scholarly journals Heritability of pain catastrophizing and associations with experimental pain outcomes

Pain ◽  
2015 ◽  
Vol 156 (3) ◽  
pp. 514-520 ◽  
Author(s):  
Zina Trost ◽  
Eric Strachan ◽  
Michael Sullivan ◽  
Tine Vervoort ◽  
Ally R. Avery ◽  
...  
2021 ◽  
Author(s):  
Hadas Nahman-Averbuch ◽  
Ian A. Boggero ◽  
Benjamin M. Hunter ◽  
Hannah Pickerill ◽  
James L. Peugh ◽  
...  

Psychological factors, such as anxiety, depression, and pain catastrophizing, may affect how healthy individuals experience experimental pain. However, current literature puts forth contradictory results, possibly due to differing study methodologies, such as the type of psychophysical measure or survey. To better understand such results, this paper analyzed the relationships between psychological factors and experimental pain outcomes across eight different studies (total n= 595) conducted in different populations of healthy adult and adolescent participants. Analyses were conducted with and without controlling for sex, age, and race. Each study was analyzed separately and as part of an aggregate analysis. Even without correction for multiple comparisons, only a few significant relationships were found for the individual studies. Controlling for demographic factors had minimal effect on the results. Importantly, even the few statistically significant models showed relatively small effect sizes; psychological factors explained no more than 20% of the variability in experimental pain sensitivity of healthy individuals. The aggregate analyses revealed relationships between anxiety and PPT / cold pain ratings and between pain catastrophizing and PPT. Sample size calculations based on the aggregate analyses indicated that several hundred participants would be required to correctly detect relationships between these psychological factors and pain measures. These overall negative findings suggest that anxiety, depression, and pain catastrophizing in healthy individuals may not be meaningfully related to experimental pain outcomes. Furthermore, positive findings in the literature may be subject to small group effects and publication bias towards positive findings.


2019 ◽  
Vol 123 ◽  
pp. 109730
Author(s):  
Ian A. Boggero ◽  
Victor J. Schneider ◽  
Priya L. Thomas ◽  
Hadas Nahman-Averbuch ◽  
Christopher D. King

2020 ◽  
Vol 21 (3) ◽  
pp. 181-193 ◽  
Author(s):  
Maja Matic ◽  
Sjoerd de Hoogd ◽  
Saskia N de Wildt ◽  
Dick Tibboel ◽  
Catherijne AJ Knibbe ◽  
...  

Aim: Investigate the potential role of OPRM1 (mu-opioid receptor) and COMT (catechol-O-methyltransferase enzyme) polymorphisms in postoperative acute, chronic and experimental thermal pain. Methods: A secondary analysis of 125 adult cardiac surgery patients that were randomized between fentanyl and remifentanil during surgery and genotyped. Results: Patients in the fentanyl group with the COMT high-pain sensitivity haplotype required less postoperative morphine compared with the average-pain sensitivity haplotype (19.4 [16.5; 23.0] vs 34.6 [26.2; 41.4]; p = 0.00768), but not to the low-pain sensitivity group (30.1 [19.1; 37.7]; p = 0.13). No association was found between COMT haplotype and other pain outcomes or OPRM1 polymorphisms and the different pain modalities. Conclusion: COMT haplotype appears to explain part of the variability in acute postoperative pain in adult cardiac surgery patients.


2011 ◽  
Vol 12 (5) ◽  
pp. 563-572 ◽  
Author(s):  
Laura Pence Forsythe ◽  
Beverly Thorn ◽  
Melissa Day ◽  
Grace Shelby

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