Predictors of controlled attenuation parameter in metabolic dysfunction
- PMID: 38141028
- PMCID: PMC11017762
- DOI: 10.1002/ueg2.12513
Predictors of controlled attenuation parameter in metabolic dysfunction
Abstract
Background & aims: Hepatic fat content can be non-invasively estimated by controlled attenuation parameter (CAP) during transient elastography. The aim of this study was to examine the determinants and predictors of CAP values in individuals with metabolic dysfunction.
Methods: We enrolled 1230 consecutive apparently healthy individuals (Liver-Bible-2022 cohort) with ≥3 metabolic dysfunction features. CAP was measured by Fibroscan. CAP determinants and predictors were identified using backward stepwise analysis and introduced in generalized linear models.
Results: Participants were predominantly males (82.9%), mean age was 53.8 ± 6.4 years, 600 (48.8%) had steatosis (CAP ≥ 275 dB/m), and 27 had liver stiffness measurement (LSM) ≥ 8 kPa. CAP values correlated with LSM (p < 10-22). In multivariable analysis, fasting insulin and abdominal circumference (AC) were the main determinants of CAP (p < 10-6), together with body mass index (BMI; p < 10-4), age, diabetes, triglycerides, ferritin, and lower HDL and thyroid stimulating hormone (TSH; p < 0.05 for all). In a subset of 592 participants with thyroid hormone measurement, we found an association between higher free triiodothyronine levels, correlating with lower TSH, and CAP values, independent of TSH and of levothyroxine treatment (p = 0.0025). A clinical CAP score based on age, BMI, AC, HbA1c, ALT, and HDL predicted CAP ≥ 275 dB/m with moderate accuracy (AUROC = 0.73), which was better than that of the Fatty Liver Index and of ALT (AUROC = 0.70/0.61, respectively) and validated it in multiple cohorts.
Conclusion: Abdominal adiposity and insulin resistance severity were the main determinants of CAP in individuals with metabolic dysfunction and may improve steatotic liver disease risk stratification. CAP values were modulated by the hypophysis-thyroid axis.
Keywords: CAP; LSM; abdominal circumference; controlled attenuation parameter; fasting insulin; fibroscan; liver stiffness measurement; metabolic syndrome; steatosis; thyroid; transient elastography.
© 2023 The Authors. United European Gastroenterology Journal published by Wiley Periodicals LLC on behalf of United European Gastroenterology.
Conflict of interest statement
The authors declare that they have no conflicts of interest relevant to the present study. LV has received speaking fees from MSD, Gilead, AlfaSigma and AbbVie, served as a consultant for Gilead, Pfizer, AstraZeneca, Novo Nordisk, Intercept, Diatech Pharmacogenetics, Ionis Pharmaceuticals, Boeringher Ingelheim, Resalis and received research grants from Gilead. DP served as a consultant for and has received speaking fees, travel grants, and research grants from Macopharma, Ortho Clinical Diagnostics, Grifols, Terumo, Immucor, Diamed, and Diatech Pharmacogenetics.
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- Gilead_IN-IT-989-5790/Gilead
- RF-2016-02364358/Ministero della Salute
- Rete Cardiologica "CV-PREVITAL"/Ministero della Salute
- Ricerca Corrente/Ministero della Salute
- Astra Zeneca Agreement for Research/AstraZeneca
- Ricerca Corrente/Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
- 101016726 - REVEAL/H2020 LEIT Information and Communication Technologies
- 777377 - Litmus project/Horizon 2020 Framework Program
- NNF20OC0063883/Novo Nordisk Project grants in Endocrinology and Metabolism
- VR 2021-005208/Vetenskapsrådet
- KAW 2017.0203/Knut och Alice Wallenbergs Stiftelse
- "Liver BIBLE" (PR-0391)/Fondazione Patrimonio Ca' Granda
- SU 2018-04276/ALF Agreement
- DIA2020-518/Diabetesförbundet
- SSF ITM17-0384/Stiftelsen för Strategisk Forskning
- 101096312 - GENIAL/HORIZON EUROPE Framework Program
- 20200191/Hjärt-Lungfonden
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