Unità Operativa di Endocrinologia, Ospedale Pediatrico Bambino Gesù, Roma, Italy.
J Inherit Metab Dis. 2012 Sep;35(5):899-907. doi: 10.1007/s10545-011-9432-3. Epub 2011 Dec 22.
X-linked adrenoleukodystrophy is a rare inherited demyelinating disorder characterized by an abnormal accumulation of very long chain fatty acids, mainly hexacosanoic acid (26:0), due to a mutation of the gene encoding for a peroxisomal membrane protein. The only available, and partially effective, therapeutic treatment consists of dietary intake of a 4:1 mixture of triolein and trierucin, called Lorenzo's oil (LO), targeted to inhibit the elongation of docosanoic acid (22:0) to 26:0. In this study we tested whether, besides inhibiting elongation, an enhancement of peroxisomal beta oxidation induced by conjugated linoleic acid (CLA), will improve somatosensory evoked potentials and modify inflammatory markers in adrenoleukodystrophy females carriers. We enrolled five heterozygous women. They received a mixture of LO (40 g/day) with CLA (5 g/day) for 2 months. The therapeutic efficacy was evaluated by the means of plasma levels of 26:0, 26:0/22:0 ratio, modification of cerebrospinal fluid (CSF) inflammatory markers and somatosensory evoked potentials. Changes of fatty acid profile, and in particular CLA incorporation, were also evaluated in CSF and plasma. The results showed that CLA promptly passes the blood brain barrier and the mixture was able to lower both 26:0 and 26:0/22:0 ratio in plasma. The mixture improved somatosensory evoked potentials, which were previously found unchanged or worsened with dietary LO alone, and reduced IL-6 levels in CSF in three out of five patients. Our data suggest that the synergic activity of CLA and LO, by enhancing peroxisomal beta-oxidation and preventing 26:0 formation, improves the somatosensory evoked potentials and reduces neuroinflammation.
X 连锁肾上腺脑白质营养不良是一种罕见的遗传性脱髓鞘疾病,其特征是由于编码过氧化物酶体膜蛋白的基因突变,导致极长链脂肪酸(主要是二十六烷酸(26:0))异常积累。唯一可用的、部分有效的治疗方法是摄入 4:1 的三油酸甘油酯和三油精混合物,称为洛伦佐油(LO),以抑制二十二烷酸(22:0)延伸为 26:0。在这项研究中,我们测试了共轭亚油酸(CLA)是否除了抑制延伸外,还能增强过氧化物酶体β氧化,从而改善肾上腺脑白质营养不良女性携带者的体感诱发电位并改变炎症标志物。我们招募了五名杂合女性。她们接受 LO(40 g/天)和 CLA(5 g/天)混合物治疗 2 个月。通过测定血浆 26:0、26:0/22:0 比值、脑脊液(CSF)炎症标志物和体感诱发电位来评估治疗效果。还评估了 CSF 和血浆中脂肪酸谱的变化,特别是 CLA 的掺入。结果表明,CLA 迅速穿透血脑屏障,该混合物能够降低血浆中 26:0 和 26:0/22:0 比值。该混合物改善了体感诱发电位,先前发现单独用 LO 饮食治疗时体感诱发电位不变或恶化,并且在五名患者中的三名中降低了 CSF 中的 IL-6 水平。我们的数据表明,CLA 和 LO 的协同作用通过增强过氧化物酶体β氧化和防止 26:0 形成,改善了体感诱发电位并减轻了神经炎症。