# Correlation between intravesical prostatic protrusion and ejaculatory dysfunction after tamsulosin treatment in men with BPH

**Authors:** Cem Tuğrul Gezmiş, Nusret Can Çilesiz, Veli Huzeyfe Kartal, Mahmut Kemal Altan, Basri Çakıroğlu, Mustafa Bahadır Can Balcı

PMC · DOI: 10.1007/s00345-026-06266-8 · World Journal of Urology · 2026-02-17

## TL;DR

This study finds that men with certain prostate shapes experience less ejaculatory dysfunction when taking tamsulosin for enlarged prostate.

## Contribution

Shows for the first time that intravesical prostatic protrusion correlates with reduced ejaculatory dysfunction during tamsulosin treatment.

## Key findings

- Tamsulosin improved urinary symptoms but reduced ejaculatory function scores in BPH patients.
- Greater intravesical prostatic protrusion was linked to smaller declines in ejaculatory function.
- Prostate length and older age also correlated with less severe ejaculatory dysfunction changes.

## Abstract

To evaluate the correlation between prostate morphological measurements and changes in ejaculatory function during short-term tamsulosin therapy in men with benign prostatic hyperplasia (BPH).

This prospective study included 214 sexually active men with moderate-to-severe lower urinary tract symptoms (LUTS) who received tamsulosin 0.4 mg/day for eight weeks. Patients with prior treatment for BPH or pre-existing sexual dysfunction were excluded. Symptom severity and ejaculatory function were evaluated using the International Prostate Symptom Score (IPSS) and the Male Sexual Health Questionnaire–Ejaculatory Dysfunction Short Form (MSHQ-EjD-SF). Prostate morphological measurements, including overall dimensions and intravesical prostatic protrusion (IPP), were obtained by transabdominal ultrasonography. Correlations between changes in MSHQ-EjD scores (ΔMSHQ-EjD) and clinical or anatomical variables were assessed using Spearman’s rank coefficients.

After eight weeks of treatment, the median IPSS significantly decreased from 18 to 14 (p < 0.001) and Qmax increased from 9.2 to 14.0 mL/s (p < 0.001). The median MSHQ-EjD-SF score declined from 11 to 7 (p < 0.001), while higher ejaculatory bother scores were observed after treatment. ΔMSHQ-EjD was negatively correlated with IPP (ρ = −0.386), prostate length (ρ = −0.250), and age (ρ = −0.334) (all p < 0.01). Patients with IPP > 10 mm showed a less pronounced decline in ejaculatory function compared with lower IPP grades (p < 0.001).

Tamsulosin improved urinary symptoms but was associated with a decline in ejaculatory function. Prostate morphological characteristics, particularly IPP > 10 mm and longer prostate length, were associated with a less pronounced decline in ejaculatory function. Although these correlations were modest, the findings may help contextualize the relationship between prostate anatomy and tamsulosin-related ejaculatory changes.

## Linked entities

- **Chemicals:** tamsulosin (PubChem CID 60147)
- **Diseases:** benign prostatic hyperplasia (MONDO:0010811)

## Full-text entities

- **Genes:** SERPINA1 (serpin family A member 1) [NCBI Gene 5265] {aka A1A, A1AT, AAT, PI, PI1, PRO2275}, NPEPPS (aminopeptidase puromycin sensitive) [NCBI Gene 9520] {aka AAP-S, MP100, PSA}, SLC12A3 (solute carrier family 12 member 3) [NCBI Gene 6559] {aka NCC, NCCT, TSC}, IPP (intracisternal A particle-promoted polypeptide) [NCBI Gene 3652] {aka KLHL27}
- **Diseases:** Prostate (MESH:D011472), multiple sclerosis (MESH:D009103), ejaculatory problems (MESH:D019973), Ejaculation (MESH:D061686), EjD (MESH:D006331), coronary artery disease (MESH:D003324), peripheral neuropathies (MESH:D010523), obsessive-compulsive disorder (MESH:D009771), thyroid dysfunction (MESH:D013959), type 1 or type 2 diabetes mellitus (MESH:D003924), erectile dysfunction (MESH:D007172), BPH (MESH:D011470), sexual side effects (MESH:D064420), urinary tract infections (MESH:D014552), chronic kidney or liver failure (MESH:D007676), LUTS (MESH:D059411), urinary retention (MESH:D016055), nerve damage (MESH:D000080902), hypertension (MESH:D006973), bladder stones (MESH:D001744), Symptom (MESH:D012816), spinal cord injury (MESH:D013119), hypogonadism (MESH:D007006), neurological disorders (MESH:D009461), major depression (MESH:D003865), hyperprolactinemia (MESH:D006966), COPD chronic obstructive pulmonary disease (MESH:D029424), function (MESH:D003291), malignancies (MESH:D009369), sexual dysfunction (MESH:D012735), renal failure (MESH:D051437), decline in ejaculatory (MESH:D060825), substance dependence (MESH:D019966), Parkinson's disease (MESH:D010300), alcohol (MESH:D000437), hematuria (MESH:D006417), prostate cancer (MESH:D011471)
- **Chemicals:** creatinine (MESH:D003404), silodosin (MESH:C095285), doxazosin (MESH:D017292), TCAs (MESH:D014238), urea (MESH:D014508), -blockers (-), Tamsulosin (MESH:D000077409)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

2 references — full list in the complete paper: https://tomesphere.com/paper/PMC12913309/full.md

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Source: https://tomesphere.com/paper/PMC12913309