Resumen
Background: Positive associations between pain and depression in the general population have been well characterized; however, the interplay between pain, depression, and early cognitive decline, characterized as mild cognitive impairment (MCI), is poorly understood. Methods: The current study examined the association of self-reported pain complaints (measured by the 36-item Short Form Health Survey) and self-reported depressive symptoms (measured by the 30-item Geriatric Depression Scale) in cognitively intact participants (n = 492) and participants with a clinical diagnosis of MCI (n = 83). Results: Depressive symptoms and subjective reports of pain were significantly associated in the entire sample (r =.29; P <.0001). Multiple logistic regression modeling (adjusted for age, education, and APOE4 status as covariates) demonstrated that while depressive symptoms were positively associated with the diagnosis of MCI (P <.001), subjective pain reports were negatively associated with MCI (P <.002). Conclusion: While the negative association of subjective pain complaints with MCI might arguably be explained by the development of anosognosia, self-reports of depressive symptoms were actually increased in these participants, suggesting preserved insight into cognitive decline-associated symptoms. It is possible that preferential involvement of limbic circuitry in MCI could explain these findings. Future studies are needed to elucidate the reasons for the dissociation of pain and depressive symptoms in MCI described in the present article.
| Idioma original | English |
|---|---|
| Páginas (desde-hasta) | 107-112 |
| Número de páginas | 6 |
| Publicación | Journal of Geriatric Psychiatry and Neurology |
| Volumen | 25 |
| N.º | 2 |
| DOI | |
| Estado | Published - jun 2012 |
Nota bibliográfica
Funding Information:The authors disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This study was approved by the University of Kentucky IRB and supported by NIH/NIA 1 P30 AG028383.
Financiación
The authors disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This study was approved by the University of Kentucky IRB and supported by NIH/NIA 1 P30 AG028383.
| Financiadores | Número del financiador |
|---|---|
| National Institutes of Health (NIH) | |
| National Institute on Aging | 1 P30 AG028383 |
| National Institute on Aging | |
| National Center for Advancing Translational Sciences (NCATS) | UL1TR000117 |
| National Center for Advancing Translational Sciences (NCATS) |
ODS de las Naciones Unidas
Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible
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Good health and well being
ASJC Scopus subject areas
- Clinical Neurology
- Geriatrics and Gerontology
- Psychiatry and Mental health
Huella
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