Effects of selenium status, dietary glucosinolate intake and serum glutathione S‐transferase α activity on the risk of benign prostatic hyperplasia
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 m...
Saved in:
Published in | BJU international Vol. 110; no. 11c; pp. E879 - E885 |
---|---|
Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Oxford, UK
Blackwell Publishing Ltd
01.12.2012
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | 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. |
---|---|
AbstractList | 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.UNLABELLEDStudy 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.• 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.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.• 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.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.• 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.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.• 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.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. 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. • 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. • 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. • 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. • 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. 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. |
Author | Linseisen, Jakob Teucher, Birgit Rohrmann, Sabine Steinbrecher, Astrid Kaaks, Rudolf Eichholzer, Monika |
Author_xml | – sequence: 1 givenname: Monika surname: Eichholzer fullname: Eichholzer, Monika – sequence: 2 givenname: Astrid surname: Steinbrecher fullname: Steinbrecher, Astrid – sequence: 3 givenname: Rudolf surname: Kaaks fullname: Kaaks, Rudolf – sequence: 4 givenname: Birgit surname: Teucher fullname: Teucher, Birgit – sequence: 5 givenname: Jakob surname: Linseisen fullname: Linseisen, Jakob – sequence: 6 givenname: Sabine surname: Rohrmann fullname: Rohrmann, Sabine |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/22882569$$D View this record in MEDLINE/PubMed |
BookMark | eNqVUUtuFDEQtVAQ-cAVkJcsmMG_bndvkCAKP0ViQZDYWR5POeOJxz3YbsjsOAIr7sFFOAQnoTq_BSuwZLlUfq9eVb1DspeGBIRQzuYcz7P1nKtWzRRnn-aCcYFZ2cn55T1ycPexdxuzvt0nh6WsGcNE2zwg-0J0nWja_oD8OPEeXC108LRAhBTGDS3V1rE8pcsA1eYdPY-jG0pIQ7QVaEjVXgC1aYmMjHD8RsIqYI_0w-9v32u2qXjItgD99ZNaV8OXUHd0SLSugOZQLia5BYqdJ7rNw6QXHF3ttpC30ZZgH5L73sYCj27eI3L26uTs-M3s9P3rt8cvTmdOaiZnVqqu0Vo4nKG3ve-U17aTrNeNW_Cud04rwXveNqA8433LOt8KsdBceQtMHpEn12Wxic8jlGo2oTiI0SYYxmK40BKv4hqhj2-g42IDS7PNYYO7MberREB3DXA4UMng7yCcmck1szaTIWYyx0yumSvXzCVSn_9FdWFayZBwlSH-R4GvIcLun4XNy3cfr0L5Bwpotbw |
CitedBy_id | crossref_primary_10_1186_s12889_024_21098_0 crossref_primary_10_1007_s11934_013_0372_3 crossref_primary_10_1159_000366210 crossref_primary_10_3390_molecules25163682 crossref_primary_10_2174_1381612825666190701144709 crossref_primary_10_1186_s13046_016_0418_8 crossref_primary_10_1038_s41698_018_0058_x crossref_primary_10_1016_j_juro_2015_11_068 |
Cites_doi | 10.1016/j.urology.2004.04.012 10.1158/1055-9965.EPI-09-0660 10.1093/jn/126.1.138 10.1038/sj.ejcn.1600565 10.1159/000012787 10.1158/1055-9965.EPI-10-0364 10.1002/ijc.24555 10.1385/BTER:73:2:113 10.1039/a806307i 10.1093/ije/26.suppl_1.S59 10.1016/j.urology.2005.07.030 10.1016/j.exger.2004.12.008 10.1007/s00394-008-2005-z 10.1210/jc.84.10.3613 10.1002/mnfr.200800103 10.1093/acprof:oso/9780195122978.001.0001 10.1007/s11884-010-0067-2 10.1016/j.febslet.2006.06.006 10.1007/s00394-008-2009-8 10.1016/j.eururo.2008.11.011 10.1159/000209266 10.1007/s00394-009-0039-5 10.1016/j.clinbiochem.2005.11.018 10.1007/s10549-009-0589-5 10.1111/j.1464-410X.2007.07345.x 10.1016/S0140-6736(00)02490-9 10.1093/ije/26.suppl_1.S71 10.1016/S0009-8981(03)00048-2 10.1016/j.juro.2007.03.103 10.1016/j.jtemb.2007.11.003 10.1159/000012788 10.3945/ajcn.2010.29642 10.1097/MOU.0b013e32834100c9 10.1093/aje/kwm389 10.1080/02841860802403721 10.1016/S0022-5347(05)67909-8 |
ContentType | Journal Article |
Copyright | 2012 BJU INTERNATIONAL 2012 BJU INTERNATIONAL. |
Copyright_xml | – notice: 2012 BJU INTERNATIONAL – notice: 2012 BJU INTERNATIONAL. |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 7X8 |
DOI | 10.1111/j.1464-410X.2012.11383.x |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed MEDLINE - Academic |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) MEDLINE - Academic |
DatabaseTitleList | MEDLINE - Academic MEDLINE |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 1464-410X |
EndPage | E885 |
ExternalDocumentID | 22882569 10_1111_j_1464_410X_2012_11383_x BJU11383 |
Genre | article Journal Article Comparative Study |
GeographicLocations | Germany |
GeographicLocations_xml | – name: Germany |
GroupedDBID | --- .3N .55 .GA .Y3 05W 0R~ 10A 1OC 23N 24P 2WC 31~ 33P 36B 3O- 3SF 4.4 50Y 50Z 51W 51X 52M 52N 52O 52P 52R 52S 52T 52U 52V 52W 52X 53G 5GY 5HH 5LA 5RE 5VS 66C 6P2 702 7PT 8-0 8-1 8-3 8-4 8-5 8UM 930 A01 A03 AAESR AAEVG AAHHS AAHQN AAIPD AAMNL AANLZ AAONW AASGY AAXRX AAYCA AAZKR ABCQN ABCUV ABDBF ABEML ABJNI ABLJU ABOCM ABPVW ABQWH ABXGK ACAHQ ACCFJ ACCZN ACFBH ACGFS ACGOF ACMXC ACPOU ACPRK ACSCC ACUHS ACXBN ACXQS ADBBV ADBTR ADEOM ADIZJ ADKYN ADMGS ADOZA ADXAS ADZMN ADZOD AEEZP AEIGN AEIMD AENEX AEQDE AEUQT AEUYR AFBPY AFEBI AFFNX AFFPM AFGKR AFPWT AFWVQ AFZJQ AHBTC AHMBA AIACR AITYG AIURR AIWBW AJBDE ALAGY ALMA_UNASSIGNED_HOLDINGS ALUQN ALVPJ AMBMR AMYDB ATUGU AZBYB AZVAB BAFTC BAWUL BFHJK BHBCM BMXJE BROTX BRXPI BY8 C45 CAG COF CS3 D-6 D-7 D-E D-F DCZOG DIK DPXWK DR2 DRFUL DRMAN DRSTM DU5 E3Z EAD EAP EBC EBD EBS EJD EMB EMK EMOBN ESX EX3 F00 F01 F04 F5P FUBAC G-S G.N GODZA H.X HF~ HGLYW HZI HZ~ IHE IX1 J0M J5H K48 KBYEO LATKE LC2 LC3 LEEKS LH4 LITHE LOXES LP6 LP7 LUTES LW6 LYRES MEWTI MK4 MRFUL MRMAN MRSTM MSFUL MSMAN MSSTM MXFUL MXMAN MXSTM N04 N05 N9A NF~ O66 O9- OIG OK1 OVD P2P P2W P2X P2Z P4B P4D PQQKQ Q.N Q11 QB0 R.K RJQFR ROL RX1 SUPJJ SV3 TEORI TUS UB1 V9Y W8V W99 WBKPD WHWMO WIH WIJ WIK WOHZO WOW WQJ WRC WVDHM WXI WXSBR X7M XG1 YFH ZGI ZXP ~IA ~WT AAYXX AEYWJ AGHNM AGYGG CITATION AAMMB AEFGJ AGXDD AIDQK AIDYY CGR CUY CVF ECM EIF NPM 7X8 |
ID | FETCH-LOGICAL-c3703-a3485772cfec9a9f84f7a830975cb189cc74219165e4f019608f622b714fae03 |
IEDL.DBID | DR2 |
ISSN | 1464-4096 1464-410X |
IngestDate | Fri Jul 11 06:14:09 EDT 2025 Mon Jul 21 06:06:47 EDT 2025 Tue Jul 01 03:49:58 EDT 2025 Thu Apr 24 23:03:19 EDT 2025 Wed Jan 22 16:26:06 EST 2025 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 11c |
Language | English |
License | 2012 BJU INTERNATIONAL. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c3703-a3485772cfec9a9f84f7a830975cb189cc74219165e4f019608f622b714fae03 |
Notes | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
PMID | 22882569 |
PQID | 1273127417 |
PQPubID | 23479 |
PageCount | 7 |
ParticipantIDs | proquest_miscellaneous_1273127417 pubmed_primary_22882569 crossref_primary_10_1111_j_1464_410X_2012_11383_x crossref_citationtrail_10_1111_j_1464_410X_2012_11383_x wiley_primary_10_1111_j_1464_410X_2012_11383_x_BJU11383 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | December 2012 2012-12-00 2012-Dec 20121201 |
PublicationDateYYYYMMDD | 2012-12-01 |
PublicationDate_xml | – month: 12 year: 2012 text: December 2012 |
PublicationDecade | 2010 |
PublicationPlace | Oxford, UK |
PublicationPlace_xml | – name: Oxford, UK – name: England |
PublicationTitle | BJU international |
PublicationTitleAlternate | BJU Int |
PublicationYear | 2012 |
Publisher | Blackwell Publishing Ltd |
Publisher_xml | – name: Blackwell Publishing Ltd |
References | 2004; 64 2010; 19 2000; 356 1997; 26 2000; 9 2006; 39 2005; 40 2010; 121 1998 2000; 73 1999; 43 1999; 84 2008; 52 2008; 167 2008; 101 1996; 126 2009; 48 2003; 330 2009; 55 2007; 178 1967; 70 2009; 54 2006; 67 2000 1999; 14 2008; 47 1987 2006; 580 2005; 52 2000; 163 2011; 21 2008; 22 1998; 52 2010; 92 2010; 5 2009; 125 e_1_2_7_5_2 e_1_2_7_4_2 e_1_2_7_3_2 e_1_2_7_2_2 e_1_2_7_9_2 e_1_2_7_8_2 e_1_2_7_7_2 e_1_2_7_6_2 e_1_2_7_19_2 Standing Committe on the Scientific Evaluation of Dietary Reference Intakes, Food and Nutrition Board, Institute of Medicine. (e_1_2_7_41_2) 2000 e_1_2_7_18_2 e_1_2_7_17_2 e_1_2_7_16_2 e_1_2_7_14_2 e_1_2_7_40_2 e_1_2_7_13_2 e_1_2_7_12_2 Dinkova‐Kostova AT (e_1_2_7_15_2) 2008; 52 e_1_2_7_42_2 e_1_2_7_11_2 e_1_2_7_43_2 e_1_2_7_10_2 e_1_2_7_27_2 e_1_2_7_28_2 Yang G (e_1_2_7_39_2) 1987 Paglia DE (e_1_2_7_29_2) 1967; 70 Lampe JW (e_1_2_7_21_2) 2000; 9 e_1_2_7_25_2 e_1_2_7_24_2 e_1_2_7_30_2 e_1_2_7_23_2 e_1_2_7_31_2 e_1_2_7_22_2 e_1_2_7_32_2 e_1_2_7_33_2 e_1_2_7_20_2 e_1_2_7_34_2 e_1_2_7_35_2 e_1_2_7_36_2 e_1_2_7_37_2 e_1_2_7_38_2 Zachara BA (e_1_2_7_26_2) 2005; 52 |
References_xml | – volume: 580 start-page: 3845 year: 2006 end-page: 52 article-title: Acute oxidative stress is associated with cell proliferation in the mouse liver publication-title: FEBS Lett – volume: 9 start-page: 787 year: 2000 end-page: 93 article-title: Modulation of human glutathione S‐transferases by botanically defined vegetable diets publication-title: Cancer Epidemiol Biomarkers Prev – volume: 47 start-page: 29 issue: 2 year: 2008 end-page: 50 article-title: Selenium and cancer: biomarkers of selenium status and molecular action of selenium supplements publication-title: Eur J Nutr – volume: 14 start-page: 109 year: 1999 end-page: 12 article-title: Determination of total selenium in serum, whole blood and erythrocytes by ICP‐MS publication-title: J Anal Atomic Spectrom – volume: 64 start-page: 504 year: 2004 end-page: 9 article-title: Association between serum concentrations of micronutrients and lower urinary tract symptoms in older men in the Third National Health and Nutrition Examination Survey publication-title: Urology – volume: 167 start-page: 925 year: 2008 end-page: 34 article-title: Dietary patterns, supplement use, and the risk of symptomatic benign prostatic hyperplasia: results from the prostate cancer prevention trial publication-title: Am J Epidemiol – volume: 52 start-page: 1261 year: 2008 end-page: 72 article-title: Selenium and the prevention of prostate and colorectal cancer publication-title: Mol Nutr Food Res – volume: 101 start-page: 853 year: 2008 end-page: 60 article-title: Dietary patterns and surgically treated benign prostatic hyperplasia: a case control study in Western Australia publication-title: BJU Int – volume: 52 start-page: S128 issue: 1 year: 2008 end-page: 38 article-title: Direct and indirect antioxidant properties of inducers of cytoprotective proteins publication-title: Mol Nutr Food Res – year: 2000 – volume: 330 start-page: 57 year: 2003 end-page: 83 article-title: The role of nutrition in preventing prostate cancer: a review of the proposed mechanism of action of various dietary substances publication-title: Clin Chim Acta – volume: 19 start-page: 2958 year: 2010 end-page: 68 article-title: Effects of selenium status and polymorphisms in selenoprotein genes on prostate cancer risk in a prospective study of European men publication-title: Cancer Epidemiol Biomarkers Prev – volume: 22 start-page: 24 year: 2008 end-page: 32 article-title: New assay for the measurement of selenoprotein P as a sepsis biomarker from serum publication-title: J Trace Elem Med Biol – volume: 70 start-page: 158 year: 1967 end-page: 69 article-title: Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase publication-title: J Lab Clin Med – volume: 39 start-page: 176 year: 2006 end-page: 9 article-title: Oxidative stress and antioxidant status in non‐metastatic prostate cancer and benign prostatic hyperplasia publication-title: Clin Biochem – volume: 126 start-page: 138 year: 1996 end-page: 45 article-title: Selenoprotein P concentration in plasma is an index of selenium status in selenium‐deficient and selenium‐supplemented Chinese subjects publication-title: J Nutr – volume: 356 start-page: 233 year: 2000 end-page: 41 article-title: The importance of selenium to human health publication-title: Lancet – year: 1998 – start-page: 589 year: 1987 end-page: 607 – volume: 52 start-page: 248 year: 2005 end-page: 54 article-title: Blood and tissue selenium concentrations and glutathione peroxidase activities in patients with prostate cancer and benign prostate hyperplasia publication-title: Neoplasma – volume: 125 start-page: 2179 year: 2009 end-page: 86 article-title: Dietary glucosinolate intake and risk of prostate cancer in the EPIC‐Heidelberg cohort study publication-title: Int J Cancer – volume: 48 start-page: 483 year: 2009 end-page: 91 article-title: Modulation of detoxification enzymes by watercress: in vitro and in vivo investigations in human peripheral blood cells publication-title: Eur J Nutr – volume: 19 start-page: 135 year: 2010 end-page: 43 article-title: Dietary glucosinolate intake, polymorphisms in selected biotransformation enzymes, and risk of prostate cancer publication-title: Cancer Epidemiol Biomarkers Prev – volume: 21 start-page: 1 year: 2011 end-page: 4 article-title: Lifestyle factors, benign prostatic hyperplasia, and lower urinary tract symptoms publication-title: Curr Opin Urol – volume: 5 start-page: 212 year: 2010 end-page: 8 article-title: Benign prostatic hyperplasia and male lower urinary tract symptoms: epidemiology and risk factors publication-title: Curr Bladder Dysfunct Rep – volume: 67 start-page: 73 year: 2006 end-page: 9 article-title: Food groups and risk of benign prostatic hyperplasia publication-title: Urology – volume: 43 start-page: 205 year: 1999 end-page: 15 article-title: Recruitment procedures of EPIC‐Germany. European Investigation into Cancer and Nutrition publication-title: Ann Nutr Metab – volume: 54 start-page: 87 year: 2009 end-page: 96 article-title: Dietary intake of individual glucosinolates in participants of the EPIC‐Heidelberg cohort study publication-title: Ann Nutr Metab – volume: 48 start-page: 452 year: 2009 end-page: 6 article-title: Whole blood selenium levels (WBSL) in patients with prostate cancer (PC), benign prostatic hyperplasia (BPH) and healthy male inhabitants (HMI) and prostatic tissue selenium levels (PTSL) in patients with PC and BPH publication-title: Acta Oncol – volume: 52 start-page: 363 year: 1998 end-page: 7 article-title: Plasma selenoprotein P levels of healthy males in different selenium status after oral supplementation with different forms of selenium publication-title: Eur J Clin Nutr – volume: 40 start-page: 121 year: 2005 end-page: 8 article-title: Benign prostatic hyperplasia: age‐related tissue‐remodeling publication-title: Exp Gerontol – volume: 47 start-page: 73 issue: 2 year: 2008 end-page: 88 article-title: The cancer chemopreventive actions of phytochemicals derived from glucosinolates publication-title: Eur J Nutr – volume: 121 start-page: 497 year: 2010 end-page: 502 article-title: No evidence for glutathione S‐transferases GSTA2, GSTM2, GSTO1, GSTO2, and GSTZ1 in breast cancer risk publication-title: Breast Cancer Res Treat – volume: 26 start-page: S71 issue: 1 year: 1997 end-page: 81 article-title: Reproducibility and relative validity of energy and macronutrient intake of a food frequency questionnaire developed for the German part of the EPIC project. European Prospective Investigation into Cancer and Nutrition publication-title: Int J Epidemiol – volume: 163 start-page: 490 year: 2000 end-page: 5 article-title: Race, ethnicity and benign prostatic hyperplasia in the health professionals follow‐up study publication-title: J Urol – volume: 26 start-page: S59 issue: 1 year: 1997 end-page: 70 article-title: Reproducibility and relative validity of food group intake in a food frequency questionnaire developed for the German part of the EPIC project. European Prospective Investigation into Cancer and Nutrition publication-title: Int J Epidemiol – volume: 92 start-page: 525 year: 2010 end-page: 31 article-title: Optimization of selenoprotein P and other plasma selenium biomarkers for the assessment of the selenium nutritional requirement: a placebo‐controlled, double‐blind study of selenomethionine supplementation in selenium‐deficient Chinese subjects publication-title: Am J Clin Nutr – volume: 73 start-page: 113 year: 2000 end-page: 25 article-title: Selenium supplementation of children in a selenium‐deficient area in China: blood selenium levels and glutathione peroxidase activities publication-title: Biol Trace Elem Res – volume: 43 start-page: 216 year: 1999 end-page: 24 article-title: Measures of quality control in the German component of the EPIC study. European Prospective Investigation into Cancer and Nutrition publication-title: Ann Nutr Metab – volume: 178 start-page: 395 year: 2007 end-page: 401 article-title: Modifiable risk factors for benign prostatic hyperplasia and lower urinary tract symptoms: new approaches to old problems publication-title: J Urol – volume: 55 start-page: 864 year: 2009 end-page: 73 article-title: Is there evidence of a relationship between benign prostatic hyperplasia and prostate cancer? Findings of a literature review publication-title: Eur Urol – volume: 84 start-page: 3613 year: 1999 end-page: 9 article-title: Ethnicity and migration as determinants of human prostate size publication-title: J Clin Endocrinol Metab – ident: e_1_2_7_25_2 doi: 10.1016/j.urology.2004.04.012 – ident: e_1_2_7_12_2 doi: 10.1158/1055-9965.EPI-09-0660 – ident: e_1_2_7_40_2 doi: 10.1093/jn/126.1.138 – ident: e_1_2_7_19_2 doi: 10.1038/sj.ejcn.1600565 – ident: e_1_2_7_27_2 doi: 10.1159/000012787 – volume: 9 start-page: 787 year: 2000 ident: e_1_2_7_21_2 article-title: Modulation of human glutathione S‐transferases by botanically defined vegetable diets publication-title: Cancer Epidemiol Biomarkers Prev – volume-title: Dietary Reference Intakes for Vitamin C, Vitamin E, Selenium, and Carotenoids year: 2000 ident: e_1_2_7_41_2 – ident: e_1_2_7_10_2 doi: 10.1158/1055-9965.EPI-10-0364 – ident: e_1_2_7_11_2 doi: 10.1002/ijc.24555 – ident: e_1_2_7_18_2 doi: 10.1385/BTER:73:2:113 – ident: e_1_2_7_30_2 doi: 10.1039/a806307i – ident: e_1_2_7_32_2 doi: 10.1093/ije/26.suppl_1.S59 – ident: e_1_2_7_7_2 doi: 10.1016/j.urology.2005.07.030 – ident: e_1_2_7_8_2 doi: 10.1016/j.exger.2004.12.008 – ident: e_1_2_7_16_2 doi: 10.1007/s00394-008-2005-z – ident: e_1_2_7_4_2 doi: 10.1210/jc.84.10.3613 – ident: e_1_2_7_17_2 doi: 10.1002/mnfr.200800103 – volume: 70 start-page: 158 year: 1967 ident: e_1_2_7_29_2 article-title: Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase publication-title: J Lab Clin Med – ident: e_1_2_7_35_2 doi: 10.1093/acprof:oso/9780195122978.001.0001 – ident: e_1_2_7_2_2 doi: 10.1007/s11884-010-0067-2 – ident: e_1_2_7_13_2 doi: 10.1016/j.febslet.2006.06.006 – ident: e_1_2_7_20_2 doi: 10.1007/s00394-008-2009-8 – start-page: 589 volume-title: Selenium in Biology and Medicine year: 1987 ident: e_1_2_7_39_2 – ident: e_1_2_7_9_2 doi: 10.1016/j.eururo.2008.11.011 – ident: e_1_2_7_34_2 doi: 10.1159/000209266 – ident: e_1_2_7_22_2 doi: 10.1007/s00394-009-0039-5 – ident: e_1_2_7_36_2 doi: 10.1016/j.clinbiochem.2005.11.018 – volume: 52 start-page: S128 issue: 1 year: 2008 ident: e_1_2_7_15_2 article-title: Direct and indirect antioxidant properties of inducers of cytoprotective proteins publication-title: Mol Nutr Food Res – ident: e_1_2_7_23_2 doi: 10.1007/s10549-009-0589-5 – ident: e_1_2_7_24_2 doi: 10.1111/j.1464-410X.2007.07345.x – ident: e_1_2_7_43_2 doi: 10.1016/S0140-6736(00)02490-9 – ident: e_1_2_7_33_2 doi: 10.1093/ije/26.suppl_1.S71 – volume: 52 start-page: 248 year: 2005 ident: e_1_2_7_26_2 article-title: Blood and tissue selenium concentrations and glutathione peroxidase activities in patients with prostate cancer and benign prostate hyperplasia publication-title: Neoplasma – ident: e_1_2_7_38_2 doi: 10.1016/S0009-8981(03)00048-2 – ident: e_1_2_7_6_2 doi: 10.1016/j.juro.2007.03.103 – ident: e_1_2_7_31_2 doi: 10.1016/j.jtemb.2007.11.003 – ident: e_1_2_7_28_2 doi: 10.1159/000012788 – ident: e_1_2_7_42_2 doi: 10.3945/ajcn.2010.29642 – ident: e_1_2_7_37_2 doi: 10.1097/MOU.0b013e32834100c9 – ident: e_1_2_7_5_2 doi: 10.1093/aje/kwm389 – ident: e_1_2_7_14_2 doi: 10.1080/02841860802403721 – ident: e_1_2_7_3_2 doi: 10.1016/S0022-5347(05)67909-8 |
SSID | ssj0014665 |
Score | 2.088003 |
Snippet | 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... 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... |
SourceID | proquest pubmed crossref wiley |
SourceType | Aggregation Database Index Database Enrichment Source Publisher |
StartPage | E879 |
SubjectTerms | Adult Aged benign prostatic hyperplasia Biomarkers - blood cohort study Dietary Supplements Follow-Up Studies Germany - epidemiology glucosinolate intake Glucosinolates - administration & dosage Glutathione Transferase - blood GPx GST‐α Humans Incidence Isoenzymes - blood Male Middle Aged Prostatic Hyperplasia - blood Prostatic Hyperplasia - diet therapy Prostatic Hyperplasia - epidemiology Retrospective Studies Risk Factors Selenium - blood SePP serum selenium |
Title | Effects of selenium status, dietary glucosinolate intake and serum glutathione S‐transferase α activity on the risk of benign prostatic hyperplasia |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1464-410X.2012.11383.x https://www.ncbi.nlm.nih.gov/pubmed/22882569 https://www.proquest.com/docview/1273127417 |
Volume | 110 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3NbtQwELaqVqq4QMvvQqkGiSNZbRI7P8cuZVVVag-llfZm2Y4DqwXvajeRECcegRPvwYv0IfokzNjZlbb0UCFuUZKxHceT-cb5ZoaxtyZTSghlo6w0VcQzE0dFYnlUobUSVYUWTNE-5Nl5dnLFT8di3PGfKBYm5IdYb7iRZvjvNSm40svbSs4jHg_GxNBKqDpJkfYJTxJ1i_DRxTqTFN7qq0oGEYTtm6SeOxvatFR_wc9NNOvN0egRm64eJLBQpv220X3z_VaOx__zpHvsYYda4Sgss322Zd1jtnvW_Zd_wn6FJMhLmNVA5ZvcpP0KFKvULt9BNbENdg6BHT9x6Ew3FiauUVMLylUoscDb8XJDVMiZs_Dx5sfPxkNqu0AzC9e_gQIwqM4FzBwgaAXixFN3Gjv75GBO0SuUfRY-o2e9mPvo0KfscvTh8v1J1FV8iEyKn55IpbwQiPcNjrlUZV3wOldFOihzYXRclMagJ48eZiYsrymzz6CosyTRecxrZQfpM7btcJQvGFjFK4UCOrWGF7bU2Ggq6FyGLpoWPZavXq40XTZ0KsrxRW54RVzSrEuadelnXX7rsXgtOQ8ZQe4h82a1fiSqL_2TUc7O2qWMET7GlEIo77HnYWGtW00SdH9EVuJY_fK4d3dyeHrlD1_-s-Qr9oDOB-LOAdtuFq19jfCr0Yds52h4PBwdegX7A8J1JXE |
linkProvider | Wiley-Blackwell |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3NbhMxELaqVipcoOU3FMogcWSj7K69P8dCqdLS9ACplJvl9XpL1OJEya6EeuIROPU9-iI8BE_CjL2JlNJDhbitsh7b63h2vvHOfMPYW50oJYQyQZLrMuCJDoMsMjwo0VqJskQLpugccnCS9E_50UiM2nJAlAvj-SGWB26kGe59TQpOB9I3tZwHPOyNKEQrovIkWdxFQLlBBb6JSH__85JLCtu6upJeBoH7aljPrT2t2qq_AOgqnnUG6eAhu1g8io9DOe82ddHVlzdYHv_Ts26xBy1whT2_07bZmrGP2Oag_TT_mF15HuQ5TCqgCk523HwDSldq5u-gHJsaRwcfID-26E_XBsa2VucGlC1RYobN8XZN0ZATa-DL7x8_a4eqzQwtLfy6BsrBoFIXMLGAuBUoLJ6GK3CwMwtTSmAhAlr4is71bOoSRJ-w4cHH4Yd-0BZ9CHSMb59AxTwTCPk1zjlXeZXxKlVZ3MtToYswy7VGZx6dzEQYXhG5Ty-rkigq0pBXyvTip2zd4iyfMzCKlwoFithonpm8wE5jQb8l6KUVosPSxb8rdUuITnU5LuSKY8QlrbqkVZdu1eX3DguXklNPCnIHmTeLDSRRg-mzjLJm0sxliAgyJBahtMOe-Z217DWK0AMSSY5zdfvjzsPJ90en7vLFP0u-Zvf6w8GxPD48-bTD7lMbH8fzkq3Xs8a8QjRWF7tOy_4A1lcoGw |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3NbtQwELZQkSou_P8sv4PEkazyYzvJESirUmiFoJX2ZjmOU1YL3tVuIqGe-giceA9ehIfok3TGzq60hUOFuEWJx3YcT-abZOYbxl4YqbUQ2kayNHXEpUmiIrU8qtFaibpGC6bpO-T-gdw94ntjMe7jnygXJvBDrD-4kWb49zUp-LxuLio5j3gSjylCK6XqJEU2RDx5lcu4pDIOO5_WVFLY1peVDDKI2zejev7a06ap-gN_bsJZb49GN9h0dSchDGU67NpqaE4ukDz-n1u9ya73sBVehX12i12x7jbb3u9_zN9hPwML8hJmDVD9JjfpvgElK3XLl1BPbIuDQwiPnzj0plsLE9fqqQXtapRYYHO83FIs5MxZ-Hx2-qP1mNou0M7C719AGRhU6AJmDhC1AgXF03AVDnbsYE7pK0Q_C1_QtV7MfXroXXY4env4ZjfqSz5EJsN3T6QzXggE_AbnXOqyKXiT6yKLy1yYKilKY9CVRxdTCssbovaJi0amaZUnvNE2zu6xLYezfMDAal5rFKgya3hhywo7zQSdk-ijVWLA8tXDVaanQ6eqHF_VhlvEFa26olVXftXV9wFL1pLzQAlyCZnnq_2jUH_pp4x2dtYtVYL4MSEOoXzA7oeNte41TdH_EbLEufrtcenh1Ou9I3_48J8ln7Htjzsj9eHdwftH7Bo1CUE8j9lWu-jsE4RibfXU69g5NFcmyg |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Effects+of+selenium+status%2C+dietary+glucosinolate+intake+and+serum+glutathione+S-transferase+%CE%B1+activity+on+the+risk+of+benign+prostatic+hyperplasia&rft.jtitle=BJU+international&rft.au=Eichholzer%2C+Monika&rft.au=Steinbrecher%2C+Astrid&rft.au=Kaaks%2C+Rudolf&rft.au=Teucher%2C+Birgit&rft.date=2012-12-01&rft.eissn=1464-410X&rft.volume=110&rft.issue=11+Pt+C&rft.spage=E879&rft_id=info:doi/10.1111%2Fj.1464-410X.2012.11383.x&rft_id=info%3Apmid%2F22882569&rft.externalDocID=22882569 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1464-4096&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1464-4096&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1464-4096&client=summon |