TY - JOUR
T1 - Motoric cognitive risk syndrome trajectories and incident dementia over 10 years
AU - Mullin, Donncha S.
AU - Gadd, Danni
AU - Russ, Tom C.
AU - Luciano, Michelle
AU - Muniz-Terrera, Graciela
N1 - Funding Information:
The present manuscript received no direct funding. DSM is undertaking a PhD Clinical Research Fellowship funded by the Masonic Charitable Foundation and the Royal College of Psychiatrists, United Kingdom. DSM and TCR are members of the Alzheimer Scotland Dementia Research Centre, which is funded by Alzheimer Scotland. All researchers are independent of their funders. Age UK's Disconnected Mind project supported data collection for the LBC1936 study, the UK's Biotechnology and Biological Sciences Research Council (BBSRC) and the Economic and Social Research Council (BB/W008793/1). The Lothian Birth Cohort 1936 study acknowledges the financial support of NHS Research Scotland (NRS) through the Edinburgh Clinical Research Facility. DAG is supported by funding from the Welcome Trust 4-year PhD in Translational Neuroscience: training the next generation of basic neuroscientists to embrace clinical research [108890/Z/15/Z].
PY - 2023
Y1 - 2023
N2 - Background: Motoric Cognitive Risk (MCR) syndrome is a high-risk state for adverse health outcomes in older adults characterised by measured slow gait speed and self-reported cognitive complaints. The recent addition to the Lothian Birth Cohort 1936 of robust dementia outcomes enabled us to assess the prognostic value of MCR for dementia and explore the various trajectories of participants diagnosed with MCR. Methods: We classified 680 community-dwelling participants free from dementia into non-MCR or MCR groups at mean [SD] age 76.3 [0.8] years. We used Cox and competing risk regression methods, adjusted for potential confounders, to evaluate the risk of developing all-cause incident dementia over 10 years of follow-up. Secondarily, we followed the trajectories for individuals with and without MCR at baseline and categorised them into subgroups based on whether MCR was still present at the next research wave, three years later. Results: The presence of MCR increased the risk of incident dementia (adjusted HR 2.34, 95%CI 1.14–4.78, p = 0.020), as did fewer years of education and higher depression symptoms. However, MCR has a heterogenous progression trajectory. The MCR progression subgroups each have different prognostic values for incident dementia. Conclusion: MCR showed similar prognostic ability for dementia in a Scottish cohort as for other populations. MCR could identify a target group for early interventions of modifiable risk factors to prevent incident dementia. This study illustrates the heterogeneous nature of MCR progression. Exploring the underlying reasons will be important work in future work.
AB - Background: Motoric Cognitive Risk (MCR) syndrome is a high-risk state for adverse health outcomes in older adults characterised by measured slow gait speed and self-reported cognitive complaints. The recent addition to the Lothian Birth Cohort 1936 of robust dementia outcomes enabled us to assess the prognostic value of MCR for dementia and explore the various trajectories of participants diagnosed with MCR. Methods: We classified 680 community-dwelling participants free from dementia into non-MCR or MCR groups at mean [SD] age 76.3 [0.8] years. We used Cox and competing risk regression methods, adjusted for potential confounders, to evaluate the risk of developing all-cause incident dementia over 10 years of follow-up. Secondarily, we followed the trajectories for individuals with and without MCR at baseline and categorised them into subgroups based on whether MCR was still present at the next research wave, three years later. Results: The presence of MCR increased the risk of incident dementia (adjusted HR 2.34, 95%CI 1.14–4.78, p = 0.020), as did fewer years of education and higher depression symptoms. However, MCR has a heterogenous progression trajectory. The MCR progression subgroups each have different prognostic values for incident dementia. Conclusion: MCR showed similar prognostic ability for dementia in a Scottish cohort as for other populations. MCR could identify a target group for early interventions of modifiable risk factors to prevent incident dementia. This study illustrates the heterogeneous nature of MCR progression. Exploring the underlying reasons will be important work in future work.
KW - cognitive impairment
KW - dementia
KW - dementia prediction
KW - motoric cognitive risk
KW - slow gait
KW - slow walking
KW - subjective cognitive complaint
KW - trajectories
UR - https://www.ed.ac.uk/lothian-birth-cohorts/data-access-collaboration
U2 - 10.1016/j.cccb.2023.100178
DO - 10.1016/j.cccb.2023.100178
M3 - Article
AN - SCOPUS:85166332284
SN - 2666-2450
VL - 5
JO - Cerebral Circulation - Cognition and Behavior
JF - Cerebral Circulation - Cognition and Behavior
M1 - 100178
ER -