Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2020 Aug 3:7:100112.
doi: 10.1016/j.bbih.2020.100112. eCollection 2020 Aug.

Sympathetic function and markers of inflammation in well-controlled HIV

Affiliations

Sympathetic function and markers of inflammation in well-controlled HIV

Jessica Robinson-Papp et al. Brain Behav Immun Health. .

Abstract

Purpose: HIV-associated autonomic neuropathy (HIV-AN) is common and may be associated with both sympathetic and parasympathetic dysfunction. Sympathetic nervous system (SNS) dysfunction occurs on a continuum of hyper-to hypo-adrenergic function, and may be a mediator between psychological stress and chronic inflammation. We sought to describe patterns of SNS dysfunction in people living with HIV, and to determine whether SNS dysfunction is associated with markers of systemic inflammation (focusing on IL-6 and TNF-α) and pain and anxiety.

Methods: Forty-seven people with well-controlled HIV and without confounding medical conditions or medications completed the Medical Outcomes Survey (MOS-HIV), quantification of a panel of 41 plasma cytokines/chemokines, and a standardized, non-invasive autonomic reflex screen (ARS). Adrenergic baroreflex sensitivity (BRSA) was calculated from the ARS as a measure of SNS function.

Results: Pain (46%) and anxiety (52%) were commonly reported on the MOS-HIV. BRSA was reduced in 30% of participants and elevated in 9% with the latter occurring only in participants with normal to mild HIV-AN. BRSA was significantly associated with IL-6, but not with TNF-α, pain or anxiety. Exploratory analyses also revealed positive associations of BRSA with numerous other cytokines with no significant inverse associations.

Conclusion: Higher BRSA, indicative of a more hyperadrenergic state, can be part of the spectrum of early HIV-AN, and may be associated with elevations in multiple cytokines including IL-6. These associations do not appear to be driven by stressors such as pain or anxiety.

Keywords: Autonomic; Cytokines; HIV; IL-6; Inflammation; Sympathetic.

PubMed Disclaimer

Conflict of interest statement

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper..

Figures

Fig. 1
Fig. 1
Figure legend. Results of an exploratory analysis in which bivariate Spearman’s rank correlations were performed between adrenergic baroreflex sensitivity (BRSA) and each of the 41 cytokines in our multiplex panel. Black bars indicate statistically significant correlations using a Benjamini-Hochberg adjustment for multiple testing, whereas asterisks indicate correlations that were statistically significant using the more conservative Bonferroni correction.

References

    1. Adlan A.M. Increased sympathetic nerve activity and reduced cardiac baroreflex sensitivity in rheumatoid arthritis. J Physiol. 2017;595(3):967–981. - PMC - PubMed
    1. Aronson D., Mittleman M.A., Burger A.J. Interleukin-6 levels are inversely correlated with heart rate variability in patients with decompensated heart failure. J. Cardiovasc. Electrophysiol. 2001;12(3):294–300. - PubMed
    1. Askgaard G. Decreased heart rate variability in HIV positive patients receiving antiretroviral therapy: importance of blood glucose and cholesterol. PloS One. 2011;6(5) - PMC - PubMed
    1. Balzan S. Bacterial translocation: overview of mechanisms and clinical impact. J. Gastroenterol. Hepatol. 2007;22(4):464–471. - PubMed
    1. Bellinger D.L., Lorton D. Sympathetic nerve hyperactivity in the spleen: causal for nonpathogenic-driven chronic immune-mediated inflammatory diseases (IMIDs)? Int. J. Mol. Sci. 2018;19(4) - PMC - PubMed

LinkOut - more resources