Picornaviruses may not play a role as persistent agents in the inflamm
atory myopathies, but it is still thought likely that they may act as
triggers of an autoimmune process. Forty one muscle biopsy specimens,
taken from three weeks to six months (mean four months) after onset, w
ere examined using three different picornaviral primers and PCR. Moder
ate to severe disease activity was evident in all specimens. The resul
ts were compared with those of 18 biopsy specimens examined later in t
he disease course, and with specimens from 27 patients with noninflamm
atory myopathies. All results were negative. Thus, even as early as th
ree weeks after clinical disease appears, picornaviruses are not detec
table in these disorders.