreased relative abundance of Ruminococcus gnavus (P = 0.001) and Prevotella copri (P = 0.025) and increased relative abundance of Parabacteroides merdae (P = 0.001) and Clostridioides difficile (P = 0.040) with higher mortality rates in patients with CDI. Moreover, these microbiota changes were correlated with the duration of PPI use. IMPORTANCE This article demonstrates that daily PPI use was the only avoidable risk factor for death. With more extended PPI use, the mortality rate was higher in patients with CDI. Decreases in Prevotella copri and Ruminococcus gnavus and increases in Parabacteroides merdae and Clostridioides difficile in line with daily PPI use duration were significantly associated with the death of CDI patients. Our findings provide in-depth insights into the cautious use of PPIs in chronically ill patients with CDI. |
| format | Article |
| id | doaj-art-e4f4be6a27914012a79a331663802d6c |
| institution | Directory of Open Access Journals |
| issn | 2165-0497 |
| language | English |
| publishDate | 2022-08-01 |
| publisher | American Society for Microbiology |
| record_format | Article |
| spelling | doaj-art-e4f4be6a27914012a79a331663802d6c2025-08-19T21:59:37ZengAmerican Society for MicrobiologyMicrobiology Spectrum2165-04972022-08-0110410.1128/spectrum.00486-22Proton Pump Inhibitor-Induced Gut Dysbiosis Increases Mortality Rates for Patients with Clostridioides difficile InfectionCheng-Yu Lin0Hao-Tsai Cheng1Chia-Jung Kuo2Yun-Shien Lee3Chang-Mu Sung4Micah Keidan5Krishna Rao6John Y. Kao7Sen-Yung Hsieh8Department of Gastroenterology and Hepatology, Chang Gung Memorial Hospital, Taoyuan, TaiwanChang Gung University College of Medicine, Taoyuan, TaiwanDepartment of Gastroenterology and Hepatology, Chang Gung Memorial Hospital, Taoyuan, TaiwanDepartment of Biotechnology, Ming Chuan University, Taoyuan, TaiwanDepartment of Gastroenterology and Hepatology, Chang Gung Memorial Hospital, Taoyuan, TaiwanDepartment of Internal Medicine, Division of Infectious Diseases, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USADepartment of Internal Medicine, Division of Infectious Diseases, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USADepartment of Internal Medicine, Division of Gastroenterology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USADepartment of Gastroenterology and Hepatology, Chang Gung Memorial Hospital, Taoyuan, TaiwanABSTRACT Clostridioides difficile infection (CDI) is associated with high mortality rates among patients with chronic illnesses. We aimed to identify avoidable risk factors to reduce the mortality rate in CDI patients. A total of 306 patients with diarrhea and clinical suspicion of CDI were enrolled, and fecal samples were gathered from 145 patients. CDI was diagnosed by fecal positivity for the C. difficile tcdB gene. Risk factors associated with death within 180 days were identified using Cox regression analysis. The fecal microbiota was determined through bacterial 16S rRNA gene sequencing. Of the patients with diarrhea, 240 (mean age, 69.1 years) were positive for CDI, and 91 died within 180 days. Multivariate analysis revealed that male sex, high Charlson Comorbidity Index and McCabe scores, high serum C-reactive protein levels, low hematocrit levels, low absolute eosinophil counts, high neutrophil/lymphocyte ratios, and daily use of proton pump inhibitors (PPIs) were independent risk factors for overall mortality. Cumulative analyses confirmed the association of duration-dependent PPI use with a high mortality rate. Fecal microbiota analyses showed associations of decreased relative abundance of Ruminococcus gnavus (P = 0.001) and Prevotella copri (P = 0.025) and increased relative abundance of Parabacteroides merdae (P = 0.001) and Clostridioides difficile (P = 0.040) with higher mortality rates in patients with CDI. Moreover, these microbiota changes were correlated with the duration of PPI use. IMPORTANCE This article demonstrates that daily PPI use was the only avoidable risk factor for death. With more extended PPI use, the mortality rate was higher in patients with CDI. Decreases in Prevotella copri and Ruminococcus gnavus and increases in Parabacteroides merdae and Clostridioides difficile in line with daily PPI use duration were significantly associated with the death of CDI patients. Our findings provide in-depth insights into the cautious use of PPIs in chronically ill patients with CDI.https://journals.asm.org/doi/10.1128/spectrum.00486-22CDI-associated gut dysbiosisPPI-induced gut dysbiosisgut microbiota |
| spellingShingle | Cheng-Yu Lin Hao-Tsai Cheng Chia-Jung Kuo Yun-Shien Lee Chang-Mu Sung Micah Keidan Krishna Rao John Y. Kao Sen-Yung Hsieh Proton Pump Inhibitor-Induced Gut Dysbiosis Increases Mortality Rates for Patients with Clostridioides difficile Infection CDI-associated gut dysbiosis PPI-induced gut dysbiosis gut microbiota |
| title | Proton Pump Inhibitor-Induced Gut Dysbiosis Increases Mortality Rates for Patients with Clostridioides difficile Infection |
| title_full | Proton Pump Inhibitor-Induced Gut Dysbiosis Increases Mortality Rates for Patients with Clostridioides difficile Infection |
| title_fullStr | Proton Pump Inhibitor-Induced Gut Dysbiosis Increases Mortality Rates for Patients with Clostridioides difficile Infection |
| title_full_unstemmed | Proton Pump Inhibitor-Induced Gut Dysbiosis Increases Mortality Rates for Patients with Clostridioides difficile Infection |
| title_short | Proton Pump Inhibitor-Induced Gut Dysbiosis Increases Mortality Rates for Patients with Clostridioides difficile Infection |
| title_sort | proton pump inhibitor induced gut dysbiosis increases mortality rates for patients with clostridioides difficile infection |
| topic | CDI-associated gut dysbiosis PPI-induced gut dysbiosis gut microbiota |
| url | https://journals.asm.org/doi/10.1128/spectrum.00486-22 |
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