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Circulating microRNAs Related to Bone Metabolism in HIV-Associated Bone Loss
Maria P Yavropoulou1,2, Artemis Kolynou3, Polyzois Makras2
1Endocrinology Unit, The First Department of Propaedeutic and Internal Medicine, Medical School, National and Kapodistrian University of Athens, 11527 Athens, Greece.
Abstract:
The pathophysiology of human immunodeficiency virus (HIV)-associated bone loss is complex and to date largely unknown. In this study, we investigated serum expression of microRNAS (miRNAs) linked to bone metabolism in HIV-associated bone loss. This was a case-control study. Thirty male individuals with HIV infection (HIV+) and osteoporosis/osteopenia (HIV+/OP+) (cases) and 30 age-matched male HIV+ individuals with normal bone mass (HIV+/OP-) (controls) were included in the analysis. Thirty male individuals matched for age without HIV infection (HIV-), were also included as second controls. The selected panel of miRNAs was as follows: hsa-miRNA-21-5p; hsa-miRNA-23a-3p; hsa-miRNA-24-2-5p; hsa-miRNA-26a-5p; hsa-miRNA-29a-3p; hsa-miRNA-124-3p; hsa-miRNA-33a-5p; and hsa-miRNA-133a-3p. Within the cohort of HIV+ individuals, relative serum expression of miRNA-21-5p and miRNA-23a-3p was significantly lower (p < 0.001) while the expression of miRNA-24-2-5p was significantly higher (p = 0.030) in HIV+/OP+ compared to HIV+/OP-. Expression of miRNA-21-5p demonstrated a sensitivity of 84.6% and a specificity of 66.7 in distinguishing HIV+/OP+ individuals. Expression of circulating miRNAs related to bone metabolism; miRNA-23a-3p, miRNA-24-2-5p, and miRNA-21-5p is significantly altered in HIV+OP+ individuals, in line with data on other causes of osteoporosis, suggesting a common pattern of circulating miRNAs independent of the underlying cause.
Insights
Serum microRNAs (miRNAs) linked to bone metabolism are altered in individuals with human immunodeficiency virus (HIV) and osteoporosis. Specific miRNA changes may help identify HIV-associated bone loss.
Area of Science:
- Endocrinology
- Virology
- Genetics
Background:
- Human immunodeficiency virus (HIV) infection is associated with complex bone loss.
- The specific mechanisms driving HIV-associated bone loss remain largely unknown.
- MicroRNAs (miRNAs) play a role in regulating bone metabolism.
Purpose of the Study:
- To investigate serum miRNA expression in individuals with HIV and bone loss.
- To identify specific miRNAs associated with osteoporosis/osteopenia in the context of HIV infection.
- To explore potential diagnostic biomarkers for HIV-associated bone disease.
Main Methods:
- A case-control study design was employed.
- Participants included male individuals with HIV and osteoporosis/osteopenia (HIV+/OP+), HIV+ individuals with normal bone mass (HIV+/OP-), and HIV-negative controls.
- Serum samples were analyzed for the expression of a panel of eight miRNAs involved in bone metabolism.
Main Results:
- Within the HIV+ cohort, significantly lower serum expression of miRNA-21-5p and miRNA-23a-3p was observed in HIV+/OP+ cases compared to HIV+/OP- controls (p < 0.001).
- Significantly higher serum expression of miRNA-24-2-5p was found in HIV+/OP+ cases versus HIV+/OP- controls (p = 0.030).
- miRNA-21-5p showed 84.6% sensitivity and 66.7% specificity in distinguishing HIV+/OP+ individuals.
Conclusions:
- Circulating miRNAs, specifically miRNA-21-5p, miRNA-23a-3p, and miRNA-24-2-5p, are significantly altered in individuals with HIV and osteoporosis.
- These altered miRNA patterns suggest a common molecular pathway in bone loss, potentially independent of the underlying cause.
- The findings highlight the potential of these miRNAs as biomarkers for HIV-associated bone loss.
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