β-Carotene concentration in buccal mucosal cells with and without dysplastic oral leukoplakia after long-term β-carotene supplementation in male smokers
To measure the beta-carotene concentration in buccal mucosal cells in smoking men who had received long-term beta-carotene (BC) supplementation in a controlled trial. To assess the association of cellular BC on the prevalence of dysplasia in oral leukoplakia. An end-of-trial examination of a part of...
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Veröffentlicht in: | European journal of clinical nutrition 1998-12, Vol.52 (12), p.872-876 |
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creator | LIEDE, K. E ALFTHAN, G HIETANEN, J. H. P HAUKKA, J. K SAXEN, L. M HEINONEN, O. P |
description | To measure the beta-carotene concentration in buccal mucosal cells in smoking men who had received long-term beta-carotene (BC) supplementation in a controlled trial. To assess the association of cellular BC on the prevalence of dysplasia in oral leukoplakia.
An end-of-trial examination of a part of subjects in the Alpha-Tocopherol, Beta Carotene Cancer Prevention Study.
343 men who for 5-7 years had received BC (20 mg/d) or alpha-tocopherol (AT) (50 mg/d), or both of these or placebo. BC concentration of buccal mucosal cells was compared in the subjects with BC supplementation (n = 173) to that of those without it (n = 170). Oral mucosae were examined clinically and lesions showing leukoplakia histopathologically.
Mean (s.d.) BC concentration in buccal mucosal cells was 7.7 (10.3)mg/kg protein in the subjects who received BC compared to 1.1 (1.7) mg/kg protein in those who did not. The BC concentration in the cells of supplemented subjects correlated with their serum BC levels (P < 0.001). AT supplementation had no effect on BC concentration nor was daily amount of smoking statistically significantly associated with the BC concentration in buccal cells. Altogether 17 subjects showed oral leukoplakia, 7 had dysplasia. In these 7 subjects, the BC concentration in buccal mucosal cells did not differ statistically significantly compared to subjects with only hyperkeratosis (n = 10) (F-test, P = 0.74).
After long-term BC supplementation, BC concentration in oral mucosal cells was 7-fold greater than without supplementation. There was no evidence to support an association between cellular BC concentration and precancerous lesions among the few subjects having them in their oral mucosae. |
doi_str_mv | 10.1038/sj.ejcn.1600646 |
format | Article |
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An end-of-trial examination of a part of subjects in the Alpha-Tocopherol, Beta Carotene Cancer Prevention Study.
343 men who for 5-7 years had received BC (20 mg/d) or alpha-tocopherol (AT) (50 mg/d), or both of these or placebo. BC concentration of buccal mucosal cells was compared in the subjects with BC supplementation (n = 173) to that of those without it (n = 170). Oral mucosae were examined clinically and lesions showing leukoplakia histopathologically.
Mean (s.d.) BC concentration in buccal mucosal cells was 7.7 (10.3)mg/kg protein in the subjects who received BC compared to 1.1 (1.7) mg/kg protein in those who did not. The BC concentration in the cells of supplemented subjects correlated with their serum BC levels (P < 0.001). AT supplementation had no effect on BC concentration nor was daily amount of smoking statistically significantly associated with the BC concentration in buccal cells. Altogether 17 subjects showed oral leukoplakia, 7 had dysplasia. In these 7 subjects, the BC concentration in buccal mucosal cells did not differ statistically significantly compared to subjects with only hyperkeratosis (n = 10) (F-test, P = 0.74).
After long-term BC supplementation, BC concentration in oral mucosal cells was 7-fold greater than without supplementation. There was no evidence to support an association between cellular BC concentration and precancerous lesions among the few subjects having them in their oral mucosae.</description><identifier>ISSN: 0954-3007</identifier><identifier>EISSN: 1476-5640</identifier><identifier>DOI: 10.1038/sj.ejcn.1600646</identifier><identifier>PMID: 9881881</identifier><language>eng</language><publisher>Basingstoke: Nature Publishing</publisher><subject>Aged ; beta Carotene - administration & dosage ; beta Carotene - analysis ; beta Carotene - therapeutic use ; Biological and medical sciences ; Carotene ; Clinical trials ; Dietary supplements ; Dysplasia ; General and cellular metabolism. Vitamins ; Humans ; Lesions ; Leukokeratosis ; Leukoplakia, Oral - metabolism ; Leukoplakia, Oral - pathology ; Male ; Medical sciences ; Men ; Middle Aged ; Mouth Mucosa - chemistry ; Mouth Neoplasms - prevention & control ; Mucosa ; Oral cancer ; Pharmacology. Drug treatments ; Proteins ; Smoking ; Smoking - adverse effects ; Tocopherol ; Vitamin A ; Vitamin E ; β-Carotene</subject><ispartof>European journal of clinical nutrition, 1998-12, Vol.52 (12), p.872-876</ispartof><rights>1999 INIST-CNRS</rights><rights>Copyright Macmillan Journals Ltd. Dec 1998</rights><rights>Macmillan Publishers Limited 1998.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c376t-6136f667f39e714b7cb0baa98e179c7775e7cce4a0b7ffa3992ecedcf7f786e23</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1625791$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9881881$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>LIEDE, K. E</creatorcontrib><creatorcontrib>ALFTHAN, G</creatorcontrib><creatorcontrib>HIETANEN, J. H. P</creatorcontrib><creatorcontrib>HAUKKA, J. K</creatorcontrib><creatorcontrib>SAXEN, L. M</creatorcontrib><creatorcontrib>HEINONEN, O. P</creatorcontrib><title>β-Carotene concentration in buccal mucosal cells with and without dysplastic oral leukoplakia after long-term β-carotene supplementation in male smokers</title><title>European journal of clinical nutrition</title><addtitle>Eur J Clin Nutr</addtitle><description>To measure the beta-carotene concentration in buccal mucosal cells in smoking men who had received long-term beta-carotene (BC) supplementation in a controlled trial. To assess the association of cellular BC on the prevalence of dysplasia in oral leukoplakia.
An end-of-trial examination of a part of subjects in the Alpha-Tocopherol, Beta Carotene Cancer Prevention Study.
343 men who for 5-7 years had received BC (20 mg/d) or alpha-tocopherol (AT) (50 mg/d), or both of these or placebo. BC concentration of buccal mucosal cells was compared in the subjects with BC supplementation (n = 173) to that of those without it (n = 170). Oral mucosae were examined clinically and lesions showing leukoplakia histopathologically.
Mean (s.d.) BC concentration in buccal mucosal cells was 7.7 (10.3)mg/kg protein in the subjects who received BC compared to 1.1 (1.7) mg/kg protein in those who did not. The BC concentration in the cells of supplemented subjects correlated with their serum BC levels (P < 0.001). AT supplementation had no effect on BC concentration nor was daily amount of smoking statistically significantly associated with the BC concentration in buccal cells. Altogether 17 subjects showed oral leukoplakia, 7 had dysplasia. In these 7 subjects, the BC concentration in buccal mucosal cells did not differ statistically significantly compared to subjects with only hyperkeratosis (n = 10) (F-test, P = 0.74).
After long-term BC supplementation, BC concentration in oral mucosal cells was 7-fold greater than without supplementation. There was no evidence to support an association between cellular BC concentration and precancerous lesions among the few subjects having them in their oral mucosae.</description><subject>Aged</subject><subject>beta Carotene - administration & dosage</subject><subject>beta Carotene - analysis</subject><subject>beta Carotene - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Carotene</subject><subject>Clinical trials</subject><subject>Dietary supplements</subject><subject>Dysplasia</subject><subject>General and cellular metabolism. Vitamins</subject><subject>Humans</subject><subject>Lesions</subject><subject>Leukokeratosis</subject><subject>Leukoplakia, Oral - metabolism</subject><subject>Leukoplakia, Oral - pathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Men</subject><subject>Middle Aged</subject><subject>Mouth Mucosa - chemistry</subject><subject>Mouth Neoplasms - prevention & control</subject><subject>Mucosa</subject><subject>Oral cancer</subject><subject>Pharmacology. Drug treatments</subject><subject>Proteins</subject><subject>Smoking</subject><subject>Smoking - adverse effects</subject><subject>Tocopherol</subject><subject>Vitamin A</subject><subject>Vitamin E</subject><subject>β-Carotene</subject><issn>0954-3007</issn><issn>1476-5640</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kdFqFTEQhoNY6rF67ZUQtHi3p8lmN9lcysGqUOiNXodszkR3TzZZkw2lr-Jj-CA-kzl2baEgBGaY-TL_DD9CryjZUsK6izRuYTR-SzkhvOFP0IY2glctb8hTtCGybSpGiHiGnqc0ElKaoj5Fp7LraHkb9PP3r2qnY1jAAzbBG_BL1MsQPB487rMx2uEpm5BKNOBcwjfD8h1rv_-bhLzg_W2anU7LYHCIBXOQD6FUDoPG2i4QsQv-W1WSCRc5808u5Xl2MBXFe8FJu1KfwgFieoFOrHYJXq7xDH29_PBl96m6uv74eff-qjJM8KXilHHLubBMgqBNL0xPeq1lB1RII4RoQRgDjSa9sFYzKWswsDdWWNFxqNkZenc3d47hR4a0qGlIx1O1h5CT4pIy0rS0gG8fgWPI0ZfdVM2bWtBasK5Qb_5LUclbWawq0MUdZGJIKYJVcxwmHW8VJeporEqjOhqrVmPLj9fr2NxPsL_nVydL_3zt61Q8s1F7M6SHsbxuRTnkDwhCsW0</recordid><startdate>19981201</startdate><enddate>19981201</enddate><creator>LIEDE, K. E</creator><creator>ALFTHAN, G</creator><creator>HIETANEN, J. H. P</creator><creator>HAUKKA, J. K</creator><creator>SAXEN, L. M</creator><creator>HEINONEN, O. P</creator><general>Nature Publishing</general><general>Nature Publishing Group</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7TK</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>19981201</creationdate><title>β-Carotene concentration in buccal mucosal cells with and without dysplastic oral leukoplakia after long-term β-carotene supplementation in male smokers</title><author>LIEDE, K. E ; ALFTHAN, G ; HIETANEN, J. H. P ; HAUKKA, J. K ; SAXEN, L. M ; HEINONEN, O. P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c376t-6136f667f39e714b7cb0baa98e179c7775e7cce4a0b7ffa3992ecedcf7f786e23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Aged</topic><topic>beta Carotene - administration & dosage</topic><topic>beta Carotene - analysis</topic><topic>beta Carotene - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Carotene</topic><topic>Clinical trials</topic><topic>Dietary supplements</topic><topic>Dysplasia</topic><topic>General and cellular metabolism. Vitamins</topic><topic>Humans</topic><topic>Lesions</topic><topic>Leukokeratosis</topic><topic>Leukoplakia, Oral - metabolism</topic><topic>Leukoplakia, Oral - pathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Men</topic><topic>Middle Aged</topic><topic>Mouth Mucosa - chemistry</topic><topic>Mouth Neoplasms - prevention & control</topic><topic>Mucosa</topic><topic>Oral cancer</topic><topic>Pharmacology. Drug treatments</topic><topic>Proteins</topic><topic>Smoking</topic><topic>Smoking - adverse effects</topic><topic>Tocopherol</topic><topic>Vitamin A</topic><topic>Vitamin E</topic><topic>β-Carotene</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>LIEDE, K. E</creatorcontrib><creatorcontrib>ALFTHAN, G</creatorcontrib><creatorcontrib>HIETANEN, J. H. P</creatorcontrib><creatorcontrib>HAUKKA, J. K</creatorcontrib><creatorcontrib>SAXEN, L. M</creatorcontrib><creatorcontrib>HEINONEN, O. P</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of clinical nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>LIEDE, K. E</au><au>ALFTHAN, G</au><au>HIETANEN, J. H. P</au><au>HAUKKA, J. K</au><au>SAXEN, L. M</au><au>HEINONEN, O. P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>β-Carotene concentration in buccal mucosal cells with and without dysplastic oral leukoplakia after long-term β-carotene supplementation in male smokers</atitle><jtitle>European journal of clinical nutrition</jtitle><addtitle>Eur J Clin Nutr</addtitle><date>1998-12-01</date><risdate>1998</risdate><volume>52</volume><issue>12</issue><spage>872</spage><epage>876</epage><pages>872-876</pages><issn>0954-3007</issn><eissn>1476-5640</eissn><abstract>To measure the beta-carotene concentration in buccal mucosal cells in smoking men who had received long-term beta-carotene (BC) supplementation in a controlled trial. To assess the association of cellular BC on the prevalence of dysplasia in oral leukoplakia.
An end-of-trial examination of a part of subjects in the Alpha-Tocopherol, Beta Carotene Cancer Prevention Study.
343 men who for 5-7 years had received BC (20 mg/d) or alpha-tocopherol (AT) (50 mg/d), or both of these or placebo. BC concentration of buccal mucosal cells was compared in the subjects with BC supplementation (n = 173) to that of those without it (n = 170). Oral mucosae were examined clinically and lesions showing leukoplakia histopathologically.
Mean (s.d.) BC concentration in buccal mucosal cells was 7.7 (10.3)mg/kg protein in the subjects who received BC compared to 1.1 (1.7) mg/kg protein in those who did not. The BC concentration in the cells of supplemented subjects correlated with their serum BC levels (P < 0.001). AT supplementation had no effect on BC concentration nor was daily amount of smoking statistically significantly associated with the BC concentration in buccal cells. Altogether 17 subjects showed oral leukoplakia, 7 had dysplasia. In these 7 subjects, the BC concentration in buccal mucosal cells did not differ statistically significantly compared to subjects with only hyperkeratosis (n = 10) (F-test, P = 0.74).
After long-term BC supplementation, BC concentration in oral mucosal cells was 7-fold greater than without supplementation. There was no evidence to support an association between cellular BC concentration and precancerous lesions among the few subjects having them in their oral mucosae.</abstract><cop>Basingstoke</cop><pub>Nature Publishing</pub><pmid>9881881</pmid><doi>10.1038/sj.ejcn.1600646</doi><tpages>5</tpages></addata></record> |
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subjects | Aged beta Carotene - administration & dosage beta Carotene - analysis beta Carotene - therapeutic use Biological and medical sciences Carotene Clinical trials Dietary supplements Dysplasia General and cellular metabolism. Vitamins Humans Lesions Leukokeratosis Leukoplakia, Oral - metabolism Leukoplakia, Oral - pathology Male Medical sciences Men Middle Aged Mouth Mucosa - chemistry Mouth Neoplasms - prevention & control Mucosa Oral cancer Pharmacology. Drug treatments Proteins Smoking Smoking - adverse effects Tocopherol Vitamin A Vitamin E β-Carotene |
title | β-Carotene concentration in buccal mucosal cells with and without dysplastic oral leukoplakia after long-term β-carotene supplementation in male smokers |
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