S. Oguma et al., STABLE HUMAN T-LYMPHOTROPIC VIRUS TYPE-I CARRIER RATES FOR 7 YEARS AMONG A TEENAGED BLOOD-DONOR COHORT OF 1986 IN KUMAMOTO, JAPAN, Leukemia research, 19(8), 1995, pp. 567-571
The human T-lymphotropic virus type I (HTLV-I) carrier rates for blood
donors in Kumamoto, Kyushu, Japan for 8 years, 1986-1993, are current
ly available. The data show that 16-19-year-olds in 1986 and 20-29-yea
r-olds in 1993 represent nearly the same cohort, because the median ag
e in both groups is 24.5 years in 1993. Therefore, comparison of the H
TLV-I positive rate for the two groups gives an estimate of the change
in the rate over 7 years within the cohort. In males, 265 of 22,143 d
onors (1.20%) were seropositive for HTLV-I among 16-19-year-olds in 19
86, and 214 were seropositive among 20,076 (1.07%) donors in 20-29-yea
r-olds in 1993. In females, 203 were seropositive among 20,677 (0.98%)
donors in 16-19-year-olds in 1986, and 154 were seropositive among 18
,660 (0.83%) donors in 20-29-year-olds in 1993. Thus, the seropositive
rates declined in both sexes. However, the average annual rate of imm
igration to Kumamoto Prefecture was 2.37%. If seropositive rates for 2
0-29-year-olds in 1993 are adjusted for the dilution effect due to imm
igration (under the assumption that all immigrants were HTLV-I negativ
e), the adjusted carrier rate for males is 1.26% and that for females
is 0.98%. The adjusted carrier rates for both sexes are almost the sam
e as those for 16-19-year-olds in 1986. This indicates that horizontal
transmission was negligible for those in the cohort who were in their
early reproductive period. Using all 8 year carrier rates for 16-19-y
ear-olds and 20-29-year-olds, chronological changes of 20-29-year-olds
in the near future was estimated. The best goodness of fit model indi
cated that the HTLV-I carrier rate will decline exponentially, and tha
t the rate will decrease by 50% approximately every 10 years for both
sexes. It is probable that in recent years south-west Japan has lost t
he conditions that are favorable for HTLV-I endemicity and the virus w
ill be virtually non-endemic within a few generations.