Abstract
Hepatic encephalopathy (HE) after transjugular intrahepatic portosystemic shunt (TIPS) insertion constitutes a frequent and severe complication. However, there is a lack of robust predictive biomarkers for post-TIPS HE, so far. This study evaluated the usefulness of neurofilament light chains (NfL) and glial fibrillary acidic protein (GFAP) in serum for predicting post-TIPS HE. Around 144 patients with cirrhosis from three centers were prospectively included and monitored for the occurrence of post-TIPS overt HE, liver transplantation, and death. Serum NfL and GFAP were evaluated before TIPS insertion using the single molecule array technology. In a subgroup of patients sequential NfL and GFAP levels were assessed at 30- and 180-days post-TIPS. While higher NfL levels (sHR 1.01, p = 0.036) were independently associated with post-TIPS OHE after adjusting for other risk factors, GFAP levels had no predictive ability. Consistently, only elevated NfL levels were associated with a higher risk of death/liver transplantation in multivariable analyses. Sequential measurements of NfL at 30 and 180 days after TIPS revealed that NfL levels remain constant until Day 30 followed by a decrease at day 180. Notably, GFAP levels did not change over time. Thus, NfL could be a valuable biomarker for identifying high-risk patients for post-TIPS HE.
| Originalsprache | Englisch |
|---|---|
| Aufsatznummer | e70475 |
| Zeitschrift | MedComm |
| Jahrgang | 6 |
| Ausgabenummer | 11 |
| DOIs | |
| Publikationsstatus | Veröffentlicht - 11.2025 |
Fördermittel
JUM: Lecture and consultant fees: Merz Therapeutics, Falk Foundation e.V., ABBVIE, AstraZeneca, Gilead; Research grants: Merz Therapeutics SB: S.B. has received honoraria from Biogen, Bristol Myers Squibb, Hexal, Merck Healthcare, Novartis, Roche, Sanofi and Teva. S.B. is supported by the Deutsche Forschungsgemeinschaft (DFG, SFB CRC TRR 355 ‐ 480846870), Novartis and the Hermann‐ and Lilly‐Schilling Foundation. This work was partly supported by the German Center for Infectious Research (no approval number available) and by the Dr. Rolf M. Schwiete Stiftung (grant number: 2022–56). SJG: Travel expenses: Ipsen and Gilead. Research grant: Schwiete Foundation. This work was partly supported by the German Center for Infectious Research (no approval number available) and by the Dr. Rolf M. Schwiete Stiftung (grant number: 2022–56). This study was supported by the Schwiete Stiftung with a grant provided to Christian Labenz and Simon J. Gairing. Martin A. Kabelitz, Alena F. Ehrenbauer, Anja Tiede and Jim B. Mauz were supported by the KlinStrucMed-Program of Hannover Medical School. The authors thank Irina Wagner, Teresa Braun, Sina Liedke, Nathalie Eckel, Falko Zucker-Reimann, Dunja Amani, Laura Schmidtke and Julia Kowalczyk for excellent technical assistance. Open access funding enabled and organized by Projekt DEAL. EMS: received travel grants from Abbvie and Advitos.
| Träger | Trägernummer |
|---|---|
| AstraZeneca | |
| Novartis | |
| Gilead | |
| Leibniz Forschungszentrum Borstel | |
| Ipsen and Gilead | |
| Schwiete Foundation | |
| Lilly‐Schilling Foundation | |
| Dr. Rolf M. Schwiete Stiftung | 2022–56 |
| Medizinischen Hochschule Hannover | |
| AbbVie | |
| Merz Therapeutics | |
| Deutsches Zentrum für Infektionsforschung | |
| Falk Foundation | |
| Deutsche Forschungsgemeinschaft | SFB CRC TRR 355 ‐ 480846870 |
UN SDGs
Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung
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SDG 3 – Gesundheit und Wohlergehen
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