Jason Flatt

Dr. Jason Flatt

University of Nevada Las Vegas, Las Vegas, NV
orcid

Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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21 December 2012 in International Psychogeriatrics
Verified
Journal Article
Open access
PDF file
THTiffany F. Hughes
Tiffany F. Hughes
Jason FlattJason Flatt
Jason Flatt
BFBo Fu
Bo Fu
CCChung-Chou H. Chang
Chung-Chou H. Chang
MGMary Ganguli
Mary Ganguli
Background: It is of considerable public health importance to prevent or delay the progression of mild cognitive impairment (MCI) to more severely impaired cognitive states. This study examines the risk of progression from mild to severe cognitive impairment in relation to engagement in social activities while mildly impaired and the concurrence of subsequent change in engagement with MCI progression.Methods: Participants were 816 older adults with cognitively defined MCI (mean age 78.0 (standard deviation or SD = 7.4) years) from the Monongahela–Youghiogheny Healthy Aging Team (MYHAT) Study – a prospective cohort study of MCI in the community. Over three years of follow-up, 78 individuals progressed from MCI to severe cognitive impairment, while 738 did not progress. Risk of progression was estimated using discrete time survival analyses. The main predictors were standardized composite measures of the variety and frequency of engagement in social activities.Results: Lower risk of progression from mild to severe cognitive impairment was associated with both a greater level of frequency of engagement in social activities while mildly impaired (OR = 0.72, 95% CI: 0.55–0.93, p = 0.01) and also with a slower rate of decline in the variety of activities over time (OR = 0.01, 95% CI: <0.001–0.38, p = 0.02).Conclusions: Greater engagement in social activities may potentially be beneficial for preventing or delaying further cognitive decline among older adults with MCI. Alternatively, lesser engagement in social activities may be a marker of impending cognitive decline in MCI.

14 February 2020 in The Journals of Gerontology, Series B: Psychological Sciences and Social Sciences
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Journal Article
Open access
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JJJulene K Johnson
Julene K Johnson
ASAnita L Stewart
Anita L Stewart
MAMichael Acree
Michael Acree
ANAnna M Nápoles
Anna M Nápoles
Jason FlattJason Flatt
Jason Flatt
SGSteven E Gregorich
Steven E Gregorich
To test effects of the Community of Voices choir intervention on the health, well-being, and health care costs of racial/ethnically diverse older adults. Twelve Administration-on-Aging-supported senior centers were cluster randomized into two groups: the intervention group started the choir immediately and a wait-list control group began the choir 6 months later. The choir program was designed for community-dwelling adults aged 60 years and older. The multimodal intervention comprises activities that engage participants cognitively, physically, and socially. Outcome measures assessed these three domains as well as health care utilization and costs. The intention-to-treat comparison was at 6 months. The sample (N = 390) had a mean age of 71.3 years (SD = 7.2); 65% were nonwhite. Six-month retention was 92%. Compared to controls, intervention group members experienced significantly greater improvements in loneliness (p = .02; standardized effect size [ES = 0.34] and interest in life (p = .008, ES = 0.39). No significant group differences were observed for cognitive or physical outcomes or for health care costs. Findings support adoption of community choirs for reducing loneliness and increasing interest in life among diverse older adults. Further efforts need to examine the mechanisms by which engagement in choirs improves aspects of well-being and reduces health disparities among older adults, including potential longer-term effects. NCT01869179 registered January 9, 2013.

9 October 2020 in PLOS ONE
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Journal Article
Open access
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ARAmy Rosenwohl-Mack
Amy Rosenwohl-Mack
STSuegee Tamar-Mattis
Suegee Tamar-Mattis
ABArlene B. Baratz
Arlene B. Baratz
KDKatharine B. Dalke
Katharine B. Dalke
AIAlesdair Ittelson
Alesdair Ittelson
Jason FlattJason Flatt
Jason Flatt
To describe the health of intersex adults (people with differences of sex development) in the U.S. using community-based research methods. In July–September 2018, we conducted a national health study of intersex adults aged 18 and older in the U.S., using a survey hosted on Qualtrics. The study describes the physical and mental health experiences of intersex adults, including differences by age (18 to 39 vs. 40 and older). Questions were derived from national (Behavioral Risk Factor Surveillance System) and intersex-related health studies. A non-probability sample of 198 intersex adults completed the survey over three months. Over 43% of participants rated their physical health as fair/poor and 53% reported fair/poor mental health. Prevalent health diagnoses included depression, anxiety, arthritis, and hypertension, with significant differences by age. Nearly a third reported difficulty with everyday tasks and over half reported serious difficulties with cognitive tasks. To our knowledge, this is the first national study of intersex adults in the U.S. Greater understanding of intersex health over the life course is essential. Findings highlight the need for longitudinal studies and further examination of potential health disparities experienced by intersex populations.

22 January 2014 in International Journal of Geriatric Psychiatry
Verified
Journal Article
Closed access
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THTiffany F. Hughes
Tiffany F. Hughes
Jason FlattJason Flatt
Jason Flatt
BFBo Fu
Bo Fu
MBMeryl A. Butters
Meryl A. Butters
CCChung-Chou H. Chang
Chung-Chou H. Chang
MGMary Ganguli
Mary Ganguli

14 June 2017 in Alzheimer's & Dementia
Verified
Journal Article
Closed access
Jason FlattJason Flatt
Jason Flatt
PGPaola Gilsanz
Paola Gilsanz
CQCharles P. Quesenberry
Charles P. Quesenberry
KAKathleen B. Albers
Kathleen B. Albers
RWRachel A. Whitmer
Rachel A. Whitmer

2 June 2016 in American Journal of Epidemiology
Verified
Journal Article
Closed access
PDF file
ARAndrea L. Rosso
Andrea L. Rosso
Jason FlattJason Flatt
Jason Flatt
MCMichelle C. Carlson
Michelle C. Carlson
GLGina S. Lovasi
Gina S. Lovasi
CRCaterina Rosano
Caterina Rosano
PGPeter J. Gianaros
Peter J. Gianaros
Neighborhood socioeconomic status (NSES) is associated with cognitive function, independently of individual demographic, health, and socioeconomic characteristics. However, research has been largely cross-sectional, and mechanisms of the association are unknown. In 1992–1993, Cardiovascular Health Study participants (n = 3,595; mean age = 74.8 years; 15.7% black) underwent cognitive testing and magnetic resonance imaging of white matter hyperintensities (WMH), and their addresses were geocoded. NSES was calculated using 1990 US Census data (block groups; 6 measures of wealth, education, and occupation). The Modified Mini-Mental State Examination (3MS) was used to assess general cognition, and the Digit Symbol Substitution Test (DSST) was used to assess speed of processing annually for 6 years. Associations of race-specific NSES tertiles with 3MS, DSST, and WMH were estimated using linear mixed-effects models accounting for geographic clustering, stratified by race, and adjusted for demographic, health, and individual socioeconomic status (education, income, lifetime occupational status) variables. In fully adjusted models, higher NSES was associated with higher 3MS scores in blacks (mean difference between highest and lowest NSES = 2.4 points; P = 0.004) and whites (mean difference = 0.7 points; P = 0.02) at baseline but not with changes in 3MS over time. NSES was marginally associated with DSST and was not associated with WMH. Adjustment for WMH did not attenuate NSES-3MS associations. Associations of NSES with cognition in late adulthood differ by race, are not explained by WMH, and are evident only at baseline.