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Published on: February 26, 2013
Cerebral Small Vessel Disease Associated With Atrial Fibrillation Among Older Adults: A Population-Based Study
Mozhu Ding1, Rui Wang1,2,3, Grégoria Kalpouzos1
1Aging Research Center, Department of Neurobiology, Care Sciences and Society (M.D., R.W., G.K., E.J.L., Y.L., L.F., C.Q.), Karolinska Institutet, Stockholm University, Sweden.
Insights
Atrial fibrillation (AF) is linked to faster progression of white matter lesions and brain ventricle enlargement in older adults. This study investigated AF
Area of Science:
- Neurology
- Cardiology
- Geriatrics
Background:
- Cerebral small vessel disease (CSVD) is a potential mechanism linking atrial fibrillation (AF) and dementia.
- The association between AF and CSVD markers is not well understood.
- Older adults are a key demographic for studying neurodegenerative processes.
Purpose of the Study:
- To investigate the association between atrial fibrillation (AF) and markers of cerebral small vessel disease (CSVD).
- To examine the progression of CSVD in older adults with and without AF.
- To understand the role of CSVD in the relationship between AF and cognitive decline.
Main Methods:
- Cohort study including 336 participants (age ≥60 years) from the Swedish National Study on Aging and Care in Kungsholmen.
- Brain magnetic resonance imaging (MRI) used to assess CSVD markers: perivascular spaces, lacunes, white matter hyperintensities, and ventricular volumes.
- Atrial fibrillation (AF) assessed via clinical examination, ECG, and medical records; analyzed using linear mixed-effects models.
Main Results:
- Prevalent AF (5.4%) and incident AF (5.6%) were identified over a 6-year follow-up.
- AF was significantly associated with accelerated annual increases in white matter hyperintensities volume (β=0.45) and lateral ventricular volume (β=0.58).
- No significant association was found between AF and annual changes in perivascular spaces or lacune number.
Conclusions:
- Atrial fibrillation (AF) is independently associated with accelerated progression of white matter lesions.
- AF is also linked to ventricular enlargement in older adults, irrespective of cerebral infarcts.
- These findings highlight the impact of AF on small vessel disease progression in the aging brain.
Background And Purpose:
Cerebral small vessel disease, as a potential mechanism underlying the association between atrial fibrillation (AF) and dementia, remains poorly investigated. In this cohort study, we sought to examine the association between AF and cerebral small vessel disease markers among older adults.
Methods:
Data on 336 participants (age ≥60 years, mean 70.2 years; 60.2% women) free of dementia, disability, and cerebral infarcts were derived from the population-based Swedish National Study on Aging and Care in Kungsholmen. Structural brain magnetic resonance imaging examinations were performed at baseline (2001–2004) and follow-ups (2004–2007 and 2007–2010). Magnetic resonance imaging markers of cerebral small vessel disease included perivascular spaces, lacunes, and volumes of white matter hyperintensities, lateral ventricles, and total brain tissue. AF was assessed at baseline and follow-ups through clinical examinations, electrocardiogram, and medical records. Data were analyzed using linear mixed-effects models.
Results:
At baseline, 18 persons (5.4%) were identified to have prevalent AF and 17 (5.6%) developed incident AF over the 6-year follow-up. After multivariable adjustment, AF was significantly associated with a faster annual increase in white matter hyperintensities volume (β coefficient=0.45 [95% CI, 0.04–0.86]) and lateral ventricular volume (0.58 [0.13–1.02]). There was no significant association of AF with annual changes in perivascular spaces number (β coefficient=0.53 [95% CI, −0.27 to 1.34]) or lacune number (−0.01 [−0.07 to 0.05]).
Conclusions:
Independent of cerebral infarcts, AF is associated with accelerated progression of white matter lesions and ventricular enlargement among older adults.
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