Increased susceptibility to Kuru of carriers of the PRNP 129 methionine/methionine genotype

被引:105
作者
Lee, HS
Brown, P
Cervenáková, L
Garruto, RM
Alpers, MP
Gajdusek, DC
Goldfarb, LG
机构
[1] NINDS, Clin Neurogenet Unit, NIH, Bethesda, MD 20892 USA
[2] NINDS, Cent Nervous Syst Studies Lab, NIH, Bethesda, MD 20892 USA
[3] Amer Red Cross, JH Holland Lab, Rockville, MD USA
[4] SUNY Binghamton, Dept Anthropol, Binghamton, NY USA
[5] Inst Med Res, Goroka, Papua N Guinea
[6] Inst Alfred Fessard, CNRS, Gif Sur Yvette, France
关键词
D O I
10.1086/317935
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Kuru reached epidemic proportions by the mid-twentieth century among the Fore people of New Guinea and disappeared after the abolition of cannibalistic rituals. To determine susceptibility to kuru and its role in the spread and elimination of the epidemic, we analyzed the PRNP gene coding sequences in 5 kuru patients; no germline mutations were found. Analysis of the PRNP 129 methionine (M)/valine (V) polymorphism in 80 patients and 95 unaffected controls demonstrated that the kuru epidemic preferentially affected individuals with the M/M genotype. A higher representation of M/M carriers was observed among the affected young Fore males entering the age of risk, whereas a lower frequency of M/M homozygotes was found among the survivors. M/V and V/V genotypes predisposed to a lower risk of disease development and longer incubation times. These findings are relevant to the current outbreak of variant Creutzfeldt-Jakob disease (vCJD) in the United Kingdom, because all vCJD patients tested thus far have been M/M carriers.
引用
收藏
页码:192 / 196
页数:5
相关论文
共 28 条
[21]  
KLITZMAN R L, 1984, Neuroepidemiology, V3, P3, DOI 10.1159/000110837
[22]   Is the neuropathology of new variant Creutzfeldt-Jakob disease and kuru similar? [J].
Lantos, PL ;
Bhatia, K ;
AlSarraj, S ;
Doshi, R ;
Beck, J ;
Collinge, J .
LANCET, 1997, 350 (9072) :187-188
[23]  
McLean CA, 1998, BRAIN PATHOL, V8, P429
[24]  
NEI M, 1972, THEOR POPUL BIOL, V3, P460, DOI 10.1016/0040-5809(72)90017-2
[25]   HOMOZYGOUS PRION PROTEIN GENOTYPE PREDISPOSES TO SPORADIC CREUTZFELDT-JAKOB DISEASE [J].
PALMER, MS ;
DRYDEN, AJ ;
HUGHES, JT ;
COLLINGE, J .
NATURE, 1991, 352 (6333) :340-342
[26]  
WEISENFELD SL, 1975, AM J HUM GENET, V27, P498
[27]  
Will RG, 2000, ANN NEUROL, V47, P575
[28]   A new variant of Creutzfeldt-Jakob disease in the UK [J].
Will, RG ;
Ironside, JW ;
Zeidler, M ;
Cousens, SN ;
Estibeiro, K ;
Alperovitch, A ;
Poser, S ;
Pocchiari, M ;
Hofman, A ;
Smith, PG .
LANCET, 1996, 347 (9006) :921-925