Published online Apr 27, 2024. doi: 10.4254/wjh.v16.i4.601
Peer-review started: November 13, 2023
First decision: January 23, 2024
Revised: February 4, 2024
Accepted: March 7, 2024
Article in press: March 7, 2024
Published online: April 27, 2024
Processing time: 162 Days and 17.2 Hours
Intrahepatic cholestasis of pregnancy (ICP) is a liver condition specific to pregnancy. Short-chain fatty acids (SCFAs), important metabolites produced by the gut microbiota, are significantly linked to several pregnancy complications.
However, the metabolic profile of SCFAs in patients with ICP is still uncertain.
The study aimed to examine the correlation between maternal and umbilical blood SCFAs and investigate the changes in SCFAs in patients with ICP and their offspring. Additionally, the research sought to assess the clinical significance and diagnostic value of these SCFAs. Ultimately, the study aimed to identify novel biomarkers for diagnosing and treating ICP by focusing on gut microbiota metabolites.
Therefore, in this study, we utilized targeted metabolomics technology to analyze SCFAs in the maternal and cord blood of patients with ICP and normal pregnant (NP) women.
The study revealed that maternal serum SCFAs in both the ICP and NP groups showed significantly higher levels of acetic acid, propionic acid, and butyric acid compared to other SCFAs. In umbilical cord blood, acetic and propionic acids were found to be the most abundant, with similar levels of butyric acid, isobutyric acid, and caproic acid, while isovaleric acid and valeric acid levels were the lowest. Furthermore, the correlation analysis indicated a negative correlation between both acetic acid and caproic acid in maternal and cord blood, and total bile acids in peripheral blood.
Significant alterations were observed in the SCFAs of maternal serum and cord blood in the ICP group, compared with the NP group. It is notable that the SCFA levels in maternal serum and cord blood were significantly positively correlated in the ICP group. Additionally, certain maternal serum SCFAs, specifically caproic and acetic acids, exhibited excellent diagnostic efficiency for ICP.
Additional in vivo and in vitro experiments are needed to clarify the mechanisms of action of SCFAs, establishing a strong theoretical basis for their use as diagnostic and therapeutic targets for ICP.