Evaluation of Liver Metabolism Biomarkers in Metabolic Associated Fatty Liver Disease According to Obesity Phenotype

被引:0
|
作者
Loureiro, Ligiane M. [1 ,2 ,3 ]
Cordeiro, Adryana [3 ,4 ,8 ]
Barboza, Leticia [3 ]
Mendes, Rodrigo [5 ]
Pereira, Silvia [3 ,6 ]
Saboya, Carlos J. [3 ,6 ]
Ramalho, Andrea [7 ]
机构
[1] Fed Univ Rio De Janeiro UFRJ, Postgrad Program, Doctorate Nutr Sci, Rio De Janeiro, Brazil
[2] Fed Univ Para UFPA, Hlth Sci Inst, Fac Nutr, Belem, Brazil
[3] Univ Fed Rio de Janeiro, Ctr Res Micronutrients NPqM, Inst Nutr Josue De Castro, Rio de Janeiro, Brazil
[4] Univ Porto, Fac Med, Biomed Dept, Biochem Unit, Porto, Portugal
[5] Pontif Catholic Univ Rio De Janeiro, Postgrad Program, Appl Math, Rio De Janeiro, Brazil
[6] Multidisciplinary Ctr Bariatr & Metab Surg, Rio De Janeiro, Brazil
[7] Univ Fed Rio de Janeiro, Inst Nutr, Dept Social & Appl Nutr, Rio de Janeiro, Brazil
[8] Fed Univ Rio De Janeiro UFRJ, Inst Nutr Josue De Castro, Ctr Res Micronutrients NPqM, Carlos Chagas Ave,373 Edificio Ctr Ciencias Saude,, BR-21941902 Rio De Janeiro, Brazil
来源
关键词
Obesity; obesity phenotype; liver biomarkers; alkaline phosphatase; MAFLD; INSULIN-RESISTANCE; NATURAL-HISTORY; VITAMIN-D; HEALTH; CHOLESTEROL; DEFICIENCY; PROGRAM; PLASMA; MASS;
D O I
10.1080/07315724.2021.2007427
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Objective To analyze the relationship between the biochemical markers of liver metabolism in different stages of Metabolic Associated Fatty Liver Disease (MAFLD) according to the obesity phenotype. Methodology This is a cross-sectional study with individuals with class III obesity classified according to the obesity phenotypes proposed by the National Cholesterol Education Program Adult Treatment Panel III (NCEP ATP III) criteria. Biochemical and anthropometric variables were analyzed according to the staging of MAFLD and obesity phenotype. Results A total of 50 subjects with MAFLD, 62% (n = 31) with steatosis and 38% (n = 19) with steatohepatitis without fibrosis; 36% were classified as metabolically healthy obesity (MHO) and 64% as metabolically unhealthy obesity (MUHO), respectively. Mean values of alkaline phosphatase were 85.44 +/- 27.27 vs. 61.92 +/- 17.57 (p = 0.006); gamma-glutamyl transpeptidase, 25.77 +/- 15.36 vs. 30.63 +/- 19.49 (p = 0.025); and albumin, 3.99 +/- 0.34 vs. 4.24 +/- 0.23 (p = 0.037), were lower and statistically significant in the MHO group with steatosis. The results show when considering individuals with IR, only AP is a predictor of unhealthy phenotype (B-0.934, 0.848- 1.029, p = 0.031). Conclusion MHO individuals with steatosis present lower severe changes related to markers of liver damage and function and AP is considered the predictor of MUHO phenotype.
引用
收藏
页码:140 / 147
页数:8
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