| Literature DB >> 25909154 |
Irene Torres-Sánchez1, Elisabeth Rodríguez-Alzueta1, Irene Cabrera-Martos1, Isabel López-Torres1, Maria Paz Moreno-Ramírez1, Marie Carmen Valenza1.
Abstract
The objectives of this study were to characterize and clarify the relationships between the various cognitive domains affected in COPD patients and the disease itself, as well as to determine the prevalence of impairment in the various cognitive domains in such patients. To that end, we performed a systematic review using the following databases: PubMed, Scopus, and ScienceDirect. We included articles that provided information on cognitive impairment in COPD patients. The review of the findings of the articles showed a significant relationship between COPD and cognitive impairment. The most widely studied cognitive domains are memory and attention. Verbal memory and learning constitute the second most commonly impaired cognitive domain in patients with COPD. The prevalence of impairment in visuospatial memory and intermediate visual memory is 26.9% and 19.2%, respectively. We found that cognitive impairment is associated with the profile of COPD severity and its comorbidities. The articles reviewed demonstrated that there is considerable impairment of the cognitive domains memory and attention in patients with COPD. Future studies should address impairments in different cognitive domains according to the disease stage in patients with COPD.Entities:
Mesh:
Year: 2015 PMID: 25909154 PMCID: PMC4428856 DOI: 10.1590/S1806-37132015000004424
Source DB: PubMed Journal: J Bras Pneumol ISSN: 1806-3713 Impact factor: 2.624
Figure 1 -Selection of the articles analyzed in this review.
Characteristics of the articles selected.
| Study | Design | Objective | Sample size and COPD severity | Characteristics of COPD participants | Intervention | Results/Conclusions |
|---|---|---|---|---|---|---|
| Dodd et al.(19) | Observational study | To assess neuropsychological performance in COPD patients hospitalized after an acute exacerbation and recovery, compared with patients with stable COPD and with healthy control subjects | 110 participants: | - | In patients hospitalized with an acute COPD exacerbation, impaired cognitive function is associated with worse health status and longer length of hospital stay. Cognitive function might not improve with recovery | |
| 30 COPD inpatients hospitalized following an exacerbation | Mean age, 70 ± 11 years; 15 (50%) were female | |||||
| 50 outpatients with stable COPD | Mean age, 69 ± 8 years; 28 (56%) were female | |||||
| 30 healthy control subjects | ||||||
| Chang et al.(20) | Cohort study | To determine the extent to which the co-occurrence of COPD and cognitive impairment leads to adverse health outcomes in older adults | 3,093 patients: | None | Patients with COPD and cognitive impairment had the highest rates of respiratory-related and all-cause hospitalizations and death | |
| 431 with COPD only | 188 (43.7%) were 65-70 years of age; 210 (48.7%) were female | |||||
| 29 with COPD and cognitive impairment | 6 (21.3%) were 65-70 years of age; 10 (34.5%) were female | |||||
| 114 with cognitive impairment only | ||||||
| 2,519 with neither COPD nor cognitive impairment | ||||||
| Dodd et al.(21) | Observational study | To evaluate whether there are significant differences between COPD patients and control subjects, in terms of white matter integrity and communication between gray matter resting-state networks, and to test the observed differences related to disease severity, comorbid cerebrovascular disease, and cognitive dysfunction | 25 non-hypoxemic COPD patients | Mean age, 67.8 ± 8.1 years; 11 (44%) were female | None | In stable, non-hypoxemic COPD, there is reduced white matter integrity throughout the brain and widespread disturbance in the functional activation of gray matter, which might contribute to cognitive dysfunction. White matter microstructural integrity is independent of smoking and comorbid cerebrovascular disease, but gray matter functional activation is not. The mechanisms remain unclear but could include cerebral small vessel disease caused by COPD |
| 25 control subjects | ||||||
| Villeneuve et al.(10) | Observational study | To determine the frequency and subtypes of MCI in COPD patients and to assess the validity of two cognitive screening tests (the MMSE and MoCA) in detecting MCI in COPD patients | 45 patients with moderate-to-severe COPD | Mean age, 68.84 ± 8.43 years; 29 (64%) were female | None | In this preliminary study, a substantial proportion of COPD patients were found to have MCI. The MoCA was better than was the MMSE at detecting MCI in COPD patients. |
| 50 healthy control subjects | ||||||
| Martin et al.(22) | Clinical trial | To determine the effect of hypoxia on cognitive performance in COPD patients with PaO2 <6.6 kPa | 10 patients with moderate-to-severe COPD | Mean age, 64 years; 3 (30%) were female | For a short period of time, patients breathed 21% O2 when PaO2 was < 6.6 kPa | Short-term exposure to hypoxia had no adverse effect on cognitive function |
| Pereira et al.(23) | Clinical trial | To evaluate the effect of a multidisciplinary pulmonary rehabilitation program on cognitive function in COPD patients, adjusting for potential confounders | 34 patients with moderate-to-severe COPD | Mean age, 65.2 ± 7 years; 17 (50%) were female | 3-month program of pulmonary rehabilitation | Even after adjusting for the sociodemographic factors that might affect cognitive function, the authors found that pulmonary rehabilitation improved cognitive performance in COPD patients. There were gender- and age-related differences in cognitive scores that persisted after rehabilitation |
| 18 healthy control subjects | ||||||
| Klein et al.(24) | Cohort study | To explore the influence of COPD on attentional functions, learning, and logical thinking | 60 COPD patients | Mean age, 63.2 ± 9.8 years; 24 (40%) were female | None | In COPD patients, there was global impairment in cognitive functions that was negatively influenced by advancing age and increased in proportion to the degree of disease severity |
| 60 control subjects | ||||||
| Thakur et al.(25) | Cohort study | To elucidate the association between COPD and the risk of cognitive impairment, in comparison with control subjects without COPD | 1,202 COPD patients | Mean age, 58.2 ± 6.2 years; 691 (57.4%) were female | None | COPD is a major risk factor for cognitive impairment. In COPD patients, hypoxemia is a major contributor to cognitive impairment and regular use of home oxygen is a protective factor. Health care providers should consider screening COPD patients for cognitive impairment |
| 302 control subjects | ||||||
| Antonelli-Incalzi et al.(14) | Observational study | To assess whether certain neuropsychological patterns are associated with various limitations to physical independence in COPD patients | 149 COPD patients | 112 (75.2%) were over 65 years of age; 14 (9.4%) were female | None | Classic indicators of the severity of COPD showed no correlation with personal autonomy |
| Borson et al.(26) | Observational study | To model the relationship between respiratory failure and domains related to brain function, including low mood, subtly impaired cognition, systemic inflammation, and structural/neurochemical brain abnormalities | 9 healthy control subjects | None | COPD is associated with slight decreases in mood and cognition. Severe COPD is associated with chronic systemic inflammation and subtle cognitive deficits (on digit symbol coding tasks). Levels of oxygen desaturation appear to mediate specific changes in brain neurochemistry and structure that suggest sustained brain damage | |
| 18 COPD patients, half of whom were oxygen-dependent | Mean age, 68.5 ± 8.0 years; 11 (64%) were female | |||||
| Orth et al.(27) | Observational study | To analyze driving performance in COPD patients and healthy control subjects | 17 COPD patients | Mean age, 55.2 ± 9.3 years | None | Compared with healthy control subjects, COPD patients are more likely to cause a traffic accident. Impaired driving performance in COPD patients cannot be predicted on the basis of the severity of the disease |
| 10 healthy control subjects | ||||||
| Pinto de Lima et al.(28) | Observational study | To test the hypothesis that clinically stable COPD patients without overt cognitive symptoms can nonetheless have subtle cognitive impairment | 30 COPD patients | Mean age, 65 ± 8 years; 10 (33%) were female | None | There might be subclinical encephalopathy in COPD, characterized by subtle impairment of global cognitive ability |
| 34 control subjects | 24 (71%) were female | |||||
| Salik et al.(29) | Observational study | To determine the relationship between cognitive function and quality of life in COPD patients with mild hypoxemia and moderate airway obstruction | 32 patients with moderate stable COPD | Mean age, 66.7 ± 2.5 years; 14 (44%) were female | None | Cognitive function in COPD patients with hypoxemia might not be impaired despite their poor quality of life status |
| 26 healthy subjects | ||||||
| Antonelli-Incalzi et al.(30) | Observational study | To evaluate the prognostic role of cognitive impairment in patients with severe COPD | 149 COPD patients who had undergone a period of in-hospital rehabilitation following an acute exacerbation | Mean age, 68.7 ± 8.5 years; 22 (16.4%) were female | None | Impaired drawing ability is a risk factor for mortality and its testing might improve the assessment of hypoxemic COPD patients |
| Corsonello et al.(31) | Observational study | To determine whether cancer is more disabling than are other chronic diseases that are highly prevalent in the elderly | 6 groups of patients: | None | Cognitive impairment was more prevalent in patients with congestive heart failure or COPD than in those with cancer | |
| Congestive heart failure (n = 832) | ||||||
| Diabetes mellitus (n = 939) | ||||||
| COPD (n = 399) | 178 (44.6%) were 65-79 years of age; 147 (36.8%) were female | |||||
| Non-metastatic solid tumors (n = 813) | ||||||
| Metastatic solid tumors (n = 259) | ||||||
| Leukemia/lymphoma (n = 326) | ||||||
| Antonelli-Incalzi et al.(32) | Observational study | To determine whether the neuropsychological performance of untreated patients with OSA conforms to a distinctive pattern | 49 newly diagnosed, untreated OSA patients | None | A minority of newly diagnosed OSA patients had distinct neuropsychological impairment. The greater body mass index of cognitively impaired OSA patients indicates that the metabolic syndrome might also be causally related to the cognitive dysfunction | |
| 27 patients with multi-infarct dementia | ||||||
| 31 patients with mild-to-moderate dementia of the Alzheimer type | ||||||
| 63 patients with severe COPD |
MMSE: Mini-Mental State Examination; MoCA: Montreal Cognitive Assessment; MCI: mild cognitive impairment; kPa: kilopascal; CHF: congestive heart failure; and OSA: obstructive sleep apnea.
Tests or batteries of tests used in the assessment of the cognitive domains under study in the articles selected.
| Neuropsychological assessment instrument or function assessed | Cognitive domain | ||||||
|---|---|---|---|---|---|---|---|
| Perception | Attention | Memory and learning | Abstract thinking and executive function | Language | Intelligence | General (global screening) | |
| Wechsler Test of Adult Reading(19,22) | X | ||||||
| Mini-Mental State Examination(10,19-21,25,28-30) | X | ||||||
| Rey Complex Figure Test-Copy and Rey Complex Figure Test-Recall(19,21,22) | X | ||||||
| Wechsler Memory Scale-III UK Word Lists(19) | X | ||||||
| Delis-Kaplan Verbal Fluency test(19) | X | ||||||
| Delis-Kaplan Trail Making Test(10,19,22) | X | ||||||
| Wechsler Adult Intelligence Scale-III UK Letter-Number Sequencing(19,21) | X | ||||||
| Wechsler Memory Scale-III UK Spatial Span(19,23) | X | ||||||
| Wechsler Adult Intelligence Scale-III Digit Symbol(19,26) | X | ||||||
| Wechsler Adult Intelligence Scale-III Symbol Search(19,21) | X | ||||||
| Montreal Cognitive Assessment(10) | X | ||||||
| Digit Span Test (Wechsler Adult Intelligence Scale-III)(10,23) | X | X | |||||
| Digit Symbol coding test (Wechsler Adult Intelligence Scale-III)(10) | X | X | |||||
| Semantic Verbal Fluency(10) | X | X | |||||
| Letter verbal fluency (P, F and L)(10) | X | X | |||||
| Rey Auditory Verbal Learning Test(10,23) | X | ||||||
| Block Design(10) | X | ||||||
| Bells Test(10) | X | ||||||
| Word Lists Learning, Delayed Recall, and Delayed Recognition (Wechsler Memory Scale-III)(21) | X | ||||||
| Verbal Fluency-FAS task (Delis-Kaplan Executive Function System)(21,23) | X | ||||||
| Stroop Color-Word Test(10,23) | X | ||||||
| Attention Network Test(24) | X | X | |||||
| Standard Progressive Matrices(24) | |||||||
| Verbal and Nonverbal Learning Test (part of the Vienna Test System)(24) | X | ||||||
| Raven’s Colored Progressive Matrices(14) | X | ||||||
| Phonemic verbal fluency test(14) | X | ||||||
| Corsi Block-Tapping task (visuospatial span)(14) | X | X | |||||
| Verbal word span(14) | X | X | |||||
| Rey Auditory 15-Word Learning test(14) | X | ||||||
| Albert’s test (visual exploration)(14) | X | ||||||
| Copying geometrical drawings with or without landmarks(14) | X | ||||||
| Immediate Visual Memory Test(14) | X | ||||||
| Sentence construction(14) | X | ||||||
| The Computer-Aided Risk Simulator (driving simulator test)(27) | X | X | |||||
| Dementia Rating Scale-2(26) | X | ||||||
| Wide Range Achievement Test-3(26) | X | ||||||
| Logical memory subtest of the Wechsler Memory Scale-III(26) | X | ||||||
| Mental Deterioration Battery(30) | X | ||||||
| 10-item Hodkinson Abbreviated Mental Test(31) | X | ||||||