CLINICAL-FEATURES OF JAPANESE LEPERS HEREDITARY OPTIC NEUROPATHY WITH MUTATION-11778 OF MITOCHONDRIAL-DNA

被引:0
|
作者
HOTTA, Y
FUJIKI, K
HAYAKAWA, M
NAKAJIMA, A
KANAI, A
MASHIMA, Y
HIIDA, Y
SHINODA, K
YAMADA, K
OGUCHI, Y
ISHIDA, M
YANASHIMA, K
WAKAKURA, M
ISHIKAWA, S
NAKAMURA, M
SAKAI, J
YAMAMOTO, M
HAYASHI, T
MITANI, I
MIYAZAKI, S
SHIMOOKU, M
IMACHI, J
KUNIYOSHI, N
NAGATAKI, S
ISASHIKI, Y
OHBA, N
机构
[1] KEIO UNIV,SCH MED,TOKYO,JAPAN
[2] NATL REHABIL CTR DISABLED,TOKOROZAWA,SAITAMA,JAPAN
[3] KITASATO UNIV,SCH MED,SAGAMIHARA,KANAGAWA 228,JAPAN
[4] KOBE UNIV,SCH MED,KOBE 650,JAPAN
[5] HYOGO MED UNIV,NISHINOMIYA,HYOGO,JAPAN
[6] UNIV RYUKYUS,FAC MED,OKINAWA,JAPAN
[7] KAGOSHIMA UNIV,FAC MED,KAGOSHIMA 890,JAPAN
关键词
CLINICAL FEATURES; LEBERS HEREDITARY OPTIC NEUROPATHY; MITOCHONDRIAL DNA; MULTIINSTITUTIONAL STUDY; 11778 POINT MUTATION;
D O I
暂无
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
The G to A transition of nucleotide position (nt) 11778 of mitochondrial DNA (mtDNA) has been frequently observed in Japanese Leber's hereditary optic neuropathy (LHON) cases. Therefore, we performed a multi-institutional study in Japan of LHON cases with this 11778 mutation of the mtDNA. Genetic and clinical data on 108 cases (90 affected and 18 carriers) in 79 unrelated families were obtained from 64 Japanese institutions. Detection of the nt11778 mutation was performed using restriction enzymes (74 cases) or dot blot with allele specific oligonucleotide (34 cases). Heteroplasmy was observed in 13 of the 90 affected cases and in 8 of the 18 carrier cases. Forty-five families had family history of LHON (44 maternal inheritance, 1 undetermined), and in 28 families (35.9%) there were isolated cases. The male-to-female ratio in the affected was 82:7 (92.1% male). The age at onset of visual loss ranged from 7 to 59 years (average: 23.4 years). All cases had bilateral involvement except one case with a blind eye resulting from ocular infection during childhood. Onset interval between the two eyes ranged from simultaneous to 17 months (average: 2.5 months), in 91.3% of cases being under 6 months. Visual acuity was 0.1 or worse in 152 (85.9%) of 177 eyes, only 6 eyes showing over 0.5. Progression of visual loss ranged from 0 to 48 months (average: 6.2 months). Central visual field abnormality was observed in 162 eyes (96.4%) of 168 eyes. Nonsuspect fundus in the ophthalmoscopic examination constituted 22.8% of eyes. Systemic corticosteroid was given to 45 (52.9%) of 85 cases and visual acuity was improved in only 2 cases (4.4%). Arrhythmia, neurological and muscular abnormality were observed as rare general complications. The present survey indicates that the male-to-female ratio is higher than the previous Japanese LHON statistics and that the visual outcome is better than in American LHON cases with the 11778 mutation.
引用
收藏
页码:96 / 108
页数:13
相关论文
共 50 条
  • [1] CLINICAL-FEATURES OF JAPANESE LEBERS HEREDITARY OPTIC NEUROPATHY WITH THE 11778 MUTATION
    HOTTA, Y
    ARA, F
    FUJIKI, K
    NAKAJIMA, A
    KANAI, A
    MASHIMA, Y
    HIIDA, Y
    SHINODA, K
    YAMADA, K
    OGUCHI, Y
    WAKAKURA, M
    ISHIKAWA, S
    NAKAMURA, M
    SAKAI, J
    YAMAMOTO, M
    HAYASHI, T
    MITANI, I
    MIYAZAKI, S
    SHIMOOKU, M
    IMACHI, J
    ISASHIKI, Y
    OHBA, N
    KUNIYOSHI, N
    NAGATAKI, S
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 1994, 35 (04) : 1542 - 1542
  • [2] THE CLINICAL-FEATURES OF LEBERS HEREDITARY OPTIC NEUROPATHY DEFINED BY THE PRESENCE OF A PATHOGENIC MITOCHONDRIAL-DNA MUTATION
    RIORDANEVA, P
    SANDERS, MD
    GOVAN, GG
    SWEENEY, MG
    DACOSTA, J
    HARDING, AE
    BRAIN, 1995, 118 : 319 - 337
  • [3] HIGH PREVALENCE OF THE NT-11778 MUTATION IN MITOCHONDRIAL-DNA IN JAPANESE LEBERS HEREDITARY OPTIC NEUROPATHY WITH CLINICAL HETEROGENEITY
    SHINODA, K
    MASHIMA, Y
    HIIDA, Y
    OGUCHI, Y
    WAKAKURA, M
    KAWASAKI, T
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 1993, 34 (04) : 1123 - 1123
  • [4] A MUTATION OF MITOCHONDRIAL-DNA IN JAPANESE FAMILIES WITH LEBERS HEREDITARY OPTIC NEUROPATHY
    FUJIKI, K
    HOTTA, Y
    HAYAKAWA, M
    SAITO, K
    ARA, F
    UEDA, S
    GOTO, T
    ISHIDA, M
    YANASHIMA, K
    SHIONO, T
    SAKAI, J
    KANAI, A
    NAKAJIMA, A
    JAPANESE JOURNAL OF HUMAN GENETICS, 1991, 36 (02): : 143 - 147
  • [5] MITOCHONDRIAL-DNA MUTATION IN LEBERS HEREDITARY OPTIC NEUROPATHY
    YEN, MY
    YEN, TC
    PANG, CY
    LIU, JH
    WEI, YH
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 1992, 33 (08) : 2561 - 2566
  • [6] MITOCHONDRIAL-DNA MUTATION ASSOCIATED WITH LEBERS HEREDITARY OPTIC NEUROPATHY
    WALLACE, DC
    SINGH, G
    LOTT, MT
    HODGE, JA
    SCHURR, TG
    LEZZA, AMS
    ELSAS, LJ
    NIKOSKELAINEN, EK
    SCIENCE, 1988, 242 (4884) : 1427 - 1430
  • [7] A MITOCHONDRIAL-DNA MUTATION AS A CAUSE OF LEBERS HEREDITARY OPTIC NEUROPATHY
    SINGH, G
    LOTT, MT
    WALLACE, DC
    NEW ENGLAND JOURNAL OF MEDICINE, 1989, 320 (20): : 1300 - 1305
  • [8] MITOCHONDRIAL-DNA MUTATION IN FAMILY WITH LEBERS HEREDITARY OPTIC NEUROPATHY
    YONEDA, M
    TSUJI, S
    YAMAUCHI, T
    INUZUKA, T
    MIYATAKE, T
    HORAI, S
    OZAWA, T
    LANCET, 1989, 1 (8646): : 1076 - 1077
  • [9] Hereditary cerebellar ataxia with Leber's hereditary optic neuropathy mitochondrial DNA 11778 mutation
    Murakami, T
    Mita, S
    Tokunaga, M
    Maeda, H
    Ueyama, H
    Kumamoto, T
    Uchino, M
    Ando, M
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 1996, 142 (1-2) : 111 - 113
  • [10] Penetrance of leber hereditary optic neuropathy in Chinese individuals with mitochondrial DNA 11778 mutation
    Zhang, Q.
    Guo, X.
    Jia, X.
    Xiao, X.
    Guo, L.
    Li, S.
    Chinese Journal of Medical Genetics, 2001, 18 (06) : 441 - 443