The sera of 38 patients with nonalcoholic fatty liver disease (NAFLD) inclu
ding nonalcoholic steatohepatitis (NASH), were tested for TT virus (TTV) DN
A by polymerase chain reaction (PCR) using three different primer pairs (UT
R PCR, N22 PCR and genotype-l PCR), and various histological features of th
e liver biopsy specimens were compared among those who were positive or neg
ative for TTV infection. By UTR PCR which detects all TTV genotypes, TTV DN
A was detected in 37 (97%) of the 38 patients. In contrast, N22 PCR which d
etects primarily TTV genotypes 1-4, detected TTV DNA in 18 patients (47%).
In the liver biopsy specimens, moderate to many acidophilic bodies, moderat
e to marked focal/ spotty necrosis of hepatocytes and marked stellate, peri
cellular or perivenular fibrosis were observed significantly more frequentl
y among those who were positive for TTV DNA by N22 PCR, than among those wh
o were negative by N22 PCR. Twelve patients (32%) were positive for TTV gen
otype 1. Moderate to marked vacuolation of nuclei, moderate to many acidoph
ilic bodies, and moderate to marked focal/spotty necrosis as well as marked
stellate, pericellular or perivenular fibrosis were found significantly mo
re frequently in the TTV genotype 1-positive group than in the TTV genotype
1-negative group. These results suggest that certain TTV genotypes includi
ng genotype 1 influence the necrosis and inflammation of hepatocytes and li
ver fibrosis in NAFLD patients. (C) 2001 Elsevier Science Ireland Ltd. All
rights reserved.