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Shade avoidance syndrome (SAS) is a strategy of major adaptive significance and typically includes elongation of the stem and petiole, leaf hyponasty, reduced branching and phototropic orientation of the plant shoot toward canopy gaps. Both cryptochrome 1 and phytochrome B (phyB) are the major photoreceptors that sense the reduction in the blue light fluence rate and the low red:far-red ratio, respectively, and both light signals are associated with plant density and the resource reallocation when SAS responses are triggered. The B-box (BBX)-containing zinc finger transcription factor BBX24 has been implicated in the SAS as a regulator of DELLA activity, but this interaction does not explain all the observed BBX24-dependent regulation in shade light. Here, through a combination of transcriptional meta-analysis and large-scale identification of BBX24-interacting transcription factors, we found that JAZ3, a jasmonic acid signaling component, is a direct target of BBX24. Furthermore, we demonstrated that joint loss of BBX24 and JAZ3 function causes insensitivity to DELLA accumulation, and the defective shade-induced elongation in this mutant is rescued by loss of DELLA or phyB function. Therefore, we propose that JAZ3 is part of the regulatory network that controls the plant growth in response to shade, through a mechanism in which BBX24 and JAZ3 jointly regulate DELLA activity. Our results provide new insights into the participation of BBX24 and JA signaling in the hypocotyl shade avoidance response in Arabidopsis.
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Proteínas de Arabidopsis , Arabidopsis , Proteínas de Arabidopsis/genética , Proteínas de Arabidopsis/metabolismo , Arabidopsis/metabolismo , Luz , Factores de Transcripción/genética , Factores de Transcripción/metabolismo , Fitocromo B/metabolismo , Regulación de la Expresión Génica de las PlantasRESUMEN
To maintain the world population demand, a sustainable agriculture is needed. Since current global vision is more friendly with the environment, eco-friendly alternatives are desirable. In this sense, plant growth-promoting rhizobacteria could be the choice for the management of soil-borne diseases of crop plants. These rhizobacteria secrete chemical compounds which act as phytohormones. Indole-3-acetic acid (IAA) is the most common plant hormone of the auxin class which regulates various processes of plant growth. IAA compound, in which structure can be found a carboxylic acid attached through a methylene group to the C-3 position of an indole ring, is produced both by plants and microorganisms. Plant growth-promoting rhizobacteria and fungi secrete IAA to promote the plant growth. In this review, IAA production and mechanisms of action by bacteria and fungi along with the metabolic pathways evolved in the IAA secretion and commercial prospects are revised.Key points⢠Many microorganisms produce auxins which help the plant growth promotion.⢠These auxins improve the plant growth by several mechanisms.⢠The auxins are produced through different mechanisms.
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Ácidos Indolacéticos , Reguladores del Crecimiento de las Plantas , Agricultura , Desarrollo de la Planta , PlantasRESUMEN
INTRODUCTION: The absence of a consensus system for full neuropathological evaluation limits clinicopathological studies and comparability between laboratories. Combined staging for Alzheimer's type and cerebral vascular pathology may allow a better classification of cases for clinical and cognitive correlation. METHODS: Cognitive and postmortem neuropathological data were obtained from 70 brains donated to the Tissue Bank of the Centro de Investigación de Enfermedades Neurológicas (CIEN) Foundation according to recently developed staging schemes for Alzheimer's type and vascular pathology. Subjects belonged to a cohort of institutionalized patients with moderate or severe dementia and a mean follow-up period of 7 years. RESULTS: Cases were classified into three groups: Alzheimer's predominant (64.1%), vascular predominant (6.3%) and mixed pathology (29.6%). Significant differences were observed in Severe Mini-Mental State Examination and verbal fluency between the vascular predominant and the other groups of patients. DISCUSSION: The combination of scales measuring cerebral vascular and Alzheimer's type pathology allowed a classification of patients that reveals differences between groups in premortem cognitive features.
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Enfermedad de Alzheimer/patología , Encéfalo/patología , Trastornos Cerebrovasculares/patología , Trastornos del Conocimiento/patología , Cognición , Anciano , Anciano de 80 o más Años , Enfermedad de Alzheimer/psicología , Trastornos Cerebrovasculares/psicología , Femenino , Humanos , Masculino , Escala del Estado Mental , Persona de Mediana Edad , Análisis de Regresión , Estudios RetrospectivosRESUMEN
Cell elongation during seedling development is antagonistically regulated by light and gibberellins (GAs). Light induces photomorphogenesis, leading to inhibition of hypocotyl growth, whereas GAs promote etiolated growth, characterized by increased hypocotyl elongation. The mechanism underlying this antagonistic interaction remains unclear. Here we report on the central role of the Arabidopsis thaliana nuclear transcription factor PIF4 (encoded by PHYTOCHROME INTERACTING FACTOR 4) in the positive control of genes mediating cell elongation and show that this factor is negatively regulated by the light photoreceptor phyB (ref. 4) and by DELLA proteins that have a key repressor function in GA signalling. Our results demonstrate that PIF4 is destabilized by phyB in the light and that DELLAs block PIF4 transcriptional activity by binding the DNA-recognition domain of this factor. We show that GAs abrogate such repression by promoting DELLA destabilization, and therefore cause a concomitant accumulation of free PIF4 in the nucleus. Consistent with this model, intermediate hypocotyl lengths were observed in transgenic plants over-accumulating both DELLAs and PIF4. Destabilization of this factor by phyB, together with its inactivation by DELLAs, constitutes a protein interaction framework that explains how plants integrate both light and GA signals to optimize growth and development in response to changing environments.
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Proteínas de Arabidopsis/metabolismo , Arabidopsis/efectos de los fármacos , Arabidopsis/efectos de la radiación , Forma de la Célula/efectos de los fármacos , Forma de la Célula/efectos de la radiación , Giberelinas/farmacología , Luz , Arabidopsis/citología , Arabidopsis/metabolismo , Proteínas de Arabidopsis/química , Proteínas de Arabidopsis/genética , Factores de Transcripción con Motivo Hélice-Asa-Hélice Básico/química , Factores de Transcripción con Motivo Hélice-Asa-Hélice Básico/genética , Factores de Transcripción con Motivo Hélice-Asa-Hélice Básico/metabolismo , Tamaño de la Célula/efectos de los fármacos , Tamaño de la Célula/efectos de la radiación , ADN de Plantas/metabolismo , Hipocótilo/genética , Hipocótilo/crecimiento & desarrollo , Hipocótilo/metabolismo , Proteínas Nucleares/química , Proteínas Nucleares/genética , Proteínas Nucleares/metabolismo , Fitocromo B/genética , Fitocromo B/metabolismo , Hojas de la Planta/metabolismo , Unión Proteica , Plantones/metabolismo , Transducción de Señal/efectos de los fármacos , Nicotiana/metabolismo , Triazoles/farmacología , Técnicas del Sistema de Dos HíbridosRESUMEN
Introduction: Although stentrievers (SRs) have been a mainstay of mechanical thrombectomy (MT), and current guidelines recommend the use of SRs in the treatment of large vessel occlusion stroke (LVO), there is a paucity of studies in the literature comparing SRs directly against each other in terms of mechanical and functional properties. Timely access to endovascular therapy and the ability to restore intracranial flow in a safe, efficient, and efficacious manner have been critical to the success of MT. This study aimed to investigate the impact of contemporary SR characteristics, including model, brand, size, and length, on the first-pass effect (FPE) in patients with acute ischemic stroke. Methods: Consecutive patients with M1 occlusion treated with a single SR+BGC were recruited from the ROSSETTI registry. The primary outcome was the FPE that was defined as modified (mFPE) or true (tFPE) for the achievement of modified thrombolysis in cerebral infarction (mTICI) grades 2b-3 or 3 after a single device pass, respectively. We compared patients who achieved mFPE with those who achieved tFPE according to SR characteristics. Results: We included 610 patients (52.3% female and 47.7% male, mean age 75.1 ± 13.62 years). mFPE was achieved in 357 patients (58.5%), whereas tFPE was achieved in 264 (43.3%). There was no significant association between SR characteristics and mFPE or tFPE. Specifically, the SR size did not show a statistically significant relationship with improvement in FPE. Similarly, the length of the SR did not yield significant differences in the mFPE and tFPE, even when the data were grouped. Conclusions: Our data indicate that contemporary SR-mediated thrombectomy characteristics, including model, brand, size, and length, do not significantly affect the FPE.
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Alzheimer's disease (AD) is the most common cause of neurodegenerative cognitive impairment. Brain stimulation techniques based on the delivery of transcranial shockwaves are currently being studied for their increasing popularity as an approach to modulate the human brain in a focal and targeted manner making this therapy a promising line of action against AD. In the present manuscript, we review for further understanding whether transcranial pulse stimulation (TPS) is a beneficial treatment for AD patients. PubMed, Google Scholar, and Cochrane databases were accessed with the search criteria set from year 2001 to 2022 and the following keywords were used: "transcranial pulse stimulation", "focused ultrasound", "noninvasive treatment and Alzheimer" and "TPS". The search was focused on papers that provide evidence on the biological bases of the method, as well as its safety and tolerability. Even though more studies are needed with greater scientific rigor, such as a doubleblind and randomized study versus a placebo, TPS is an excellent and safe therapeutic option for AD. This novel approach accompanies currently available treatments and complements them, helping to maintain greater stability of the disease and slowing its progression. The biological effects and potential mechanisms of action of TPS for the improvement of cognitive function are further discussed.
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The role of the tetraamine spermine in plant defense against pathogens was investigated by using the Arabidopsis (Arabidopsis thaliana)-Pseudomonas viridiflava pathosystem. The effects of perturbations of plant spermine levels on susceptibility to bacterial infection were evaluated in transgenic plants (35S::spermine synthase [SPMS]) that overexpressed the SPMS gene and accumulated spermine, as well as in spms mutants with low spermine levels. The former exhibited higher resistance to P. viridiflava than wild-type plants, while the latter were more susceptible. Exogenous supply of spermine to wild-type plants also increased disease resistance. Increased resistance provided by spermine was partly counteracted by the polyamine oxidase inhibitor SL-11061, demonstrating that the protective effect of spermine partly depends on its oxidation. In addition, global changes in gene expression resulting from perturbations of spermine levels were analyzed by transcript profiling 35S::SPMS-9 and spms-2 plants. Overexpression of 602 genes was detected in 35S::SPMS-9 plants, while 312 genes were down-regulated, as compared to the wild type. In the spms-2 line, 211 and 158 genes were up- and down-regulated, respectively. Analysis of gene ontology term enrichment demonstrated that many genes overexpressed only in 35S::SPMS-9 participate in pathogen perception and defense responses. Notably, several families of disease resistance genes, transcription factors, kinases, and nucleotide- and DNA/RNA-binding proteins were overexpressed in this line. Thus, a number of spermine-responsive genes potentially involved in resistance to P. viridiflava were identified. The obtained results support the idea that spermine contributes to plant resistance to P. viridiflava.
Asunto(s)
Arabidopsis/inmunología , Arabidopsis/microbiología , Perfilación de la Expresión Génica , Regulación de la Expresión Génica de las Plantas , Pseudomonas/fisiología , Espermina Sintasa/genética , Espermina/metabolismo , Arabidopsis/enzimología , Arabidopsis/genética , Recuento de Colonia Microbiana , Regulación Enzimológica de la Expresión Génica , Genes de Plantas/genética , Mutación/genética , Oxidación-Reducción , Plantas Modificadas Genéticamente , Pseudomonas/crecimiento & desarrollo , ARN Mensajero/genética , ARN Mensajero/metabolismo , Especies Reactivas de Oxígeno/metabolismo , Espermina Sintasa/metabolismo , Factores de Tiempo , Transcripción GenéticaRESUMEN
Alzheimer's Disease is a complex, multifactorial, and comorbid condition. The asymptomatic behavior in the early stages makes the identification of the disease onset particularly challenging. Mild cognitive impairment (MCI) is an intermediary stage between the expected decline of normal aging and the pathological decline associated with dementia. The identification of risk factors for MCI is thus sorely needed. Self-reported personal information such as age, education, income level, sleep, diet, physical exercise, etc. is called to play a key role not only in the early identification of MCI but also in the design of personalized interventions and the promotion of patients empowerment. In this study, we leverage a large longitudinal study on healthy aging in Spain, to identify the most important self-reported features for future conversion to MCI. Using machine learning (random forest) and permutation-based methods we select the set of most important self-reported variables for MCI conversion which includes among others, subjective cognitive decline, educational level, working experience, social life, and diet. Subjective cognitive decline stands as the most important feature for future conversion to MCI across different feature selection techniques.
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Disfunción Cognitiva/patología , Anciano , Anciano de 80 o más Años , Enfermedad de Alzheimer/patología , Estudios de Cohortes , Dieta , Ejercicio Físico/fisiología , Femenino , Humanos , Estudios Longitudinales , Aprendizaje Automático , Masculino , Pruebas Neuropsicológicas , Factores de Riesgo , Sueño/fisiología , EspañaRESUMEN
BACKGROUND: Detecting cognitive impairment is a priority for health systems. The aim of this study is to create normative data on screening tests (MMSE, GDS and MFE) for middle-aged and older Spanish adults, considering the effects of sociodemographic factors. METHOD: A total of 2,030 cognitively intact subjects who lived in the community, aged from 50 to 88 years old, participated voluntarily in SCAND consortium studies. The statistical procedure included the conversion of percentile ranges into scalar scores. Secondly, the effects of age, educational level and gender were verified. Linear regressions were used to calculate the scalar adjusted scores. Cut-off values for each test were also calculated. RESULTS: Scalar scores and percentiles corresponding to MMSE, GDS-15 and MFE are shown. An additional table is provided which shows the points that must be added or subtracted from MMSE score depending on the subject's educational level. CONCLUSIONS: The current norms should provide clinically useful data for evaluating Spanish people aged 50 to 88 years old and should contribute to improving the detection of initial symptoms of cognitive impairment in people living in the community, taking into account the influence of gender, age and educational level
ANTECEDENTES: detectar el deterioro cognitivo es una prioridad del sistema sanitario. El objetivo de este estudio es la presentación de datos normativos de pruebas de cribado (MMSE, GDS y MFE) para adultos españoles de mediana edad y adultos mayores, considerando los efectos de factores sociodemográficos. MÉTODO: en los estudios realizados por el consorcio SCAND participaron voluntariamente 2.030 personas cognitivamente sanas, de 50 a 88 años, residentes en su comunidad. El procedimiento estadístico supuso la conversión de rangos percentiles en puntuaciones escalares. Posteriormente, se comprobaron los efectos de la edad, el nivel educativo y el género. Se utilizaron regresiones lineales para calcular las puntuaciones escalares ajustadas. También se calcularon los puntos de corte para cada prueba. RESULTADOS: se muestran las puntuaciones escalares y los percentiles correspondientes a MMSE, GDS-15 y MFE. Además, se presenta una tabla que muestra los puntos que deben sumarse o restarse a la puntuación del MMSE dependiendo del nivel educativo del individuo. CONCLUSIONES: los datos normativos presentados tienen una utilidad clínica para evaluar a población española de 50 a 88 años, y contribuyen a mejorar la detección de los síntomas iniciales del deterioro cognitivo teniendo en cuenta la influencia del género, la edad y el nivel educativo
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Humanos , Masculino , Femenino , Adulto , Persona de Mediana Edad , Anciano , Anciano de 80 o más Años , Disfunción Cognitiva/diagnóstico , Pruebas de Estado Mental y Demencia/normas , Envejecimiento Cognitivo/psicología , Escala del Estado Mental/normas , Pruebas Neuropsicológicas/normas , Disfunción Cognitiva/psicología , Evaluación Geriátrica/estadística & datos numéricos , Modelos Lineales , EscolaridadRESUMEN
The MAPT H1 haplotype has been linked to several disorders, but its relationship with Alzheimer's disease (AD) remains controversial. A rare variant in MAPT (p.A152T) has been linked with frontotemporal dementia (FTD) and AD. We genotyped H1/H2 and p.A152T MAPT in 11,572 subjects from Spain (4,327 AD, 563 FTD, 648 Parkinson's disease (PD), 84 progressive supranuclear palsy (PSP), and 5,950 healthy controls). Additionally, we included 101 individuals from 21 families with genetic FTD. MAPT p.A152T was borderline significantly associated with FTD [odds ratio (OR)â=â2.03; pâ=â0.063], but not with AD. MAPT H1 haplotype was associated with AD risk (ORâ=â1.12; pâ=â0.0005). Stratification analysis showed that this association was mainly driven by APOE É4 noncarriers (ORâ=â1.14; pâ=â0.0025). MAPT H1 was also associated with risk for PD (ORâ=â1.30; pâ=â0.0003) and PSP (ORâ=â3.18; pâ=â8.59 × 10-8) but not FTD. Our results suggest that the MAPT H1 haplotype increases the risk of PD, PSP, and non-APOE É4 AD.
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Enfermedad de Alzheimer/genética , Predisposición Genética a la Enfermedad/genética , Polimorfismo de Nucleótido Simple/genética , Proteínas tau/genética , Anciano , Anciano de 80 o más Años , Apolipoproteína E4/genética , Femenino , Demencia Frontotemporal/genética , Haplotipos , Humanos , Modelos Logísticos , Masculino , Persona de Mediana Edad , EspañaRESUMEN
The use of anticholinergic drugs is common in the elderly, even in people with cognitive impairment. A systematic search was conducted in PubMed (anticholinergic effects, anticholinergic and dementia) to define the effects of anticholinergic drugs in the elderly. We emphasized the search in patterns of use, the combined use with AChEIs, the measurement of the Serum Anticholinergic Activity, and the short-term and long-term cognitive effects. The conclusions are that the use of anticholinergic drugs is common in the elderly, even more so than the medical prescription of AChEIs in Alzheimer's disease. The use of anticholinergic drugs may result in cognitive impairment. In long-term use it may generate a worsening of cognitive functions. It can lead to a wrong diagnosis of mild cognitive impairment or dementia, and they can also initiate signs of dementia. Greater cognitive effects appear when there is a previous deficit, but cognitive effects from anticholinergic drugs disappear in severe dementia. The presence of ApoEÉ4 increases the vulnerability for cognitive impairment when these drugs are employed.
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Antagonistas Colinérgicos/efectos adversos , Trastornos del Conocimiento/inducido químicamente , Anciano , Anciano de 80 o más Años , Apolipoproteína E4/genética , Antagonistas Colinérgicos/uso terapéutico , Inhibidores de la Colinesterasa/uso terapéutico , Trastornos del Conocimiento/diagnóstico , Trastornos del Conocimiento/epidemiología , Trastornos del Conocimiento/genética , Trastornos del Conocimiento/prevención & control , Comorbilidad , Estudios Transversales , Errores Diagnósticos , Utilización de Medicamentos , Femenino , Predisposición Genética a la Enfermedad , Humanos , Masculino , Polifarmacia , Prevalencia , Receptores Muscarínicos/efectos de los fármacos , Receptores Muscarínicos/fisiología , Estudios RetrospectivosRESUMEN
INTRODUCTION: Alzheimer's disease (AD) is a major threat for the well-being of an increasingly aged world population. The physiopathological mechanisms of late-onset AD are multiple, possibly heterogeneous, and not well understood. Different combinations of variables from several domains (i.e., clinical, neuropsychological, structural, and biochemical markers) may predict dementia conversion, according to distinct physiopathological pathways, in different groups of subjects. METHODS: We launched the Vallecas Project (VP), a cohort study of non-demented people aged 70-85, to characterize the social, clinical, neuropsychological, structural, and biochemical underpinnings of AD inception. Given the exploratory nature of the VP, multidimensional and machine learning techniques will be applied, in addition to the traditional multivariate statistical methods. RESULTS: A total of 1169 subjects were recruited between October 2011 and December 2013. Mean age was 74.4 years (SD 3.9), 63.5% of the subjects were women, and 17.9% of the subjects were carriers of at least one ε4 allele of the apolipoprotein E gene. Cognitive diagnoses at inclusion were as follows: normal cognition 93.0% and mild cognitive impairment (MCI) 7.0% (3.1% amnestic MCI, 0.1% non-amnestic MCI, 3.8% mixed MCI). Blood samples were obtained and stored for future determinations in 99.9% of the subjects and 3T magnetic resonance imaging study was conducted in 89.9% of the volunteers. The cohort is being followed up annually for 4 years after the baseline. CONCLUSION: We have established a valuable homogeneous single-center cohort which, by identifying groups of variables associated with high risk of MCI or dementia conversion, should help to clarify the early physiopathological mechanisms of AD and should provide avenues for prompt diagnosis and AD prevention.
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The circadian clock acts as central coordinator of plant activity, and it regulates key traits for plant fitness such as flowering time, gas exchange, growth, and stress responses. In the May issue of the Proceedings of the National Academy of Science we describe the circadian regulation of gibberellin (GA) signaling, through transcriptional control of GA receptor genes (GID1a and GID1b). We show that, in short day photocycles, the expression of GA receptors oscillates in seedlings, yielding a window of strong GA activity at the end of the night that overlaps with the period of maximum growth. This clock-mediated control of GA signaling is not only crucial for the establishment of rhythmic patterns of growth but also affects the expression of many circadian-controlled genes that participate in a wide range of biological processes. Here we propose a possible mechanism that might operate for the transcriptional control of GID1 expression by the circadian clock.
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Proteínas de Arabidopsis/genética , Arabidopsis/genética , Arabidopsis/fisiología , Relojes Circadianos/fisiología , Giberelinas/farmacología , Plantas Modificadas Genéticamente/genética , Plantas Modificadas Genéticamente/fisiología , Receptores de Superficie Celular/genética , Arabidopsis/efectos de los fármacos , Relojes Circadianos/genética , Regulación de la Expresión Génica de las Plantas/efectos de los fármacos , Regulación de la Expresión Génica de las Plantas/genética , Plantas Modificadas Genéticamente/efectos de los fármacos , Plantones/efectos de los fármacos , Plantones/genética , Plantones/fisiología , Transducción de Señal/efectos de los fármacos , Transducción de Señal/genéticaRESUMEN
El empleo de fármacos anticolinérgicos es frecuente en personas mayores, incluso con deterioro cognitivo. Se ha realizado una revisión bibliográfica en PubMed (anticholinergic effects y anticholinergic and dementia) acerca de los efectos de los fármacos anticolinérgicos en población anciana. Se ha enfatizado en determinar patrones de consumo, uso combinado con fármacos inhibidores de la acetilcolinesterasa (IACE), medida de la carga anticolinérgica y efectos cognitivos a corto y a largo plazo. Las conclusiones son que estos fármacos se emplean de forma habitual en población anciana, incluso tras la prescripción de IACE en la enfermedad de Alzheimer. Su empleo puede producir alteraciones cognitivas. Si el consumo es prolongado puede provocar un empeoramiento de la cognición a largo plazo originando falsos diagnósticos de deterioro, o incluso precipitando cuadros de demencia. Los efectos cognitivos son mayores ante un déficit preexistente, pero desaparecen en la demencia avanzada. La presencia de ApoE ¿4 marca una vulnerabilidad a la afectación cognitiva por estos fármacos (AU)
The use of anticholinergic drugs is common in the elderly, even in people with cognitive impairment. A systematic search was conducted in PubMed (anticholinergic effects, anticholinergic and dementia) to define the effects of anticholinergic drugs in the elderly. We emphasized the search in patterns of use, the combined use with AChEIs, the measurement of the Serum Anticholinergic Activity, and the short-term and long-term cognitive effects. The conclusions are that the use of anticholinergic drugs is common in the elderly, even more so than the medical prescription of AChEIs in Alzheimers disease. The use of anticholinergic drugs may result in cognitive impairment. In long-term use it may generate a worsening of cognitive functions. It can lead to a wrong diagnosis of mild cognitive impairment or dementia, and they can also initiate signs of dementia. Greater cognitive effects appear when there is a previous deficit, but cognitive effects from anticholinergic drugs disappear in severe dementia. The presence of ApoE ¿4 increases the vulnerability for cognitive impairment when these drugs are employed (AU)
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Humanos , Masculino , Femenino , Anciano , Enfermedad de Alzheimer/tratamiento farmacológico , Antagonistas Colinérgicos/uso terapéutico , Disfunción Cognitiva , Colinérgicos/efectos adversos , Inhibidores de la Colinesterasa/uso terapéuticoRESUMEN
Fundamento y objetivo: la enfermedad de Alzheimer (EA) se acompaña frecuentemente de patología vascular (PV). La utilización de un sistema de clasificación que combine ambos tipos de patología permitiría realizar un diagnóstico diferencial preciso. En el presente trabajo se aplican de manera conjunta criterios neuropatológicos de EA y PV para clasificar una cohorte de pacientes con demencia avanzada. Material y método: se analizaron los datos neuropatológicos post mórtem de 40 cerebros donados al Banco de Tejidos de la Fundación CIEN. Todos los sujetos eran mayores de 70 años (edad = 85,42 ± 7,06; 75 % mujeres) y residentes del Centro Alzheimer de la Fundación Reina Sofía. Resultados: EA y PV no mostraron ninguna relación entre sí. Las puntuaciones cognitivas correlacionaron de forma inversamente proporcional con la EA, pero no mostraron asociación con la PV. Utilizando una escala de EA y otra de PV, los casos se clasificaron en tres grupos (57,5% EA, 12,5 % demencia vascular y 30 % demencia mixta) y se estudió su rendimiento en los test cognitivos. Conclusiones: el grupo vascular evidenció un rendimiento cognitivo superior a los otros dos. Los resultados apoyan el uso combinado de escalas de EA y PV para clasificar a los pacientes con demencia avanzada (AU)
Introduction and aim: Alzheimers (AD) disease is often accompanied by vascular pathology (VP). The use of a classification system combining both types of pathologies would enable a precise differential diagnosis. In this paper neuropathological criteria of AD and VP are applied in order to classify a cohort of patients with advanced dementia. Material and method: Postmortem neuropathological data from 40 brains donated to the CIEN Foundation Bank Tissue were analyzed. All participants were over 70 years old (mean age = 85.42 ± 7.06; 75% women) and they were institutionalized at the Alzheimer Center Reina Sofia Foundation. Results: AD and VP did not show any relation between them. Cognitive scores correlated inversely proportional with AD, but no association with VP was found. Combination of both scales allowed a classification of cases in three groups (57.5% AD, 12.5% vascular dementia, and 30% mixed dementia). Cognitive performance of those groups was studied. Discussion: Vascular group showed a higher cognitive performance than the other two groups. These results support the combination of AD and VP scales to classify a cohort of patients with advanced dementia (AU)
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Humanos , Masculino , Femenino , Anciano , Anciano de 80 o más Años , Enfermedades Vasculares/epidemiología , Enfermedad de Alzheimer/complicaciones , Clasificación Internacional de Enfermedades , Estudios de Casos y Controles , Trastornos del Conocimiento/epidemiología , Trastornos Cerebrovasculares/fisiopatologíaRESUMEN
En los últimos años, ha existido un interés creciente por entender la naturaleza del lenguaje en el envejecimiento, no solo por tratar de describir el modo en que este dominio cambia con la edad, sino también por la particular cualidad que su complejidad e interdependencia con otros procesos cognitivos le confieren sirviendo de marco en el desarrollo de teorías generales sobre el envejecimiento, al tiempo que brindando la oportunidad de examinar los sustratos neurobiológicos asociados al deterioro funcional y la preservación cognitiva. Aunque el procesamiento lingüístico parece resistir el avance de la edad, lo cierto es que cambios asociados al proceso de envejecimiento surgen también en el lenguaje. Sin embargo, el envejecimiento no afecta al lenguaje de un modo global, sino específicamente produciendo asimetrías, entre las que destaca un marcado deterioro de la producción frente a un relativo mantenimiento de la comprensión o un aumento del vocabulario. El propósito de este trabajo es revisar los principales cambios estructurales y funcionales que acontecen en el cerebro con la edad, así como los declives que a nivel cognitivo de ellos se derivan, con particular interés en el efecto que estos cambios pueden tener en el lenguaje, y en especial en los procesos de recuperación léxica. Se considera también el efecto de factores sociales, tales como el nivel educativo y la posición socioeconómica. El artículo aborda además los déficits de acceso léxico asociados a enfermedad neurológica, concretamente a deterioro cognitivo leve y enfermedad de Alzheimer (AU)
In the last few years, interest in understanding the nature of language in aging has grown. This interest concerns how this domain changes with age. Furthermore, because of its complexity and interdependence with other cognitive processes, language provides a framework to develop general theories on aging and to examine the neurobiological substrates in relation to functional impairment and cognitive preservation. Although linguistic processes seem not to be impaired as a result of age, age-related changes do affect language. However, not all linguistic processes are affected equally. Aging causes a marked deterioration in language production versus a relative preservation of comprehension or an increase in vocabulary. The aim of this study was to review age-related changes in brain structure and function, as well as the resulting cognitive decline, with particular focus on the effect that these changes might have on language, especially on the processes of lexical retrieval. The role of social variables, such as education and socioeconomic status are also considered. Deficits in lexical access related to neurological disorders such as mild cognitive impairment and Alzheimer's disease are also discussed (AU)