• 沒有找到結果。

FOK JUDGMENT AND NEUROCOGNITIVE PERFORMANCES

In order to examine the relationship between FOK judgment and neurocognitive

performance, correlations were calculated (see Table 6). Previous analyses revealed the

misses on the FOK “yes” judgment was sensitive in distinguishing HC from other

groups. Thus, special attention was paid on the relationships between misses on the

FOK “yes” judgment and three neurocognitive measures. Pearson’s r correlation was

performed. However, the relationship with neurocognitive measures did not examine in

the auditory-based FOK performance due to violation to the assumption of Pearson’s.

The misses on the “yes” judgment was negatively correlated with executive

function in both HC (r(30) = -.370, p = .044) and SCD (r(33) = -.420, p = .015); no

correlation was found in MCI (r(18) = .118, p = .641) and AD (r(7) = -.347, p = .445).

In addition to executive function, the misses was also negatively correlated with

immediate recall in HC (r(30) = -.572, p = .001). Contrary to the results of Souchay et

al. (2002), no correlation with memory score was found in all four groups.

Since literature has suggested that the aging-related decline of executive function

and episodic memory behaving similarly and being strongly correlated to each other

(McCabe, Roediger, McDaniel, Balota, & Hambrick, 2010), further correlations were

done to examine the relationship between executive function and other two measures.

Pearson’s r correlations showed that executive function measure was positively

correlated with immediate recall measure in both HC (r(30) = .782, p < .001) and SCD

(r(33) = .453, p = .008). A z-test was conducted (Eid, Gollwitzer, & Schmitt, 2017)

comparing the correlations in SCD and HC. The result was statistically significant (z =

2.119, p = .017, one-tailed) that the HC group showed a stronger correlation between

executive function and immediate recall when compared to SCD. Positive correlations

between executive function and delayed recall were also found in both HC (r(30) = .694,

p < .001) and SCD (r(33) = .409, p = .018). However, no significant correlation difference was reported (z = 1.588, p = .056, one-tailed).

(INSERT TABLE 6 HERE).

DISCUSSION

The present study examined memory monitoring performance in individuals with

SCD by applying the FOK paradigm in episodic memory tests, which examined

whether individuals with SCD exhibit differences across different modalities.

Individuals with SCD did not exhibit differences on the overall performance of

making memory-monitoring judgment as compared to healthy elders in the present

study. This finding supports a previous study wherein individuals with SCD judged

their memory performance no worse than did healthy elders (Perrotin et al., 2012).

However, the current study revealed the difference between individuals with SCD and

healthy elders while comparing them to patients with MCI and AD. While healthy

elders consistently exhibited significantly better memory monitoring performances than

did patients across domains, individuals with SCD only excelled on the auditory-based

test. That is, despite no statistical difference was reported between healthy elders and

individuals with SCD, our results also demonstrated insignificant differences between

individuals with SCD and patients with MCI and AD on visual-based test. A possible

explanation for the aforementioned results is that the subtle cognitive changes in

individuals with SCD were compensated for by other neurocognitive mechanisms (Erk

et al., 2011), leading to a decline that was not detectable when compared to healthy

elders (Koppara et al., 2015). This is in line with the cognitive decline depicted in the

study of Jessen et al. (2014); the slope of cognitive decline did not steeply drop during

the preclinical phase. In other words, our finding might suggest individuals with SCD

lying at the intermediate position between healthy elders and patients with MCI, as

Figure 1a showed a gradually increasing trend in the proportion of poor performance

from healthy elders, individuals with SCD, to pathological patients. Moreover, a recent

study has addressed the relationship between SCD and MCI from a different perspective.

It stated that the boundary between MCI and SCD is artificial in nature, and thus the

issue requires further study establishing an optimal distinction (Molinuevo et al., 2017).

Our results support the idea that auditory-based tests are better in the context of

detecting episodic memory deficits (Albert et al., 2011; Mortamais et al., 2017).

However, our discoveries in the visual-based test contradict previous findings of the

picture superiority effect in patients with AD and MCI (Ally, 2012; Ally et al., 2009;

Embree, Budson, & Ally, 2012). The reasons might be multifold. First, the visual

stimuli we used in this study were highly abstract, without concrete general concept that

was familiar to participants. The figure placed a high demand on information processing

(Shin, Park, Park, Seol, & Kwon, 2006), differing from concrete pictures used in

previous studies. Therefore, instead of an unequal performance caused by test modality,

it is possible that the difference was created by the level of abstraction embodied in the

information (Vallet et al., 2016). Recent research has also indicated that patients with

mild AD exhibit a relatively intact cued performance when the cues are focused on

distinctive conceptual information related to the target item (Deason, Hussey, Flannery,

& Ally, 2015). Second, our study mainly focused on the accuracy of monitoring

memory prospectively in relation to subsequent recognition. Despite a previous study

reporting that patients with MCI demonstrate a coherent performance on rating their

confidence and recognizing presented picture is new or old (Embree et al., 2012), our

results from the comparison with healthy elders provide evidence that MCI patients’

ability to deal with visual items is not superior than auditory item at memory monitoring.

Third, the tests selected for the FOK paradigm might have been of varying levels from

their cognitive substrates to test procedures. For example, RCFT requires attentive

learning during encoding phase (Shin et al., 2006) whereas Word list subtest of

WMS-III uses semantically-associated learning during encoding (Chang et al., 2018).

Thus, these memory tests require different cognitive abilities while processing provided

stimuli. Moreover, it is unlikely that these tests were comparable given the fact that they

use different approaches to measure the memory performance other than visual versus

auditory stimulus difference only. Therefore, the discrepant results between our study

and previous literature might need further studies to clarify given the possibility that

FOK performances in two selected tests might actually reflect different cognitive

components.

In comparison with healthy elders, further analyses suggest a discrepant

relationship between memory monitoring and neurocognitive functions in individuals

with SCD. Unlike the finding in patients with AD (Souchay et al., 2002), executive

function was negatively correlated with the overestimation of accuracy in both healthy

elders and individuals with SCD. This finding supports previous studies that found

memory monitoring performance measured by the FOK paradigm to be associated with

executive function in aging-related decline (Isingrini et al., 2008; Souchay & Isingrini,

2004). However, a negative correlation between the immediate recall score indicating

learning functioning and the accuracy overestimation of the FOK task was only evident

in our HC group. As the learning index indicated participants’ ability to learn new

information, reflecting a partial characteristic of episodic memory (Albert et al., 2011),

our results might suggest that individuals with SCD has a tendency to less use memory

resources in proceeding memory monitoring compared to healthy elders. Such findings

appear to be in line with a recent proposal suggesting that within-person variability

across cognitive domains is more valuable in predicting late-life cognitive decline

(Salthouse & Soubelet, 2014). However, further follow-up studies on this issue are

needed.

Several limitations were noted in the current study. First, our study used a

relatively small sample size in each group, particularly the patient groups. In order to

obtain sufficient information to examine differences between groups, it is advised that

future studies involve larger sample sizes. Second, we are aware of the debate about the

influence of recruiting sites for individuals with SCD (Perrotin et al., 2017;

Rodriguez-Gomez, Abdelnour, Jessen, Valero, & Boada, 2015). Thus, information

regarding depressive mood, medical records, and judgment regarding one’s own

memory decline were collected to eliminate possible confounding variables. Third, it is

likely that our results were biased by participants’ response preference in the FOK

paradigm. In other words, all participants tended to state “yes,” firmly assured of their

following accuracy, which the base rate for “yes” judgment was enlarged enough to

show variation. However, this tendency was observed across groups, and no significant

difference was reported between groups. Thus, this is unlikely to have led to the final

results. Another similar statistical limitation was from our data distribution. That is, the

selected auditory episodic memory test had items with high familiarity or high semantic

association to help memorizing. According to our data, it is clear that cognitively

normal participants almost excelled in every trial in the auditory-based test, leading to a

violation of the parametric assumption. This makes data analysis problematic as some

useful kits could not be performed. Fourth, our study requires extra caution while

explaining the FOK test results between SCD and HC given the fact that no direct

differences were observed. It is possible that the insignificance, other than the gradual

decline during the AD pathology, is rooted from the visual stimulus item lacking in

sensitivity differentiating SCD from HC. Future study on this issue is merited.

However, to our knowledge, the current study is the first to use an objective

method to examine how individuals with SCD monitor their memory. Despite the fact

that there was no significant difference in comparison with healthy elders, our results

suggest that individuals with SCD are at the intermediate position between normal

aging and pathological aging. This finding is in line with a recent hypothesis depicting

AD as a continuum (Jack et al., 2018). Moreover, a recent study simulated the AD

disease progression through data-driven model and found multifactorial interactions,

rather than linear cascade event, are responsible for the progression (Veitch et al., In

press). In addition, out study might provide an objective measure targeting individuals

with SCD who might be in risk for pathological change. Future follow-up study on this

issue is thus needed.

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