Functional Connectivity, Physical Activity, and Behavioral Abnormality in Patients with Vascular Cognitive Impairment

Research Article

Phys Med Rehabil Int. 2023; 10(3): 1221.

Functional Connectivity, Physical Activity, and Behavioral Abnormality in Patients with Vascular Cognitive Impairment

Ya-Ting Chang, MD, PhD1,2; Chun-Ting Liu, MD3,4; Shih-Wei Hsu, MD5; Chen-Chang Lee, PhD5; Pei-Ning Huang, BS1

1Department of Neurology, Kaohsiung Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Taiwan

2Department of Psychiatry, Osaka University Graduate School of Medicine, Japan

3Department of Chinese Medicine, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Taiwan

4Graduate Institute of Integrated Medicine, College of Chinese Medicine, China Medical University, Taiwan

5Department of Radiology, Kaohsiung Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Taiwan

*Corresponding author: Ya-Ting Chang Department of Neurology, Kaohsiung Chang Gung Memorial Hospital 123, Ta-Pei Road, Niaosung, Kaohsiung 83301, Taiwan. Tel: +886-7-731-7123 ext. 3389 Email: emily0606@cgmh.org.tw

Received: November 21, 2023 Accepted: December 19, 2023 Published: December 26, 2023

Abstract

Purpose of the research: Neuropsychiatric Symptoms (NPSs) can negatively impact the survival and quality of life in Vascular Cognitive Impairment (VCI) patients. Physical Activity (PA) has been shown to reduce NPSs in dementia patients, possibly by influencing synaptic plasticity. This study investigates the relationship between NPSs, Default Mode Network (DMN), and PA in patients with VCI.

Methods: The study included 42 VCI patients. Functional Connectivity (FC) within the DMN and neurobehavioral performance was assessed. NPSs were categorized. The severity of Hyperactivity and Behavioral Symptoms (HBS) was quantified using a Hyperactivity and Behavioral Composite Score (HBCS). Patients’ PA levels were measured using Fitbit Charge 2.

Principal results: After accounting for disease severity, increased FC between the left Posterior Cingulate Cortex (PCC) seed and the right inferior parietal gyrus was linked to more severe HBS. There was an inverse correlation between HBCS and average step counts per day (steps/d) as well as average distance per day (km/d). This suggests that higher levels of PA were associated with less severe HBS. HBCS was also inversely correlated with steps/d and km/d, reinforcing the idea that increased PA was linked to reduced symptom severity.

Major conclusions: The study concludes that increased FC within the DMN is associated with more severe HBS in VCI patients. Greater levels of PA (measured by step counts and distance) were associated with a reduction in the severity of HBS. This suggests that FC within the DMN may play a role in the modulation of HBS by PA in VCI patients.

Keywords: Actigraphy; Brain network; Cognition; Functional connectivity; Neuropsychiatric symptoms; Physical activity

Abbreviations: ACS: Affective Composite Scores; AD: Alzheimer’s Disease; HBCS: Hyperactivity and Behavioral Composite Scores; HBS: Hyperactivity and Behavioral Symptoms; CDR: Clinical Dementia Rating; CVVLT-10 min: free recall of number of items retrieved over four learning trials of a 9-word list 10 minutes after Chinese Version Verbal Learning Test (CVVLT); FC: Functional Connectivity; FDS: Forward Digital Span; FLAIR: Fluid-Attenuated-Inversion-Recovery; IADL: Instrumental Activities of Daily Living; IPG: Inferior Parietal Gyrus; IQR: Interquartile Range; MoCA: Montreal Cognitive Assessment; MMSE: Mini-Mental State Examination; MNI: Montreal Neurological Institute; MRI: Magnetic Resonance Imaging; rs-fMRI: Rest State Functional MRI; NPS: Neuropsychiatric Symptoms; PA: Physical Activity; PCC: Posterior Cingulate Cortex; PCS: Psychotic Composite Scores; PS: Psychotic Symptoms; PSD: Post-Stroke Depression; ROCF-copy: Modified Rey-Osterrieth Complex Figure copy; ROCF-recall: Modified Rey-Osterrieth Complex Figure recall; TMB: Trail Making Test B; VCI: Vascular Cognitive Impairment; VOSP: Visual Object and Space Perception; WATs: Wearable Activity Trackers

Introduction

Vascular Cognitive Impairment (VCI) is indeed a broad term that encompasses a range of cognitive disorders resulting from Cerebrovascular Diseases (CVDs) [1,2]. These diseases can lead to reduced blood flow to the brain due to blockages or damage to blood vessels. This reduced blood flow can result in cognitive decline [1,2]. It encompasses various conditions, including individuals who exhibit both the pathological changes associated with Alzheimer's Disease (AD) (such as amyloid plaques and neurofibrillary tangles) and vascular diseases (related to blood vessel issues in the brain) [3].

Neuropsychiatric Aymptoms (NPSs) are a common and challenging aspect of various forms of cognitive decline, including VCI. These symptoms can have significant consequences for both the individuals with dementia and their caregivers. NPSs are associated with a more rapid cognitive decline in individuals with VCI [4]. This means that when these symptoms are present, the cognitive abilities of the person with VCI may deteriorate more quickly compared to those without such symptoms. This can make the management of the condition more challenging. Research has shown that the presence of NPSs in VCI can have a negative impact on survival [5]. Individuals who experience these symptoms may have a shorter lifespan compared to those without them. The reasons for this association are complex but could be related to factors like increased stress, physical health complications, and reduced quality of care. NPSs significantly worsen the quality of life for both individuals with VCI and their caregivers [6]. These symptoms can be distressing, disruptive, and challenging to manage. They may lead to social isolation, impaired daily functioning, and a decreased overall sense of well-being for the person with VCI. Caregivers also experience increased stress and burden when managing these symptoms. Some of the common NPSs that frequently occur in VCI include delusions, depression, aggression/agitation, disinhibition, apathy, anxiety [7].

The idea behind clustering similar NPSs together is to improve the effectiveness of studying their underlying causes (pathogenesis) and potential treatments [8]. This approach helps researchers and healthcare professionals gain a better understanding of how certain symptoms may be related and how they can be addressed collectively. Here are the clusters of NPSs that are commonly used in studies [9-11]: Affective Symptoms (AS), Hyperactivity and Behavioral Symptoms (HBS), and Psychotic Symptoms (PS).

AS includes symptoms related to mood and emotions. It typically encompasses conditions such as depression, anxiety, apathy, and sometimes includes sleep or appetite disorders. HBS focuses on symptoms related to hyperactivity and behavior. It includes symptoms like agitation, disinhibition, irritability, and aberrant motor behavior. PS involves symptoms related to psychosis, including hallucinations and delusions. Grouping them together allows for more targeted research and management strategies.

Default Mode Network (DMN) is a network of brain regions that are active when an individual is not focused on the outside world and the brain is at rest, such as during daydreaming or self-reflection [12,13]. Dysfunctions in the DMN have been observed in various neurological and psychiatric conditions. Functional Connectivity (FC) refers to the strength of communication or interaction between different brain regions. Increased or decreased FC between specific brain regions can indicate abnormalities or dysfunctions in the brain's neural networks [12,13]. While there is existing research showing a connection between DMN dysfunctions and NPSs in AD, there is limited research on the same relationship in VCI [14,15]. Treatments that target neural synapses and brain networks are suggested to improve cognitive and NPSs in individuals with neurological disorders [16,17]. Understanding the relationship between NPSs and FC alterations in VCI is important because it could provide insights into potential interventions for managing NPSs in VCI patients. Such interventions may involve modifying neural synapses and brain networks to improve cognitive and behavioral symptoms in individuals with VCI, similar to approaches being explored in AD.

In patients with VCI, there is an increased FC of the Posterior Cingulate Cortex (PCC) with various brain regions within the DMN, including the right inferior temporal gyrus, the left middle temporal gyrus, and the left superior parietal lobule [18]. This altered connectivity may be related to NPSs in VCI. Several studies have explored the relationship between NPSs and FC in patients with a history of stroke [14,15]. For example, in patients with Post-Stroke Depression (PSD), the severity of depression is positively correlated with the FC between the DMN and the salience network [14]. Another study shows decreased FC in the left Inferior Parietal Gyrus (IPG) and increased FC in the left superior frontal gyrus within the DMN in PSD patients [15]. Sub-acute ischemic stroke patients with PSD and/or anxiety symptoms have been found to have increased FC in the left IPG and the left basal nuclei within the DMN when compared to stroke controls [19]. The relationship between increased FC within DMN and NPSs suggests that NPSs in patients with VCI are associated with increased FC within the DMN. This hypothesis is based on the efficacy of antipsychotic [20,21] and antiepileptic [22,23] drugs in managing NPSs, which may be related to modulating hyperactivity within brain networks like the DMN.

Increased Physical Activity (PA) would be associated with reduced NPSs in patients with VCI. This hypothesis is supported by the idea that PA has been found to have beneficial effects on NPSs in people with dementia, especially in community-dwelling individuals [24]. Regular exercise can improve mood, reduce agitation, and enhance overall well-being [24]. When patients engage in PA, it can potentially lead to a reduction in NPSs, making care giving less stressful and burdensome for family members and caregivers [25]. PA may play a role in modulating the activity and connectivity within the DMN.

PA can increase cerebral blood flow, which is important for maintaining brain health and function. Improved blood flow can potentially enhance the functioning of brain regions involved in the DMN. Regular PA is known to reduce oxidative stress, which can be harmful to brain cells. Reduced oxidative stress may help protect brain regions associated with the DMN from damage. PA has been linked to the promotion of neurogenesis and synaptogenesis. These processes can contribute to the brain's ability to adapt and recover from damage, which may be relevant to DMN functioning [26].

To summarize, this study aims to investigate the relationship between NPSs, FC within the DMN, and PA in patients with VCI. The objectives of the present study were to: (1) perform a direct relationship analysis between the NPSs scores and the quantified measures of PA; (2) investigate the relationships among scores of NPSs, measures of PA, and strength of FC within the DMN. Through these analyses, we explored the influence of PA on FC within the DMN and on NPSs in patients with VCI.

Materials and Methods

Study Design and Subjects

The Institutional Review Committee on Human Research at Chang Gung Memorial Hospital granted approval for this study. We obtained informed consents from participants with a Clinical Dementia Rating (CDR) score of 0.5 (n=36). For participants with a CDR score of 1.0 (n=6), their designated caregivers gave informed consent. Within a four-week window, we conducted cognitive tests and Magnetic Resonance Imaging (MRI). A total of forty-two VCI patients were recruited from the Neurology Department at Chang Gung Memorial Hospital. The VCI diagnosis was determined collectively by neurologists and neuroradiologists, adhering to the criteria set by the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition [27]. The causes could range from multiple or single territorial infarcts to small or strategic ones. The pathology might also encompass both neurodegenerative and cerebrovascular issues [28,29]. We excluded participants if they: (1) had significant systemic diseases, such as gastrointestinal, renal, hepatic, or respiratory issues, or (2) had other conditions or were on medication that might influence cognitive abilities.

The criteria based on MRI results are as follows: There should be no signs of cortical or watershed infarcts, hemorrhages, hydrocephalus, or specific cause White Matter Lesions (WMLs) like multiple sclerosis. Additionally, there should be no atrophy in the hippocampal or entorhinal cortex, aligning with a zero score on Schelten’s medial temporal lobe atrophy scale [30]. The MRI might show multiple supratentorial subcortical small infarcts (measuring between 3–20 mm in diameter), or any extent of WMLs, or moderate to severe WMLs (with a Fazekas score of 2 or higher [31]). It might also display multiple or single territorial infarcts or small to strategic infarcts.

Neurobehavioral Assessments

Participants underwent a general cognitive assessment using the Montreal Cognitive Assessment (MoCA). Subsequently, these MoCA scores were translated into Mini-Mental State Examination (MMSE) scores [32]. For the assessment of delayed verbal memory, we employed the Chinese Version Verbal Learning Test (CVVLT) [33]. This involved recalling a list of 9 words after a 10-minute interval (termed CVVLT-10 min) over four learning trials [34]. Memory functions were gauged using both CVVLT-10 min [34] and the modified Rey-Osterrieth complex figure recall (ROCF-recall) [35]. To measure visual-spatial capabilities, tools like the Visual Object and Space Perception (VOSP) [36] and the modified ROCF copy (ROCF-copy) [35] were utilized. The Forward Digital Span (FDS) [37] was implemented to test attention. Executive Function (EF) in participants was determined using the corrected Trail Making Test B (TMB) as well as the TMB's time to completion (measured in seconds) [38]. Lastly, the independence of each participant was gauged using the Instrumental Activities of Daily Living (IADL) scores [39].

Patients' Neuropsychiatric Symptoms (NPSs) were assessed using the NPI-12 [9,11]. The NPI-12 scores determined the severity of different symptom syndromes. The AS was represented by the Affective Composite Score (ACS), which combined scores from depression, anxiety, sleep, appetite, and apathy. The HBS was denoted by the Hyperactivity and Behavioral Composite Score (HBCS), aggregating scores from agitation/aggression, aberrant motor behavior, disinhibition, and irritability. Meanwhile, the severity of the PS was represented by the Psychotic Composite Score (PCS), derived from the combined scores of delusion and hallucination [9,11].

MRI Acquisition and Pre-processing

MRI scans for all participants were conducted using a Siemens 3T scanner, with each session lasting approximately 20 minutes. The T1-weighted imaging followed a 3D-MPRAGE protocol in a steady-state sequence featuring a 256×256 mm field of view, a 1-mm slice thickness, and a Repetition Time (TR)/Echo Time (TE) set at 2600 ms/3.15 ms. This scan spanned 5 minutes and 50 seconds.

For the Resting State Functional MRI (rs-fMRI), participants were advised to refrain from sleep deprivation, caffeine, and sedatives for eight hours prior to the scan. They were instructed to remain still, keep their eyes closed, stay awake, and avoid focusing on any specific thoughts during the procedure. Post-scan, participants were questioned about potential sleep, anxiety, or agitation incidents, with none reporting any issues. All patients had been on consistent medical treatment for a minimum of three months to minimize any impact on FC.

The rs-fMRI followed a protocol of TR=2500 ms/TE=27 ms with a voxel size of 3.4×3.4×3.4, taking 8 minutes and 27 seconds. The CONN toolbox (http://www.nitrc.org/projects/conn) [40] was utilized for artifact removal in rs-fMRI. The average signal fluctuation of blood oxygen levels between scans should not exceed 1%. The framewise displacement should stay below 0.25 mm/TR. Images underwent detrending and filtering within a 0.008 to 0.09 Hz range. The CONN toolbox also facilitated the regression of noise such as head movement, white matter signals, and cerebrospinal fluid signals from individual voxels. Our data preprocessing mirrored our past study's approach, incorporating slice time correction, realignment, segmentation, normalization to Montreal Neurological Institute (MNI) standards, spatial smoothing with a 6 mm Gaussian Kernel, and resampling to 2×2×2mm3 [41,42].

For the assessment of WMLs and hemorrhages, both Fluid-Attenuated-Inversion-Recovery (FLAIR) and T2*-weighted MRI sequences were captured. The FLAIR MRI sequence followed a protocol with TR=5000 ms/TE=393 ms and a 1 mm slice thickness, lasting 4 minutes and 37 seconds. The T2*-weighted MRI sequence took 2 minutes.

Seed-based FC

The correlation coefficients between the PCC seeds and all notable clusters depict the voxel-wise FC for every PCC seed. For the ROI-centric functional connectivity analysis, the DMN was rooted in PCC seeds on both sides, characterized by two 10 mm-radius spheres aligned with MNI coordinates (x=±2, y=-51, z=41) [43]. These PCC seeds have shown extensive connectivity with other PCC/precuneus regions and cortical zones [43]. The FC within brain structures rooted on each PCC seed underwent analysis [44].

The DMN's FC was linked to ACS, HBCS, and PCS, and this connectivity was further related to PA metrics. Employing multiple regression analysis through the CONN toolbox [40], each PA measure was associated with FC spanning each network seed and voxels across the entire brain, rooted in the average resting-state BOLD time sequence within individual correlation maps (http://www.nitrc.org/projects/conn) [40,45]. A significance bar was set with an uncorrected p-value threshold of < 0.001 at the peak level and a false discovery rate-adjusted p-value of <0.05 at the cluster level, leveraging the second-level analysis of relative inter-regional functional covariance. All-brain correlation maps underwent a conversion into z-score maps via a Fisher’s r-to-z transformation. Post determining the correlation between each NPS-CS and FC within brain networks, the FC between every seed and peak cluster was additionally extracted [40] for association with each PA metric.

The Activity Monitoring

Participants were provided with Fitbit Charge 2 devices (https://www.fitbit.com/au/charge2) and were guided on how to activate them and authorize data sharing. Fitbit Charge 2 is a GPS-equipped health band that facilitates phone-independent running and captures essential data such as steps taken, distance covered (in kilometers), and calories expended (https://www.fitbit.com/au/one). Moreover, its associated app mainly serves as the control hub for Fitbit Charge 2, supporting account setup and Bluetooth connectivity. The walking data could seamlessly integrate with Smarttrack (https://www.fitbit.com/au/smarttrack). This setup allowed the research team to view participants' live device data. When near the user’s Bluetooth-enabled smartphone, the device autonomously sent activity information to Fitbit's servers. Previous studies have verified the accuracy and consistency of the Fitbit Charge 2 in recording steps, distance [46,47], and caloric burn [48]. This activity monitor, produced by Fitbit, San Francisco, CA (https://www.fitbit.com/au/home), was utilized to gauge Physical Activity (PA). It features a 3-axis accelerometer that identifies step thresholds based on movement patterns typically associated with walking. The device supports wireless auto-syncing with smartphones and offers a battery lifespan of around 14 days.

Participants were instructed to wear the devices continuously for a minimum of 7 days. We collected PA metrics such as daily steps, distance, and calories for every participant. Preliminary checks were conducted to scrutinize data completeness, anomalies, and implausible values.

We accumulated each PA metric over the 7 days, and then determined average PA values by dividing the total by seven. Initially, daily PA data (steps, distance in kilometers, and calories burned) was collated for each participant. Subsequently, we calculated average daily PA metrics (steps/day, km/day, calories/day) for each individual. Our subsequent analyses primarily used these average daily PA values. Adherence to using the smartwatch was verified through the app's logs. Heart rates of participants were monitored at 5-minute intervals, with continuous heart rate graphs available on the app. If a participant displayed any non-adherence, evident from a recorded heart rate dropping to zero, they were asked to continue wearing the device for additional days to ensure a complete seven-day PA log.

Statistical Analyses

All results were presented as the mean ± standard deviation. For data that didn't adhere to a normal distribution, they were displayed as median with the Interquartile Range (IQR). To examine the relationships between patient-level average PA metrics, each NPS Composite Score (CS), and the strength of FC within brain networks based on each PCC seed for all VCI patients, we employed Spearman’s correlation. Statistical analyses were performed using the SPSS software (version 18 for Windows®, SPSS Inc., Chicago, IL), with a P-value<0.05 (two-tailed) deemed as statistically significant.

Results

Demographic Data

Forty-two patients diagnosed with VCI successfully finished the study (Table 1). Given that the education (in years), glycohemoglobin (HbA1c) (%), MMSE score, NPI score, each NPSs CS, along with scores from CVVLT-10 min, ROCF-recall, FDS, TMB (corrected), TMB time to completion (in seconds), VOSP, ROCF-copy, and IADL did not follow a normal distribution, these data points were subsequently presented as median (IQR) in Table 1.

Citation: Chang YT, Liu CT, Hsu SW, Lee CC, Huang PN. Functional Connectivity, Physical Activity, and Behavioral Abnormality in Patients with Vascular Cognitive Impairment. Phys Med Rehabil Int. 2023; 10(3): 1221.