HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Atypical Skeletal Muscle Profiles in Human Immunodeficiency Virus-Infected Asymptomatic Middle-Aged Adults.

AbstractBackground:
Human immunodeficiency virus (HIV)-infected individuals are at increased risk of age-associated functional impairment, even with effective antiretroviral therapy (ART). A concurrent characterization of skeletal muscle, physical function, and immune phenotype in aviremic middle-aged HIV-infected adults represents a knowledge gap in prognostic biomarker discovery.
Methods:
We undertook a prospective observational study of 170 middle-aged, HIV-infected ambulatory men and women with CD4+ T-cell counts of at least 350/µL and undetectable plasma viremia while on effective ART, and uninfected control participants. We measured biomarkers for inflammation and immune activation, fatigue, the Veterans Aging Cohort Study mortality index, and physical function. A subset also received a skeletal muscle biopsy and computed tomography scan.
Results:
Compared to the uninfected participants, HIV-infected participants displayed increased immune activation (P < .001), inflammation (P = .001), and fatigue (P = .010), and in a regression model adjusting for age and sex displayed deficits in stair-climb power (P < .001), gait speed (P = .036), and predicted metabolic equivalents (P = .019). Skeletal muscle displayed reduced nuclear peroxisome proliferator-activated receptor-γ coactivator 1α-positive myonuclei (P = .006), and increased internalized myonuclei (P < .001) that correlated with immune activation (P = .003) and leukocyte infiltration (P < .001). Internalized myonuclei improved a model for HIV discrimination, increasing the C-statistic from 0.84 to 0.90.
Conclusions:
Asymptomatic HIV-infected middle-aged adults display atypical skeletal muscle profiles, subclinical deficits in physical function, and persistent inflammation and immune activation. Identifying biomarker profiles for muscle dysregulation and risk for future functional decline in the HIV-infected population will be key to developing and monitoring preventive interventions.
Clinical Trials Registration:
NCT03011957.
AuthorsThanh Tran, Viola Guardigni, Karol M Pencina, Anthony A Amato, Michael Floyd, Brooke Brawley, Brian Mozeleski, Jennifer McKinnon, Erin Woodbury, Emily Heckel, Zhuoying Li, Tom Storer, Paul E Sax, Monty Montano
JournalClinical infectious diseases : an official publication of the Infectious Diseases Society of America (Clin Infect Dis) Vol. 66 Issue 12 Pg. 1918-1927 (06 01 2018) ISSN: 1537-6591 [Electronic] United States
PMID29293942 (Publication Type: Clinical Trial, Journal Article, Observational Study, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Chemical References
  • Biomarkers
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
Topics
  • Aged
  • Asymptomatic Infections
  • Biomarkers
  • Biopsy
  • Fatigue (etiology, virology)
  • Female
  • HIV (isolation & purification)
  • HIV Infections (complications, immunology)
  • Humans
  • Inflammation
  • Male
  • Middle Aged
  • Muscle, Skeletal (pathology, virology)
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha (analysis)
  • Prospective Studies
  • T-Lymphocytes (immunology)
  • Viremia
  • Walking Speed

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: