Chronic back pain is associated with decreased prefrontal and thalamic gray matter density

被引:1030
作者
Apkarian, AV
Sosa, Y
Sonty, S
Levy, RM
Harden, RN
Parrish, TB
Gitelman, DR
机构
[1] Northwestern Univ, Feinberg Sch Med, Dept Physiol, Chicago, IL 60611 USA
[2] Northwestern Univ, Feinberg Sch Med, Inst Neurosci, Chicago, IL 60611 USA
[3] Northwestern Univ, Feinberg Sch Med, Dept Neurol, Chicago, IL 60611 USA
[4] Northwestern Univ, Feinberg Sch Med, Dept Neurosurg, Chicago, IL 60611 USA
[5] Northwestern Univ, Feinberg Sch Med, Dept Radiol, Chicago, IL 60611 USA
[6] Northwestern Univ, Feinberg Sch Med, Rehabil Inst Chicago, Chicago, IL 60611 USA
关键词
chronic pain; morphometry; frontal cortex; thalamus; neuropathic back pain; aging;
D O I
10.1523/JNEUROSCI.2541-04.2004
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The role of the brain in chronic pain conditions remains speculative. We compared brain morphology of 26 chronic back pain (CBP) patients to matched control subjects, using magnetic resonance imaging brain scan data and automated analysis techniques. CBP patients were divided into neuropathic, exhibiting pain because of sciatic nerve damage, and non-neuropathic groups. Pain-related characteristics were correlated to morphometric measures. Neocortical gray matter volume was compared after skull normalization. Patients with CBP showed 5-11% less neocortical gray matter volume than control subjects. The magnitude of this decrease is equivalent to the gray matter volume lost in 10-20 years of normal aging. The decreased volume was related to pain duration, indicating a 1.3 cm(3) loss of gray matter for every year of chronic pain. Regional gray matter density in 17 CBP patients was compared with matched controls using voxel-based morphometry and nonparametric statistics. Gray matter density was reduced in bilateral dorsolateral prefrontal cortex and right thalamus and was strongly related to pain characteristics in a pattern distinct for neuropathic and non-neuropathic CBP. Our results imply that CBP is accompanied by brain atrophy and suggest that the pathophysiology of chronic pain includes thalamocortical processes.
引用
收藏
页码:10410 / 10415
页数:6
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