ABSTRACT
Interest in the role of dietary patterns has been consistently emerging in recent years due to much research that has documented the impact of metabolism on erectile dysfunction (ED) and/or benign prostatic hyperplasia (BPH). We conducted a non-systematic review of English articles published from 1964 to September 2021. The search terms were: ("dietary patterns" OR "diet") AND/OR ("erectile dysfunction") AND/OR ("benign prostatic hyperplasia"). In the present review, we have highlighted how the association between dietary patterns and two of the most frequent pathologies in urology, namely erectile dysfunction and benign prostatic hyperplasia, is present in the literature. The data suggested that a diet that is more adherent to the Mediterranean diet or that emphasizes the presence of vegetables, fruits, nuts, legumes, and fish or other sources of long-chain (n-3) fats, in addition to reduced content of red meat, may have a beneficial role on erectile function. At the same time, the same beneficial effects can be transferred to BPH as a result of the indirect regulatory effects on prostatic growth and smooth muscle tone, thus determining an improvement in symptoms. Certainly, in-depth studies and translational medicine are needed to confirm these encouraging data.
Subject(s)
Diet/adverse effects , Eating/physiology , Erectile Dysfunction/etiology , Feeding Behavior/physiology , Prostatic Hyperplasia/etiology , Diet, Mediterranean , Erectile Dysfunction/diet therapy , Humans , Male , Prostatic Hyperplasia/diet therapyABSTRACT
BACKGROUND: and aims: Benign Prostatic hyperplasia (BPH) is an important public health problem. Roughly half of all men will suffer from BPH related symptoms later in life. The prostate gland, a hormone dependent part of the male reproductive system, is susceptible to internal and external disruptions of regulatory systems. We attempt in this paper to collect available evidence on influence of lifestyle modifications, and naturally occurring substances, plants, micronutrients and supplements on BPH symptoms. METHODS: Systematic review was performed within the MEDLINE database and Cochrane Library Central Search using a combination of Medical Subject Headings (MeSH) and keywords. RESULTS: Moderate exercise and the type and amount of protein intake have a considerable influence on BPH symptoms. The intake of zinc and vitamin D also positively influence BPH symptoms, and so do certain supplements, such as saw palmetto, cemilton and pygeum extracts. CONCLUSIONS: Lifestyle changes, diet modification and certain nutritional supplements can favorably influence BPH symptoms.
Subject(s)
Diet , Nutritional Status , Prostatic Hyperplasia/diet therapy , Prostatic Hyperplasia/etiology , Prostatic Hyperplasia/physiopathology , Databases, Factual , Dietary Supplements , Humans , Inflammation/diet therapy , Life Style , Male , Micronutrients , Plant Extracts , Prostatic Hyperplasia/epidemiology , Serenoa , Vitamin D , ZincABSTRACT
PURPOSE: The study was designed to assess and predict patient-reported goal achievement after treatment of benign prostatic hyperplasia (BPH) patients with tamsulosin. MATERIALS AND METHODS: From November 2013 to October 2015, 272 patients initially diagnosed with BPH were prospectively enrolled in nine different centers. Before the treatment, subjective final goals were recorded by all patients. Every four weeks, the treatment outcomes were evaluated using international prostate symptom score (IPSS) and uroflowmetry, and adverse events were recorded. Patient-reported goal achievements were assessed after 12 weeks of treatment. RESULTS: Of the enrolled patients, 179 patients completed the study. The pretreatment patients' goals included the frequency improvement, nocturia improvement, residual urine sense improvement, well voiding, hesitancy improvement, weak urine stream improvement, urgency improvement, and voiding-related discomfort improvement. Of the 179 patients, 129 patients (72.1%) reported that they achieved their primary goals after three months of medical therapy. Logistic regression analysis revealed that pretreatment quality of life (OR = 8.621, 95% CI: 2.154-9.834), and improvement of quality of life (OR = 6.740, 95% CI: 1.908-11.490) were independent predictors of patient-reported goal achievement after tamsulosin monotherapy. CONCLUSION: Overall patient-reported goal achievement after medical therapy for BPH was high and the scores of pretreatment quality of life and improvement of quality of life can be important factors to predict the achievement of treatment goals.
Subject(s)
Adrenergic alpha-Antagonists/therapeutic use , Patient Reported Outcome Measures , Prostatic Hyperplasia/diet therapy , Tamsulosin/therapeutic use , Aged , Humans , Male , Middle Aged , Prospective Studies , Time FactorsABSTRACT
OBJECTIVES: To evaluate the impact of serum vitamin D level on male lower urinary tract symptoms (LUTS). PATIENTS AND METHODS: Men with LUTS who visited the outpatient clinic of the urology department at one of two hospitals between March 2014 and April 2017 were eligible for inclusion in the study. The impact of vitamin D on LUTS was evaluated using multivariate analysis to adjust for age, body mass index, prostate-specific antigen, testosterone, glycated haemoglobin, physical activity and prostate volume. To exclude the effect of seasons, we also analysed the impact during each season. RESULTS: Vitamin D level was lowest in winter. According to the International Prostate Symptom Score (IPSS) and Overactive Bladder Symptom Score (OABSS), the severity of LUTS peaked in winter. There were no seasonal differences between prostate volume, maximum urinary flow rate (Qmax ) and post-void residual urine volume (PVR). For all patients, multivariate analysis showed that lower vitamin D level was significantly associated with higher total OABSS, whereas it was not associated with prostate volume, Qmax , PVR or total IPSS. In winter, lower vitamin D level was significantly associated with higher total OABSS based on multivariate analysis, whereas it was not during other seasons. In patients with vitamin D deficiency, the total OABSS significantly decreased after vitamin D replacement. The greatest improvement in total OABSS was associated with lower pre-treatment total OABSS and higher post-treatment vitamin D level. CONCLUSIONS: Vitamin D deficiency in men with LUTS may play a role in aggravated overactive bladder (OAB) symptoms, especially in winter. Increasing vitamin D level in patients with vitamin D deficiency appears to alleviate OAB symptoms.
Subject(s)
Hydroxycholecalciferols/blood , Hydroxycholecalciferols/therapeutic use , Lower Urinary Tract Symptoms/blood , Lower Urinary Tract Symptoms/diet therapy , Urinary Bladder, Overactive/blood , Urinary Bladder, Overactive/diet therapy , Vitamin D Deficiency/pathology , Aged , Cohort Studies , Humans , Lower Urinary Tract Symptoms/etiology , Lower Urinary Tract Symptoms/pathology , Male , Middle Aged , Organ Size , Predictive Value of Tests , Prostate/drug effects , Prostate/pathology , Prostate-Specific Antigen/blood , Prostatic Hyperplasia/diet therapy , Prostatic Hyperplasia/pathology , Testosterone/blood , Urinary Bladder, Overactive/etiology , Urinary Bladder, Overactive/pathology , Vitamin D Deficiency/blood , Vitamin D Deficiency/complications , Vitamins/blood , Vitamins/therapeutic useABSTRACT
Secoisolariciresinol diglucoside (SDG), a lignan extracted from flaxseed, has been shown to suppress benign prostatic hyperplasia (BPH). However, little is known about the mechanistic basis for its anti-BPH activity. The present study showed that enterolactone (ENL), the mammalian metabolite of SDG, shared the similar binding site of G1 on a new type of membranous estrogen receptor, G-protein-coupled estrogen eceptor 1 (GPER), by docking simulations method. ENL and G1 (the specific agonist of GPER) inhibited the proliferation of human prostate stromal cell line WPMY-1 as shown by MTT assay and arrested cell cycle at the G0/G1 phase, which was displayed by propidium iodide staining following flow cytometer examination. Silencing GPER by short interfering RNA attenuated the inhibitory effect of ENL on WPMY-1 cells. The therapeutic potential of SDG in the treatment of BPH was confirmed in a testosterone propionate-induced BPH rat model. SDG significantly reduced the enlargement of the rat prostate and the number of papillary projections of prostatic alveolus and thickness of the pseudostratified epithelial and stromal cells when comparing with the model group. Mechanistic studies showed that SDG and ENL increased the expression of GPER both in vitro and in vivo. Furthermore, ENL-induced cell cycle arrest may be mediated by the activation of GPER/ERK pathway and subsequent upregulation of p53 and p21 and downregulation of cyclin D1. This work, in tandem with previous studies, will enhance our knowledge regarding the mechanism(s) of dietary phytochemicals on BPH prevention and ultimately expand the scope of adopting alternative approaches in BPH treatment.
Subject(s)
4-Butyrolactone/analogs & derivatives , Antineoplastic Agents, Phytogenic/metabolism , Butylene Glycols/metabolism , Flax/chemistry , Glucosides/metabolism , Lignans/metabolism , Models, Molecular , Prostatic Hyperplasia/metabolism , Receptors, G-Protein-Coupled/agonists , 4-Butyrolactone/chemistry , 4-Butyrolactone/metabolism , Animals , Antineoplastic Agents, Phytogenic/chemistry , Antineoplastic Agents, Phytogenic/therapeutic use , Binding Sites , Butylene Glycols/chemistry , Butylene Glycols/therapeutic use , Cell Line, Tumor , Cell Proliferation , Dietary Supplements , Gene Expression Regulation, Neoplastic , Glucosides/chemistry , Glucosides/therapeutic use , Glycosides/chemistry , Glycosides/metabolism , Glycosides/therapeutic use , Humans , Lignans/chemistry , Lignans/therapeutic use , Male , Molecular Docking Simulation , Neoplasm Proteins/agonists , Neoplasm Proteins/chemistry , Neoplasm Proteins/genetics , Neoplasm Proteins/metabolism , Prostate/metabolism , Prostate/pathology , Prostatic Hyperplasia/diet therapy , Prostatic Hyperplasia/pathology , RNA Interference , Random Allocation , Rats , Rats, Wistar , Receptors, Estrogen/chemistry , Receptors, Estrogen/genetics , Receptors, Estrogen/metabolism , Receptors, G-Protein-Coupled/chemistry , Receptors, G-Protein-Coupled/genetics , Receptors, G-Protein-Coupled/metabolism , Seeds/chemistryABSTRACT
INTRODUCTION: We studied the effect of dutasteride on bone mineral density (BMD) in aging male patients with lower urinary tract symptoms (LUTS) and prostatic enlargement. METHODS: We prospectively studied 17 patients with LUTS and prostatic enlargement. Before and 1 year after dutasteride (0.5 mg daily), we assessed International Prostate Symptom Score (IPSS), prostatic volume (PV), serum prostatic-specific antigen (PSA) and testosterone. BMD in the lumbar and femur was measured by DEXA method. RESULTS: Dutasteride significantly reduced PV (from 51 ± 24 to 34 ± 17 ml, p < 0.001) and improved IPSS (from 15.1 ± 9.8 to 11.7 ± 10.3, p < 0.05). Serum PSA was significantly decreased (from 3.2 ± 2.6 to 1.0 ± 0.8 ng/ml, p < 0.001), while serum testosterone "was not changed" significantly. BMD of the lumbar "was not changed" significantly after dutasteride. BMD of the femur was significantly improved (from 0.75 ± 0.14 to 0.82 ± 0.16 g/cm(2), p < 0.01). In nine patients whose testosterone was increased after dutasteride, BMD of the lumbar (from 1.18 ± 0.26 to 1.22 ± 0.25 g/cm(2), p < 0.05) and femur (from 0.76 ± 0.12 to 0.84 ± 0.16 g/cm(2), p < 0.05) was significantly improved. CONCLUSIONS: Dutasteride has a potential to improve BMD with elevation of serum testosterone in aging male patients with LUTS and prostatic enlargement.
Subject(s)
5-alpha Reductase Inhibitors/therapeutic use , Bone Density/drug effects , Dutasteride/therapeutic use , Lower Urinary Tract Symptoms/drug therapy , Prostatic Hyperplasia/diet therapy , Aged , Aged, 80 and over , Humans , Male , Middle Aged , Organ Size/drug effects , Pilot Projects , Prospective Studies , Prostate/drug effects , Prostate/pathology , Prostate-Specific Antigen/blood , Prostatic Hyperplasia/pathology , TestosteroneABSTRACT
The prostate is an androgen-sensitive organ that needs proper androgen/androgen receptor (AR) signals for normal development. The progression of prostate diseases, including benign prostate hyperplasia (BPH) and prostate cancer (PCa), also needs proper androgen/AR signals. Tissue recombination studies report that stromal, but not epithelial, AR plays more critical roles via the mesenchymal-epithelial interactions to influence the early process of prostate development. However, in BPH and PCa, much more attention has been focused on epithelial AR roles. However, accumulating evidence indicates that stromal AR is also irreplaceable and plays critical roles in prostate disease progression. Herein, we summarize the roles of stromal AR in the development of normal prostate, BPH, and PCa, with evidence from the recent results of in vitro cell line studies, tissue recombination experiments, and AR knockout animal models. Current evidence suggests that stromal AR may play positive roles to promote BPH and PCa progression, and targeting stromal AR selectively with AR degradation enhancer, ASC-J9, may allow development of better therapies with fewer adverse effects to battle BPH and PCa.
Subject(s)
Neoplasm Proteins/metabolism , Prostate/metabolism , Prostatic Hyperplasia/metabolism , Prostatic Neoplasms/metabolism , Receptors, Androgen/metabolism , Signal Transduction , Animals , Curcumin/analogs & derivatives , Curcumin/therapeutic use , Humans , Male , Neoplasm Proteins/genetics , Prostate/pathology , Prostatic Hyperplasia/diet therapy , Prostatic Hyperplasia/genetics , Prostatic Hyperplasia/pathology , Prostatic Neoplasms/drug therapy , Prostatic Neoplasms/genetics , Prostatic Neoplasms/pathology , Receptors, Androgen/geneticsABSTRACT
The pathogenesis of prostate cancer (CaP) involves alterations in a gene structure of the androgen receptor (AR). The single nucleotide polymorphism AR-E211 G > A localized in exon 1 of the AR gene (G1733A) was detected using direct polymerase chain reaction and restriction digestion (PCR-RFLP) method on blood and tissue samples without prior DNA isolation. We used blood samples of patients with a diagnosis of benign prostatic hyperplasia (BPH) or CaP. From monitored group of CaP patients were selected specimen in formalin-fixed paraffin-embedded tissue blocks with morphology of BPH and CaP. The main objective of our study was to develop a method based the direct PCR-RFLP analysis from blood and tissue without prior DNA isolation for faster genotyping analysis of a large number of samples. We found no statistically significant differences in allelic % of the AR-E211 G > A polymorphism between BPH and CaP patients (p ≤ 0.8462). Genotyping of the AR-E211 G > A variant in blood was not identical with tumor tissue genotyping analysis. Significant agreement between blood and tissue AR-E211 G > A polymorphism only in non-tumor tissue focus was confirmed. Although we analyzed a limited number of the tissue samples, we suppose that a presence of the minor allele A may be associated with cancer transformation-induced changes of the modified AR gene.
Subject(s)
Blood Chemical Analysis/methods , Polymorphism, Single Nucleotide/genetics , Prostatic Neoplasms/genetics , Receptors, Androgen/genetics , Adult , Aged , Aged, 80 and over , Alleles , Blood , DNA/analysis , DNA/genetics , Genotype , Humans , Male , Middle Aged , Prostatic Hyperplasia/blood , Prostatic Hyperplasia/diet therapy , Prostatic Hyperplasia/genetics , Prostatic Hyperplasia/metabolism , Prostatic Neoplasms/blood , Prostatic Neoplasms/diagnosis , Prostatic Neoplasms/metabolism , Receptors, Androgen/blood , Receptors, Androgen/metabolismABSTRACT
PURPOSE OF REVIEW: Nutrition seems to modify the pathogenesis of benign prostatic hyperplasia (BPH) effect symptomology in men suffering from lower urinary tract symptoms (LUTS). Although there are numerous pharmaceuticals and procedures for these conditions, nutrition may improve outcomes as a primary approach or in tandem with BPH medications or procedures. The purpose of this review is to highlight the benefits of nutrition and dietary supplements in men with BPH and LUTS. RECENT FINDINGS: Dietary factors have an impact on metabolic disorders that lead to diabetes and obesity - both of which inversely effect BPH and LUTS. Dietary patterns associated with increased risks include starches and red meats, whereas moderate alcohol intake and polyunsaturated fat and vegetable consumption decrease risks. Dietary supplements of zinc, saw palmetto, and beta-sitosterol in relieving BPH symptoms have had mixed results. Randomized clinical trials of nutritional practices and other lifestyle alterations such as exercise for the prevention or treatment of BPH and LUTS have yet to be performed. SUMMARY: Nutritional practices may provide for the prevention and treatment of BPH and LUTS while positively affecting other systemic parameters. Whereas there are a few clinical randomized trials for the prevention and treatment of BPH and LUTS, nutritional modifications may have a healthy lifestyle alternative with minimal to no adverse effects.
Subject(s)
Dietary Supplements , Nutrition Therapy , Prostatic Hyperplasia/diet therapy , Prostatic Hyperplasia/prevention & control , Humans , Life Style , Lower Urinary Tract Symptoms/diet therapy , Lower Urinary Tract Symptoms/prevention & control , Male , Plant Extracts/therapeutic use , Secale , Sitosterols/therapeutic useABSTRACT
UNLABELLED: Study Type--Prognosis (case control) Level of Evidence 2. What's known on the subject? and What does the study add? Geographical and ethnic differences in the distribution of BPH and the results of migrant studies indicate that not only age, androgens and genetics, but also modifiable factors may play a role in the aetiology of BPH. Oxidative stress induced by chronic inflammation could be a cause and antioxidants, including selenoproteins, may reduce the risk. The published data related to this topic are scarce and are mainly based on cross-sectional and case-control studies. In a nested case-control study, we observed a significant inverse association between serum selenium concentrations and the risk of BPH. These results need to be confirmed in larger, prospective epidemiological studies. Prostate enlargement is an increasing health problem as a result of an ageing population in many countries. Modifiable factors may also play a role. In the present study, before this antioxidant can be recommended as a preventive measure. OBJECTIVE: ⢠To determine whether geographical differences in the distribution of benign prostatic hyperplasia (BPH) and migrant studies indicate that modifiable factors play a role in the aetiology of BPH. Oxidative stress produced by chronic inflammation could represent one of the causes, and antioxidants, including selenoproteins, may reduce the risk. SUBJECTS AND METHODS: ⢠Conditional logistic regression was used to examine the associations of serum selenium and selenoprotein P concentrations and glutathione peroxidase activity with respect to the risk of BPH in a case-control study nested in the European Prospective Investigation into Cancer and Nutrition-Heidelberg cohort, including 111 cases and 214 matched controls. ⢠In addition, dietary glucosinolate intake and the serum glutathione S-transferase α concentration was investigated. RESULTS: ⢠The risk of BPH significantly decreased with an increasing serum selenium concentration; the risk estimate was 0.83 (35% CI 0.69-0.99) per 10 µg/L increase in serum selenium concentration. ⢠However, no significant association was present for serum selenoprotein P concentration or glutathione peroxidase activity. Risk estimates for BPH decreased with a higher intake of glucosinolates, although the results were not statistically significant. CONCLUSION: ⢠A low serum selenium concentration may increase the risk of BPH, although the findings reported in the present study need to be confirmed in larger, well-designed epidemiological studies.
Subject(s)
Glucosinolates/administration & dosage , Glutathione Transferase/blood , Isoenzymes/blood , Prostatic Hyperplasia/blood , Selenium/blood , Adult , Aged , Biomarkers/blood , Dietary Supplements , Follow-Up Studies , Germany/epidemiology , Humans , Incidence , Male , Middle Aged , Prostatic Hyperplasia/diet therapy , Prostatic Hyperplasia/epidemiology , Retrospective Studies , Risk FactorsABSTRACT
Introdução: No dito popular, o tomate, fonte principal de licopeno, é útil para doenças da bexiga e próstata. Naindicação médica formal o licopeno inexiste.Objetivo: Verificar na literatura científica estudos com boa qualidade metodológica sobre licopeno que nos dessemevidências para indicá-lo na saúde.Métodos: Pelo grau de evidência, procuramos estudos inicialmente na Colaboração Cochrane e, depois, na Medline,Lilacs, Pubmed, procurando evidenciar os estudos com melhor qualidade metodológica.Resultados: Encontramos três revisões sistemáticas. Duas delas foram em câncer de próstata e não encontraramevidências da efetividade do licopeno. Uma delas foi em câncer de próstata com metásteses, também inconclusiva. Um "megatrial" com quase 10.000 participantes não encontrou relação do uso de licopeno com melhora ou piora docâncer de próstata. Um ensaio clínico randomizado realizado em pacientes portadores de hiperplasia prostática benigna não encontrou diferenças estatisticamente significantes entre os grupos na redução do antígeno prostático específico (PSA). Um estudo piloto não randomizado encontrou uma diminuição significativa do PSA. Um estudo foi realizado emvoluntários saudáveis para verificar o potencial de expressão gênica para câncer de próstata com e sem licopeno e foi encontrado um resultado favorável ao licopeno em altas doses.Conclusão: Evidências fracas sugerem que apenas uma porção de tomates ou produtos de tomate ingeridosdiariamente podem apresentar um efeito protetor contra danos no DNA. Não existem evidências na literatura científica até o momento que indiquem o uso do licopeno com elemento único, seguro e efetivo para prevenção ou tratamento das doenças referentes a próstata, benigna ou maligna. Ensaios clínicos randomizados bem desenhados, contendoum número elevado de participantes, são necessários para estabelecer o papel de tomates e produtos do tomate na prevenção e terapia das doenças prostáticas.
Subject(s)
Humans , Male , Prostatic Hyperplasia/diet therapy , Prostatic Hyperplasia/prevention & control , Solanum lycopersicum , Prostatic Neoplasms/diet therapy , Prostatic Neoplasms/prevention & control , Prostate-Specific AntigenABSTRACT
The usefulness of diet containing Telfairia occidentalis seeds, in managing benign prostatic hyperplasia (BPH) in rats was studied. Twenty male Wistar rats were divided into four equal groups. BPH was induced by sub-cutaneous injection of dihydrotestosterone (DHT) and estradiol valerate (ratio, 10:1) every other day for 28 days. Rats in the test group were placed on the test diet for 7 days following disease induction. One control group (DC) was fed on a normal diet for 7 days following disease induction. Two other control groups, HC and HDC, were given sub-cutaneous olive oil (vehicle) for the same duration, and placed on the test diet and normal diet, respectively. Markers of BPH, and hormone profile were determined using standard methods. The results show that relative prostate weight and protein content of the prostates were lower [albeit not significantly (p>0.05)] in the test group, relative to the DC group. Serum prostatic acid phosphatase concentrations (U/L) decreased significantly (p<0.05) from 2.9 ± 0.2 in the DC group to 2.1 ± 0.7 in the test group. Histological findings corroborate these data. The testosterone: estradiol ratio (× 10(3)) was increased from 4.0 ± 0.2 in the DC group to 4.6 ± 0.2 in the test group. The test diet reduced the mass and secretory activity of the enlarged prostate and may act by increasing the testosterone: estradiol ratio.
Subject(s)
Cucurbita/chemistry , Plant Extracts/therapeutic use , Prostatic Hyperplasia/diet therapy , Seeds/chemistry , Seeds/metabolism , Testosterone/blood , Acid Phosphatase , Animals , Dihydrotestosterone/adverse effects , Dihydrotestosterone/blood , Disease Management , Estradiol/adverse effects , Estradiol/analogs & derivatives , Estradiol/blood , Humans , Immunoenzyme Techniques , Male , Nigeria , Organ Size , Prostate/metabolism , Prostate/pathology , Prostatic Hyperplasia/chemically induced , Prostatic Hyperplasia/pathology , Protein Tyrosine Phosphatases , Rats , Rats, WistarABSTRACT
La hiperplasia prostática benigna es muy común en la población general, tanto desde el punto devista histológico como del clínico. El papel en ella de diversos factores se ha definido por medio deestudios epidemiológicos. Entre ellos está el consumo regular de algunos alimentos que podríaactuar como un factor protector o de riesgo para el posterior desarrollo de la enfermedad. Entre loscompuestos demostrados como benéficos para la salud prostática están los licopenos, losfitoestrógenos y las verduras. Por otro lado, entre los que podrían aumentar el riesgo de sufrir lahiperplasia prostática benigna se incluyen las dietas hipercalóricas y con alto contenido graso. Eneste artículo se revisan los principales estudios al respecto, con miras a que el médico tenga un mejorconocimiento de los patrones dietéticos que pueden incidir en la frecuencia y síntomas de estaenfermedad.
Relationship between diet and benign prostatic hyperplasiaBenign prostatic hyperplasia is very common in the general population, both from the histologicaland the clinical points of view. The role of different factors in its development has been definedby means of epidemiological studies. One such factor is the composition of the diet, as theregular consumption of certain foods may either protect against benign prostatic hyperplasia orincrease the risk of its development. Among foods which may play a protective role are lycopene,phytoestrogens and vegetables. On the other hand, the risk of developing the disease may beincreased by a diet rich in fat and calories. In this article the main clinical trials concerning thisrelationship are reviewed, as a way of informing physicians on the dietetic patterns that mayinfluence the frequency or the symptoms of this disease.
Subject(s)
Humans , Diet , Prostatic Hyperplasia/diet therapy , Diet TherapyABSTRACT
BACKGROUND: Little is known about dietary correlates of lower urinary tract symptoms (LUTS). OBJECTIVE: To examine associations between dietary intakes of total energy, carbohydrates, protein, fats, cholesterol, and sodium and LUTS in men. DESIGN, SETTING, AND PARTICIPANTS: Cross-sectional study of 1545 men aged 30-79 yr in the Boston Area Community Health survey (2002-2005), a random population-based sample. Dietary data were assessed by validated self-administered food frequency questionnaire. LUTS and covariate data were collected during in-person interviews. Primary analyses used multivariate logistic regression. MEASUREMENTS: Outcomes were moderate to severe LUTS, storage symptoms, and voiding symptoms as measured by the American Urological Association Symptom Index. RESULTS AND LIMITATIONS: Greater total energy intake was associated with higher LUTS symptom score (p(trend)<0.01) and increased likelihood of storage symptoms. No associations were observed with total, saturated, or monounsaturated fat intake or carbohydrates. Men who consumed more protein were less likely to report LUTS, particularly voiding symptoms (quintile 5 vs quintile 1 OR=0.35; 95% CI, 0.17-0.74; p=0.006). Sodium intake had positive linear associations with LUTS (p(trend)=0.01) and storage symptom score (p(trend)=0.004); this finding should be confirmed by studies using biomarkers of sodium exposure. Storage symptoms increased slightly with greater polyunsaturated fat intake (p(trend)=0.006). Data on specific polyunsaturated fats were unavailable. CONCLUSIONS: This community-based study of men found that total energy and sodium intake were positively associated with LUTS, whereas greater protein intake was inversely associated with LUTS.
Subject(s)
Diet , Energy Intake , Urination Disorders/epidemiology , Urination Disorders/prevention & control , Adult , Age Distribution , Aged , Alcohol Drinking/epidemiology , Body Mass Index , Cholesterol, Dietary/administration & dosage , Confidence Intervals , Cross-Sectional Studies , Dietary Carbohydrates/administration & dosage , Dietary Fats/administration & dosage , Dietary Proteins/administration & dosage , Follow-Up Studies , Humans , Incidence , Logistic Models , Male , Micronutrients/administration & dosage , Middle Aged , Multivariate Analysis , Obesity/epidemiology , Odds Ratio , Probability , Prostatic Hyperplasia/diet therapy , Prostatic Hyperplasia/epidemiology , Prostatic Hyperplasia/prevention & control , Risk Assessment , Severity of Illness Index , Smoking/epidemiology , Sodium, Dietary/administration & dosage , Surveys and Questionnaires , Urination Disorders/diet therapyABSTRACT
The consumption of tomatoes and tomato products has been associated with a reduced risk of prostate cancer. We observed a decrease of 10.77% in prostate-specific antigen (PSA) levels in patients with benign prostate hyperplasia who were submitted to daily ingestion of tomato paste. This was an experimental rather than a controlled study with a sample of 43 men ranging in age from 45 to 75 years, all with histological diagnoses of benign prostate hyperplasia and plasma PSA levels of 4-10 ng/mL. All patients received 50 g of tomato paste once a day for 10 consecutive weeks and PSA levels were analyzed before, during and after the consumption of tomato paste. ANOVA for repeated measures was used to compare PSA levels before, during and after the consumption of tomato paste. The mean +/- SD PSA level was 6.51 +/- 1.48 ng/mL at baseline and 5.81 +/- 1.58 ng/mL (P = 0.005) after 10 weeks. Acceptance was good in 88.3, regular in 9.3, and poor in 2.3% of the patients. Dietary ingestion of 50 g of tomato paste per day for 10 weeks significantly reduced mean plasma PSA levels in patients with benign prostate hyperplasia, probably as a result of the high amount of lycopene in tomato paste. This was not a prostate cancer prevention study, but showed some action of tomato paste in prostate biology. The development of prostate cancer is typically accompanied by an increase in plasma PSA levels, thus any intervention that affects plasma PSA levels can suggest an impact in the progression of disease.
Subject(s)
Anticarcinogenic Agents/administration & dosage , Carotenoids/administration & dosage , Prostate-Specific Antigen/blood , Prostatic Hyperplasia/diet therapy , Solanum lycopersicum/chemistry , Aged , Analysis of Variance , Humans , Lycopene , Male , Middle Aged , Nutritive Value , Prostate-Specific Antigen/drug effects , Prostatic Hyperplasia/bloodABSTRACT
The consumption of tomatoes and tomato products has been associated with a reduced risk of prostate cancer. We observed a decrease of 10.77 percent in prostate-specific antigen (PSA) levels in patients with benign prostate hyperplasia who were submitted to daily ingestion of tomato paste. This was an experimental rather than a controlled study with a sample of 43 men ranging in age from 45 to 75 years, all with histological diagnoses of benign prostate hyperplasia and plasma PSA levels of 4-10 ng/mL. All patients received 50 g of tomato paste once a day for 10 consecutive weeks and PSA levels were analyzed before, during and after the consumption of tomato paste. ANOVA for repeated measures was used to compare PSA levels before, during and after the consumption of tomato paste. The mean ± SD PSA level was 6.51 ± 1.48 ng/mL at baseline and 5.81 ± 1.58 ng/mL (P = 0.005) after 10 weeks. Acceptance was good in 88.3, regular in 9.3, and poor in 2.3 percent of the patients. Dietary ingestion of 50 g of tomato paste per day for 10 weeks significantly reduced mean plasma PSA levels in patients with benign prostate hyperplasia, probably as a result of the high amount of lycopene in tomato paste. This was not a prostate cancer prevention study, but showed some action of tomato paste in prostate biology. The development of prostate cancer is typically accompanied by an increase in plasma PSA levels, thus any intervention that affects plasma PSA levels can suggest an impact in the progression of disease.
Subject(s)
Aged , Humans , Male , Middle Aged , Anticarcinogenic Agents/administration & dosage , Carotenoids/administration & dosage , Solanum lycopersicum/chemistry , Prostate-Specific Antigen/blood , Prostatic Hyperplasia/diet therapy , Analysis of Variance , Nutritive Value , Prostate-Specific Antigen/drug effects , Prostatic Hyperplasia/bloodABSTRACT
OBJECTIVES: Dietary factors may influence the prostate and have an impact on prostatic growth and disease. A small number of studies have suggested that flaxseed-supplemented, fat-restricted diets may thwart prostate cancer growth in both animals and humans. Unknown, however, is the potential effect of such a diet on benign prostatic epithelium. METHODS: We undertook a pilot study to explore whether a flaxseed-supplemented, fat-restricted diet affects the proliferation rates in benign epithelium. We also explored the effects on circulating levels of prostate-specific antigen (PSA), total testosterone, and cholesterol. Fifteen men who were scheduled to undergo repeat prostate biopsy were instructed to follow a low-fat (less than 20% kcal), flaxseed-supplemented (30 g/day) diet and were provided with a supply of flaxseed to last throughout the 6-month intervention period. The PSA, total testosterone, and cholesterol levels were determined at baseline and at 6 months of follow-up. Reports from the original and repeat biopsies were compared, and proliferation (MIB-1) rates were quantified in the benign prostatic epithelium. RESULTS: Statistically significant decreases in PSA (8.47 +/- 3.82 to 5.72 +/- 3.16 ng/mL; P = 0.0002) and cholesterol (241.1 +/- 30.8 to 213.3 +/- 51.2 mg/dL; P = 0.012) were observed. No statistically significant change was seen in total testosterone (434.5 +/- 143.6 to 428.3 +/- 92.5 ng/dL). Although 6-month repeat biopsies were not performed in 2 cases because of PSA normalization, of the 13 men who underwent repeat biopsy, the proliferation rates in the benign epithelium decreased significantly from 0.022 +/- 0.027 at baseline to 0.007 +/- 0.014 at 6 months of follow-up (P = 0.0168). CONCLUSIONS: These pilot data suggest that a flaxseed-supplemented, fat-restricted diet may affect the biology of the prostate and associated biomarkers. A randomized controlled trial is needed to determine whether flaxseed supplementation, a low-fat diet, or a combination of the two regimens may be of use in controlling overall prostatic growth.