Differential effects of a computerized cognitive stimulation program on older adults with mild cognitive impairment according to the severity of white matter hyperintensities.

OBJECTIVE: This study aimed to explore whether a computerized cognitive stimulation program (CCS) induced differential effects in older adults with mild cognitive impairment (MCI) according to the severity of white matter hyperintensities (WMH), which are associated with cognitive impairment and increased risk of progression to Alzheimer's disease because of the damage they cause to cortical and subcortical networks. PATIENTS AND METHODS: Twenty-nine MCI patients with no or little WMH (MCI-non-WMH) and 22 MCI patients with moderate or severe WMH (MCI-WMH) attended a 24-session CCS program (two sessions per week for a duration of 3 months) focused on executive functions, attention, and processing speed. Cognitive and psychosocial assessments were performed at baseline, postintervention, and 3 months after the intervention.
RESULTS: Both groups improved on several cognitive measures after the intervention. However, the MCI-non-WMH group improved on a higher number of cognitive measures than the MCI-WMH group. At postintervention assessment, CCS had a more beneficial effect on the MCI-non-WMH group than on the MCI-WMH group with regard to improving categorical fluency (4.6±6.8 vs 0.4±6.4; effect size=0.37; p=0.002). During the 3-month follow-up assessment, significantly higher score improvements were observed in the MCI-non-WMH group for the paired-associate learning test (6.4±3 vs 4.7±3.5 points; effect size=0.43; p=0.005) as well as categorical fluency (3.8±7.8 vs -0.7±6 points; effect size=0.55; p=0.0003).
CONCLUSIONS: These findings suggest that WMH severity was related to cognitive improvement induced by a CCS program and highlight the importance of considering WMH in interventional studies on subjects with MCI.

Introduction

Mild cognitive impairment (MCI) is commonly regarded as being a transitional phase between normal aging and early Alzheimer’s disease (AD), the most common cause of dementia. Older adults with MCI have a higher risk of developing dementia (10%–15% per year),1 compared to the general older population (1%–2% per year).2 In the absence of effective treatment for dementia, MCI is becoming of interest for pharmacologic and nonpharmacologic interventions, in order to prevent further cognitive decline.

It is now well established that cognitive interventions such as cognitive training, cognitive rehabilitation, and cognitive stimulation3 could help maintain or enhance cognitive and functional abilities in MCI subjects.4,5 The last decade has seen the emergence of various computerized cognitive intervention programs, which seem promising for these patients.6–9 Computerized programs involve both cognitive training and novel learning experiences. On one hand, participants are required to focus on tasks tapping into either multiple or specific cognitive domains. On the other hand, older adults who are not familiar with digital devices need to acquire new skills, which in turn stimulates several cognitive functions.10 However, there is a lack of consensus regarding their efficacy, in part due to the heterogeneity of MCI, a factor that may affect intervention outcome.4,5,11,12 MCI is a heterogeneous clinical entity, encapsulating different cognitive profiles, underlying brain pathologies and follow-up outcomes. In most of the studies on cognitive interventions in MCI, underlying brain lesions are rarely taken into consideration. However, it has been suggested that MCI patients with more severe brain lesions might benefit less or differently from cognitive interventions than those with less severe brain lesions.9

In biologic terms, AD is commonly defined as the accumulation of beta-amyloid protein and the deposition of neurofibrillary tangles. However, increasing evidence shows that white matter hyperintensities (WMH) also contribute to the development of MCI and AD.13,14 WMH are visualized as increased signal on T2-weighted fluid-attenuated inversion recovery magnetic resonance imaging (MRI) sequences. WMH are often considered to be markers of cerebral small-vessel disease and are frequently observed in older adults with MCI and AD.15,16 It is hypothesized that WMH might precipitate the clinical manifestation of MCI and AD.17,18 Neuroimaging studies have shown that WMH may cause a frontal-subcortical pathway disruption, leading to executive, attentional, and processing speed impairment19–21 as well as memory deficits, due to retrieval impairment.17,22,23 WMH have been observed in amnestic and nonamnestic subtypes of MCI.15,17,24,25

To address the lack of literature regarding the effects of cognitive intervention programs according to brain lesions, this study aimed to compare effects of a computerized cognitive stimulation (CCS) program in MCI patients according to the severity of WMH.

Patients and methods

Design

This is a prospective, single-blind, parallel-group, quasi-experimental study. The flow chart of the study is reported in Figure 1.

Figure 1

The flow chart of the study.

Notes: T0, baseline; T3, postintervention; T6, 3-month follow-up after the intervention.

Abbreviations: MCI, mild cognitive impairment; MCI-WMH, MCI with moderate or severe white matter hyperintensities; MCI-non-WMH, MCI with no or little white matter hyperintensities.

Participants

Participants were recruited in Broca Hospital’s memory clinic between 2015 and 2016.

To be included in the study, participants must have had 1) a diagnosis of MCI:26 subjective memory complaints, preferably corroborated by an informant, objective impairment on more than one of the neuropsychological tests used in the memory clinic (French version of the Free and Cued Selective Reminding Test,27 Frontal Assessment Battery,28 Digit Span,29 verbal fluency,30 Trail Making Test parts A and B [TMT-B],31 80-item naming test,32 Praxic Ability Scale;33 1.5 SD below the mean for age and education or below the cutoff score), preserved global intellectual function, preserved or minimal impairment in daily living activities, and the absence of dementia; 2) MRI evidence indicating the severity of WMH. The severity of WMH was estimated by an experienced neurologist using the Fazekas Scale,34 providing two different scores for periventricular WMH and deep WMH, rated on four points (0–3). Periventricular WMH were rated as 0=no lesions; 1=“caps” or pencil-thin lining; 2=smooth “halo”; and 3=irregular lesions extending into the deep white matter. Deep WMH were rated as 0=no lesions; 1=punctuate foci; 2=beginning confluence of foci; and 3=large confluent areas. We classified participants into two groups according to the severity of WMH, taking into account both periventricular and deep WMH: MCI subjects with no or little WMH (MCI-non-WMH; grade 0 and 1) vs MCI subjects with moderate to severe WMH (MCI-WMH; grades 2 and 3).

The exclusion criteria were 1) psychiatric and neurologic disorders (eg, bipolar disorder, Parkinson’s disease, epilepsy); 2) history of alcohol or other substance abuse; 3) sensory and/or motor deficits that could interfere with the use of a digital device; 4) participation in another intervention. Two hundred and twenty-five patients were screened. Of the 58 participants eligible for the study, seven subjects dropped out (three participants without WMH and four with WMH), yielding 51 patients who completed the intervention program (39 women and 12 men; age=75.3±6.2 years) as well as pre-and postintervention assessments. Fourteen participants did not complete the follow-up assessment (seven MCI-WMH and seven MCI-non-WMH). Written informed consent was obtained from all participants. This study was approved by the ethical committee from Paris Descartes University’s Institutional Review Board (N°IRB: 20161300001072) and was registered at ClinicalTrials.gov as NCT03195803.

Intervention

All participants benefited from the same CCS program, developed using the concept of cognitive stimulation,35–37 an ecologic approach based on engaging participants in a range of cognitive exercises in a group setting, thus aiming to stimulate cognitive functions and promote social interactions. The participants attended a 1 and a half hour session twice a week, during a period of 3 months (24 sessions in total) in Broca hospital. Three experienced neuropsychologists conducted group sessions with five to seven participants per group.

The cognitive exercises were selected from the “KODRO” software (Altera-Group, Paris, France), a web-based platform, developed for older adults. We chose KODRO for its large content of playful cognitive exercises and for the ecologic nature of some of the exercises, which can be applied in everyday life. These cognitive exercises targeted several cognitive processes, such as mental flexibility, processing speed, working memory, planning/organization, categorization, attention, reaction time, inhibition, and visual tracking. An example of one of these exercises is “Instruction” (tapping into mental flexibility, divided attention, and processing speed), which consists in touching specific stimuli (with different shapes and colors), among multiple distractors, as quickly as possible within the time allocated (indicated by a countdown timer). Within this series of exercises, participants must pay attention to the countdown timer while touching target stimuli. At the end of each countdown timer, instructions change and participants are then required to touch stimuli of another color and shape. Neuropsychologists managed the sessions and the difficulty level of the exercises, thanks to an iPad linked to a TV screen and to each participant’s tablet-PC. The neuro psychologist’s iPad displayed the success and failure rate for each exercise, and participants’ tablet-PCs display feedback (good, very good, and excellent) at the end of each step of the exercise, in order to encourage them. The TV screen displayed the date at the beginning of the session and the instructions for each exercise, allowing the participants to refer to them when necessary. The content of the exercises was scheduled to change every 2 weeks.

During the first session, the participants introduced themselves. Explanations about the outline of the program were given. They were trained to use some basic functionalities of a tablet-PC.

The remaining sessions were structured as follows:

Greeting and discussion about personal events and the news, to foster exchanges before cognitive exercises (5 minutes).

Cognitive exercises with a tablet-PC: four 15-minute cognitive exercises (60 minutes).

Brief conclusion/debriefing with feedback about the session (5 minutes).

Outcomes

Participants were assessed at baseline (T0), immediately after the 3-month intervention (T3) and during a 3-month follow-up postintervention (T6). Neuropsychologists involved in data collection at any point of the assessment process were blinded to which group participants were part of. Outcomes were composed of neuropsychological and psychosocial measures.

At baseline, we collected sociodemographic data such as age and sex as well as education level and premorbid intelligence, as assessed by the French adaptation of the National Adult Reading Test.38 The presence or absence of hippocampal atrophy was also recorded.

Mini Mental State Evaluation (MMSE)39 assessing global cognitive efficiency (score range: 0–30).

Rey Auditory Verbal Learning Test (RAVLT)40 for the assessment of episodic memory. Two scores were used: the sum of all correct immediate recall scores across five consecutive trials (score range: 0–75) and the delayed recall score (score range: 0–15).

Paired-associate learning test (associative memory; score range: 0–12) and logical memory (trial 1 and trial 2; score range: 0–12) subtests from the Cognitive Efficiency Profile.41

TMT-A and TMT-B31 assessing processing speed, attention, and executive functions. The completion time was recorded. A completion time of 300 seconds was assigned if a subject failed to complete the TMT-B.

Symbol Digit Modalities Test (SDMT) of the Wechsler Adult Intelligent Scale-Fourth Edition (WAIS-IV)29 measuring processing speed/attentional control (score range: 0–133).

Backward Digit Span from the WAIS-IV29 assessing working memory (score range: 0–14).

Verbal fluency (“letter P” for phonemic fluency and “animals” for categorical fluency, 2 minutes) measuring verbal ability and executive control.30

Rey–Osterrieth Complex Figure (ROCF) assessing planning and organization, visual memory, and visuospatial processing.42,43 Copy completion time, copy score (score range: 0–36), and 3-minute immediate recall score (score range: 0–36) were recorded.

Neuropsychological measures

To reduce the risk of test performances improving following CCS because of the learning effect of repeated assessments, parallel versions were used when available.

French versions of the Cognitive Difficulties Scale44 assessing subjective memory complaints.

Geriatric Depression Scale (30-item GDS)45 assessing symptoms of depression.

Goldberg Anxiety Scale46 assessing symptoms of anxiety.

Quality of life was assessed using the Quality of Life Scale for older French People (Echelle de Qualité de Vie adaptée aux Personnes Agées; EQVPA).47

French version of the Rosenberg Self-esteem Scale assessing global self-worth.48

Level of motivation, with regard to interest in participating in this study and in future interventions like this, was assessed using a 20-point Likert Scale (not at all=0 to very motivated=20).

Statistical analysis

Data were summarized in the form of mean and SD for quantitative variables and count and percentage for categorical variables. Baseline characteristics and assessments were compared between the two groups (MCI-non-WMH vs MCI-WMH) using Fisher’s exact test. The main analysis focused on postintervention assessment and secondary analysis on follow-up assessment. Differences between postintervention (T3) and baseline (T0) and between follow-up (T6) and baseline (T0) were compared within each group using paired t-tests. Intervention effects at T3 and T6 were compared between the two groups, using analysis of covariance, with the baseline score being the covariate and groups being the factor. All models were adjusted for age, sex, education, and hippocampal atrophy. To estimate the magnitude of difference between the two groups with regard to change over time, effect size index was calculated using Cohen’s f2. Effect size is categorized as small (f2=0.10), medium (f2=0.25), or large (f2=0.40).49

All tests were two-sided, with a significance level of 0.05. No corrections were made for multiple comparisons because of the exploratory nature of the analyses. Analyses were carried out using R statistical software version 3.3.2 (R Foundation for Statistical Computing, Vienna, Austria).

Results

The MCI-non-WMH group included 29 MCI subjects who presented no or minimal WMH (grades 0 and 1), and the MCI-WMH group was composed of 22 MCI subjects who presented moderate-to-severe WMH (grades 2 and 3). Demographics and clinical data for the two groups are summarized in Table 1. There were no significant differences in sex, education, premorbid intelligence, or presence of hippocampal atrophy between the two groups. However, MCI-WMH subjects were significantly older than those in the MCI-non-WMH group.

Table 1

Baseline characteristics and demographics of the subjects

Characteristics	MCI-WMH (n=22)	MCI-non-WMH (n=29)	p-value
Age (years)	76.6 (6.3)	74.2 (6.0)	0.03*
Sex, female, n (%)	19 (86.4)	20 (69)	0.26
fNART	31.5 (4.4)	54.5 (12)	0.99
Education level, >college degree, n (%)	13 (59.1)	17 (58.6)	0.94
Hippocampal atrophy, n (%)	14 (48.3)	10 (45.5)	0.99
Right ≥3 severity	2 (9.1)	2 (6.9)	0.93
Left ≥3 severity	2 (9.1)	3 (10.3)	0.91

Notes: Values are given as mean (SD) or n (%); hippocampal atrophy: absence of hippocampal atrophy;

p<0.05.

Abbreviations: fNART, French version of Adult Reading Test; MCI-WMH, mild cognitive impairment with moderate or severe white matter hyperintensities; MCI-non-WMH, MCI with no or little white matter hyperintensities; ROCF, Rey–Osterrieth Complex Figure.

Baseline assessments

Neuropsychological and psychosocial scores are summarized in Table 2. The MCI-non-WMH group outperformed the MCI-WMH group on the MMSE (p=0.039), two measures of the RAVLT (p=0.039 and 0.029 for immediate recall and delayed recall, respectively) and ROCF copy completion time (p=0.033). No significant difference was found on other measures.

Table 2

Comparison between two groups on cognitive and psychosocial measures at baseline assessment

Variable	MCI-WMH (n=22)	MCI-non-WMH (n=29)	p-values
Cognitive measures
MMSE	26.5±2.5	27.9±1.8	0.039*
RAVLT-immediate recall	41.3±12.9	49±12.8	0.039*
RAVLT-delayed recall	7.8±4.4	10.5±4	0.029*
Logic memory-trial 1	10.3±4.5	12±4	0.17
Logic memory-trial 2	14±5.5	15.4±4.2	0.34
Paired-associated learning test	3.9±3.2	4.4±3.2	0.55
TMT-A	49.3±18.4	44.3±11.7	0.28
TMT-B	143±62	112.9±54.5	0.079
Backward Digit Span	4±1	4.1±1	0.59
Symbol Digit Modalities Test	45.3±10.2	49.8±9.9	0.12
ROCF (copy)	29.7±4.4	29.7±4.2	0.98
ROCF (completion time)	190.9±73	151.6±45.4	0.033*
ROCF (recall)	12.4±5.2	12.3±5.6	0.97
Phonemic verbal fluency	23.2±6.6	23.6±5.9	0.86
Categorical verbal fluency	22.3±8.3	24.1±6.7	0.41
Psychosocial measures
Motivation	16.1±2.9	16±3.3	0.88
Rosenberg Self-esteem Scale	29.4±7.2	31.1±5.8	0.38
EQVPA (Quality of Life Scale)	9.4±3.6	10.4±2.8	0.27
Cognitive Difficulty Scale	21.4±6.2	22.2±7.8	0.66
Geriatric Depression Scale	11±5.3	9.4±6.8	0.35
Goldberg Anxiety Scale	5.1±2.1	4.7±2.5	0.51

Notes: Values are given as mean (SD).

p<0.05.

Abbreviations: EQVPA, Échelle de Qualité de Vie adaptée aux Personnes Agées; MCI-WMH, mild cognitive impairment with moderate or severe white matter hyperintensities; MCI-non-WMH, MCI with no or little white matter hyperintensities; MMSE, Mini Mental State Evaluation; RAVLT, Rey Auditory Verbal Learning Test; ROCF, Rey-Osterrieth Complex Figure; TMT, Trail Making Test.

Cognitive and psychosocial changes after the intervention within each group

Changes in scores for cognitive and psychosocial measures after the intervention are presented in Tables 3 and 4.

Table 3

Score changes on cognitive measures from baseline (T0) to postintervention (T3) and 3-month follow-up (T6) in two groups and comparison between groups for score changes

Variable	T3–T0				T6–T0				Group comparison for cognitive changes (T3–T0) ANCOVA			Group comparison for cognitive changes (T6–T0) ANCOVA
	MCI-WMH (n=22)		MCI-non-WMH (n=29)		MCI-WMH (n=15)		MCI-non-WMH (n=22)
	Mean ± SD	p-value	Mean ± SD	p-value	Mean ± SD	p-value	Mean ± SD	p-value	F (1.44)1	p-value	ES f2	F (1.30)1	p-value	ES f2
MMSE	0.9±1.8	0.027*	0.7±2.1	0.10	0.2±2.3	0.75	0.6±1.9	0.13	0.97	0.33	0.1	3.03	0.092	0.24
RAVLT-immediate recall	3.8±9.8	0.085	2.4±10.3	0.22	7.9±6.7	0.0005*	3.2±12.1	0.23	0.07	0.79	0.04	0.65	0.43	0.02
RAVLT-delayed recall	0.8±2.5	0.16	1±2.9	0.080	2.3±2.1	0.0008*	1±3	0.14	1.81	0.18	0.12	0.82	0.37	0.09
Logic memory-trial 1	0±3.8	0.96	0.4± 3.2	0.53	0.7±4.2	0.17	0.9±3.2	0.23	1.36	0.25	0.19	0.06	0.80	0.05
Logic memory-trial 2	0.9±3.6	0.28	1.2±3.8	0.10	0.7±4.2	0.55	1.5±3.5	0.067	0.91	0.35	0.14	0.83	0.37	0.21
Paired-associated memory test	3.7±3.9	0.0003*	4.4±3.6	<0.0001*	4.7±3.5	0.0001*	6.4±3	<0.0001*	1.49	0.23	0.14	0.43	0.005*	0.43
TMT-A	−5.5±11.8	0.041*	−3.4±9.1	0.054*	−9.4±13.3	0.016*	−5.9±9.8	0.010*	0	0.98	0.03	0.42	0.52	0.07
TMT-B	−29.1±60.4	0.035*	−15.4±44.1	0.071	−29.4±73.6	0.14	1.7±32.2	0.81	0.35	0.56	0.02	0.15	0.70	0.12
Backward Digit Span	0.3±1.2	0.31	0.5±1.2	0.023*	0.3±1.1	0.27	0.2±1.1	0.33	1.3	0.26	0.17	0.11	0.74	0.09
Symbol Digit Modalities Test	0.9±7.8	0.59	2.8±6.8	0.037*	1.9±6	0.23	1.1±8.8	0.57	2.65	0.11	0.16	0.1	0.76	0.04
ROCF (copy)	0.9±4.8	0.38	2.9±5.3	0.007*	3.1±4.4	0.015*	3±5.6	0.021*	3.42	0.071	0.31	0.03	0.86	0.01
ROCF (completion time)	−19±54.5	0.12	1.4±57.8	0.90	−31.9±69	0.095	−3.6±37.7	0.66	0.01	0.91	0.01	0.01	0.93	0.04
ROCF (recall)	0.5±5.1	0.62	3±4.5	0.001*	1.2±6.8	0.31	4.4±4	<0.0001*	3.69	0.061	0.2	3.97	0.055	0.22
Phonemic verbal fluency	0±8.1	0.98	2.8±5.2	0.007*	1.7±5.3	0.25	1.2±7.3	0.45	3.1	0.085	0.26	0.63	0.43	0.27
Categorical verbal fluency	0.4±6.4	0.79	4.6±6.8	0.001*	−0.7±6	0.65	3.8±7.8	0.033*	11.09	0.002*	0.37	17.24	0.0003*	0.55

Notes:

p<0.05.

Abbreviations: ANCOVA, analysis of covariance; ES, effect size; MCI-WMH, mild cognitive impairment with moderate or severe white matter hyperintensities; MCI-non-WMH, MCI with no or little white matter hyperintensities; MMSE, Mini Mental State Evaluation; RAVLT, Rey Auditory Verbal Learning Test; ROCF, Rey -Osterrieth Complex Figure; TMT, Trail Making Test.

Table 4

Score changes on mood and psychosocial measures from baseline (T0) to postintervention (T3) and 3-month follow-up (T6) in two groups and comparison between groups for score changes

Variable	T3–T0				T6–T0				Group comparison for changes (T3–T0), ANCOVA			Group comparison for changes (T6–T0) ANCOVA
	MCI-WMH (n=22)		MCI-non-WMH (n=29)		MCI-WMH (n=15)		MCI-non-WMH (n=22)
	Mean ± SD	p-value	Mean ± SD	p-value	Mean ± SD	p-value	Mean ± SD	p-value	F (1,48)	p-value	ES (f2)	F (1.34)	p-value	ES (f2)
Motivation	2±2.4	0.001*	1.8±3.4	0.010*	0.9±2.4	0.19	2.2±3.5	0.009*	0.31	0.58	0.05	0.13	0.72	0.04
Rosenberg Self-esteem Scale	0.1±4.5	0.89	0.3±3.5	0.67	−1.9±8.7	0.13	1.1±4.4	0.24	0.55	0.46	0.03	2.83	0.10	0.19
EQVPA (Quality of Life Scale)	0.3±2.7	0.64	0.6±2.1	0.17	1±2.4	0.13	−0.3±2.5	0.55	1.19	0.18	0.1	1.1	0.30	0.11
Cognitive Difficulty Scale	1.7±6.5	0.23	0.1±5	0.94	0.8±4	0.45	0.6±4.8	0.56	0.88	0.35	0.07	0	0.95	0.04
Geriatric Depression Scale	0±3.6	0.95	−1±4.3	0.22	−1.3±3.7	0.18	−0.2±3.5	0.81	1.83	0.18	0.17	0.66	0.42	0
Goldberg Anxiety Scale	0±2.3	0.93	−0.4±1.8	0.23	−1.1±2.5	0.10	−0.5±1.7	0.14	1.06	0.31	0.1	0.74	0.40	0.01

Note:

p<0.05.

Abbreviations: ANCOVA, analysis of covariance; EQVPA, Echelle de Qualité de Vie adaptée aux Personnes Agées; ES, effect size; MCI-WMH, mild cognitive impairment with moderate or severe white matter hyperintensities; MCI-non-WMH, MCI with no or little white matter hyperintensities.

From baseline to postintervention, the MCI-WMH group showed significant improvement on the MMSE (p=0.027), the paired-associate learning test (p=0.0003), TMT-A (p=0.041), TMT-B (p=0.035), and motivation (p=0.001). The MCI-non-WMH group improved on a higher number of outcome measures, namely the paired-associate learning test (p<0.0001), TMT-A (p=0.054), Backward Digit Span (p=0.023), digit symbol test (p=0.037), ROCF copy (p=0.007), ROCF recall (p=0.001), phonemic fluency (p=0.007), categorical fluency (p=0.001), and motivation (p=0.01).

Between the baseline and the 3-month follow-up, improvement in the MCI-WMH group was found for the immediate and the delayed recall of the RAVLT (p=0.0005 and 0.0008, respectively), the paired-associate learning test (p=0.0001), TMT-A (0.016), and ROCF copy score (p=0.015). Once again, improvement on a higher number of outcome measures was found in the MCI-non-WMH group, namely on the paired-associate learning test (p<0.0001), TMT-A (p=0.01), ROCF copy (p=0.021), ROCF recall (p<0.0001), categorical fluency (p=0.033), and motivation (p=0.009).

Figures 2 and 3 depict the performances for the immediate recall and the delayed recall of the RAVLT in the two groups, at the three assessment points. The performances for the paired-associate memory test and categorical fluency are depicted in Figures 4 and 5, respectively.

Figure 2

RAVLT the sum of five immediate recall scores in the MCI-WMH vs MCI-non-WMH at baseline (T0), postintervention (T3), and 3-month follow-up (T6).

Abbreviations: MCI, mild cognitive impairment; MCI-WMH, MCI with moderate or severe white matter hyperintensities; MCI-non-WMH, MCI with no or little white matter hyperintensities; RAVLT, Rey Auditory Verbal Learning Test.

Figure 3

RAVLT delayed recall scores in the MCI-WMH vs MCI-non-WMH at baseline (T0), postintervention (T3), and 3-month follow-up (T6).

Abbreviations: MCI, mild cognitive impairment; MCI-WMH, MCI with moderate or severe white matter hyperintensities; MCI-non-WMH, MCI with no or little white matter hyperintensities; RAVLT, Rey Auditory Verbal Learning Test.

Figure 4

Paired-associate memory test scores in the MCI-WMH vs MCI-non-WMH at baseline (T0), postintervention (T3), and 3-month follow-up (T6).

Abbreviations: MCI, mild cognitive impairment; MCI-WMH, MCI with moderate or severe white matter hyperintensities; MCI-non-WMH, MCI with no or little white matter hyperintensities.

Figure 5

Categorical verbal fluency scores in the MCI-WMH vs MCI-non-WMH at baseline (T0), postintervention (T3), and 3-month follow-up (T6).

Abbreviations: MCI, mild cognitive impairment; MCI-WMH, MCI with moderate or severe white matter hyperintensities; MCI-non-WMH, MCI with no or little white matter hyperintensities.

Differences between groups in changes on outcome measures

At postintervention assessment, CCS had a more beneficial effect on the MCI-non-WMH group than on the MCI-WMH group with regard to improving categorical fluency (4.6±6.8 vs 0.4±6.4 points; effect size=0.37; p=0.002).

With regard to the 3-month follow-up assessment, significantly higher score gains were observed in the MCI-non-WMH group on the paired-associate learning test (6.4±3 vs 4.7±3.5 points; effect size=0.43; p=0.005) and categorical fluency (3.8±7.8 vs −0.7±6 points; effect size=0.55; p=0.0003).

Discussion

In this study, we investigated whether a CCS program induced differential effects in older adults diagnosed with MCI, according to the severity of WMH. All participants attended 24 sessions of the CCS program over a period of 3 months. The main findings were that 1) at baseline, in comparison with the MCI-non-WMH group, the subjects in MCI-WMH group were older and presented lower global cognitive efficiency and worse episodic memory, and needed more time to copy a complex figure; 2) the two groups improved on several cognitive measures after the intervention; 3) the MCI-non-WMH group improved on a higher number of cognitive measure than the MCI-WMH group, suggesting that the CCS program seemed to be more beneficial for MCI subjects without WMH; 4) although two cognitive measures were improved in both groups, the differential improvements for the other cognitive measures depend on the group status.

The baseline differences between the two groups in our study are not surprising. It is reported that WMH is associated not only with older age,50 but also with impairment of perceptual/processing speed,51,52 global cognition, executive functions, working memory, episodic memory, and semantic memory.13,53–55

Both groups improved on the paired-associate learning test and the TMT-A at postintervention. The improvement persisted for another 3 months after the intervention had been discontinued. The paired-associate learning test requires several memory strategies, such as semantic processing, visual imagery categorization, association, and organization.56 A significant time reduction on the TMT-A suggests an improvement of processing speed. These improvements could be attributed to several cognitive exercises used within the CCS program, which were focused on stimulating these cognitive processes.

Aside from the two measures mentioned above, the MCI-WMH group improved on global cognitive efficiency and motivation at postintervention. However, the improvement was not observed during the 3-month follow-up. It is worth noting that these subjects improved their performance on the immediate and delayed recall of the RAVLT as well as the ROCF copy score during the 3-month follow-up. Compared with MCI-non-WMH subjects, MCI-WMH subjects had impaired retrieval and long-term consolidation processes at baseline. However, they could still improve these cognitive functions, thanks to the CCS intervention, suggesting potential cognitive and brain plasticity in these patients. Previous studies have shown that in both younger and older adulthood, cognitive training can modify white matter microstructure57 and that there is a significant link between memory improvement and changes in white matter.58 Our findings are in concordance with a recent study on the effects of a training program focusing on attentional processes (weekly 2-hour sessions for 20 weeks) in MCI patients with moderate-to-severe WMH. The authors also found improvements on the immediate recall of the RAVLT and ROCF copy in MCI patients receiving the intervention, compared with the no-treatment group.59

MCI patients with no or little WMH improved their performance on a higher number of cognitive measures than those with moderate-to-severe WMH at postintervention and during the follow-up assessments. At postintervention, they improved on the Backward Digit Span, the SDMT, and phonemic fluency, although these improvements did not last. However, improvements on copy and recall of the ROCF and categorical fluency were observed both at postintervention and during the 3-month follow-up assessments. Moreover, significantly higher score gains with medium-to-large effect sizes, favoring the MCI-non-WMH group, were observed on the paired-associate memory test during the 3-month follow-up and on categorical fluency both at postintervention and during follow-up assessments. Overall, these findings suggest that MCI patients with WMH did not benefit from the CCS program as much as those with no or little WMH, with regard to enhancing specific cognitive functions. Taken together, our findings suggest that severity of WMH was related to baseline cognitive performance and cognitive improvement induced by a CCS program. These findings conflict with those of a study exploring the effects of working memory training on cognitive functions in MCI subjects and healthy older adults, in which authors found that hippocampal atrophy, instead of WMH, may be a predictor of cognitive training outcome.9

Finally, the two groups did not improve on psychosocial measures, except for motivation, which was initially high, being enhanced after the intervention for both groups. The enhancement persisted through to the follow-up assessment only for the MCI-non-WMH group. This finding suggests that this short-term cognitive intervention was not effective with regard to enhancing psychosocial functioning in MCI subjects.

Limitations

One of the limitations of the study is the lack of a control group, which did not receive the CCS intervention. However, our principal objective was to compare the effects of the CCS program on two clinical samples in order to understand if WMH affect intervention outcome. A randomized controlled trial is required to determine the efficacy of the CCS as a clinical intervention. In addition, the small sample size keeps us from analyzing the intervention effects according to the periventricular or deep nature of the WMH, as some studies reported that these two types of lesions may differentially impact the clinical presentation.52,60–63

Conclusions

This study constitutes a preliminary exploration, which aims to highlight the importance of considering WMH in interventions in MCI patients. Our findings suggest that both MCI subjects with and without WMH could benefit from this type of CCS program, with improvements being observed within several cognitive domains, and some improvements being maintained through to a short-term follow-up. However, the differential effects in the two groups suggest that brain lesions could influence intervention outcomes. MCI-non-WMH subjects improved on a higher number of cognitive measures than MCI-WMH subjects, for whom no improvement was observed for certain cognitive functions. Interestingly, our findings did show that MCI-WMH subjects could improve on some components of executive functions, processing speed, and memory, suggesting potential cognitive plasticity in these patients, who are at higher risk of worsening cognitive decline with the progression of lesions, and of developing AD and dementia. These findings are encouraging and should be confirmed in a randomized controlled trial. We also suggest that in future cognitive intervention studies, brain lesions, such as hippocampal atrophy and WMH, should be taken into consideration when analyzing intervention effects on patients with MCI.