Genetics Division, Department of Pediatrics, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
J Pediatr. 2013 May;162(5):999-1003. doi: 10.1016/j.jpeds.2012.10.015. Epub 2012 Nov 16.
To determine whether levels of melatonin in blood and urine can serve as a peripheral biomarker to reflect brain serotonin synthesis in individuals with phenylketonuria (PKU).
We measured the levels of melatonin, a serotonin metabolite in the pinealocytes, in the blood and urine of individuals with PKU in a randomized double-blind placebo controlled crossover study consisting of three 3-week phases in 10 adults with PKU: phase 1 (washout), phase 2 (supplementation of large neutral amino acid [LNAA] tablets or placebo), and phase 3 (alternate supplementation). An overnight protocol to measure blood melatonin and urine 6-sulfatoxymelatonin and dopamine in first void urine specimens was conducted after each phase for subjects with PKU and once in 10 controls.
Significantly lower concentrations of these neurotransmitter metabolites were observed in subjects with PKU after phase 1 compared with controls (serum melatonin P = .008, urine melatonin P = .0043, urine dopamine P < .0001), with significant increases after LNAA supplementation compared with the placebo phase (serum melatonin P = .0008, urine melatonin P = .0008, urine dopamine P = .0005). The mean tryptophan/LNAA and tyrosine/LNAA ratios were markedly lower in subjects with PKU compared with controls, and these ratios were significantly increased in the LNAA phase compared with the placebo phase (P = .016, P = .0003, respectively). Blood phenylalanine levels in subjects with PKU were not significantly different between placebo and LNAA phases (P = .74).
Blood and urine melatonin levels may serve as biomarkers reflecting brain serotonin synthesis in subjects with PKU. Because this cannot be evaluated using blood phenylalanine levels, it may provide information on neurotransmitter metabolism for optimal dietary management.
确定血液和尿液中的褪黑素水平是否可以作为反映苯丙酮尿症(PKU)个体大脑 5-羟色胺合成的外周生物标志物。
我们在一项随机、双盲、安慰剂对照交叉研究中测量了 10 名 PKU 患者的血液和尿液中的褪黑素水平,该研究包括三个为期 3 周的阶段:第 1 阶段(洗脱期)、第 2 阶段(补充大中性氨基酸 [LNAA] 片剂或安慰剂)和第 3 阶段(交替补充)。在每个阶段结束后,对 PKU 患者进行了一夜之间的协议,以测量血液褪黑素和首次晨尿标本中的 6-硫酸褪黑素和多巴胺,并且在 10 名对照者中进行了一次测量。
与对照组相比,第 1 阶段后 PKU 患者的这些神经递质代谢物的浓度明显降低(血清褪黑素 P =.008,尿液褪黑素 P =.0043,尿液多巴胺 P <.0001),与安慰剂阶段相比,LNAA 补充后明显增加(血清褪黑素 P =.0008,尿液褪黑素 P =.0008,尿液多巴胺 P =.0005)。与对照组相比,PKU 患者的色氨酸/LNAA 和酪氨酸/LNAA 比值明显降低,与安慰剂阶段相比,LNAA 阶段的这些比值明显升高(P =.016,P =.0003)。PKU 患者的血液苯丙氨酸水平在安慰剂和 LNAA 阶段之间无显著差异(P =.74)。
血液和尿液中的褪黑素水平可能作为反映 PKU 个体大脑 5-羟色胺合成的生物标志物。因为这不能通过血液苯丙氨酸水平来评估,所以它可以为最佳饮食管理提供有关神经递质代谢的信息。