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Extracellular vesicle-encapsulated microRNAs and respiratory health among American Indians in the Strong Heart Study.
Eckhardt, Christina M; Wu, Haotian; Jackson, Gabriela; Sobel, Marisa H; Bloomquist, Tessa; Divjan, Adnan; da Silva, Hadler; Best, Lyle G; Cole, Shelley; Umans, Jason; Zhang, Ying; de Hoff, Peter; Laurent, Louise C; Perzanowski, Matthew S; Cheng, Ke; Baccarelli, Andrea A; Sanchez, Tiffany R.
Affiliation
  • Eckhardt CM; Columbia University Vagelos College of Physicians and Surgeons, Division of Pulmonary, Allergy and Critical Care Medicine, Department of Medicine, New York, NY, USA; Columbia University Mailman School of Public Health, Department of Environmental Health Sciences, New York, NY, USA. Electronic addres
  • Wu H; Columbia University Mailman School of Public Health, Department of Environmental Health Sciences, New York, NY, USA.
  • Jackson G; Columbia University Mailman School of Public Health, Department of Environmental Health Sciences, New York, NY, USA.
  • Sobel MH; Columbia University Mailman School of Public Health, Department of Environmental Health Sciences, New York, NY, USA.
  • Bloomquist T; Columbia University Mailman School of Public Health, Department of Environmental Health Sciences, New York, NY, USA.
  • Divjan A; Columbia University Mailman School of Public Health, Department of Environmental Health Sciences, New York, NY, USA.
  • da Silva H; Columbia University Mailman School of Public Health, Department of Environmental Health Sciences, New York, NY, USA.
  • Best LG; Missouri Breaks Industries Research, Inc., Eagle Butte, South Dakota, USA.
  • Cole S; Population Health Program, Texas Biomedical Research Institute, San Antonio, Texas, USA.
  • Umans J; Center for Clinical and Translational Sciences, Georgetown/Howard Universities, Washington, DC, USA; MedStar Health Research Institute, Washington, DC, USA.
  • Zhang Y; Center for American Indian Health Research, Department of Biostatistics and Epidemiology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, USA.
  • de Hoff P; University of California, San Diego, Department of Obstetrics, Gynecology, and, Reproductive Sciences, La Jolla, CA, USA.
  • Laurent LC; University of California, San Diego, Department of Obstetrics, Gynecology, and, Reproductive Sciences, La Jolla, CA, USA.
  • Perzanowski MS; Columbia University Mailman School of Public Health, Department of Environmental Health Sciences, New York, NY, USA.
  • Cheng K; Columbia University, Department of Biomedical Engineering, New York, NY, USA.
  • Baccarelli AA; Harvard T.H. Chan School of Public Health, Boston, MA, USA.
  • Sanchez TR; Columbia University Mailman School of Public Health, Department of Environmental Health Sciences, New York, NY, USA.
Chest ; 2024 Aug 16.
Article in En | MEDLINE | ID: mdl-39154798
ABSTRACT

BACKGROUND:

American Indian populations have experienced marked disparities in respiratory disease burden. Extracellular vesicle-encapsulated microRNAs (EV-miRNAs) are a novel class of biomarkers that may improve recognition of lung damage in indigenous populations. RESEARCH QUESTION Are plasma EV-miRNAs viable biomarkers of respiratory health in American Indian populations? STUDY DESIGN AND

METHODS:

The Strong Heart Study is a prospective cohort study that enrolled American Indians aged 45-74 years. EV-miRNA expression was measured in plasma (1993-1995). Respiratory health outcomes including pre-bronchodilator forced expiratory volume in 1 second (FEV1), forced vital capacity (FVC), and respiratory symptom burden were ascertained in the same study visit. Club cell secretory protein (CC-16), an anti-inflammatory pneumoprotein implicated in COPD pathogenesis, was measured in serum. Linear and logistic regression were used for statistical analyses. Biological pathway analyses were used to elucidate gene targets of significant EV-miRNAs.

RESULTS:

Among 853 American Indian adults, three EV-miRNAs were associated with FEV1, four EV-miRNAs were associated with FVC, and one EV-miRNA was associated with FEV1/FVC (P<0.05). Increased miR-1294 expression was associated with higher odds of airflow limitation (OR 1.29, 95% CI 1.07-1.55), while increased expression of miR-1294 (OR 1.32, 95% CI 1.07-1.63) and miR-532-5p (OR 1.57, 95% CI 1.02-2.40) was associated with higher odds of restriction. Increased miR-451a expression was associated with lower odds of exertional dyspnea (OR 0.71, 95% CI 0.59-0.85). Twenty-two EV-miRNAs were associated with serum CC-16 levels (q<0.05), suggesting EV-miRNAs may play a role in the pathway linking CC-16 to COPD pathogenesis. A pathway analysis showed key EV-miRNAs targeted biological pathways that modulate inflammation, immunity, and structural integrity in the lungs.

INTERPRETATION:

Circulating EV-miRNAs are novel mechanistic biomarkers of respiratory health and may facilitate the early detection and treatment of lung damage in American Indian populations that have been disproportionately affected by chronic lung diseases.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Chest Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Chest Year: 2024 Document type: Article