Thrombotic microangiopathy is one of the complications of bone marrow trans
plantation and is related to other complications such as graft-versus-host
disease, veno-occlusive disease, diffuse alveolar hemorrhage, and cytomegal
ovirus infection. Thrombotic microangiopathy occurred in three out of 12 pa
tients who underwent allogeneic bone marrow transplantation over the past 1
year at our department. We compared the changes in cytokines and other mol
ecules between patients with and without microangiopathy from before condit
ioning to the early post-transplantation period. All three patients with mi
croangiopathy showed a significant increase of interleukin-12 at the time o
f leukocyte recovery after transplantation (two-way layout analysis of vari
ance; P < 0.05), while none of the patients without microangiopathy showed
an increase of interleukin-12. No significant differences were found betwee
n the two groups with respect to the other cytokines and molecules that wer
e tested. These findings suggested that thrombotic microangiopathy might be
predicted at an early stage after bone marrow transplantation by detecting
an increase of interleukin-12 at the time of leukocyte recovery. The possi
bility that thrombotic microangiopathy is related to inflammation or autoim
munity was also suggested.