A morphometric study of the peripheral nervous system at autopsy was u
ndertaken in 11 AIDS patients and 10 controls, The left L4, L5, and Sf
dorsal root ganglia (DRG) and samples of the sciatic nerve at the but
tock, tibial nerve at the knee, and sural nerve at the ankle were coll
ected. Indices of neuronal/axonal degeneration and of segmental demyel
ination/ remyelination were measured at each level. The small number o
f cases and evidence of neuropathy in a number of the control cases re
sulted in statistical significance for only a limited number of compar
isons. Nodules of Nageotte in the DRG were increased fivefold in AIDS
cases compared with controls, and axonal degeneration in single-teased
nerve fibers was increased 9-fold in the sciatic nerve, 28-fold in th
e tibial nerve, and 12-fold in the sural nerve. The ratios of AIDS to
controls for the density of remaining DRG neurons and large myelinated
axons were reduced to 0.71 in the DRG, 0.84 in the sciatic nerve, 0.8
4 in the tibial nerve, and 0.66 in the sural nerve. Axonal regeneratio
n in single-teased nerve fibers was increased threefold at the sciatic
nerve level in AIDS, but was markedly reduced at distal levels. Acute
segmental demyelination in single-teased nerve fibers was present to
a greater extent than in controls at all levels of the peripheral nerv
es in the AIDS cases. Remyelinating fibers were increased compared wit
h controls only in the proximal sciatic nerve, No case showed the chan
ges of cytomegalovirus infection. In a parallel immunohistochemical st
udy of these AIDS peripheral nerves, T-cell and macrophage infiltratio
n, with cytokine expression, was demonstrated. The pathological proces
s in the neuropathy of terminal AIDS appears to be a multifocal immuno
logically mediated inflammatory disease, with increased density of mac
rophages and T cells at all levels of the peripheral nervous system, p
roducing segmental demyelination and axonal degeneration. Reparative p
rocesses (axonal regeneration and remyelination) occurred only at the
most proximal levels of the nerves. (C) 1998 John Wiley & Sons, Inc.