TY - JOUR
T1 - Efficacy and Safety of Phosphodiesterase-5 Inhibitors for Erectile Dysfunction in Schizophrenia
T2 - A Systematic Review and Meta-Analysis
AU - Saito, Akiyoshi
AU - Sakuma, Kenji
AU - Iwata, Nakao
AU - Kishi, Taro
N1 - Publisher Copyright:
© 2025 Saito et al.
PY - 2025
Y1 - 2025
N2 - Background: The benefits of phosphodiesterase-5 inhibitors in the treatment of sexual dysfunction and psychopathology of schizophrenia remain unclear. This systematic review and meta-analysis aimed to address the above clinical question. Methods: Our primary outcome includes erectile dysfunction (ED) assessed using standardized questionnaires. Other efficacy outcomes involve overall sexual dysfunction, overall schizophrenia symptoms, positive symptoms, and negative symptoms. Further, we included all-cause discontinuation, discontinuation due to adverse events, discontinuation due to consent withdrawal, headache, loss of appetite, and somnolence. A meta-analysis was conducted for outcomes if at least two studies in each drug group had sufficient data to conduct a meta-analysis for a specific outcome. Results: Our systematic review included five double-blind, randomized, placebo-controlled trials (n=155, mean age=37.18 years, male proportion=91.61%), consisting of one lodenafil, three sildenafil, and one tadalafil study. Among the three studies on sildenafil, only one reported outcomes on sexual dysfunction; however, it demonstrated that sildenafil improved ED in males with schizophrenia. Another study reported that sildenafil also outperformed placebo in terms of schizophrenia symptom improvement, especially negative symptoms. However, our meta-analysis revealed no significant differences in outcomes associated with psychopathology, all-cause discontinuation, discontinuation due to adverse events, discontinuation due to consent withdrawal, headache, loss of appetite, and somnolence between sildenafil and placebo. Tadalafil outperformed placebo in terms of ED improvement although this finding was derived from one study. Conclusion: Sildenafil and tadalafil may be treatment options for ED, although our meta-analysis of safety outcomes did not include tadalafil. Our meta-analysis revealed that sildenafil was well accepted and well tolerated, despite involving only two studies.
AB - Background: The benefits of phosphodiesterase-5 inhibitors in the treatment of sexual dysfunction and psychopathology of schizophrenia remain unclear. This systematic review and meta-analysis aimed to address the above clinical question. Methods: Our primary outcome includes erectile dysfunction (ED) assessed using standardized questionnaires. Other efficacy outcomes involve overall sexual dysfunction, overall schizophrenia symptoms, positive symptoms, and negative symptoms. Further, we included all-cause discontinuation, discontinuation due to adverse events, discontinuation due to consent withdrawal, headache, loss of appetite, and somnolence. A meta-analysis was conducted for outcomes if at least two studies in each drug group had sufficient data to conduct a meta-analysis for a specific outcome. Results: Our systematic review included five double-blind, randomized, placebo-controlled trials (n=155, mean age=37.18 years, male proportion=91.61%), consisting of one lodenafil, three sildenafil, and one tadalafil study. Among the three studies on sildenafil, only one reported outcomes on sexual dysfunction; however, it demonstrated that sildenafil improved ED in males with schizophrenia. Another study reported that sildenafil also outperformed placebo in terms of schizophrenia symptom improvement, especially negative symptoms. However, our meta-analysis revealed no significant differences in outcomes associated with psychopathology, all-cause discontinuation, discontinuation due to adverse events, discontinuation due to consent withdrawal, headache, loss of appetite, and somnolence between sildenafil and placebo. Tadalafil outperformed placebo in terms of ED improvement although this finding was derived from one study. Conclusion: Sildenafil and tadalafil may be treatment options for ED, although our meta-analysis of safety outcomes did not include tadalafil. Our meta-analysis revealed that sildenafil was well accepted and well tolerated, despite involving only two studies.
KW - lodenafil
KW - phosphodiesterase-5 inhibitors
KW - schizophrenia
KW - sildenafil
KW - systematic review and meta-analysis
KW - tadalafil
UR - https://www.scopus.com/pages/publications/105015088201
UR - https://www.scopus.com/pages/publications/105015088201#tab=citedBy
U2 - 10.2147/NDT.S548538
DO - 10.2147/NDT.S548538
M3 - Review article
AN - SCOPUS:105015088201
SN - 1176-6328
VL - 21
SP - 1935
EP - 1943
JO - Neuropsychiatric Disease and Treatment
JF - Neuropsychiatric Disease and Treatment
ER -