New meta-analyis below [1].
"Current evidence suggests that vitamin D supplementation in conjunction with standard of care (e.g. chemotherapy, radiation therapy) may confer clinical benefits such as a decrease in serum PSA levels and VDR expression but further research is required to ascertain these results. Calcitriol supplementation in doses ranging from 250-1000 mg for 3-8 weeks or a lower dose of 45 mg for 18.3 months, appear most beneficial regarding outcomes of PC progression and survival."
Note. Calcitriol is the active hormonal form of vitamin D [1,25-D]. The inactive circulating reservoir is calcidiol [25-D]. I believe that many men maintain good 25-D levels while unknowingly inhibiting conversion to 1,25-D.
-Patrick
[1] ncbi.nlm.nih.gov/pubmed/310...
Int J Vitam Nutr Res. 2019 Apr 30:1-13. doi: 10.1024/0300-9831/a000494. [Epub ahead of print]
Effect of Vitamin D Supplementation in Prostate Cancer: A Systematic Review of Randomized Control Trials.
Petrou S1, Mamais I2, Lavranos G3, Tzanetakou IP1, Chrysostomou S1.
Author information
1
1 Department of Life Sciences, European University Cyprus, Nicosia-Cyprus.
2
2 Department of Hygiene, Epidemiology and Medical Statistics, Medical School, National and Kapodistrian University of Athens, Greece.
3
3 Department of Health Sciences, European University Cyprus, Nicosia-Cyprus.
Abstract
Vitamin D is important in many cellular functions including cell cycling and proliferation, differentiation, and apoptosis. Via the induction of cell cycle arrest and/or apoptosis, vitamin D inhibits normal prostatic epithelial cells growth. Review the evidence of the effect of vitamin D supplementation on prostate cancer (PC) biomarkers and patient survival and assess optimal dosage, formulation and duration. Pubmed, Medline and Ebsco Host databases were systematically searched for relevant literature. 8 Randomized Controlled Trials were included in this review. All studies, besides one, were of high methodological quality. 4 studies used calcitriol (0,5-45 pg/weekly), 2 studies have used vitamin D3 (150-1000 μg/daily) and 2 other studies have used 1α-hydroxy Vitamin D2 (10 μg/daily or weekly). Duration of supplementation varied between 28 days up to 18.3 months. Two studies had positive effects on prostate specific antigen (PSA) (p < .05), 1 study had a significant positive effect on median survival (p < .05) and 1 study showed a significant reduction of vitamin D receptor (VDR) expression (p < .05). The remaining studies showed negative or no effect on PC characteristics, clinical outcomes and/or survival. Current evidence suggests that vitamin D supplementation in conjunction with standard of care (e.g. chemotherapy, radiation therapy) may confer clinical benefits such as a decrease in serum PSA levels and VDR expression but further research is required to ascertain these results. Calcitriol supplementation in doses ranging from 250-1000 mg for 3-8 weeks or a lower dose of 45 mg for 18.3 months, appear most beneficial regarding outcomes of PC progression and survival.
KEYWORDS:
Calcitriol; PC; PSA; VDR; Vitamin D; randomized controlled trial
PMID: 31038028 DOI: 10.1024/0300-9831/a000494