Effective connectivity predicts future placebo analgesic response: A dynamic causal modeling study of pain processing in healthy controls.
Effective connectivity predicts future placebo analgesic response: A dynamic causal modeling study of pain processing in healthy controls.
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DOI:
10.1016/j.neuroimage.2015.01.056
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发表时间:
2015-04-15
期刊:
影响因子:
5.7
通讯作者:
Robinson ME
中科院分区:
文献类型:
--
作者:
Sevel LS;O'Shea AM;Letzen JE;Craggs JG;Price DD;Robinson ME
A better understanding of the neural mechanisms underlying pain processing and analgesia may aid in the development and personalization of effective treatments for chronic pain. Clarification of the neural predictors of individual variability in placebo analgesia (PA) could aid in this process. The present study examined whether the strength of effective connectivity (EC) among pain-related brain regions could predict future placebo analgesic response in healthy individuals. In Visit 1, fMRI data were collected from 24 healthy subjects (13 female, mean age=22.56, SD=2.94) while experiencing painful thermal stimuli. During Visit 2, subjects were conditioned to expect less pain via a surreptitiously lowered temperature applied at two of the four sites on their feet. They were subsequently scanned again using the Visit 1 (painful) temperature. Subjects used an electronic VAS to rate their pain following each stimulus. Differences in ratings at conditioned and unconditioned sites were used to measure placebo response (PA scores). Dynamic causal modeling was used to estimate the EC among a set of brain regions related to pain processing at Visit 1 (periaqueductal gray, thalamus, rostral anterior cingulate cortex, dorsolateral prefrontal cortex). Individual PA scores from Visit 2 were regressed on salient EC parameters estimates from Visit 1. Results indicate that both greater left hemisphere modulatory DLPFC→PAG connectivity and right hemisphere, endogenous thalamus→DLPFC connectivity were significantly predictive of future placebo response (R2 = 0.82). To our knowledge, this is the first study to identify the value of EC in understanding individual differences in PA, and may suggest the potential modifiability of endogenous pain modulation.
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影响因子:
5.7
作者:
Craggs, Jason G.;Price, Donald D.;Robinson, Michael M.
通讯作者:
Robinson, Michael M.
影响因子:
7.4
作者:
Bingel, U;Lorenz, J;Büchel, C
通讯作者:
Büchel, C
DOI:
10.1523/jneurosci.3420-10.2011
发表时间:
2011-01-12
期刊:
The Journal of neuroscience : the official journal of the Society for Neuroscience
影响因子:
--
作者:
Wager TD;Atlas LY;Leotti LA;Rilling JK
通讯作者:
Rilling JK
影响因子:
4.3
作者:
Penny WD;Stephan KE;Daunizeau J;Rosa MJ;Friston KJ;Schofield TM;Leff AP
通讯作者:
Leff AP
影响因子:
5.3
作者:
Schweinhardt, Petra;Seminowicz, David A.;Bushnell, M. Catherine
通讯作者:
Bushnell, M. Catherine