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PMID: 34409538 Published · ppublish English Journal Article

Depression explains the association between pain intensity and pain interference among adults with neurofibromatosis.

Journal of neuro-oncology ·Vol. 154 ·No. 2 ·2021-09-00 ·页码 257-263

Doorley JD, Greenberg J, Bakhshaie J, Fishbein NS, Vranceanu AM

Abstract

Neurofibromatoses (NFs; NF1, NF2 and Schwannomatosis) are incurable genetic syndromes characterized by nerve sheath tumors and often accompanied by substantial emotional distress (e.g., depression and anxiety). Pain is also common but understudied in adults with NF and interferes with daily living. In other medical populations, depression and anxiety have a strong association with pain interference. However, research has not explored the relationship of depression and anxiety to pain interference among adults with NF experiencing pain. The aim of this study was to test the hypothesis that depression and anxiety will mediate the association between pain intensity and pain interference among geographically diverse adults with NF who endorse pain. We used baseline data from an RCT of a mind-body intervention aimed at improving quality of life in adults with NF. Participants (N = 214) who endorsed pain completed measures of demographics, clinical characteristics, baseline pain intensity, pain interference, depression, and anxiety. We constructed a multiple mediation model in R using the lavaan package to test our hypothesis. Preliminary analyses showed differences in pain interference by NF diagnostic subtype (F(2, 206) = 6.82, p = 001). In a model that controlled for NF diagnostic subtype, we found that depression (β = .07, p = .017), but not anxiety (β = -.003, p = .878), partially mediated the association between pain intensity and pain interference. Improving depression has the potential to decrease pain interference among people with NF who experience pain. Clinicaltrials.gov Registration #: NCT03406208.

Keywords
Anxiety Depression Mediation Neurofibromatosis Pain Pain interference
作者与单位
共 5 位作者,点击展开单位 / ORCID
Doorley James D ORCID
Integrated Brain Health Clinical and Research Program, Massachusetts General Hospital, 1 Bowdoin Square, Suite 100, 1st Floor, Boston, MA, 02114, USA. | Harvard Medical School, Boston, MA, 02115, USA.
Greenberg Jonathan ORCID
Integrated Brain Health Clinical and Research Program, Massachusetts General Hospital, 1 Bowdoin Square, Suite 100, 1st Floor, Boston, MA, 02114, USA. | Harvard Medical School, Boston, MA, 02115, USA.
Bakhshaie Jafar ORCID
Integrated Brain Health Clinical and Research Program, Massachusetts General Hospital, 1 Bowdoin Square, Suite 100, 1st Floor, Boston, MA, 02114, USA. | Harvard Medical School, Boston, MA, 02115, USA.
Fishbein Nathan S ORCID
Integrated Brain Health Clinical and Research Program, Massachusetts General Hospital, 1 Bowdoin Square, Suite 100, 1st Floor, Boston, MA, 02114, USA.
Vranceanu Ana-Maria ORCID
Integrated Brain Health Clinical and Research Program, Massachusetts General Hospital, 1 Bowdoin Square, Suite 100, 1st Floor, Boston, MA, 02114, USA. avranceanu@mgh.harvard.edu. | Harvard Medical School, Boston, MA, 02115, USA. avranceanu@mgh.harvard.edu.
Article Info
Journal
Journal of neuro-oncology
Abbr.
J Neurooncol
ISSN
1573-7373
Corresponding email
Published
2021-09-00
电子出版
2021-00-19
页码
257-263
Language
English
Country/Region
United States
NLM ID
8309335
基金资助
U.S. Department of Defense · W81XWH-17-1-0121
数据资源
ClinicalTrials.gov
NCT03406208
Analysis Services
Analysis Services

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