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Infection01:20

Infection

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When a pathogen enters the body and reproduces, it can cause an infection, damage body cells, and cause illness symptoms that eventually lead to disease. Therefore, its prevention requires breaking the chain of infection.
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Urinary Tract Infection II: Pathophysiology01:25

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The pathophysiology of urinary tract infections (UTIs) encompasses several progressive stages, beginning with bacterial colonization and culminating in potential systemic complications if untreated. UTIs are primarily initiated by bacteria, such as Escherichia coli, which often originate from the gastrointestinal tract and migrate to the urinary system through the periurethral area. This migration can occur via several routes, including improper hygiene practices, sexual activity, or...
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Cystic Fibrosis: Pathogenesis01:23

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Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
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Pneumonia II: Pathophysiology01:29

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The pathophysiology of pneumonia involves the following steps:
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Stages of Infection01:26

Stages of Infection

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Stages of infection describe what happens to a susceptible host once a pathogen invades the human body. The stages of infection are incubation, prodromal, illness, stage of decline, and convalescence. The incubation stage is the period from exposure to a pathogen until symptoms start. The infected person is unaware of impending illness as the pathogens grow and multiply within the body. The duration may vary depending on the type of infection. The incubation period of measles averages ten to...
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Defense Against Bacterial Pathogens01:31

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The human immune system is a complex network of cells, tissues, and organs that work together to defend the body against bacterial infections. It consists of various immune cells, each playing a specific role in the defense mechanism.
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Mouse Footpad Inoculation Model to Study Viral-Induced Neuroinflammatory Responses
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Ciencia básica y patogénesis

Katelyn Elizabeth Mooney1, Cristian O Mojica2, Courtney Thomas Tobin3

  • 1University of California, Los Angeles Neuroscience Interdepartmental Program (NSIDP), Los Angeles, CA, USA.

Alzheimer's & dementia : the journal of the Alzheimer's Association
|December 24, 2025
PubMed
Resumen
Este resumen es generado por máquina.

Los factores sociales como la discriminación no alteraron los efectos del gen TOMM40 en el deterioro cognitivo. Sin embargo, la discriminación predijo un declive más rápido en los portadores de APOE-ε4+, lo que sugiere una vulnerabilidad genética a los factores estresantes sociales.

Palabras clave:
determinantes socialesdeterioro cognitivogenéticaAPOETOMM40adultos mayores negrosdiscriminaciónsoledadneurocienciaepidemiología social

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Área de la Ciencia:

  • Neurociencia
  • Genética
  • Epidemiología Social

Sus antecedentes:

  • Los determinantes sociales como la discriminación y la soledad están relacionados con el deterioro cognitivo en los estadounidenses negros.
  • Las variantes genéticas de TOMM40, en particular TOMM40-'523-S, interactúan con el genotipo APOE e influyen en las trayectorias cognitivas.
  • El impacto combinado de los factores sociales y TOMM40-'523-S en la cognición en adultos mayores negros sigue siendo poco estudiado.

Objetivo del estudio:

  • Investigar si los factores sociales (discriminación, soledad) modifican la asociación entre el genotipo TOMM40-'523-S y el deterioro cognitivo.
  • Examinar la interacción entre TOMM40-'523-S, el genotipo APOE y los factores sociales en la predicción de las trayectorias cognitivas en una cohorte de adultos mayores negros.

Principales métodos:

  • Se utilizaron modelos lineales de efectos mixtos con datos de 436 participantes no hispanos negros libres de demencia.
  • Se evaluaron los efectos de las copias de TOMM40-'523-S (0, 1 o 2) dentro de los genotipos APOE (ε3/ε3 o ε4+) y los factores sociales (discriminación, soledad) en la cognición global y específica de dominio.
  • Se controlaron la edad, la educación, el sexo/género y el tiempo desde la línea de base durante un seguimiento promedio de 9,5 años.

Principales resultados:

  • Los factores sociales no mediaron la relación entre TOMM40-'523-S y el deterioro cognitivo.
  • Los portadores de APOE-ε4+ que experimentaron discriminación mostraron un declive acelerado en la memoria de trabajo y la velocidad de percepción.
  • La soledad no se asoció con el deterioro cognitivo, pero los efectos de base de la discriminación y la soledad variaron según el genotipo APOE.

Conclusiones:

  • Los factores sociales no influyen en el efecto de TOMM40-'523-S en el deterioro cognitivo.
  • La discriminación predice el deterioro cognitivo específicamente en los portadores de APOE-ε4+, lo que resalta su mayor vulnerabilidad.
  • La cognición basal se ve afectada de manera diferencial por los factores sociales según el genotipo APOE.