Hirano M, Cleary J M, Stewart A M, Lincoff N S, Odel J G, Santiesteban R, Santiago Luis R
H. Houston Merritt Clinical Research Center for Muscular Dystrophy and Related Disorders, Department of Neurology, Columbia University College of Physicians and Surgeons, New York, NY 10032.
Neurology. 1994 May;44(5):843-5. doi: 10.1212/wnl.44.5.843.
Since October 1991, nearly 51,000 Cubans have been afflicted in an outbreak of optic and peripheral neuropathies. To begin an investigation of the possible role of mitochondrial DNA (mtDNA) mutations in the outbreak, we studied mtDNA from 14 affected and two unaffected Cubans for the 12 mutations associated with Leber's hereditary optic neuropathy. Eleven probands (12 patients) had optic neuropathy and two had peripheral neuropathy only. We also studied two unaffected relatives of one proband. We identified two mtDNA mutations, at nucleotides 11778 and 3460, in two of the 11 probands with optic neuropathy. Although this data set is too small to reach statistically valid conclusions, it does suggest that mtDNA mutations might be contributing to the outbreak of optic neuropathy in Cuba.
自1991年10月以来,近5.1万名古巴人在一场视神经和周围神经病变疫情中患病。为了调查线粒体DNA(mtDNA)突变在此次疫情中可能起到的作用,我们研究了14名患病古巴人和2名未患病古巴人的mtDNA,检测与Leber遗传性视神经病变相关的12种突变。11名先证者(12名患者)患有视神经病变,2名仅患有周围神经病变。我们还研究了一名先证者的两名未患病亲属。在11名患有视神经病变的先证者中,我们在两名患者身上发现了位于核苷酸11778和3460处的两种mtDNA突变。尽管这个数据集太小,无法得出具有统计学意义的有效结论,但确实表明mtDNA突变可能与古巴视神经病变疫情有关。