The relationship between indoleamine 2,3-dioxygenase activity and post-stroke cognitive impairment
© Gold et al; licensee BioMed Central Ltd. 2011
Received: 25 November 2010
Accepted: 16 February 2011
Published: 16 February 2011
Activation of indoleamine 2,3-dioxygenase (IDO) and higher concentrations of several kynurenine metabolites have been observed post-stroke, where they have been associated with increased mortality. While lower tryptophan or a higher ratio of kynurenine/tryptophan (K/T) in peripheral blood have been associated with dementia and the severity of cognitive symptoms in Alzheimer's disease, the association between K/T ratios and post-stroke cognitive impairment (PSCI) has not been investigated.
Patients were recruited from the acute stroke unit of a general hospital within 1 month post-stroke. Assessments included the Standardized Mini-Mental State Examination (sMMSE) for cognition, the National Institutes of Health Stroke Scale (NIHSS) for stroke severity, and the Center for Epidemiological Studies-Depression Scale (CES-D) for depressive symptoms. Tryptophan and kynurenine concentrations were determined by high-performance liquid chromatography.
A total of 41 patients with ischemic stroke ([mean ± SD] age 72.3 ± 12.2 years, 53.7% male, sMMSE 25.6 ± 4.1, NIHSS 7.27 ± 5.55) were recruited. Higher K/T ratios were associated with lower post-stroke global cognition (i.e. sMMSE scores; β = -.327, P = .037). A backward stepwise elimination linear regression (F1,40=6.15, P=.005, adjusted R2=.205) showed that the highest K/T ratio tertile (β = -.412, P = .006) predicted lower sMMSE scores, controlling for age (β = -.253, p = .081), with NIHSS (β = -.027, P = 0.859), and lesion volume (β = -.066, P = 0.659) removed from the model. In receiver operating characteristic analysis, a K/T ratio of 78.3 μmol/mmol (top tertile) predicted significant cognitive impairment (sMMSE score ≤ 24) with 67% sensitivity and 86% specificity (area under the curve = 0.730, p = .022).
These data suggest an inflammatory response characterized by IDO activation may be relevant to the development of PSCI. Since the neuroactivity of kynurenine metabolites may be amenable to pharmacotherapeutic intervention, the K/T ratio may be a clinically important biomarker.
Stroke affects 15 million individuals annually world-wide, and the risk of having a stroke more than doubles each decade after the age of 55. Most stroke survivors live with residual impairments that diminish independence and quality of life. For older patients with ischemic stroke, post-stroke cognitive impairment (PSCI) is particularly important and frequent, occurring in approximately one third of all patients and having a significant negative impact on rehabilitation outcomes, quality of life and risk of dementia. A recent meta-analysis has confirmed several risk factors, including previous symptomatic stroke, previous asymptomatic stroke seen on imaging, multiple stroke lesions, aphasia, stroke severity, and stroke location, are associated with PSCI as defined by Mini-Mental State Examination (MMSE) scores less than 24, Diagnostic and Statistical Manual of Mental Disorders IV (DSM-IV) or International Classification of Disease-10 (ICD-10) criteria, within 1 year after stroke. The prevalence of post-stroke MMSE scores less than 24, indicative of significant cognitive impairment, was much higher than the prevalence of dementia diagnosed by standard criteria, which included the DSM-IV or ICD-10. The majority of these and other known risk factors for PSCI including older age, lower level of education, family history of dementia  are not readily amenable to treatment. Therefore, there is considerable need to identify pathophysiological mechanisms that may contribute to PSCI.
The systemic inflammatory response to acute ischemic stroke involves increases in several pro-inflammatory cytokines and C-reactive protein (CRP)[9–11], which have also been associated with the development of cognitive deficits and dementia in aging populations. We have recently demonstrated a relationship between PSCI and two inflammatory biomarkers, CRP and interleukin-6 (IL-6). Pro-inflammatory cytokines can activate the indoleamine-2,3-dioxygenase (IDO) enzyme, leading to the depletion of tryptophan (TRP) and the production of kynurenine, increasing the kynurenine/tryptophan (K/T) ratio in peripheral blood, which acts as a clinical measure of IDO activity. Elevations in the K/T ratio and in the concentrations of several kynurenine metabolites have been observed post-stroke, where they have been associated with mortality. While lower peripheral blood tryptophan concentrations or higher K/T ratios have been associated with dementia and the severity of cognitive symptoms in Alzheimer's disease[16, 17], the association between K/T ratios and PSCI has not been investigated.
Tryptophan metabolites along the kynurenine pathway can produce excitatory and oxidative neurotoxicity, but also protect neurons from inflammatory damage and attenuate excitatory neurotoxicity via NMDA receptor antagonism[18–23]. Therefore, it is of interest to determine whether kynurenine production might be associated with clinical cognitive outcomes, and if so, at which concentrations.
The purpose of this study was to test the hypothesis that IDO activation is associated with the presence of cognitive symptoms post-stroke. We measured plasma concentrations of kynurenine and tryptophan in acute ischemic stroke patients and explored the relationship between the K/T ratio and cognitive deficits, as measured by the MMSE, a commonly used cognitive screening instrument.
This cross-sectional observational study recruited participants admitted to an acute care regional stroke centre within 30 days of an ischemic stroke. The study was approved by local research ethics boards, and all participants provided written informed consent.
Consecutive patients meeting the National Institute of Neurological and Communicative Disorders and Stroke (NINCDS) and World Health Organization Multinational Monitoring of Trends and Determinants in Cardiovascular Disease (WHO-MONICA) criteria for stroke were invited to participate in this study. Acute ischemic infarcts were verified from computed tomography (CT) or magnetic resonance imaging (MRI) reports performed at the time of admission in all patients. Inclusion criteria also required participants to speak and understand English. Exclusion criteria were: pre-stroke diagnosis of dementia or significant cognitive impairment, primary hemorrhagic stroke (which have a different etiology and clinical course), decreased level of consciousness, severe aphasia or dysarthria (which would interfere with the ability to complete the study assessments), significant acute medical illness (which would be associated with significant inflammatory burden of its own; e.g. infection, autoimmune disease, cancer), significant acute neurological illness other than stroke, and the presence of a premorbid axis I psychiatric disorder. A history of major depression was permitted, and controlled for in statistical analyses as needed.
After obtaining written informed consent, the Mini-Mental State Examination (MMSE) was administered. The MMSE was selected as a cognitive screening instrument because it is a brief, widely used, and validated scale in acute care settings. Although not sensitive to subtle cognitive impairment, scores on the MMSE correlate strongly with the more thorough yet lengthy CAMCOG (cognitive and self-contained part of the Cambridge Examination for Mental Disorders of the Elderly) in a stroke rehabilitation setting. Given the exploratory nature of this study and the potentially low tolerability of a longer assessment in an acute stroke setting, a brief yet validated and clinically meaningful cognitive instrument was selected. MMSE scores were adjusted according to physical ability post-stroke as recommended by the Standardized Mini Mental State Examination (sMMSE).
Stroke severity was assessed using the National Institutes of Health Stroke Scale (NIHSS), either as completed by clinicians at the time of patient admission and obtained through chart review, or extracted from the chart information using a standardized method as has been done before . Depressive symptoms were assessed using the Center for Epidemiological Studies-Depression Scale (CES-D). Information regarding demographic characteristics and medical history was collected via chart review and consultation with participants.
Blood sampling and plasma analyses
Fasting blood was collected via venipuncture in EDTA (ethylenediaminetetraacetic acid) BD Vacutainer ® (New Jersey, USA) tubes at 7:30 am ± 30 minutes on the morning after the clinical assessments were conducted. Blood samples were centrifuged at 1000 × g for 10 min at 4°C and plasma was separated and stored at -80°C until the time of assay. Tryptophan and kynurenine concentrations were determined by high-performance liquid chromatography (HPLC), as described elsewhere[33, 34]. Tryptophan was measured by isocratic reverse phase HPLC without derivatization and fluorescence detection. For kynurenine, an equal volume of 3% perchloric acid was used for protein precipitation. After centrifugation, the concentration of L-kynurenine in the supernatant was measured by HPLC with UV detection at 258 nm. The mobile phase consisted of 9% acetonitrile in 0.05 M potassium phosphate mono basic, pumped through a reverse phase 5 μm ODS column, 250 mm × 4.6 mm (Symmetry; Waters Corporation, Milford, Massachusetts, United States of America). Biochemical assays were performed blinded to all clinical information.
Lesion characteristics were determined from CT scans obtained without a contrast agent on a General Electric LightSpeed VCT series scanner (General Electric Healthcare, Waukesha, WI). Ischemic lesions were manually traced on these images using Medical Image Processing, Analysis, and Visualization (MIPAV; National Institutes of Health, Bethesda, MD). Stroke volume was calculated using a slice-by-slice planimetric methodology employing these manual lesion tracings.
Continuous measures were summarized using means and standard deviations whereas categorical measures were summarized using percentages. Tryptophan and kynurenine were determined by mass and converted to molar units. Their quotient was multiplied by 1000 to obtain the K/T ratio in units of μmol/mmol. The naturally skewed nature of the data resulted in absolute values of kurtosis and skewedness being greater than 2 SD of the error, so K/T values were log transformed to obtain a normal distribution. All statistical analyses were performed using transformed values or tertiles.
For initial descriptive analyses, the relationship between sMMSE scores and K/T ratio, as well as possible covariates such as age, gender, stroke severity, time since stroke, level of education, cumulative burden of cerebrovascular risk factors (i.e. the number of vascular risk factors including diabetes, smoking, hypertension, hyperlipidemia, and obesity summed), and lesion volume were analyzed with bivariate Pearson correlations or analyses of variance (ANOVA) as appropriate.
To test our hypothesis, a backward elimination multiple linear regression model was used to examine the association between K/T ratios and sMMSE scores as continuous variables with age, stroke severity, and lesion volume entered into the initial model. In addition, to determine if an elevated K/T ratio predicted poorer sMMSE scores, patients were divided into tertiles based on the K/T ratio, and a backward elimination multiple linear regression analysis with patients dichotomized by those in the top tertile vs. others was used. A removal criterion of P > .1 was used in backward regression models. Finally, a receiver operating characteristic (ROC) analysis was performed to determine a K/T ratio optimum (sensitivity vs. specificity) that predicts significant cognitive impairment (sMMSE score ≤24) .
Given the strong commonly observed relationships between depressive symptoms, inflammatory activation and cognitive impairment[36, 37], the impact of depressive symptoms or a history of depression on the observed relationship between K/T ratio top tertile and sMMSE was explored by adding CES-D scores or history of depression into the final regression model. Similarly, given the observed relationship between vascular risk factors and cognitive impairment, the number of cerebrovascular risk factors was added to the final regression model. Time since stroke, gender, and level of education were also explored as covariates.
All patient information was de-identified for statistical analyses using SPSS statistical software (version 17; SPSS Inc., Chicago, Illinois).
Sample size and study power calculation
A sample size of 39 subjects achieves a power of 80% to detect an association between the K/T ratio and sMMSE scores with an effect size (f2) of 0.35 given a two-tailed significance level of 0.05. A sample size of at least 41 subjects allows adjustment with up to 3 additional covariates.
Clinical characteristics and correlations with cognitive impairment (n = 41)
MEAN ± SD OR %
r- OR F* VALUE
72.3 ± 12.2 years
25.6 ± 4.1
7.27 ± 5.55
13.8 ± 12.8
History of Depression
Level of Education > high school
Time Since Stroke
9.17 ± 5.03 days
Cerebrovascular Risk Factors
Obesity (BMI ≥ 30kg/m2)
Total number risk factors
2.15 ± 1.28
Lesion Volume (cm3)
31.72 ± 55.09
K/T ratio ‡
67.40 ± 42.46
Linear regression model predicting sMMSE scores*
K/T top tertile
This study demonstrates an association between elevated K/T ratios and the extent of cognitive impairment among acute ischemic stroke patients. Age, stroke severity and lesion volume did not significantly modify this relationship suggesting that the clinical importance of the K/T ratio may extend beyond their relationships with these established risk factors for PSCI. The association between the K/T ratio and cognition following acute stroke was sufficiently robust to be detected with the MMSE, a practical and clinically meaningful cognitive screening instrument.
Inflammatory activation is a key process in the ischemic cascade that leads to secondary brain damage. We have previously reported that plasma CRP concentrations were able to explain 20% of the variance in MMSE scores among acute stroke patients and that plasma IL-6 concentrations also predicted MMSE scores. Interestingly, high plasma concentrations of the pleiotrophic cytokine, IL-6, have been associated with a greater lesion volume, however lesion volume did not predict sMMSE scores in our population. Pro-inflammatory cytokines induce the expression of IDO which catalyzes the committal and rate-limiting step in the production of kynurenine from tryptophan. In the present study, having a K/T ratio in the top tertile explained 21% of the variance in MMSE scores.
An elevated K/T ratio has been associated with inflammatory and neurodegenerative conditions and with clinically important outcomes, including mortality in the very old, poorer cognitive function in those with Alzheimer's disease, and the severity of depressive symptoms in those receiving interferon therapy or in those with cardiovascular disease. The K/T ratio and poorer MMSE scores may be related to the burden of neurotoxic or neuroactive metabolites such as quinolinic acid (QUIN), an NMDA receptor agonist and excitatory neurotoxin, 3-hydroxyanthranilic acid, an oxidative neurotoxin, or kynurenic acid (KYNA), an antagonist at both NMDA and α7 cholinergic receptors. The production of these neuroactive metabolites has been previously associated with depression[44, 45], cognitive impairment, and deficits in learning, retrieval, and long-term memory[40, 46]. For instance, the concentration of KYNA is elevated in the caudate nucleus and putamen of Alzheimer disease patients and it has been suggested that NMDA or α7 cholinergic inhibition by KYNA might impair learning and memory. In a study by Widner et al., Alzheimer's disease patients showed significantly higher peripheral blood K/T ratios as compared to age-matched controls and Alzheimer's disease patients with the lowest MMSE scores had significantly higher K/T ratios than those with the highest MMSE scores. A second study by Gulaj et al. did not find a correlation between K/T ratios and MMSE scores; however they observed an association between the KYNA/KYN ratio and MMSE scores, suggesting a possible protective effect of KYNA relative to the production of kynurenine and other metabolites. This effect may be attributable to opposing effects of KYNA and quinolinic acid at NMDA or α7 nicotinic cholinergic receptors. The association between increased concentrations of kynurenine metabolites, especially KYNA and 3-hydroxyanthranilic acid, and mortality observed post-stroke suggests the potential clinical importance of these metabolites in this population.
Identification of the K/T ratio as a PSCI biomarker may represent an important step in improving stroke outcomes because the kynurenine metabolites might be amenable to pharmacological manipulation. In the central nervous system, kynurenine aminotransferase II, expressed primarily in astrocytes, is responsible for KYNA synthesis while kynurenine 3-monooxygenase (KMO) produces the 3-hydroxykynurenine metabolite that gives rise to QUIN, predominantly from the microglia. In animal models of cerebral ischemia, administration of kynurenine sulfate exerts neuroprotective effects and notably increases cerebral concentrations of KYNA[50, 51]. It is now appreciated that cerebral 3-hydroxykynurenine and quinolinic acid concentrations can be manipulated, selectively without altering KYNA concentrations, by inhibition of KMO, an approach which shows neuroprotective effects in animal models of cerebral ischemia. In addition, a newly synthesized compound, ZL006, which acts downstream of NMDA receptor activation, has been demonstrated to ameliorate focal ischemic cerebral damage induced by middle cerebral artery occlusion in mice and rats. The implication of endogenous excitotoxicity in the present study suggests that ZL006 might also be evaluated to improve cognitive outcomes.
In the present study, the K/T ratio was able to identify subjects at risk of significant PSCI (i.e. those with sMMSE scores ≤ 24). While larger studies would be needed to confirm a clinically important cut-off value for the K/T ratio, the ROC presented in the present study suggested a 67% sensitivity and 86% specificity for a K/T ratio cut-off of 78.3 μM/mM. While higher K/T ratios were associated with lower MMSE scores in the entire population, this effect was most significant for subjects with a K/T ratio in the highest tertile. A K/T ratio in this range is comparable to that found in subjects with HIV-1 infection in association with cognitive symptoms and AIDS dementia complex[53–55], but much higher than that found in normal healthy aged controls or subjects with cardiovascular disease without a history of stroke. If replicated in larger populations, these data suggest potential clinical utility of the K/T ratio as a discriminating biomarker.
This study demonstrates a relationship between cognitive impairment and activation of the kynurenine pathway post-stroke. It is, however, limited by its use of a brief cognitive screening instrument and a relatively small sample size. Although stroke severity was assessed and included as a covariate, the timing of administration of the NIHSS relative to the stroke and cognitive assessment varied between assessments. Because NIHSS scores commonly fluctuate post-stroke, this measure may not have been adequate to control for stroke severity. However, in recognition of this, we also evaluated lesion volume and found that it was not significantly related to the severity of PSCI in this population. Additionally, the type of cognitive impairment observed post-stroke varies; often including deficits in measures of global cognition, as well as domain-specific impairments involving executive function, language, visuospatial ability, and memory. Some previously identified risk factors for the development of PSCI, including family history of dementia and individual cardiovascular risk factors, could not be controlled for given the sample size. Although all efforts were made to control for potentially confounding variables, pre-stroke cognitive capacity and white matter disease burden were not assessed. Finally, the cross-sectional design of this study was useful in establishing an initial relationship between PSCI and elevated K/T ratios post-stroke, but subsequent longitudinal studies will be necessary to determine the value of K/T ratio in predicting long-term cognitive outcomes.
In summary, an acute inflammatory response characterized by IDO activation may be relevant to the development of PSCI. Since the neuroactivities of kynurenine metabolites may be amenable to pharmacotherapeutic intervention, the K/T ratio may be a clinically important biomarker. Longitudinal observational and intervention studies will improve our understanding of the role of IDO activity in PSCI.
This study was supported by the Heart and Stroke Foundation of Canada (T6383 and NA5857) and the Alzheimer Society of Canada (10 61). The authors gratefully acknowledge the Heart and Stroke Foundation Centre for Stroke Recovery for fellowship support for ABG as well as Amy Wong, MSc, and Philip Francis, MSc, for their contributions to recruitment and neuroimaging, respectively.
- Lloyd-Jones D, Adams R, Carnethon M, De Simone G, Ferguson TB, Flegal K, Ford E, Furie K, Go A, Greenlund K, Haase N, Hailpern S, Ho M, Howard V, Kissela B, Kittner S, Lackland D, Lisabeth L, Marelli A, McDermott M, Meigs J, Mozaffarian D, Nichol G, O'Donnell C, Roger V, Rosamond W, Sacco R, Sorlie P, Stafford R, Steinberger J, Thom T, Wasserthiel-Smoller S, Wong N, Wylie-Rosett J, Hong Y: Heart disease and stroke statistics--2009 update: a report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee. Circulation. 2009, 119: 480-486. 10.1161/CIRCULATIONAHA.108.191259.View ArticlePubMedGoogle Scholar
- Nakayama H, Jørgensen HS, Raaschou HO, Olsen TS: The influence of age on stroke outcome. The Copenhagen Stroke Study. Stroke. 1994, 25: 808-813.View ArticlePubMedGoogle Scholar
- Tatemichi TK, Desmond DW, Stern Y, Paik M, Sano M, Bagiella E: Cognitive impairment after stroke: frequency, patterns, and relationship to functional abilities. J Neurol Neurosurg Psychiatry. 1994, 57: 202-207. 10.1136/jnnp.57.2.202.PubMed CentralView ArticlePubMedGoogle Scholar
- Pohjasvaara T, Vataja R, Leppavuori A, Kaste M, Erkinjuntti T: Cognitive functions and depression as predictors of poor outcome 15 months after stroke. Cerebrovasc Dis. 2002, 14: 228-233. 10.1159/000065667.View ArticlePubMedGoogle Scholar
- Nys GM, van Zandvoort MJ, van der Worp HB, de Haan EH, de Kort PL, Jansen BP, Kappelle LJ: Early cognitive impairment predicts long-term depressive symptoms and quality of life after stroke. J Neurol Sci. 2006, 247: 149-156. 10.1016/j.jns.2006.04.005.View ArticlePubMedGoogle Scholar
- Rockwood K, Howard K, MacKnight C, Darvesh S: Spectrum of disease in vascular cognitive impairment. Neuroepidemiology. 1999, 18: 248-254. 10.1159/000026219.View ArticlePubMedGoogle Scholar
- Pendlebury ST, Rothwell PM: Prevalence, incidence, and factors associated with pre-stroke and post-stroke dementia: a systematic review and meta-analysis. Lancet Neurol. 2009, 8: 1006-1018. 10.1016/S1474-4422(09)70236-4.View ArticlePubMedGoogle Scholar
- Khedr EM, Hamed SA, El-Shereef HK, Shawky OA, Mohamed KA, Awad EM, Ahmed MA, Shehata GA, Eltahtawy MA: Cognitive impairment after cerebrovascular stroke: Relationship to vascular risk factors. Neuropsychiatr Dis Treat. 2009, 5: 103-116.PubMed CentralPubMedGoogle Scholar
- Kostulas N, Pelidou SH, Kivisakk P, Kostulas V, Link H: Increased IL-1beta, IL-8, and IL-17 mRNA expression in blood mononuclear cells observed in a prospective ischemic stroke study. Stroke. 1999, 30: 2174-2179.View ArticlePubMedGoogle Scholar
- Tarkowski E, Rosengren L, Blomstrand C, Wikkelso C, Jensen C, Ekholm S, Tarkowski A: Early intrathecal production of interleukin-6 predicts the size of brain lesion in stroke. Stroke. 1995, 26: 1393-1398.View ArticlePubMedGoogle Scholar
- Liebau C, Baltzer AW, Schmidt S, Roesel C, Karreman C, Prisack JB, Bojar H, Merk H: Interleukin-12 and interleukin-18 induce indoleamine 2,3-dioxygenase (IDO) activity in human osteosarcoma cell lines independently from interferon-gamma. Anticancer Res. 2002, 22: 931-936.PubMedGoogle Scholar
- Schram MT, Euser SM, de Craen AJ, Witteman JC, Frolich M, Hofman A, Jolles J, Breteler MM, Westendorp RG: Systemic markers of inflammation and cognitive decline in old age. J Am Geriatr Soc. 2007, 55: 708-716. 10.1111/j.1532-5415.2007.01159.x.View ArticlePubMedGoogle Scholar
- Rothenburg LS, Herrmann N, Swardfager W, Black SE, Tennen G, Kiss A, Gladstone DJ, Ween J, Snaiderman A, Lanctôt KL: The relationship between inflammatory markers and post stroke cognitive impairment. J Geriatr Psychiatry Neurol. 2010, 23: 199-205. 10.1177/0891988710373598.View ArticlePubMedGoogle Scholar
- Widner B, Laich A, Sperner-Unterweger B, Ledochowski M, Fuchs D: Neopterin production, tryptophan degradation, and mental depression--what is the link?. Brain Behav Immun. 2002, 16: 590-595. 10.1016/S0889-1591(02)00006-5.View ArticlePubMedGoogle Scholar
- Darlington LG, Mackay GM, Forrest CM, Stoy N, George C, Stone TW: Altered kynurenine metabolism correlates with infarct volume in stroke. Eur J Neurosci. 2007, 26: 2211-2221. 10.1111/j.1460-9568.2007.05838.x.View ArticlePubMedGoogle Scholar
- Gulaj E, Pawlak K, Bien B, Pawlak D: Kynurenine and its metabolites in Alzheimer's disease patients. Adv Med Sci. 2010, 55: 204-211. 10.2478/v10039-010-0023-6.View ArticlePubMedGoogle Scholar
- Widner B, Leblhuber F, Walli J, Tilz GP, Demel U, Fuchs D: Tryptophan degradation and immune activation in Alzheimer's disease. J Neural Transm. 2000, 107: 343-353. 10.1007/s007020050029.View ArticlePubMedGoogle Scholar
- Matysiak M, Stasiołek M, Orłowski W, Jurewicz A, Janczar S, Raine CS, Selmaj K: Stem cells ameliorate EAE via an indoleamine 2,3-dioxygenase (IDO) mechanism. J Neuroimmunol. 2008, 193: 12-23. 10.1016/j.jneuroim.2007.07.025.PubMed CentralView ArticlePubMedGoogle Scholar
- Moroni F, Carpenedo R, Cozzi A, Meli E, Chiarugi A, Pellegrini-Giampietro DE: Studies on the neuroprotective action of kynurenine mono-oxygenase inhibitors in post-ischemic brain damage. Adv Exp Med Biol. 2003, 527: 127-136.View ArticlePubMedGoogle Scholar
- Yan Y, Zhang GX, Gran B, Fallarino F, Yu S, Li H, Cullimore ML, Rostami A, Xu H: IDO upregulates regulatory T cells via tryptophan catabolite and suppresses encephalitogenic T cell responses in experimental autoimmune encephalomyelitis. J Immunol. 2010, 185: 5953-5961. 10.4049/jimmunol.1001628.PubMed CentralView ArticlePubMedGoogle Scholar
- Sas K, Robotka H, Rozsa E, Agoston M, Szenasi G, Gigler G, Marosi M, Kis Z, Farkas T, Vecsei L, Toldi J: Kynurenine diminishes the ischemia-induced histological and electrophysiological deficits in the rat hippocampus. Neurobiol Dis. 2008, 32: 302-308. 10.1016/j.nbd.2008.07.013.View ArticlePubMedGoogle Scholar
- Kwidzinski E, Bechmann I: IDO expression in the brain: a double-edged sword. J Mol Med. 2007, 85: 1351-1359. 10.1007/s00109-007-0229-7.View ArticlePubMedGoogle Scholar
- Stone TW, Darlington LG: Endogenous kynurenines as targets for drug discovery and development. Nat Rev Drug Discov. 2002, 1: 609-620. 10.1038/nrd870.View ArticlePubMedGoogle Scholar
- Folstein MF, Folstein SE, McHugh PR: "Mini-mental state". A practical method for grading the cognitive state of patients for the clinician. J Psychiatr Res. 1975, 12: 189-198. 10.1016/0022-3956(75)90026-6.View ArticlePubMedGoogle Scholar
- Foulkes MA, Wolf PA, Price TR, Mohr JP, Hier DB: The Stroke Data Bank: design, methods, and baseline characteristics. Stroke. 1988, 19: 547-554.View ArticlePubMedGoogle Scholar
- The World Health Organization MONICA Project (monitoring trends and determinants in cardiovascular disease): a major international collaboration. WHO MONICA Project Principal Investigators. J Clin Epidemiol. 1988, 41: 105-114. 10.1016/0895-4356(88)90084-4.Google Scholar
- Tombaugh TN, McIntyre NJ: The mini-mental state examination: a comprehensive review. J Am Geriatr Soc. 1992, 40: 922-935.View ArticlePubMedGoogle Scholar
- Winkel-Witlox AC, Post MW, Visser-Meily JM, Lindeman E: Efficient screening of cognitive dysfunction in stroke patients: comparison between the CAMCOG and the R-CAMCOG, Mini Mental State Examination and Functional Independence Measure-cognition score. Disabil Rehabil. 2008, 30: 1386-1391. 10.1080/09638280701623000.View ArticleGoogle Scholar
- Molloy DW, Standish TI: A guide to the standardized Mini-Mental State Examination. Int Psychogeriatr. 1997, 9 (Suppl 1): 87-94. 10.1017/S1041610297004754. discussion 143-150View ArticlePubMedGoogle Scholar
- Brott T, Marler JR, Olinger CP, Adams HP, Tomsick T, Barsan WG, Biller J, Eberle R, Hertzberg V, Walker M: Measurements of acute cerebral infarction: lesion size by computed tomography. Stroke. 1989, 20: 871-875.View ArticlePubMedGoogle Scholar
- Williams LS, Yilmaz EY, Lopez-Yunez AM: Retrospective assessment of initial stroke severity with the NIH Stroke Scale. Stroke. 2000, 31: 858-862.View ArticlePubMedGoogle Scholar
- Radloff L: The CES-D scale: A self-report depression scale for research in the general population. Applied Psychological Measurement. 1977, 1: 385-401. 10.1177/014662167700100306.View ArticleGoogle Scholar
- Anderson GM, Purdy WC: Liquid chromatographic-fluorometric system for the determination of indoles in physiological samples. Anal Chem. 1979, 51: 283-286. 10.1021/ac50038a030.View ArticlePubMedGoogle Scholar
- Forrest CM, Mackay GM, Stoy N, Egerton M, Christofides J, Stone TW, Darlington LG: Tryptophan loading induces oxidative stress. Free Radic Res. 2004, 38: 1167-1171. 10.1080/10715760400011437.View ArticlePubMedGoogle Scholar
- Pucak ML, Kaplin AI: Unkind cytokines: current evidence for the potential role of cytokines in immune-mediated depression. Int Rev Psychiatry. 2005, 17: 477-483. 10.1080/02646830500381757.View ArticlePubMedGoogle Scholar
- Hackett ML, Anderson CS: Predictors of depression after stroke: a systematic review of observational studies. Stroke. 2005, 36: 2296-2301. 10.1161/01.STR.0000183622.75135.a4.View ArticlePubMedGoogle Scholar
- Narushima K, Chan KL, Kosier JT, Robinson RG: Does cognitive recovery after treatment of poststroke depression last? A 2-year follow-up of cognitive function associated with poststroke depression. Am J Psychiatry. 2003, 160: 1157-1162. 10.1176/appi.ajp.160.6.1157.View ArticlePubMedGoogle Scholar
- Kivipelto M, Ngandu T, Fratiglioni L, Viitanen M, Kareholt I, Winblad B, Helkala EL, Tuomilehto J, Soininen H, Nissinen A: Obesity and vascular risk factors at midlife and the risk of dementia and Alzheimer disease. Arch Neurol. 2005, 62: 1556-1560. 10.1001/archneur.62.10.1556.View ArticlePubMedGoogle Scholar
- Brouns R, De Deyn PP: The complexity of neurobiological processes in acute ischemic stroke. Clin Neurol Neurosurg. 2009, 111: 483-495. 10.1016/j.clineuro.2009.04.001.View ArticlePubMedGoogle Scholar
- Park SB, Coull JT, McShane RH, Young AH, Sahakian BJ, Robbins TW, Cowen PJ: Tryptophan depletion in normal volunteers produces selective impairments in learning and memory. Neuropharmacology. 1994, 33: 575-588. 10.1016/0028-3908(94)90089-2.View ArticlePubMedGoogle Scholar
- Pertovaara M, Raitala A, Lehtimaki T, Karhunen PJ, Oja SS, Jylha M, Hervonen A, Hurme M: Indoleamine 2,3-dioxygenase activity in nonagenarians is markedly increased and predicts mortality. Mech Ageing Dev. 2006, 127: 497-499.View ArticlePubMedGoogle Scholar
- Bonaccorso S, Marino V, Puzella A, Pasquini M, Biondi M, Artini M, Almerighi C, Verkerk R, Meltzer H, Maes M: Increased depressive ratings in patients with hepatitis C receiving interferon-alpha-based immunotherapy are related to interferon-alpha-induced changes in the serotonergic system. J Clin Psychopharmacol. 2002, 22: 86-90. 10.1097/00004714-200202000-00014.View ArticlePubMedGoogle Scholar
- Swardfager W, Herrmann N, Dowlati Y, Oh PI, Kiss A, Walker SE, Lanctôt KL: Indoleamine 2,3-dioxygenase activation and depressive symptoms in patients with coronary artery disease. Psychoneuroendocrinology. 2009, 34: 1560-1566. 10.1016/j.psyneuen.2009.05.019.View ArticlePubMedGoogle Scholar
- Cowen PJ, Parry-Billings M, Newsholme EA: Decreased plasma tryptophan levels in major depression. J Affect Disord. 1989, 16: 27-31. 10.1016/0165-0327(89)90051-7.View ArticlePubMedGoogle Scholar
- Lucca A, Lucini V, Catalano M, Alfano M, Smeraldi E: Plasma tryptophan to large neutral amino acids ratio and therapeutic response to a selective serotonin uptake inhibitor. Neuropsychobiology. 1994, 29: 108-111. 10.1159/000119071.View ArticlePubMedGoogle Scholar
- Riedel WJ, Klaassen T, Deutz NE, van Someren A, van Praag HM: Tryptophan depletion in normal volunteers produces selective impairment in memory consolidation. Psychopharmacology (Berl). 1999, 141: 362-369. 10.1007/s002130050845.View ArticleGoogle Scholar
- Baran H, Jellinger K, Deecke L: Kynurenine metabolism in Alzheimer's disease. J Neural Transm. 1999, 106: 165-181. 10.1007/s007020050149.View ArticlePubMedGoogle Scholar
- Potter MC, Elmer GI, Bergeron R, Albuquerque EX, Guidetti P, Wu HQ, Schwarcz R: Reduction of endogenous kynurenic acid formation enhances extracellular glutamate, hippocampal plasticity, and cognitive behavior. Neuropsychopharmacology. 2010, 35: 1734-1742.PubMed CentralPubMedGoogle Scholar
- Amori L, Guidetti P, Pellicciari R, Kajii Y, Schwarcz R: On the relationship between the two branches of the kynurenine pathway in the rat brain in vivo. J Neurochem. 2009, 109: 316-325. 10.1111/j.1471-4159.2009.05893.x.PubMed CentralView ArticlePubMedGoogle Scholar
- Nozaki K, Beal MF: Neuroprotective effects of L-kynurenine on hypoxia-ischemia and NMDA lesions in neonatal rats. J Cereb Blood Flow Metab. 1992, 12: 400-407.View ArticlePubMedGoogle Scholar
- Gigler G, Szénási G, Simó A, Lévay G, Hársing LG, Sas K, Vécsei L, Toldi J: Neuroprotective effect of L-kynurenine sulfate administered before focal cerebral ischemia in mice and global cerebral ischemia in gerbils. Eur J Pharmacol. 2007, 564: 116-122. 10.1016/j.ejphar.2007.02.029.View ArticlePubMedGoogle Scholar
- Zhou L, Li F, Xu HB, Luo CX, Wu HY, Zhu MM, Lu W, Ji X, Zhou QG, Zhu DY: Treatment of cerebral ischemia by disrupting ischemia-induced interaction of nNOS with PSD-95. Nat Med. 2010, 16: 1439-1443. 10.1038/nm.2245.View ArticlePubMedGoogle Scholar
- Gendelman HE, Zheng J, Coulter CL, Ghorpade A, Che M, Thylin M, Rubocki R, Persidsky Y, Hahn F, Reinhard J, Swindells S: Suppression of inflammatory neurotoxins by highly active antiretroviral therapy in human immunodeficiency virus-associated dementia. J Infect Dis. 1998, 178: 1000-1007. 10.1086/515693.View ArticlePubMedGoogle Scholar
- Suarez S, Baril L, Stankoff B, Khellaf M, Dubois B, Lubetzki C, Bricaire F, Hauw JJ: Outcome of patients with HIV-1-related cognitive impairment on highly active antiretroviral therapy. Aids. 2001, 15: 195-200. 10.1097/00002030-200101260-00008.View ArticlePubMedGoogle Scholar
- Huengsberg M, Winer JB, Gompels M, Round R, Ross J, Shahmanesh M: Serum kynurenine-to-tryptophan ratio increases with progressive disease in HIV-infected patients. Clin Chem. 1998, 44: 858-862.PubMedGoogle Scholar
- Hachinski V, Iadecola C, Petersen RC, Breteler MM, Nyenhuis DL, Black SE, Powers WJ, DeCarli C, Merino JG, Kalaria RN, et al: National Institute of Neurological Disorders and Stroke-Canadian Stroke Network vascular cognitive impairment harmonization standards. Stroke. 2006, 37: 2220-2241. 10.1161/01.STR.0000237236.88823.47.View ArticlePubMedGoogle Scholar
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