Interorgan Cross Talk Between Fatty Acid Metabolism, Tissue Inflammation, and FADS2 Genotype in Humans with Obesity

被引:29
作者
Vaittinen, Maija [1 ,2 ]
Mannisto, Ville [3 ,4 ]
Kakela, Pirjo [4 ,5 ]
Agren, Jyrki [6 ]
Tiainen, Mika [7 ]
Schwab, Ursula [1 ,8 ]
Pihlajamaki, Jussi [1 ,8 ]
机构
[1] Univ Eastern Finland, Inst Publ Hlth & Clin Nutr, Kuopio, Finland
[2] Turku Univ Hosp, Turku PET Ctr, Turku, Finland
[3] Univ Eastern Finland, Dept Med, Kuopio, Finland
[4] Kuopio Univ Hosp, Kuopio, Finland
[5] Univ Eastern Finland, Dept Surg, Kuopio, Finland
[6] Univ Eastern Finland, Inst Biomed, Kuopio, Finland
[7] Univ Eastern Finland, Sch Pharm, Kuopio, Finland
[8] Kuopio Univ Hosp, Clin Nutr & Obes Ctr, Kuopio, Finland
基金
芬兰科学院;
关键词
ADIPOSE-TISSUE; NONALCOHOLIC STEATOHEPATITIS; DESATURASE ACTIVITIES; INSULIN-RESISTANCE; SERUM-LIPIDS; RISK-FACTORS; LIVER; ASSOCIATIONS; DIET;
D O I
10.1002/oby.21753
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Fatty acid (FA) composition affects obesity-associated low-grade inflammation. It has been shown that the fatty acid desaturase (FADS) 2 gene polymorphism associates with FA metabolism and adipose tissue (AT) inflammation. This study aimed to investigate the relationship between FA metabolism and inflammation in different tissues and the possible interorgan cross talk. Methods: Cross-sectional baseline data from 155 individuals with obesity (both male and female) participating in the Roux-en-Y gastric bypass operation in the ongoing Kuopio Obesity Surgery Study were used. Gas chromatograph for FA composition, liver histology, and targeted RNA expression for gene expression profile were performed. Results: It was demonstrated that the saturated fatty acid (SFA) proportion in AT correlated positively with inflammation in subcutaneous AT (SAT) and visceral AT (VAT) but not in the liver, while the monounsaturated fatty acid (MUFA) proportion in SAT and VAT correlated negatively with AT inflammation. Notably, there was a positive correlation between AT n-6 polyunsaturated fatty acids (PUFAs), but not AT SFAs or MUFAs, and liver inflammation. This correlation was modified by the FADS2 genotype. Conclusions: The AT FA profile relates with AT inflammation. Additionally, there seems to be a complex interaction, partly regulated by the FADS2 genotype, regulating the interaction between FAs in AT and liver inflammation.
引用
收藏
页码:545 / 552
页数:8
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