P. Brown et al., IATROGENIC CREUTZFELDT-JAKOB-DISEASE - AN EXAMPLE OF THE INTERPLAY BETWEEN ANCIENT GENES AND MODERN MEDICINE, Neurology, 44(2), 1994, pp. 291-293
We tested DNA from 15 centrally infected cases of iatrogenic Creutzfel
dt-Jakob disease (CJD) (dura mater or corneal homografts and stereotac
tic EEG electrodes), 11 peripherally infected cases (native human grow
th hormone or gonadotrophin), and 110 control individuals for the pres
ence of mutations in the chromosome 20 amyloid gene. No patient or con
trol had any of the known pathogenic point or insert mutations found i
n familial disease, but allelic homozygosity at polymorphic codon 129
was present in all but two (92%) of the 26 patients, compared with 54
(50%) of the 110 controls (p < 0.001). Pooled data from all identified
and tested cases of iatrogenic disease yielded a worldwide total of 5
6 patients, of whom all but four were homozygous at codon 129 (p < 0.0
01). These findings support the thesis that homozygosity at codon 129
enhances susceptibility to iatrogenic infections of both central and p
eripheral origin, with evident implications for the population of dura
mater homograft and pituitary hormone recipients whose lives have bee
n complicated by the possibility of exposure to the infectious agent o
f CJD.