Elevated stearoyl-CoA desaturase 1 activity is associated with alcohol-associated liver disease.

Elevated stearoyl-CoA desaturase 1 activity is associated with alcohol-associated liver disease.
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DOI:
10.1016/j.alcohol.2022.04.001
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发表时间:
2022-08
期刊:
影响因子:
2.3
通讯作者:
Ramchandani, V. A.
Ramchandani, V. A.
中科院分区:
医学4区
文献类型:
--
作者:
Klepp, T. D.;Sloan, M. E.;Soundararajan, Soundarya;Ramsden, C. E.;Cinar, R.;Schwandt, M. L.;Diazgranados, N.;Vatsalya, V.;Ramchandani, V. A.

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Chronic binge drinking induces hepatic lipid accumulation, but only certain individuals develop alcohol-associated liver disease (ALD). Specific patterns of lipid accumulation are thought to be associated with ALD, but this has not been comprehensively investigated to date. We analyzed plasma fatty acid levels quantified by gas chromatography-mass spectrometry in a sample of patients with alcohol use disorder (AUD). Given that elevation in serum alanine aminotransferase (ALT) levels are strongly associated with ALD, patients were stratified into two groups based on ALT levels: an ALD group (ALT > 40 IU/L) and a non-ALD group (ALT ≤ 40 IU/L). There was a shift towards greater concentrations of monounsaturated fatty acids in the ALD group compared to the non-ALD group. Steroyl-CoA desaturase (SCD1) activity in the ALD group was then estimated as the ratio of palmitoleic acid (16:1) to palmitic acid (16:0). SCD1 activity was greater in the ALD than the non-ALD group. A series of linear regression models demonstrated that SCD1 activity mediated the association between binge drinking and ALD. These findings provide initial evidence that SCD1 activity may be associated with ALD. If validated prospectively, elevated SCD1 activity could potentially be used as a biomarker to identify individuals at high risk for developing ALD.
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