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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.
The chain begins with pathogens: bacteria, viruses, fungi, prions, or parasites such as protozoa helminths. These can be present on the skin as transient or resident flora, or they can be acquired from the environment. Identifying and treating the type of infection and...
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Urinary Tract Infection II: Pathophysiology01:25

Urinary Tract Infection II: Pathophysiology

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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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Updated: Jan 8, 2026

Mouse Footpad Inoculation Model to Study Viral-Induced Neuroinflammatory Responses
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Ciencia básica y patogénesis

Justina P Tavana1, Maegan Leary1, James E Galvin2

  • 1Brigham Young University, Provo, UT, USA.

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

Los alelos APOE ε2 y ε4 no predicen el deterioro cognitivo leve (DCL) en poblaciones nativas hawaianas e isleñas del Pacífico (NHPI). Este estudio destaca la necesidad de conjuntos de datos diversos en la investigación de la enfermedad de Alzheimer (EA).

Palabras clave:
Enfermedad de AlzheimerDeterioro cognitivo leveAPOE ε2APOE ε4Nativos hawaianosIsleños del PacíficoGenéticaFactores de riesgoPoblaciones subrepresentadas

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Área de la Ciencia:

  • Neurociencia
  • Genética
  • Salud Pública

Sus antecedentes:

  • Los conjuntos de datos de investigación de la enfermedad de Alzheimer (EA) son predominantemente blancos, lo que limita la utilidad clínica y puede causar disparidades poblacionales.
  • Las poblaciones nativas hawaianas e isleñas del Pacífico (NHPI) exhiben un mayor riesgo de EA, un inicio más temprano y peores puntuaciones cognitivas.
  • Los NHPI están significativamente subrepresentados en los principales repositorios de investigación de la EA.

Objetivo del estudio:

  • Investigar la asociación de los alelos APOE ε2 y ε4 con el deterioro cognitivo leve (DCL) en poblaciones NHPI.
  • Abordar la falta de datos genéticos para los NHPI en la investigación de la EA.
  • Comparar las frecuencias de SNP de APOE en NHPI con otras poblaciones mundiales.

Principales métodos:

  • Se reclutaron aproximadamente 2.000 NHPI mayores en Utah, Hawái, Samoa Americana y Tonga.
  • Se recolectaron especímenes biológicos y se administró la prueba de deterioro cognitivo AD8.
  • Se genotiparon los SNP de APOE ε2 (rs7412) y ε4 (rs429358), analizando las frecuencias y la asociación con el DCL.

Principales resultados:

  • La cohorte comprendió 1.367 adultos NHPI, con 1.325 de ascendencia única de diversos grupos polinesios.
  • Los NHPI tienen una frecuencia de alelos menores (MAF) de ε2 comparable pero una MAF de ε4 duplicada (∼25%) en comparación con otras poblaciones.
  • Ni APOE ε2 ni ε4 se correlacionaron significativamente con el DCL en esta cohorte (valores p ≈ 1).

Conclusiones:

  • Los alelos APOE ε2 y ε4 no parecen predecir el DCL en poblaciones nativas hawaianas e isleñas del Pacífico.
  • A pesar de un tamaño de cohorte relativamente pequeño, el estudio tuvo suficiente poder para detectar tamaños de efecto similares a los de otras poblaciones.
  • Los hallazgos coinciden con investigaciones en otras poblaciones indígenas que muestran una correlación no significativa entre APOE y demencia.