Serum levels of prostate specific antigen, free PSA, [-2]proPSA, fPSA/tPSA ratio, Prostate Health Index, and glycosylation patterns of free PSA in patients with benign prostatic hyperplasia pharmacotherapy
Language English Country United States Media print-electronic
Document type Journal Article
Grant support
"COOPERATIO" Program, research area Pharmaceutical Sciences
project BBMRI. cz, reg. no. LM2023033
Faculty Hospital in Pilsen-FNPl, 00669806
PubMed
39327946
PubMed Central
PMC11609895
DOI
10.1002/pros.24801
Knihovny.cz E-resources
- Keywords
- 5‐alpha reductase inhibitors, PSA, alpha‐blockers, antimuscarinic agents, benign prostate hyperplasia, prostate cancer,
- MeSH
- Adrenergic alpha-Antagonists therapeutic use MeSH
- Muscarinic Antagonists * therapeutic use MeSH
- Glycosylation MeSH
- Prostatic Hyperplasia * blood drug therapy MeSH
- 5-alpha Reductase Inhibitors therapeutic use MeSH
- Middle Aged MeSH
- Humans MeSH
- Prostatic Neoplasms blood drug therapy MeSH
- Prostate pathology metabolism MeSH
- Prostate-Specific Antigen * blood MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Adrenergic alpha-Antagonists MeSH
- Muscarinic Antagonists * MeSH
- 5-alpha Reductase Inhibitors MeSH
- Prostate-Specific Antigen * MeSH
BACKGROUND: The medication used to treat benign prostate hyperplasia (BPH), a common condition in men over 50 years of age, can alter the levels of biomarkers used in prostate cancer detection. Commonly used medications for BPH include alpha-blockers, 5-alpha reductase inhibitors (5-ARIs), and muscarinic antagonists. We studied the impact of these drugs on total prostate-specific antigen (tPSA), free PSA (fPSA), [-2]proPSA, fPSA/tPSA ratio, and the Prostate Health Index (PHI), as well as novel potential biomarkers in the form of glycan composition of fPSA. PATIENTS AND METHODS: Serum samples were collected from 564 males with BPH, with a mean age of 68.5 years. The samples were used to measure levels of tPSA, fPSA, and [-2]proPSA. The fPSA/tPSA and PHI were then calculated. The glycan composition of fPSA was analyzed using lectin-based glycoprofiling. Pharmacotherapy data was collected from the patients' medical records. RESULTS: Alpha-blocker monotherapy was associated with higher fPSA and fPSA/tPSA ratio, and decreased PHI. Levels of tPSA were not impacted. Alpha-blocker and 5-ARI dual therapy was associated with reduced levels of fPSA, [-2]proPSA, and PHI. Therapy combining alpha-blockers and antimuscarinic agents did not significantly influence biomarker levels apart from an increase in a Maackia amurensis lectin-recognized glycan originating in fPSA. CONCLUSION: BPH pharmacotherapy notably affects prostate cancer biomarkers. Recognizing the impact of pharmacotherapy is crucial for achieving an accurate diagnosis of prostate cancer and for planning treatment.
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