Background
Late-life depression (LLD) is a major public health issue [
1]. It is associated with lower quality of life, poorer physical health and higher disability [
2], as well as greater mortality risk [
3]. LLD has specific characteristics, including the chronicity of symptoms [
4], frequent comorbidities and the high prevalence of subsyndromal depression [
5]. Cognitive impairments are very common in LLD, with executive dysfunction and decreased information processing speed being the most predominant [
6‐
8]. Impairments in visuospatial skills and verbal fluency have also been reported as well as poor performance in episodic memory, learning and recall [
8‐
11]. Cognitive dysfunction is furthermore predictive of poor response to pharmacological and psychological treatments of depression [
12].
While there are arguments supporting antidepressant effectiveness and a favourable benefit-risk ratio for major depression [
13], a much lower efficacy has been found for subsyndromal depression [
14]. In particular, the potential positive effect of antidepressants on cognitive functioning in depressed elderly patients is still debated, and deleterious effects on cognition have also been reported. Several antidepressants, such as tricyclic antidepressants (TCAs), may have a detrimental impact notably due to their anticholinergic properties and selective serotonin reuptake inhibitors (SSRIs) may have a negative cognitive impact in non-responders [
15]. The inappropriate use of antidepressants in subsyndromal depression may increase the risk of drug interactions and adverse reactions as aging is also associated with pharmacodynamic alterations (decreased renal clearance, altered hepatic metabolism and increased elimination half-lives). Given the risks associated with reduced cognitive competency in the elderly, the benefit-risk balance of antidepressants in relation to cognition should be given careful consideration.
In a systematic review of 43 clinical trials with a median follow-up of 8 weeks, a small effect size favouring active monotherapy was observed for verbal memory while a small effect size favouring placebo was observed for processing speed [
16]. The few existing elderly community cohort studies with longer follow-up [
17,
18] generally suffer from several biases notably due to limited consideration of potential confounders (e.g. use of other medications), of patterns of antidepressant use and treatment chronicity, and of channelling bias (related to underlying burden of physical and mental illness). Distinguishing the effect of depression from that of antidepressant treatment is notably a critical point [
19].
The purpose of this study was to prospectively examine the association between antidepressant use and 10-year decline in five cognitive domains in a large elderly community-dwelling cohort, taking into account multiple potential confounding factors including residual depressive symptoms.
Methods
Study sample
Participants were recruited as part of the Three-City Cohort study of community-dwelling persons aged 65 years and over from the electoral rolls of three French cities (Bordeaux, Dijon and Montpellier) between 1999 and 2001 [
20]. Of the persons contacted, the participation rate was 37%. The study protocol was approved by the Ethics Committee of the Bicêtre University-Hospital (France) and written informed consent was obtained from each participant. A standardised evaluation with a face-to-face interview and a clinical examination was undertaken at baseline and after 2, 4, 7, and 10 years.
Of the 9294 participants included in the cohort, 214 were excluded because of a diagnosis of prevalent dementia at baseline and 1159 because of they missed the 2-year follow-up examination, which was necessary for antidepressant exposure assessment as defined below. The study sample was further limited to those using the same class of antidepressant at both baseline and the 2-year visit and to those not treated with antidepressant at both visits, thus excluding a further 511 participants. Among the latter, 157 stopped taking their antidepressant between the two visits, 278 began antidepressant treatment during the 2-year period, 32 were taking two different classes of antidepressant at the same visit, and 44 changed class of antidepressant between the two visits. Twenty-nine participants missing all follow-up cognitive evaluations were also excluded. The present analyses were thus conducted on 7381 subjects. As compared with the analysed sample, the non-demented excluded participants were older (P < 0.0001) and more likely to have activity limitations, visual impairment and ischemic pathologies (P < 0.0001), respiratory diseases (P = 0.002), and diabetes (P = 0.005). They had lower levels of education and cognitive scores and higher levels of depressive and anxiety symptoms (P < 0.0001). They also had higher rates of use of antidepressants, benzodiazepines, anticholinergic drugs and other drugs acting on the central nervous system (P < 0.0001).
Cognitive outcome measures
A battery of cognitive tests administered by a neuropsychologist assessed different cognitive domains. The Isaac’s Set Test [
21] was used to provide a measure of verbal fluency or semantic access which is sensitive to changes in both frontal and temporal areas. Fluency was assessed as the total score corresponding to the sum of the number of words generated in four semantic categories within 30 seconds (animals, colours, cities, fruits). Benton’s Visual Retention Test (BVRT) [
22] was used to assess visual memory, psychomotor speed and executive function were assessed using the Trail Making Tests A and B, respectively (TMTA and TMTB) (time in seconds) [
23], and the Mini Mental State Examination (MMSE) was used as a global measure of cognitive function [
24]. All of the cognitive tests were administered at baseline and at each wave of the follow-up, except the TMTA and B, which were not given in the 2-year wave. Consequently, and because of sparse missing data, the analyses finally involved 7364 participants for MMSE, 7262 for BVRT, 7291 for Isaac’s test, 6090 for TMTA, and 5857 for TMTB.
Antidepressant exposure
An inventory of all drugs regularly used during the preceding month was registered at baseline and each follow-up examination. To reduce underreporting, participants were asked to provide medical prescriptions, drug packages and any other relevant material. The drugs were systematically coded using the Anatomical Therapeutic Chemical classification system. Drug exposure has previously been validated in this cohort in comparison with the reimbursement data from the healthcare insurance system. The validity of antidepressant exposure measured from participant interviews was very high, with a sensitivity of 80% and a specificity of 98% [
25,
26]. Three classes of antidepressants were considered: the TCAs (non-selective monoamine reuptake inhibitors), the SSRIs and the other antidepressants, which included serotonin norepinephrine reuptake inhibitors, monoamine oxidase inhibitors and mianserin, tianeptine, viloxazine, and mirtazapine. For a given class, the treated group included participants who used this class at both baseline and the first follow-up and we considered their follow-up cognitive data until the last consecutive follow-up with a report of antidepressant use of the same class. The reference group included those who were untreated at both evaluations using their cognitive data until the last consecutive follow-up without report of antidepressant.
Socio-demographic and clinical variables
The standardised interview included questions on socio-demographic characteristics, alcohol, caffeine, fruit and vegetable consumption, and visual impairment. Use of benzodiazepines, drugs with anticholinergic effects other than antidepressants [
27], and other central nervous system drugs, as well as the total number of other medications, were derived from reported drugs (see above). Fasting blood samples were taken at baseline for glycaemia and APOE ε4 genotyping [
28]. Diabetes was defined as treated or glycaemia ≥ 7 mmol/L and body mass index as weight divided by height squared. History of ischemic pathologies (stroke, angina pectoris, myocardial infarction and cardiovascular surgery) was established according to standardised questions. Respiratory pathologies included self-reported chronic bronchitis and asthma attacks (over the last 12 months). Potential cases of dementia were reviewed by an independent committee of neurologists in order to obtain a consensus on the diagnosis according to the DSM-IV criteria. A hierarchical indicator of disability [
29] combined three scales, namely the Rosow and Breslau mobility scale [
30], Lawton-Brody Instrumental Activity of Daily Living (IADL) scale [
31], and Katz’s Activity of Daily Living (ADL) scale [
32]. This indicator defines four levels of disability: full independence, mild disability (only mobility restriction), moderate disability (mobility and IADL limitation), and severe disability (mobility, IADL and ADL limitation). Severity of depressive symptoms was assessed by the Center for Epidemiologic Studies-Depression scale (CES-D) [
33] and history of major depressive episode (MDE) was diagnosed using the Mini International Neuropsychiatric Interview [
34]. Spielberger’s State-Trait Anxiety Inventory was used to measure trait anxiety symptoms [
35].
Statistical analyses
Comparison of baseline characteristics between included and excluded participants as well as between antidepressant users and non-users was performed using χ2 tests and unpaired Wilcoxon rank-sum tests. We used linear random-effect models to analyse the association between antidepressant use and 10-year change on cognitive scores taken as continuous variables. In order to normalise the distributions, cognitive variables were transformed using (15-Benton)1/2, (30-MMSE)1/2 and natural logarithm of TMT. Each model included time, antidepressant group, time*antidepressant group interaction and covariates. In the tables, the term ‘antidepressant’ represents the intercept point differences on cognitive scores and corresponds to the baseline differences between antidepressant treated and untreated groups. The term ‘time’ indicates the linear evolution per year on the cognitive test. The term for interaction ‘antidepressant*time’ represents the additional annual modification on the selected cognitive tests for antidepressant users expressed as a score change per year.
We used multiple imputations to permit multivariate analysis of all participants who had baseline and at least one follow-up cognitive evaluation. We generated five replications of the original data set, in which missing values (2.1% of data) for 17 covariates considered in the analysis were replaced by values generated according to the Markov Chain Monte Carlo method [
36] using the PROC MI SAS procedure. Each imputed data set was then analysed using the linear mixed models described above and the results were pooled to calculate mean estimates and their standard error using the PROC MIANALYZE procedure.
To control for confounding effects, two nested models were examined. The first model was adjusted for sex, centre, baseline age, and education and for significant interactions: age*time, centre*time, and education*time. The multi-adjusted model included additional covariates and their time interactions (with age, centre, education and APOE ε4) that were associated with at least one of the cognitive scores (
P ≤ 0.10 in the first model). We also conducted three sensitivity analyses, namely (1) excluding paroxetine users from the SSRI group as this drug has been reported to have a high anticholinergic activity in comparison with other SSRIs [
37], (2) excluding participants with history of MDE to reduce the impact of past depression on cognition, and (3) excluding participants with incident dementia to control for the protopathic bias where antidepressants are prescribed for an early manifestation of a dementia not yet diagnostically detected. A last analysis was performed keeping in the models the follow-up cognitive data after antidepressant treatment changes in order to have similar lengths of follow-up between groups. All analyses were conducted using the statistical software SAS version 9.4 for Windows.
Discussion
In this large prospective study, 4.0% of community-dwelling elderly people were taking antidepressants, mainly SSRIs and TCAs. Differences in baseline performance levels and decline over time were observed according to cognitive domains with SSRIs and TCAs but not with the other antidepressants. Compared to non-users, the TCA users showed lower baseline performances of 9% for verbal fluency, 5% for visual memory (BVRT) and 9% for psychomotor speed (TMTA), and the SSRI users of 3% for verbal fluency and 7% for psychomotor speed. On the other hand, no significant differences were found at baseline for global cognitive performances (MMSE) or executive function (TMTB) irrespective of the treatment groups. Regarding changes over time, only a slow additional improvement (0.7% per year) was observed on verbal fluency for the TCA group, which was not significant when the analyses were performed without censoring cognitive data. Hence, regardless of the cognitive domains, we did not observe statistically significant accelerated cognitive decline over time in treated participants, meaning that the differences found at inclusion remained constant over the 10-year follow-up.
Hence, our study indicates that TCAs and SSRIs are principally associated with relatively weak cognitive impairment at baseline, mainly related to verbal fluency, visual memory and psychomotor skills, but the question remains as to whether this occurred before or at treatment initiation. Impairment in executive function, psychomotor speed and, although less consistently, verbal fluency have been associated with depression [
6‐
8,
11]. Our results remained significant after adjustment for other possible co-determinants of cognitive impairment, including current anxiety and depressive symptoms, and also when participants with past history of MDE were excluded, suggesting that the antidepressants themselves rather than the underlying burden of illness could be associated with impaired cognitive performance. However, the effect of TCAs on baseline cognitive visual memory may be more related to psychological comorbidity as it became statistically non-significant when participants with a history of MDE were excluded. Baseline cognitive impairment may be the consequence of the unknown level of depressive symptoms just before initiation of treatment and of a limited capacity of antidepressants to improve cognitive performance. It is thus difficult to disentangle the initial effect of treatment on cognitive performances from that of depression prior to inclusion. Impairment in executive function is also a common hallmark of poor responders to psychopharmacologic interventions, which may persist even after treatment cessation [
7,
38]. We observed lower executive function only in participants treated with SSRIs and without history of MDE. Whether this may correspond to under-treated or resistant late-onset depression remains to be determined. Antidepressants, and in particular SSRIs, may also be prescribed for symptoms associated with suspected mild cognitive impairment. In this prodromal dementia group, the cognitive deficit may persist over time. In line with this hypothesis, when we removed the participants with incident dementia, the baseline associations were weakened and remained only significant for TCAs and the Isaac’s test.
In our study, TCA and SSRI intake were not associated with substantial accelerated cognitive decline over time after multiple adjustments including residual depressive symptoms. So far, few large prospective studies have examined the relationship between antidepressant use and cognitive decline in elderly populations. These studies had, however, probable confounding bias (see above) and they mainly focused on global cognitive change on the MMSE, which is highly likely to have a ceiling effect in non-demented participants. Our results support and extend to specific cognitive domains and longer follow-up, recent data of a nationally representative cohort of US residents showing that antidepressant use did not modify the course of 6-year global cognitive change [
18]. In a poorly adjusted analysis of a Canadian prescription database, antidepressant use was also not associated with global cognitive changes from baseline among patients with or without major depression, but was moderately associated with an MMSE score increase over time in patients with minor depression [
39]. Conversely, both SSRIs and TCAs were associated with an increased risk of mild cognitive impairment in a large cohort of elderly women [
17]. However, this study did not take into account possible confounding by other psychotropic drugs and potential prodromal dementia symptoms. In our study, the main confounders for baseline differences were depressive symptom score, anxiety score and benzodiazepine use. Additionally, people taking drugs with anticholinergic properties are known to be at increased risk for cognitive decline and dementia [
27], and this has rarely been considered previously. Antidepressants, mainly TCAs, but also the SSRI paroxetine, may have high anticholinergic effects [
37]. In our study, when paroxetine was removed from the SSRI group, the associations with baseline verbal fluency and psychomotor speed became non-significant, suggesting that paroxetine may be the principle compound responsible for the effect of SSRIs at baseline. However, the lower statistical power in the restricted group precludes drawing a definite conclusion.
The study has several strengths. First, the multicentric longitudinal design and the size of the sample with more than 7300 elderly participants from the general population, of whom half were followed for 10 years. Second, antidepressant use was ascertained at baseline and during follow-up by examining the prescriptions and boxes, thus minimising exposure misclassification. Exposure to both current and chronic antidepressant medication has previously been shown within this cohort to be highly valid in comparison with the reimbursement data from the healthcare insurance system [
25,
26]. Third, although in observational studies residual confounding may always subsist, our analyses overcame several limitations of previous studies. To our knowledge, this is the first study which adjusted for such a large range of different key factors, including ApoE4 genotype, behavioural characteristics, activity limitations, physical and mental health as well as anticholinergic drugs and other psychotropic drugs. Fourth, the linear mixed models took into account the influence of confounders on cognitive changes including all significant terms for interactions with time (age, education, ApoE4). Sixth, the cognitive evaluation included a battery of tests examining different and complementary cognitive domains.
Our study has several limitations. No information about dose and frequency of reported treatment was available in our study nor on the duration and type of treatment before inclusion. The antidepressant treatment was initiated before inclusion of participants in the present study and the cognitive state was unknown at treatment initiation. We thus cannot conclude if the observed baseline loss of performance is due to an effect that rapidly appears after treatment onset without further worsening over the follow-up or to the consequence of pre-treatment depression, which we could not fully control. Studying each cognitive test separately conducted to statistical multiple testing and we did not correct for inflated Type 1 error rates. However, each selected cognitive test examined different cognitive domains. Using linear mixed models, we assumed that dropouts and missing data were missing at random [
40]; however, some dropouts may be related to unexpected cognitive decline and this can lead to under- or overestimated effects. Finally, bias could have been introduced by the exclusion of participants with incomplete information on exposure who were more likely to be frail and thus susceptible to cognitive decline.
Acknowledgments
Not applicable.