Publications by authors named "Gustavo Galicia-Negrete"

Purpose: The protease inhibitor S (PiS) and Z (PiZ) variants have been stated as the only genetic cause of chronic obstructive pulmonary disease (COPD) in Caucasians. However, its frequency in admixed populations is low. We aimed to identify genetic susceptibility between PiS (rs17580) and PiZ (rs28929474) polymorphisms with COPD related to tobacco smoking and biomass-burning smoke as well as to determine its frequencies in Mestizo and Amerindian populations from Mexico.

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Background: Asthma is a complex and chronic inflammatory airway disease. Asthma's etiology is unknown; however, genetic and environmental factors could affect disease susceptibility. We designed a case-control study aimed to evaluate the role of single-nucleotide polymorphisms (SNP), and copy-number variants (CNV) in the and genes in asthma susceptibility and their participation in plasma cytokine levels depending on genotypes Methods: We include 486 subjects, divided into asthma patients (AP, = 141) and clinically healthy subjects (CHS, = 345).

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There is an increase in the prevalence of asthma and obesity, constituting a public health problem at national and global levels. The association between the two pathologies has not been clearly determined; however, a certain synergy has been proposed, which leads to more severe bronchospasms, longer recovery time, and more prolonged use of medications in obese asthmatic patients. The discovery of leptin, an adipokine that is directly related to the amount of total body fat and the production of proinflammatory cytokines, has generated greater interest in white adipose tissue.

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Article Synopsis
  • AERD is a condition that involves chronic sinus issues, asthma, and sensitivity to aspirin, potentially linked to COX-1 inhibition and increased leukotriene production.
  • Current research is exploring genetic factors, specifically the roles of IL1B and IL8 gene polymorphisms, in understanding AERD.
  • A study found a significant association between the AA genotype of IL1B in AERD patients compared to those with aspirin-tolerant asthma, suggesting a need for further investigation into IL1β's role and its genetic connections in AERD.
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