Age‐ and sex‐specific cumulative rate and risk of ATLL for HTLV‐I carriers
We have surveyed the incidence of adult T‐cell leukemia/lymphoma (ATLL) in an endemic area of 290,464 inhabitants for 7 years. We now revise our previous results on the basis of additional findings and estimate the age‐ and sex‐specific cumulative rate for HTLV‐I carriers, the adoption of which is r...
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creator | Kondo, Toshifumi Kono, Hidehisa Miyamoto, Naoaki Yoshida, Ryouichi Toki, Hironobu Matsumoto, Isao Hara, Masamichi Inoue, Hiroo Inatsuki, Akira Funatsu, Takashi Yamano, Norio Bando, Fumihiro Iwao, Eiichi Miyoshi, Isao Hinuma, Yorio Hanaoka, Masao |
description | We have surveyed the incidence of adult T‐cell leukemia/lymphoma (ATLL) in an endemic area of 290,464 inhabitants for 7 years. We now revise our previous results on the basis of additional findings and estimate the age‐ and sex‐specific cumulative rate for HTLV‐I carriers, the adoption of which is recommended by current cancer epidemiology as a new age‐standardized incidence rate. An unequivocal age‐dependent increase in seroprevalence was observed for both sexes with a characteristic predominance in females. The age‐dependent seroconversion in females may be partly explained by additional infection from infected husbands to their wives but the reason for men remains obscure. The mean annual number of incident cases of ATLL was 11.4, giving 3.9 ATLL patients annually per 105 inhabitants, 6.1 per 105 inhabitants aged over 30, and 85.0 per 105 seropositives aged over 30. Crude annual incidence rate of ATLL among 105 male seropositives aged over 30 was 145.3 and that for females was 55.2 and 95% confidence intervals of ATLL incidence rates were 34.8 to 255.7 for males and 6.4 to 104.1 for females, respectively. Although the sex ratio of 80 ATLL patients was 1.35, males are more prone to the disease (46 male patients among 4,522 male seropositives aged over 30 vs. 34 female patients among 8,801 female seropositives aged over 30; p < 0.001) for unknown reason(s). Morbidity in male seropositives aged over 30 is 2.6 times as high as that of females. Decennial incidence rates in males in their fifties and sixties were significantly higher than those in females. The remarkable male preponderance in oncogenicity of HTLV‐I may be due to the fact that men are more prone to the disease and the number of female carriers in the denominator used to calculate the incidence rate is larger than that of males. The whole life span (0–79) cumulative risk for males was 6.9% and significantly higher than that of females (2.95%). |
doi_str_mv | 10.1002/ijc.2910430618 |
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We now revise our previous results on the basis of additional findings and estimate the age‐ and sex‐specific cumulative rate for HTLV‐I carriers, the adoption of which is recommended by current cancer epidemiology as a new age‐standardized incidence rate. An unequivocal age‐dependent increase in seroprevalence was observed for both sexes with a characteristic predominance in females. The age‐dependent seroconversion in females may be partly explained by additional infection from infected husbands to their wives but the reason for men remains obscure. The mean annual number of incident cases of ATLL was 11.4, giving 3.9 ATLL patients annually per 105 inhabitants, 6.1 per 105 inhabitants aged over 30, and 85.0 per 105 seropositives aged over 30. Crude annual incidence rate of ATLL among 105 male seropositives aged over 30 was 145.3 and that for females was 55.2 and 95% confidence intervals of ATLL incidence rates were 34.8 to 255.7 for males and 6.4 to 104.1 for females, respectively. Although the sex ratio of 80 ATLL patients was 1.35, males are more prone to the disease (46 male patients among 4,522 male seropositives aged over 30 vs. 34 female patients among 8,801 female seropositives aged over 30; p < 0.001) for unknown reason(s). Morbidity in male seropositives aged over 30 is 2.6 times as high as that of females. Decennial incidence rates in males in their fifties and sixties were significantly higher than those in females. The remarkable male preponderance in oncogenicity of HTLV‐I may be due to the fact that men are more prone to the disease and the number of female carriers in the denominator used to calculate the incidence rate is larger than that of males. The whole life span (0–79) cumulative risk for males was 6.9% and significantly higher than that of females (2.95%).</description><identifier>ISSN: 0020-7136</identifier><identifier>EISSN: 1097-0215</identifier><identifier>DOI: 10.1002/ijc.2910430618</identifier><identifier>PMID: 2732000</identifier><identifier>CODEN: IJCNAW</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Age Factors ; AIDS/HIV ; Biological and medical sciences ; Carrier State - epidemiology ; Carrier State - immunology ; Hematologic and hematopoietic diseases ; HTLV-I Antibodies - analysis ; HTLV-I Infections - epidemiology ; HTLV-I Infections - immunology ; Humans ; Japan ; Leukemia-Lymphoma, Adult T-Cell - epidemiology ; Leukemia-Lymphoma, Adult T-Cell - immunology ; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis ; Medical sciences ; Population Surveillance ; Retrospective Studies ; Risk Factors ; Sex Factors</subject><ispartof>International journal of cancer, 1989-06, Vol.43 (6), p.1061-1064</ispartof><rights>Copyright © 1989 Wiley‐Liss, Inc., A Wiley Company</rights><rights>1989 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3508-dc3d2a9284ac83e3f65edcbe17484d9fdf0f657c5eae5dcf19cc8e846e1bff293</citedby><cites>FETCH-LOGICAL-c3508-dc3d2a9284ac83e3f65edcbe17484d9fdf0f657c5eae5dcf19cc8e846e1bff293</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fijc.2910430618$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fijc.2910430618$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27928,27929,45578,45579</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7280445$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2732000$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kondo, Toshifumi</creatorcontrib><creatorcontrib>Kono, Hidehisa</creatorcontrib><creatorcontrib>Miyamoto, Naoaki</creatorcontrib><creatorcontrib>Yoshida, Ryouichi</creatorcontrib><creatorcontrib>Toki, Hironobu</creatorcontrib><creatorcontrib>Matsumoto, Isao</creatorcontrib><creatorcontrib>Hara, Masamichi</creatorcontrib><creatorcontrib>Inoue, Hiroo</creatorcontrib><creatorcontrib>Inatsuki, Akira</creatorcontrib><creatorcontrib>Funatsu, Takashi</creatorcontrib><creatorcontrib>Yamano, Norio</creatorcontrib><creatorcontrib>Bando, Fumihiro</creatorcontrib><creatorcontrib>Iwao, Eiichi</creatorcontrib><creatorcontrib>Miyoshi, Isao</creatorcontrib><creatorcontrib>Hinuma, Yorio</creatorcontrib><creatorcontrib>Hanaoka, Masao</creatorcontrib><title>Age‐ and sex‐specific cumulative rate and risk of ATLL for HTLV‐I carriers</title><title>International journal of cancer</title><addtitle>Int J Cancer</addtitle><description>We have surveyed the incidence of adult T‐cell leukemia/lymphoma (ATLL) in an endemic area of 290,464 inhabitants for 7 years. We now revise our previous results on the basis of additional findings and estimate the age‐ and sex‐specific cumulative rate for HTLV‐I carriers, the adoption of which is recommended by current cancer epidemiology as a new age‐standardized incidence rate. An unequivocal age‐dependent increase in seroprevalence was observed for both sexes with a characteristic predominance in females. The age‐dependent seroconversion in females may be partly explained by additional infection from infected husbands to their wives but the reason for men remains obscure. The mean annual number of incident cases of ATLL was 11.4, giving 3.9 ATLL patients annually per 105 inhabitants, 6.1 per 105 inhabitants aged over 30, and 85.0 per 105 seropositives aged over 30. Crude annual incidence rate of ATLL among 105 male seropositives aged over 30 was 145.3 and that for females was 55.2 and 95% confidence intervals of ATLL incidence rates were 34.8 to 255.7 for males and 6.4 to 104.1 for females, respectively. Although the sex ratio of 80 ATLL patients was 1.35, males are more prone to the disease (46 male patients among 4,522 male seropositives aged over 30 vs. 34 female patients among 8,801 female seropositives aged over 30; p < 0.001) for unknown reason(s). Morbidity in male seropositives aged over 30 is 2.6 times as high as that of females. Decennial incidence rates in males in their fifties and sixties were significantly higher than those in females. The remarkable male preponderance in oncogenicity of HTLV‐I may be due to the fact that men are more prone to the disease and the number of female carriers in the denominator used to calculate the incidence rate is larger than that of males. The whole life span (0–79) cumulative risk for males was 6.9% and significantly higher than that of females (2.95%).</description><subject>Age Factors</subject><subject>AIDS/HIV</subject><subject>Biological and medical sciences</subject><subject>Carrier State - epidemiology</subject><subject>Carrier State - immunology</subject><subject>Hematologic and hematopoietic diseases</subject><subject>HTLV-I Antibodies - analysis</subject><subject>HTLV-I Infections - epidemiology</subject><subject>HTLV-I Infections - immunology</subject><subject>Humans</subject><subject>Japan</subject><subject>Leukemia-Lymphoma, Adult T-Cell - epidemiology</subject><subject>Leukemia-Lymphoma, Adult T-Cell - immunology</subject><subject>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</subject><subject>Medical sciences</subject><subject>Population Surveillance</subject><subject>Retrospective Studies</subject><subject>Risk Factors</subject><subject>Sex Factors</subject><issn>0020-7136</issn><issn>1097-0215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkLtOAzEQRS0EgvBo6ZBcILoNY-_TZRTxCFoJikC7cmbHyGE3G-wskI5P4Bv5EhYSBTqqGc2ce2d0GTsW0BcA8txOsS-VgCiERGRbrCdApQFIEW-zXgdAkIow2WP73k8BhIgh2mW7Mg0lAPTY3eCRPt8_uJ6V3NNb1_o5oTUWObZ1W-mFfSHu9IJ-EGf9E28MH4zznJvG8etx_tCJRhy1c5acP2Q7Rleejtb1gN1fXoyH10F-ezUaDvIAwxiyoMSwlFrJLNKYhRSaJKYSJyTSKItKZUoD3SjFmDTFJRqhEDPKooTExBipwgN2tvKdu-a5Jb8oauuRqkrPqGl9kSoQqUriDuyvQHSN945MMXe21m5ZCCi-Iyy6CIvfCDvBydq5ndRUbvB1Zt3-dL3XHnVlnJ6h9RsslRlE0fddtcJebUXLf44Wo5vhnxe-ANMni_c</recordid><startdate>19890615</startdate><enddate>19890615</enddate><creator>Kondo, Toshifumi</creator><creator>Kono, Hidehisa</creator><creator>Miyamoto, Naoaki</creator><creator>Yoshida, Ryouichi</creator><creator>Toki, Hironobu</creator><creator>Matsumoto, Isao</creator><creator>Hara, Masamichi</creator><creator>Inoue, Hiroo</creator><creator>Inatsuki, Akira</creator><creator>Funatsu, Takashi</creator><creator>Yamano, Norio</creator><creator>Bando, Fumihiro</creator><creator>Iwao, Eiichi</creator><creator>Miyoshi, Isao</creator><creator>Hinuma, Yorio</creator><creator>Hanaoka, Masao</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</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>7X8</scope></search><sort><creationdate>19890615</creationdate><title>Age‐ and sex‐specific cumulative rate and risk of ATLL for HTLV‐I carriers</title><author>Kondo, Toshifumi ; Kono, Hidehisa ; Miyamoto, Naoaki ; Yoshida, Ryouichi ; Toki, Hironobu ; Matsumoto, Isao ; Hara, Masamichi ; Inoue, Hiroo ; Inatsuki, Akira ; Funatsu, Takashi ; Yamano, Norio ; Bando, Fumihiro ; Iwao, Eiichi ; Miyoshi, Isao ; Hinuma, Yorio ; Hanaoka, Masao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3508-dc3d2a9284ac83e3f65edcbe17484d9fdf0f657c5eae5dcf19cc8e846e1bff293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Age Factors</topic><topic>AIDS/HIV</topic><topic>Biological and medical sciences</topic><topic>Carrier State - epidemiology</topic><topic>Carrier State - immunology</topic><topic>Hematologic and hematopoietic diseases</topic><topic>HTLV-I Antibodies - analysis</topic><topic>HTLV-I Infections - epidemiology</topic><topic>HTLV-I Infections - immunology</topic><topic>Humans</topic><topic>Japan</topic><topic>Leukemia-Lymphoma, Adult T-Cell - epidemiology</topic><topic>Leukemia-Lymphoma, Adult T-Cell - immunology</topic><topic>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</topic><topic>Medical sciences</topic><topic>Population Surveillance</topic><topic>Retrospective Studies</topic><topic>Risk Factors</topic><topic>Sex Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kondo, Toshifumi</creatorcontrib><creatorcontrib>Kono, Hidehisa</creatorcontrib><creatorcontrib>Miyamoto, Naoaki</creatorcontrib><creatorcontrib>Yoshida, Ryouichi</creatorcontrib><creatorcontrib>Toki, Hironobu</creatorcontrib><creatorcontrib>Matsumoto, Isao</creatorcontrib><creatorcontrib>Hara, Masamichi</creatorcontrib><creatorcontrib>Inoue, Hiroo</creatorcontrib><creatorcontrib>Inatsuki, Akira</creatorcontrib><creatorcontrib>Funatsu, Takashi</creatorcontrib><creatorcontrib>Yamano, Norio</creatorcontrib><creatorcontrib>Bando, Fumihiro</creatorcontrib><creatorcontrib>Iwao, Eiichi</creatorcontrib><creatorcontrib>Miyoshi, Isao</creatorcontrib><creatorcontrib>Hinuma, Yorio</creatorcontrib><creatorcontrib>Hanaoka, Masao</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>MEDLINE - Academic</collection><jtitle>International journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kondo, Toshifumi</au><au>Kono, Hidehisa</au><au>Miyamoto, Naoaki</au><au>Yoshida, Ryouichi</au><au>Toki, Hironobu</au><au>Matsumoto, Isao</au><au>Hara, Masamichi</au><au>Inoue, Hiroo</au><au>Inatsuki, Akira</au><au>Funatsu, Takashi</au><au>Yamano, Norio</au><au>Bando, Fumihiro</au><au>Iwao, Eiichi</au><au>Miyoshi, Isao</au><au>Hinuma, Yorio</au><au>Hanaoka, Masao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Age‐ and sex‐specific cumulative rate and risk of ATLL for HTLV‐I carriers</atitle><jtitle>International journal of cancer</jtitle><addtitle>Int J Cancer</addtitle><date>1989-06-15</date><risdate>1989</risdate><volume>43</volume><issue>6</issue><spage>1061</spage><epage>1064</epage><pages>1061-1064</pages><issn>0020-7136</issn><eissn>1097-0215</eissn><coden>IJCNAW</coden><abstract>We have surveyed the incidence of adult T‐cell leukemia/lymphoma (ATLL) in an endemic area of 290,464 inhabitants for 7 years. We now revise our previous results on the basis of additional findings and estimate the age‐ and sex‐specific cumulative rate for HTLV‐I carriers, the adoption of which is recommended by current cancer epidemiology as a new age‐standardized incidence rate. An unequivocal age‐dependent increase in seroprevalence was observed for both sexes with a characteristic predominance in females. The age‐dependent seroconversion in females may be partly explained by additional infection from infected husbands to their wives but the reason for men remains obscure. The mean annual number of incident cases of ATLL was 11.4, giving 3.9 ATLL patients annually per 105 inhabitants, 6.1 per 105 inhabitants aged over 30, and 85.0 per 105 seropositives aged over 30. Crude annual incidence rate of ATLL among 105 male seropositives aged over 30 was 145.3 and that for females was 55.2 and 95% confidence intervals of ATLL incidence rates were 34.8 to 255.7 for males and 6.4 to 104.1 for females, respectively. Although the sex ratio of 80 ATLL patients was 1.35, males are more prone to the disease (46 male patients among 4,522 male seropositives aged over 30 vs. 34 female patients among 8,801 female seropositives aged over 30; p < 0.001) for unknown reason(s). Morbidity in male seropositives aged over 30 is 2.6 times as high as that of females. Decennial incidence rates in males in their fifties and sixties were significantly higher than those in females. The remarkable male preponderance in oncogenicity of HTLV‐I may be due to the fact that men are more prone to the disease and the number of female carriers in the denominator used to calculate the incidence rate is larger than that of males. The whole life span (0–79) cumulative risk for males was 6.9% and significantly higher than that of females (2.95%).</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>2732000</pmid><doi>10.1002/ijc.2910430618</doi><tpages>4</tpages></addata></record> |
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subjects | Age Factors AIDS/HIV Biological and medical sciences Carrier State - epidemiology Carrier State - immunology Hematologic and hematopoietic diseases HTLV-I Antibodies - analysis HTLV-I Infections - epidemiology HTLV-I Infections - immunology Humans Japan Leukemia-Lymphoma, Adult T-Cell - epidemiology Leukemia-Lymphoma, Adult T-Cell - immunology Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis Medical sciences Population Surveillance Retrospective Studies Risk Factors Sex Factors |
title | Age‐ and sex‐specific cumulative rate and risk of ATLL for HTLV‐I carriers |
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