Mild cognitive impairment and the uncertainties of diagnosis: reviewing the accuracy of the Montreal Cognitive Assessment and exploring the process of psychosocial adjustment
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Abstract
Background: Mild Cognitive Impairment (MCI) is a clinical construct reputed to
represent an intermediate stage on a continuum between normal aging and cognitive
decline. Conceptual and prognostic ambiguity can lead to significant diagnostic
challenges and there is a need for accurate screening tests which can assist clinicians
with decision-making. A diagnosis of MCI is also associated with considerable
uncertainty for patients who may be adjusting to cognitive difficulties along with an
increased risk of developing dementia. Beliefs about MCI may influence psychosocial
adjustment, and individual differences in ‘psychological flexibility (PF)’, as
conceptualised by the Acceptance and Commitment Therapy (ACT) model, may also
be involved in this process.
Objectives: In order to evaluate the accuracy and clinical utility of a recently
developed screening tool for MCI, the Montreal Cognitive Assessment (MoCA), a
systematic review of validation and diagnostic test accuracy (DTA) studies for this
measure was conducted. Psychosocial adjustment to a diagnosis of MCI was also a
key focus. An empirical study was therefore carried out with the aim of evaluating the
possible relationships between cognitive impairment, illness representations about
MCI, psychological wellbeing and quality of life (QoL), and to assess the potential
involvement of PF.
Method: Following a systematic search of relevant electronic databases and reference
lists, validation and DTA studies of the MoCA were identified and evaluated for
methodological quality. For the empirical study, patients recently diagnosed with MCI
were recruited from local NHS memory clinic services and completed the MoCA and
a questionnaire pack assessing illness representations, PF, mood, anxiety and QoL.
Results: The systematic review identified 18 validation and DTA studies. Few of the
studies achieved high ratings for methodological quality and problems with
representativeness and generalisability were identified. Nevertheless, sensitivity levels
appeared robust across studies, though specificity was variable. For the present
empirical study, participants reported a spectrum of positive and negative beliefs about
MCI. Distress attributed to MCI was associated with anxiety, along with perceptions
of more serious illness consequences, while higher PF was associated with higher
perceived QoL and mood. Lived experience of MCI appeared to have more relevance
to psychosocial adjustment than objective cognitive impairment.
Conclusions: The results of the systematic review indicate that while the MoCA is a
robust tool overall in the identification of cognitive impairment, estimates of accuracy
may be exaggerated by inter-study variation and bias. More rigorous validation studies
are therefore needed. Implications for clinical decision-making regarding MCI are
discussed and recommendations for future accuracy studies are outlined.
The empirical study supported the findings of previous studies of the relevance of
illness representations to psychosocial adjustment in MCI and added to the evidence
base by providing preliminary support for the possible involvement of PF. The results
suggest that both cognitive content and PF may represent possible vehicles for
therapeutic change in patients with adjustment difficulties, and indicate that further
investigation of these factors is warranted. Conclusions are limited, however, by small
sample size and low statistical power. Replication of these findings with a larger and
more representative sample is therefore recommended.
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