The Mitochondrial and Metabolic Disease Center, University of California San Diego School of Medicine, San Diego, California, United States of America.
Department of Medicine, Division of Medical Genetics, University of California San Diego School of Medicine, San Diego, California, United States of America.
PLoS One. 2019 Jul 26;14(7):e0219531. doi: 10.1371/journal.pone.0219531. eCollection 2019.
More than 230,000 veterans-about 1/3 of US personnel deployed in the 1990-1991 Persian Gulf War-developed chronic, multi-symptom health problems now called "Gulf War illness" (GWI), for which mechanisms and objective diagnostic signatures continue to be sought.
Targeted, broad-spectrum serum metabolomics was used to gain insights into the biology of GWI. 40 male participants, included 20 veterans who met both Kansas and CDC diagnostic criteria for GWI and 20 nonveteran controls without similar symptoms that were 1:1 matched to GWI cases by age, sex, and ethnicity. Serum samples were collected and archived at -80° C prior to testing. 358 metabolites from 46 biochemical pathways were measured by hydrophilic interaction liquid chromatography and tandem mass spectrometry.
Veterans with GWI, compared to healthy controls, had abnormalities in 8 of 46 biochemical pathways interrogated. Lipid abnormalities accounted for 78% of the metabolic impact. Fifteen ceramides and sphingomyelins, and four phosphatidylcholine lipids were increased. Five of the 8 pathways were shared with the previously reported metabolic phenotype of males with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS). However, 4 of the 5 shared pathways were regulated in opposite directions; key pathways that were up-regulated in GWI were down-regulated in ME/CFS. The single pathway regulated in the same direction was purines, which were decreased.
Our data show that despite heterogeneous exposure histories, a metabolic phenotype of GWI was clearly distinguished from controls. Metabolomic differences between GWI and ME/CFS show that common clinical symptoms like fatigue can have different chemical mechanisms and different diagnostic implications. Larger studies will be needed to validate these findings.
超过 230,000 名退伍军人——约占 1990-1991 年波斯湾战争中部署的美国人员的 1/3——出现了慢性、多症状的健康问题,现在被称为“海湾战争病”(GWI),目前仍在寻找其发病机制和客观诊断特征。
采用靶向、广谱血清代谢组学方法深入了解 GWI 的生物学特性。共纳入 40 名男性参与者,包括 20 名符合堪萨斯和疾病控制与预防中心(CDC)GWI 诊断标准的退伍军人和 20 名无类似症状的非退伍军人对照者,通过年龄、性别和种族与 GWI 病例 1:1 匹配。在检测前,将血清样本收集并保存在-80°C。通过亲水相互作用液相色谱和串联质谱法测量了来自 46 种生化途径的 358 种代谢物。
与健康对照组相比,患有 GWI 的退伍军人在 46 种生化途径中有 8 种出现异常。脂质异常占代谢影响的 78%。15 种神经酰胺和神经鞘磷脂以及 4 种磷脂酰胆碱脂质增加。与先前报道的男性肌痛性脑脊髓炎/慢性疲劳综合征(ME/CFS)的代谢表型共享的有 8 种途径中的 5 种。然而,在 GWI 中上调的 4 个途径与 ME/CFS 相反;在 GWI 中上调的关键途径在 ME/CFS 中下调。在相同方向调节的唯一途径是嘌呤,其减少。
我们的数据表明,尽管接触史存在异质性,但 GWI 的代谢表型与对照组明显不同。GWI 和 ME/CFS 之间的代谢差异表明,像疲劳这样的常见临床症状可能具有不同的化学机制和不同的诊断意义。需要更大规模的研究来验证这些发现。