TY - JOUR
T1 - Afamin predicts the prevalence and incidence of nonalcoholic fatty liver disease
AU - Pitkänen, Niina
AU - Finkenstedt, Armin
AU - Lamina, Claudia
AU - Juonala, Markus
AU - Kähönen, Mika
AU - Mäkelä, Kari-Matti
AU - Dieplinger, Benjamin
AU - Viveiros, Andre
AU - Melmer, Andreas
AU - Leitner, Isabella
AU - Kedenko, Ludmilla
AU - Seppälä, Ilkka
AU - Viikari, Jorma S.A.
AU - Mueller, Thomas
AU - Kronenberg, Florian
AU - Paulweber, Bernhard
AU - Lehtimäki, Terho
AU - Zoller, Heinz
AU - Raitakari, Olli T.
AU - Dieplinger, Hans
N1 - Funding Information:
Research funding: The Young Finns Study has been financially supported by the Academy of Finland: Grants 322098, 286284, 134309 (Eye), 126925, 121584, 124282, 129378 (Salve), 117787 (Gendi), and 41071 (Skidi); the Social Insurance Institution of Finland; Competitive State Research Financing of the Expert Responsibility area of Kuopio, Tampere and Turku University Hospitals (Grant X51001); Juho Vainion Foundation; Paavo Nurmi Foundation; Finnish Foundation for Cardiovascular Research; Finnish Cultural Foundation; The Sigrid Juselius Foundation; Tampere Tuberculosis Foundation; Emil Aaltonen Foundation; Yrjö Jahnsson Foundation; Signe and Ane Gyllenberg Foundation; Diabetes Research Foundation of Finnish Diabetes Association. This project has received funding from the European Union’s Horizon 2020 Research and Innovation Program under Grant Agreements No. 848146 for To Aition and Grant Agreement No. 755320 for TAXINOMISIS; European Research Council (Grant 742927 for MULTIEPIGEN project); Tampere University Hospital Supporting Foundation and Finnish Society of Clinical Chemistry. The Austrian contribution to this work has received support from grants of the Austrian Research Fund (P19969-B11) to H.D., Standortagentur Tirol and the Austrian Heart Fund to F.K., and Kamillo-Eisner Stiftung and Medizinische Forschungsgesellschaft Salzburg to B.P.
Publisher Copyright:
© 2021 Niina Pitkänen et al., published by De Gruyter, Berlin/Boston.
PY - 2022
Y1 - 2022
N2 - Objectives: In the general population, increased afamin concentrations are associated with the prevalence and incidence of metabolic syndrome as well as type 2 diabetes. Although metabolic syndrome is commonly associated with nonalcoholic fatty liver disease (NAFLD), there exist no information on afamin and NAFLD. Methods: Afamin concentrations were cross-sectionally measured in 146 Austrian patients with NAFLD, in 45 patients without NAFLD, and in 292 age- and sex-matched healthy controls. Furthermore, the feasibility of afamin to predict incident NAFLD was evaluated in 1,434 adult participants in the population-based Cardiovascular Risk in Young Finns Study during a 10-year follow-up. Results: Median afamin concentrations were significantly higher in NAFLD patients (83.6 mg/L) than in patients without NAFLD (61.6 mg/L, p<0.0001) or in healthy controls (63.9 mg/L, p<0.0001). In age- and sex-adjusted logistic regression analyses a 10 mg/L increase of afamin was associated with a 1.5-fold increase of having NAFLD as compared with patients without NAFLD and the risk was even two-fold when compared with healthy controls. In the population-based cohort, afamin concentrations at baseline were significantly lower in participants without NAFLD (n=1,195) than in 239 participants who developed NAFLD (56.5 vs. 66.9 mg/L, p<0.0001) during the 10-year follow up, with highest afamin values observed in individuals developing severe forms of NAFLD. After adjustment for several potentially confounding parameters, afamin remained an independent predictor for the development of NAFLD (OR=1.37 [95% CI 1.23-1.54] per 10 mg/L increase, p<0.0001). Conclusions: Afamin concentrations are increased in patients with NAFLD and independently predict the development of NAFLD in a population-based cohort.
AB - Objectives: In the general population, increased afamin concentrations are associated with the prevalence and incidence of metabolic syndrome as well as type 2 diabetes. Although metabolic syndrome is commonly associated with nonalcoholic fatty liver disease (NAFLD), there exist no information on afamin and NAFLD. Methods: Afamin concentrations were cross-sectionally measured in 146 Austrian patients with NAFLD, in 45 patients without NAFLD, and in 292 age- and sex-matched healthy controls. Furthermore, the feasibility of afamin to predict incident NAFLD was evaluated in 1,434 adult participants in the population-based Cardiovascular Risk in Young Finns Study during a 10-year follow-up. Results: Median afamin concentrations were significantly higher in NAFLD patients (83.6 mg/L) than in patients without NAFLD (61.6 mg/L, p<0.0001) or in healthy controls (63.9 mg/L, p<0.0001). In age- and sex-adjusted logistic regression analyses a 10 mg/L increase of afamin was associated with a 1.5-fold increase of having NAFLD as compared with patients without NAFLD and the risk was even two-fold when compared with healthy controls. In the population-based cohort, afamin concentrations at baseline were significantly lower in participants without NAFLD (n=1,195) than in 239 participants who developed NAFLD (56.5 vs. 66.9 mg/L, p<0.0001) during the 10-year follow up, with highest afamin values observed in individuals developing severe forms of NAFLD. After adjustment for several potentially confounding parameters, afamin remained an independent predictor for the development of NAFLD (OR=1.37 [95% CI 1.23-1.54] per 10 mg/L increase, p<0.0001). Conclusions: Afamin concentrations are increased in patients with NAFLD and independently predict the development of NAFLD in a population-based cohort.
KW - afamin
KW - non-alcoholic liver disease
KW - population-based studies
KW - prediction
KW - risk factors
KW - vitamin E-binding protein
U2 - 10.1515/cclm-2021-0837
DO - 10.1515/cclm-2021-0837
M3 - Article
AN - SCOPUS:85120636521
SN - 1434-6621
VL - 60
JO - CLINICAL CHEMISTRY AND LABORATORY MEDICINE
JF - CLINICAL CHEMISTRY AND LABORATORY MEDICINE
IS - 2
ER -