Thursday, November 21, 2024
11/21/2024
Aphasia is a multi-modality disturbance of language that is more common than disorders such as Parkinson’s disease and has a greater negative impact on quality of life than Alzheimer’s disease and many cancers. Persons with Aphasia (PWAs) are thought to be at a higher risk for depression than other stroke survivors. Depression is also thought to worsen language and cognitive performance in PWAs and decrease their quality of life. However, identifying depression in PWAs is challenging as their language disturbances make it difficult to assess depressive symptoms using traditional methods such as questionnaires and interviews as these methods require PWAs to report on their inner experiences (e.g., their sadness, experience of pleasure, etc.). An alternative approach to diagnostic interviews or questionnaires is to utilize laboratory-assessed biomarkers that require minimal language abilities and have shown to robustly identify depression in neurologically healthy individuals. A goal of this study is thus to assess the ability of three laboratory tests to detect depression in PWAs (N=46): (a) heart-rate variability at rest, (b) pupil dilation, and (c) gaze duration (a measure of biased attention) to negatively and positively valenced images. A challenge of this study is that without a gold-standard way to assess depression in PWAs, it is difficult to truly know whether the three biomarkers are validly assessing depression in people who have difficulty verbally reporting on their inner experiences. Aim 1 of the study will therefore apply a novel convergent validity approach and use as its validator a composite reference standard based on multiple indicators or proxies of depression - specifically, informant (e.g., family member, caregiver) report of PWAs (a) depression symptoms, (b) pre-morbid history of PWAs depression (a robust predictor of future depression in non-neurological and neurological patients), and (c) a self-report depression scale adapted for PWAs. Composite reference standards are routinely employed to evaluate new tests when gold-standard and imperfect diagnostic tests exist, but this approach has not been used to assess depression in PWA. Aim 2 will test whether laboratory- assessed biomarkers predict PWAs day-to-day experiences of affect and social interaction (a critical factor for successful rehabilitation), using experience sampling methodology (ESM). ESM is an approach that requires brief, frequent (multiple per day), at-home assessments (in this case, from caregivers). ESM minimizes recall bias and increases ecological validity of assessments. Lastly, aim 3 will establish the retest reliability of laboratory-assessed biomarkers of depression by re-administering all measures to PWAs 7 days later. The proposed project has the potential for high impact for PWAs since accurate diagnosis of depression in PWAs can lead to better management of depression, which can positively impact linguistic and cognitive functioning and improve PWA’s quality of life. The project will lay the foundation for a future research platform for the early- stage PI that examines whether the laboratory-assessed biomarkers predict different depression treatment responses and language and functional improvements related to the treatments longitudnally.
HHS’ Tracking Accountability in Government Grants System (TAGGS) website provides access to detailed descriptions of grants, loans, aggregated direct payments and other types of financial assistance awarded by the HHS Operating Divisions (OPDIVs) and the Office of the Secretary Staff Divisions (STAFFDIVs).
