Association of Serum and Fecal Bile Acid Patterns With Liver Fibrosis in Biopsy-Proven Nonalcoholic Fatty Liver Disease: An Observational Study. Issue 7 (26th July 2022)
- Record Type:
- Journal Article
- Title:
- Association of Serum and Fecal Bile Acid Patterns With Liver Fibrosis in Biopsy-Proven Nonalcoholic Fatty Liver Disease: An Observational Study. Issue 7 (26th July 2022)
- Main Title:
- Association of Serum and Fecal Bile Acid Patterns With Liver Fibrosis in Biopsy-Proven Nonalcoholic Fatty Liver Disease: An Observational Study
- Authors:
- Kasai, Yuki
Kessoku, Takaomi
Tanaka, Kosuke
Yamamoto, Atsushi
Takahashi, Kota
Kobayashi, Takashi
Iwaki, Michihiro
Ozaki, Anna
Nogami, Asako
Honda, Yasushi
Ogawa, Yuji
Kato, Shingo
Imajo, Kento
Higurashi, Takuma
Hosono, Kunihiro
Yoneda, Masato
Usuda, Haruki
Wada, Koichiro
Kawanaka, Miwa
Kawaguchi, Takumi
Torimura, Takuji
Kage, Masayoshi
Hyogo, Hideyuki
Takahashi, Hirokazu
Eguchi, Yuichiro
Aishima, Shinichi
Kobayashi, Noritoshi
Sumida, Yoshio
Honda, Akira
Oyamada, Shunsuke
Shinoda, Satoru
Saito, Satoru
Nakajima, Atsushi
… (more) - Abstract:
- Abstract : INTRODUCTION: No reports on both blood and fecal bile acids (BAs) in patients with nonalcoholic fatty liver disease (NAFLD) exist. We simultaneously assessed the serum and fecal BA patterns in healthy participants and those with NAFLD. METHODS: We collected stool samples from 287 participants from 5 hospitals in Japan (healthy control [HC]: n = 88; mild fibrosis: n = 104; and advanced fibrosis group: n = 95). Blood samples were collected and analyzed for serum BAs and 7α-hydroxy-4-cholesten-3-one (C4)—a surrogate marker for BA synthesis ability—from 141 patients. Concentrations of BAs, including cholic acid (CA), deoxycholic acid (DCA), chenodeoxycholic acid, ursodeoxycholic acid, and lithocholic acid (LCA), were measured using liquid chromatography-mass spectrometry. RESULTS: The total fecal BA concentration was significantly higher in the NAFLD group with worsening of fibrosis than in the HC group. Most of the fecal BAs were secondary and unconjugated. In the fecal BA fraction, CA, DCA, chenodeoxycholic acid, ursodeoxycholic acid, and LCA were significantly higher in the NAFLD than in the HC group. The total serum BA concentration was higher in the NAFLD group with worsening of fibrosis than in the HC group. In the serum BA fraction, CA, LCA, and C4 concentrations were significantly higher in the NAFLD than in the HC group. DISCUSSION: Fecal and serum BA and C4 concentrations were high in patients with NAFLD with worsening of fibrosis, suggesting involvement ofAbstract : INTRODUCTION: No reports on both blood and fecal bile acids (BAs) in patients with nonalcoholic fatty liver disease (NAFLD) exist. We simultaneously assessed the serum and fecal BA patterns in healthy participants and those with NAFLD. METHODS: We collected stool samples from 287 participants from 5 hospitals in Japan (healthy control [HC]: n = 88; mild fibrosis: n = 104; and advanced fibrosis group: n = 95). Blood samples were collected and analyzed for serum BAs and 7α-hydroxy-4-cholesten-3-one (C4)—a surrogate marker for BA synthesis ability—from 141 patients. Concentrations of BAs, including cholic acid (CA), deoxycholic acid (DCA), chenodeoxycholic acid, ursodeoxycholic acid, and lithocholic acid (LCA), were measured using liquid chromatography-mass spectrometry. RESULTS: The total fecal BA concentration was significantly higher in the NAFLD group with worsening of fibrosis than in the HC group. Most of the fecal BAs were secondary and unconjugated. In the fecal BA fraction, CA, DCA, chenodeoxycholic acid, ursodeoxycholic acid, and LCA were significantly higher in the NAFLD than in the HC group. The total serum BA concentration was higher in the NAFLD group with worsening of fibrosis than in the HC group. In the serum BA fraction, CA, LCA, and C4 concentrations were significantly higher in the NAFLD than in the HC group. DISCUSSION: Fecal and serum BA and C4 concentrations were high in patients with NAFLD with worsening of fibrosis, suggesting involvement of abnormal BA metabolism in NAFLD with fibrosis progression. Abnormalities in BA metabolism may be a therapeutic target in NAFLD with fibrosis. … (more)
- Is Part Of:
- Clinical and translational gastroenterology. Volume 13:Issue 7(2022)
- Journal:
- Clinical and translational gastroenterology
- Issue:
- Volume 13:Issue 7(2022)
- Issue Display:
- Volume 13, Issue 7 (2022)
- Year:
- 2022
- Volume:
- 13
- Issue:
- 7
- Issue Sort Value:
- 2022-0013-0007-0000
- Page Start:
- e00503
- Page End:
- Publication Date:
- 2022-07-26
- Subjects:
- Stomach -- Diseases -- Periodicals
Intestines -- Diseases -- Periodicals
Gastroenterology
Gastrointestinal Diseases
Liver Diseases
Intestines -- Diseases
Stomach -- Diseases
Periodical
Periodicals
Fulltext
Internet Resources
Periodicals
Electronic journals
616.33 - Journal URLs:
- http://bibpurl.oclc.org/web/52768 ↗
http://www.nature.com/ctg ↗
http://www.ncbi.nlm.nih.gov/pmc/journals/1564/ ↗
https://journals.lww.com/ctg/pages/default.aspx ↗
http://www.nature.com/ ↗ - DOI:
- 10.14309/ctg.0000000000000503 ↗
- Languages:
- English
- ISSNs:
- 2155-384X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 24068.xml