Department of Medicine, Endoscopy Unit, Kuopio University Hospital, 70029 Kuopio, Finland.
Institute of Public Health and Clinical Nutrition, University of Eastern Finland, 70210 Kuopio, Finland.
Nutrients. 2024 Jan 16;16(2):261. doi: 10.3390/nu16020261.
The GG genotype of the Patatin-like phosphatase domain-containing 3 (), dietary fat, short-chain fatty acids (SCFA) and branched-chain amino acids (BCAA) are linked with non-alcoholic fatty liver disease. We studied the impact of the quality of dietary fat on plasma (p) and fecal (f) SCFA and p-BCAA in men homozygous for the rs738409 variant (I148M). Eighty-eight randomly assigned men (age 67.8 ± 4.3 years, body mass index 27.1 ± 2.5 kg/m) participated in a 12-week diet intervention. The recommended diet (RD) group followed the National and Nordic nutrition recommendations for fat intake. The average diet (AD) group followed the average fat intake in Finland. The intervention resulted in a decrease in total p-SCFAs and iso-butyric acid in the RD group ( = 0.041 and = 0.002). Valeric acid (p-VA) increased in participants with the GG genotype regardless of the diet (RD, 3.6 ± 0.6 to 7.0 ± 0.6 µmol/g, = 0.005 and AD, 3.8 ± 0.3 to 9.7 ± 8.5 µmol/g, = 0.015). Also, genotype relation to p-VA was seen statistically significantly in the RD group (CC: 3.7 ± 0.4 to 4.2 ± 1.7 µmol/g and GG: 3.6 ± 0.6 to 7.0 ± 0.6 µmol/g, = 0.0026 for time and = 0.004 for time and genotype). P-VA, unlike any other SCFA, correlated positively with plasma gamma-glutamyl transferase ( = 0.240, = 0.025). Total p-BCAAs concentration changed in the AD group comparing CC and GG genotypes (CC: 612 ± 184 to 532 ± 149 µmol/g and GG: 587 ± 182 to 590 ± 130 µmol/g, = 0.015 for time). Valine decreased in the RD group ( = 0.009), and leucine decreased in the AD group ( = 0.043). RD decreased total fecal SCFA, acetic acid (f-AA), and butyric acid (f-BA) in those with CC genotype ( = 0.006, 0.013 and 0.005, respectively). Our results suggest that the genotype modifies the effect of dietary fat modification for p-VA, total f-SCFA, f-AA and f-BA, and total p-BCAA.
GG 基因型的 patatin 样磷酸酶域包含 3 (),膳食脂肪,短链脂肪酸(SCFA)和支链氨基酸(BCAA)与非酒精性脂肪性肝病有关。我们研究了膳食脂肪质量对男性同型纯合子 rs738409 变异(I148M)血浆(p)和粪便(f)SCFA 和 p-BCAA 的影响。88 名随机分配的男性(年龄 67.8 ± 4.3 岁,体重指数 27.1 ± 2.5 kg/m)参加了为期 12 周的饮食干预。推荐饮食(RD)组遵循国家和北欧营养建议的脂肪摄入量。平均饮食(AD)组遵循芬兰的平均脂肪摄入量。干预导致 RD 组总 p-SCFA 和异丁酸降低(= 0.041 和 = 0.002)。戊酸(p-VA)在无论饮食如何的 GG 基因型参与者中增加(RD,3.6 ± 0.6 至 7.0 ± 0.6 µmol/g,= 0.005 和 AD,3.8 ± 0.3 至 9.7 ± 8.5 µmol/g,= 0.015)。此外,在 RD 组中还观察到基因型与 p-VA 的统计学显著关系(CC:3.7 ± 0.4 至 4.2 ± 1.7 µmol/g 和 GG:3.6 ± 0.6 至 7.0 ± 0.6 µmol/g,= 0.0026 用于时间和= 0.004 用于时间和基因型)。与任何其他 SCFA 不同,p-VA 与血浆γ-谷氨酰转移酶呈正相关(= 0.240,= 0.025)。与 CC 基因型相比,AD 组中总 p-BCAA 浓度发生变化(CC:612 ± 184 至 532 ± 149 µmol/g 和 GG:587 ± 182 至 590 ± 130 µmol/g,= 0.015 用于时间)。RD 组缬氨酸减少(= 0.009),AD 组亮氨酸减少(= 0.043)。RD 降低了 CC 基因型的总粪便 SCFA、乙酸(f-AA)和丁酸(f-BA)(= 0.006、0.013 和 0.005)。我们的结果表明,基因型修饰了饮食脂肪修饰对 p-VA、总 f-SCFA、f-AA 和 f-BA 以及总 p-BCAA 的影响。