Serum vitamin D level may be a novel potential risk factor for premature ejaculation: a comparative study
Alaa Mohamed Abd El Aal1, Sameh Fayek GamalEl Din1, Laila Ahmed Rashed2
1Andrology & STDs Department, Kasr Alainy Faculty of Medicine, Cairo University, Cairo, Egypt.
Insights
Low vitamin D levels are linked to lifelong premature ejaculation (LPE). This study found significantly lower 25(OH)D in LPE patients, correlating with ejaculation latency and diagnostic tool scores.
Area of Science:
- Urology
- Endocrinology
- Nutritional Science
Background:
- Premature ejaculation (PE) is a common male sexual dysfunction.
- The role of vitamin D in sexual health, particularly PE, requires further investigation.
Purpose of the Study:
- To compare serum 25-hydroxyvitamin D [25(OH)D] levels between men with lifelong premature ejaculation (LPE) and healthy controls.
- To investigate the correlation between vitamin D levels and parameters of ejaculatory function.
Main Methods:
- A case-control study involving 40 men with LPE and 40 healthy controls.
- Exclusion criteria included hormonal disorders, obesity, chronic diseases, and relevant medications.
- Premature ejaculation diagnostic tool (PEDT) and intra-vaginal ejaculation latency time (IELT) were used for assessment. Serum 25(OH)D was measured via venous blood analysis.
Main Results:
- 20% of participants exhibited vitamin D insufficiency/deficiency, all within the LPE group.
- Serum 25(OH)D levels were significantly lower in LPE patients (35.75 ng/ml) compared to controls (58.92 ng/ml) (p < 0.001).
- 25(OH)D showed significant negative correlations with IELT (r²=0.349) and PEDT scores (r²=0.425). A cut-off of 50.65 ng/ml for 25(OH)D predicted LPE with 85% sensitivity and specificity.
Conclusions:
- Vitamin D deficiency is significantly associated with lifelong premature ejaculation.
- Lower vitamin D levels correlate with reduced ejaculation latency and higher PE diagnostic scores.
- Vitamin D status is a potential modifiable factor in managing LPE.
Purpose:
To compare serum level of vitamin D [25(OH)D] in patients with life-long premature ejaculation (LPE) versus healthy controls.
Methods:
Healthy married potent males were recruited from February 2017 to January 2018. Group A included 40 patients suffering from LPE who were compared versus 40 healthy controls (Group B). Participants suffering from hormonal disorders, obesity, neurological, psychological, or chronic diseases or taking medications that may affect ejaculatory function, serum level of vitamin D, or the accuracy of intra-vaginal ejaculation latency time (IELT) were excluded. LPE was self-reported by the patients with subsequent feelings of frustration and measured by premature ejaculation diagnostic tool (PEDT) and IELT using stopwatch handled by their partners. 25(OH)D was measured by obtaining 2 ml of venous blood. Statistical analysis was performed using Student t, Mann-Whitney, Chi square tests, logistic regression analysis, and Spearman correlation.
Results:
Sixteen (20%) participants had vitamin D insufficiency/deficiency. All of them were in PE group. 25(OH)D correlated significantly with IELT (r2 = 0.349; p < 0.001) and PEDT (r2 = 0.425; p < 0.001). There was no statistically significant difference in age (p = 0.341), BMI (p = 1) or IIEF-5 (p = 0.408) in both groups. 25(OH)D was significantly lower in patients than controls (35.75 vs. 58.92 ng/ml, p < 0.001). ROC analysis revealed that the best cut-off value of 25(OH)D to detect patients suffering from LPE was 50.65 ng/ml with a sensitivity and specificity of 85% for both. 25(OH)D remained a significant risk factor for LPE in the logistic regression analysis (p < 0.001).
Conclusions:
The current study showed that vitamin D has significant association with LPE and correlates significantly with IELT and PEDT.
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