A multisite validation of brain white matter pathways of resilience to chronic back pain.
Autor: | Mišić M; Institute of Cognitive and Clinical Neuroscience, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany., Lee N; Department of Psychiatry, University of Rochester Medical Center, Rochester, United States., Zidda F; Institute of Cognitive and Clinical Neuroscience, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany., Sohn K; Department of Statistics and Operations Research, University of North Carolina, Chapel Hill, Rochester, United States., Usai K; Institute of Cognitive and Clinical Neuroscience, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany., Löffler M; Institute of Cognitive and Clinical Neuroscience, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.; Department of Experimental Psychology, Heinrich Heine University Düsseldorf, Düsseldorf, Germany., Uddin MN; Department of Neurology, University of Rochester Medical Center, Rochester, United States., Farooqi A; Department of Psychiatry, University of Rochester Medical Center, Rochester, United States., Schifitto G; Department of Neurology, University of Rochester Medical Center, Rochester, United States., Zhang Z; Department of Statistics and Operations Research, University of North Carolina, Chapel Hill, Rochester, United States., Nees F; Institute of Cognitive and Clinical Neuroscience, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.; Institute of Medical Psychology and Medical Sociology, University Medical Center Schleswig Holstein, Kiel University, Kiel, Germany., Geha P; Department of Psychiatry, University of Rochester Medical Center, Rochester, United States., Flor H; Institute of Cognitive and Clinical Neuroscience, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany. |
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Jazyk: | angličtina |
Zdroj: | ELife [Elife] 2024 Dec 24; Vol. 13. Date of Electronic Publication: 2024 Dec 24. |
DOI: | 10.7554/eLife.96312 |
Abstrakt: | Chronic back pain (CBP) is a global health concern with significant societal and economic burden. While various predictors of back pain chronicity have been proposed, including demographic and psychosocial factors, neuroimaging studies have pointed to brain characteristics as predictors of CBP. However, large-scale, multisite validation of these predictors is currently lacking. In two independent longitudinal studies, we examined white matter diffusion imaging data and pain characteristics in patients with subacute back pain (SBP) over 6- and 12-month periods. Diffusion data from individuals with CBP and healthy controls (HC) were analyzed for comparison. Whole-brain tract-based spatial statistics analyses revealed that a cluster in the right superior longitudinal fasciculus (SLF) tract had larger fractional anisotropy (FA) values in patients who recovered (SBPr) compared to those with persistent pain (SBPp), and predicted changes in pain severity. The SLF FA values accurately classified patients at baseline and follow-up in a third publicly available dataset (Area under the Receiver Operating Curve ~0.70). Notably, patients who recovered had FA values larger than those of HC suggesting a potential role of SLF integrity in resilience to CBP. Structural connectivity-based models also classified SBPp and SBPr patients from the three data sets (validation accuracy 67%). Our results validate the right SLF as a robust predictor of CBP development, with potential for clinical translation . Cognitive and behavioral processes dependent on the right SLF, such as proprioception and visuospatial attention, should be analyzed in subacute stages as they could prove important for back pain chronicity. Competing Interests: MM, NL, FZ, KS, KU, ML, MU, AF, GS, ZZ, FN, PG, HF No competing interests declared (© 2024, Mišić, Lee et al.) |
Databáze: | MEDLINE |
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