• J Pain · Jun 2022

    The relationship between experienced discrimination and pronociceptive processes in Native Americans: Results from the Oklahoma Study of Native American Pain Risk.

    • Yvette M Güereca, Parker A Kell, Bethany L Kuhn, Natalie Hellman, Cassandra A Sturycz, Tyler A Toledo, Felicitas A Huber, Mara Demuth, Edward W Lannon, Shreela Palit, Joanna O Shadlow, and Jamie L Rhudy.
    • Department of Psychology, The University of Tulsa, Tulsa, Oklahoma.
    • J Pain. 2022 Jun 1; 23 (6): 100610241006-1024.

    AbstractNative Americans (NAs) have higher pain rates than the general U.S. population. It has been found that increased central sensitization and reduced pain inhibition are pronociceptive processes that increase pain risk; yet, little attention has focused on the influence of psychosocial factors. Discrimination is a psychosocial factor associated with increased pain in other minoritized groups; however, it is unclear whether it also promotes pain in NAs. This study analyzed data from 269 healthy, pain-free participants (N = 134 non-Hispanic whites [NHWs], N = 135 NAs) from the Oklahoma Study of Native American Pain Risk. Experienced discrimination was measured using the Everyday Discrimination Scale (EDS). Nociceptive processes were measured via static measures of spinal sensitivity (nociceptive flexion reflex [NFR] threshold, 3-stimulation NFR threshold), temporal summation of pain (TS-Pain) and nociceptive flexion reflex (TS-NFR), and conditioned pain modulation of pain (CPM-Pain) and NFR (CPM-NFR). Results demonstrated that greater discrimination was associated with enhanced TS-NFR and impaired CPM-NFR but not static measures of spinal sensitivity or measures of pain modulation (TS-Pain, CPM-Pain). Although the effects of discrimination on outcomes were similar in both groups (not moderated by ethnicity), NAs experienced higher levels of discrimination and therefore discrimination mediated a relationship between ethnicity and impaired CPM-NFR. This indicates experienced discrimination may promote a pain risk phenotype in NAs that involves spinal sensitization resulting from impaired inhibition of spinal nociception without sensitization of pain experience. PERSPECTIVE: This study found that discrimination was associated with spinal sensitization and impaired descending inhibition of spinal nociception. These findings bolster our understanding of how social stressors experienced disproportionately by minoritized groups can contribute to pain outcomes.Copyright © 2022 United States Association for the Study of Pain, Inc. All rights reserved.

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