Bioinformatics Research Center, University of North Carolina at Charlotte, USA.
FASEB J. 2010 Aug;24(8):2962-75. doi: 10.1096/fj.09-154054. Epub 2010 Apr 6.
Choline is an essential nutrient, and deficiency causes liver and muscle dysfunction. Common genetic variations alter the risk of developing organ dysfunction when choline deficient, probably by causing metabolic inefficiencies that should be detectable even while ingesting a normal choline-adequate diet. We determined whether metabolomic profiling of plasma at baseline could predict whether humans will develop liver dysfunction when deprived of dietary choline. Fifty-three participants were fed a diet containing 550 mg choline/70 kg/d for 10 d and then fed < 50 mg choline/70 kg/d for up to 42 d. Participants who developed organ dysfunction on this diet were repleted with a choline-adequate diet for > or = 3 d. Plasma samples, obtained at baseline, end of depletion, and end of repletion, were used for targeted and nontargeted metabolomic profiling. Liver fat was assessed using magnetic resonance spectroscopy. Metabolomic profiling and targeted biochemical analyses were highly correlated for the analytes assessed by both procedures. In addition, we report relative concentration changes of other small molecules detected by the nontargeted metabolomic analysis after choline depletion. Finally, we show that metabolomic profiles of participants when they were consuming a control baseline diet could predict whether they would develop liver dysfunction when deprived of dietary choline.
胆碱是一种必需的营养物质,缺乏会导致肝脏和肌肉功能障碍。常见的遗传变异会增加在胆碱缺乏时发生器官功能障碍的风险,这可能是由于代谢效率低下所致,即使在摄入正常胆碱充足的饮食时,这些代谢效率低下也应该是可以检测到的。我们确定了基线时血浆代谢组学分析是否可以预测人类在缺乏饮食胆碱时是否会发生肝功能障碍。53 名参与者在 10 天内摄入含有 550mg 胆碱/70kg/d 的饮食,然后摄入<50mg 胆碱/70kg/d,最长可达 42 天。在这种饮食下出现器官功能障碍的参与者用胆碱充足的饮食补充>或=3 天。在基线、耗竭结束和补充结束时采集血浆样本,用于靶向和非靶向代谢组学分析。使用磁共振波谱法评估肝脂肪。代谢组学分析和靶向生化分析对于两种方法评估的分析物高度相关。此外,我们还报告了在胆碱耗尽后通过非靶向代谢组学分析检测到的其他小分子的相对浓度变化。最后,我们表明,参与者在摄入对照基线饮食时的代谢组学特征可以预测他们在缺乏饮食胆碱时是否会发生肝功能障碍。