TY - JOUR
T1 - Elevated serum hepatic transaminases in apical periodontitis individuals
AU - Bordagaray, María José
AU - Pellegrini, Elizabeth
AU - Garrido, Mauricio
AU - Hernández-Ríos, Patricia
AU - Villalobos, Thomas
AU - Fernández, Alejandra
AU - Hernández, Marcela
N1 - Publisher Copyright:
© 2024 British Endodontic Society. Published by John Wiley & Sons Ltd.
PY - 2024
Y1 - 2024
N2 - Aim: Apical periodontitis (AP) is the chronic inflammation of the periradicular tissues in response to root canal infection. Whilst AP has been linked with systemic inflammation and noncommunicable diseases, its potential association with nonalcoholic fatty liver disease (NAFLD) is unknown. We aimed to evaluate the serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels as surrogate markers of hepatic injury, and the systemic inflammatory burden in otherwise healthy individuals with and without AP diagnosis. Methodology: Cross-sectional study. Individuals with AP (n = 30) and healthy controls (n = 29) were recruited. The number, mean diameter (mm) and periapical index of the apical lesions of endodontic origin (ALEO) were assessed. ALT and AST levels (pg/mL) were measured through enzyme-linked immunosorbent assays. The serum levels of TNF-α, IL-4, IL-9, IL-10, IL-17A and IL-22 were evaluated by Multiplex assay. Inferential analysis was performed using t-test or Mann–Whitney tests according to data distribution and linear regression models. Data were analysed with StataV16 (p <.05). Results: ALT and AST levels were significantly higher in individuals with AP compared to controls (p <.05). Serum inflammatory biomarkers showed no significant differences between the study groups. Bivariate and multivariate analyses confirmed that AP diagnosis was independently associated with ALT and AST elevations (p <.05). Additionally, the number of ALEO positively influenced AST levels (p =.002). IL-22 on the other hand, was associated with reduced ALT levels (p =.043). Conclusion: AP is associated with higher serum hepatic transaminases ALT and AST, potentially contributing to NAFLD physiopathology in young adults.
AB - Aim: Apical periodontitis (AP) is the chronic inflammation of the periradicular tissues in response to root canal infection. Whilst AP has been linked with systemic inflammation and noncommunicable diseases, its potential association with nonalcoholic fatty liver disease (NAFLD) is unknown. We aimed to evaluate the serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels as surrogate markers of hepatic injury, and the systemic inflammatory burden in otherwise healthy individuals with and without AP diagnosis. Methodology: Cross-sectional study. Individuals with AP (n = 30) and healthy controls (n = 29) were recruited. The number, mean diameter (mm) and periapical index of the apical lesions of endodontic origin (ALEO) were assessed. ALT and AST levels (pg/mL) were measured through enzyme-linked immunosorbent assays. The serum levels of TNF-α, IL-4, IL-9, IL-10, IL-17A and IL-22 were evaluated by Multiplex assay. Inferential analysis was performed using t-test or Mann–Whitney tests according to data distribution and linear regression models. Data were analysed with StataV16 (p <.05). Results: ALT and AST levels were significantly higher in individuals with AP compared to controls (p <.05). Serum inflammatory biomarkers showed no significant differences between the study groups. Bivariate and multivariate analyses confirmed that AP diagnosis was independently associated with ALT and AST elevations (p <.05). Additionally, the number of ALEO positively influenced AST levels (p =.002). IL-22 on the other hand, was associated with reduced ALT levels (p =.043). Conclusion: AP is associated with higher serum hepatic transaminases ALT and AST, potentially contributing to NAFLD physiopathology in young adults.
KW - alanine transaminase
KW - aspartate aminotransferase
KW - periapical periodontitis
UR - http://www.scopus.com/inward/record.url?scp=85195989675&partnerID=8YFLogxK
U2 - 10.1111/iej.14109
DO - 10.1111/iej.14109
M3 - Article
AN - SCOPUS:85195989675
SN - 0143-2885
VL - 57
SP - 1395
EP - 1403
JO - International Endodontic Journal
JF - International Endodontic Journal
IS - 10
ER -