Familial heterogeneity of colon cancer risk
The authors have assembled detailed family histories of cancer on 857 cancer probands, of whom 180 manifested colorectal carcinoma. This study determines if some families had a greater risk for colorectal cancer than others, and if so, what factors were associated with an increase in risk. To test f...
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Veröffentlicht in: | Cancer 1986-05, Vol.57 (10), p.2089-2096 |
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creator | Lynch, Henry T. Kimberling, William J. Biscone, Karen A. Lynch, Jane F. Wagner, Cindy A. Brennan, Kathleen Mailliard, James A. Johnson, P. Steven Soori, Janet S. McKenna, Patrick J. |
description | The authors have assembled detailed family histories of cancer on 857 cancer probands, of whom 180 manifested colorectal carcinoma. This study determines if some families had a greater risk for colorectal cancer than others, and if so, what factors were associated with an increase in risk. To test for the possibility of heterogeneity of risk, a parameter called the Z‐score, was calculated for each family. The Z‐score is a measure of the number of cancer cases in the family adjusted for the number of expected cases. A permutation test was employed to test whether or not the variance of Z‐scores from the sample was greater then expected by random chance. The variance for families ascertained through colon cancer probands, but not in any of the other groups, was significantly increased. Of the colon group, 10.6% fell into a high‐risk category, as did 5.56% of the rectal cancer families, but only 3.95% of the other groups combined were at high risk. Anatomic sites (in the proband) with the highest Z‐score variances were sigmoid and transverse colon, whereas lower variances were seen for cecum and descending colon. Risk status therefore may be partially dependent upon exact anatomic sites within the colon. The effect of proband's age of diagnosis was not significant, but did show the possibility of an effect on heterogeneity of risk for both the younger and older groups. |
doi_str_mv | 10.1002/1097-0142(19860515)57:10<2089::AID-CNCR2820571034>3.0.CO;2-J |
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Steven ; Soori, Janet S. ; McKenna, Patrick J.</creator><creatorcontrib>Lynch, Henry T. ; Kimberling, William J. ; Biscone, Karen A. ; Lynch, Jane F. ; Wagner, Cindy A. ; Brennan, Kathleen ; Mailliard, James A. ; Johnson, P. Steven ; Soori, Janet S. ; McKenna, Patrick J.</creatorcontrib><description>The authors have assembled detailed family histories of cancer on 857 cancer probands, of whom 180 manifested colorectal carcinoma. This study determines if some families had a greater risk for colorectal cancer than others, and if so, what factors were associated with an increase in risk. To test for the possibility of heterogeneity of risk, a parameter called the Z‐score, was calculated for each family. The Z‐score is a measure of the number of cancer cases in the family adjusted for the number of expected cases. A permutation test was employed to test whether or not the variance of Z‐scores from the sample was greater then expected by random chance. The variance for families ascertained through colon cancer probands, but not in any of the other groups, was significantly increased. Of the colon group, 10.6% fell into a high‐risk category, as did 5.56% of the rectal cancer families, but only 3.95% of the other groups combined were at high risk. Anatomic sites (in the proband) with the highest Z‐score variances were sigmoid and transverse colon, whereas lower variances were seen for cecum and descending colon. Risk status therefore may be partially dependent upon exact anatomic sites within the colon. The effect of proband's age of diagnosis was not significant, but did show the possibility of an effect on heterogeneity of risk for both the younger and older groups.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/1097-0142(19860515)57:10<2089::AID-CNCR2820571034>3.0.CO;2-J</identifier><identifier>PMID: 3955516</identifier><identifier>CODEN: CANCAR</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Age Factors ; Analysis of Variance ; Biological and medical sciences ; Colonic Neoplasms - genetics ; Female ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; Male ; Medical sciences ; Middle Aged ; Rectal Neoplasms - genetics ; Risk ; Sex Factors ; Statistics as Topic ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Tumors</subject><ispartof>Cancer, 1986-05, Vol.57 (10), p.2089-2096</ispartof><rights>Copyright © 1986 American Cancer Society</rights><rights>1986 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c5014-cfb7071e73dfbea5056c8c5aa5e826e5e048680b5d2cfffdb9954ca8ce74fb603</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8718498$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3955516$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lynch, Henry T.</creatorcontrib><creatorcontrib>Kimberling, William J.</creatorcontrib><creatorcontrib>Biscone, Karen A.</creatorcontrib><creatorcontrib>Lynch, Jane F.</creatorcontrib><creatorcontrib>Wagner, Cindy A.</creatorcontrib><creatorcontrib>Brennan, Kathleen</creatorcontrib><creatorcontrib>Mailliard, James A.</creatorcontrib><creatorcontrib>Johnson, P. Steven</creatorcontrib><creatorcontrib>Soori, Janet S.</creatorcontrib><creatorcontrib>McKenna, Patrick J.</creatorcontrib><title>Familial heterogeneity of colon cancer risk</title><title>Cancer</title><addtitle>Cancer</addtitle><description>The authors have assembled detailed family histories of cancer on 857 cancer probands, of whom 180 manifested colorectal carcinoma. This study determines if some families had a greater risk for colorectal cancer than others, and if so, what factors were associated with an increase in risk. To test for the possibility of heterogeneity of risk, a parameter called the Z‐score, was calculated for each family. The Z‐score is a measure of the number of cancer cases in the family adjusted for the number of expected cases. A permutation test was employed to test whether or not the variance of Z‐scores from the sample was greater then expected by random chance. The variance for families ascertained through colon cancer probands, but not in any of the other groups, was significantly increased. Of the colon group, 10.6% fell into a high‐risk category, as did 5.56% of the rectal cancer families, but only 3.95% of the other groups combined were at high risk. Anatomic sites (in the proband) with the highest Z‐score variances were sigmoid and transverse colon, whereas lower variances were seen for cecum and descending colon. Risk status therefore may be partially dependent upon exact anatomic sites within the colon. The effect of proband's age of diagnosis was not significant, but did show the possibility of an effect on heterogeneity of risk for both the younger and older groups.</description><subject>Age Factors</subject><subject>Analysis of Variance</subject><subject>Biological and medical sciences</subject><subject>Colonic Neoplasms - genetics</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Rectal Neoplasms - genetics</subject><subject>Risk</subject><subject>Sex Factors</subject><subject>Statistics as Topic</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Tumors</subject><issn>0008-543X</issn><issn>1097-0142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1986</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkFFrFDEUhYModa3-BGEeRCwy600yd5JZpVCmVluKC6Lgg3DJZG_q2Nmdmuwi---dYdcFfRB8CuF8OTl8QpxLmEoA9UpCZXKQhXohK1sCSjxBM5PwRoGtZrOzy_O8_lB_VFYBGgm6ONVTmNbz1yq_uicmh-f3xQQAbI6F_vJQPErp-3A1CvWRONIVIspyIl5euGXbta7LvvGaY3_DK27X26wPme-7fpV5t_Ics9im28fiQXBd4if781h8vnj7qX6fX8_fXdZn17nH4d_ch8aAkWz0IjTsELD01qNzyFaVjAyFLS00uFA-hLBoqgoL76xnU4SmBH0snu9672L_Y8NpTcs2ee46t-J-k8iUBiso1QB-3YE-9ilFDnQX26WLW5JAo0saZdAog367JDRjOrokGlzSny5JE1A9J0VXQ_3T_Y5Ns-TFoXwvb8if7XOXvOtCHFS16YBZI21R2QG72WE_2463_znxnwv_SvQvUnKd4w</recordid><startdate>19860515</startdate><enddate>19860515</enddate><creator>Lynch, Henry T.</creator><creator>Kimberling, William J.</creator><creator>Biscone, Karen A.</creator><creator>Lynch, Jane F.</creator><creator>Wagner, Cindy A.</creator><creator>Brennan, Kathleen</creator><creator>Mailliard, James A.</creator><creator>Johnson, P. Steven</creator><creator>Soori, Janet S.</creator><creator>McKenna, Patrick J.</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>19860515</creationdate><title>Familial heterogeneity of colon cancer risk</title><author>Lynch, Henry T. ; Kimberling, William J. ; Biscone, Karen A. ; Lynch, Jane F. ; Wagner, Cindy A. ; Brennan, Kathleen ; Mailliard, James A. ; Johnson, P. Steven ; Soori, Janet S. ; McKenna, Patrick J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5014-cfb7071e73dfbea5056c8c5aa5e826e5e048680b5d2cfffdb9954ca8ce74fb603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1986</creationdate><topic>Age Factors</topic><topic>Analysis of Variance</topic><topic>Biological and medical sciences</topic><topic>Colonic Neoplasms - genetics</topic><topic>Female</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Rectal Neoplasms - genetics</topic><topic>Risk</topic><topic>Sex Factors</topic><topic>Statistics as Topic</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lynch, Henry T.</creatorcontrib><creatorcontrib>Kimberling, William J.</creatorcontrib><creatorcontrib>Biscone, Karen A.</creatorcontrib><creatorcontrib>Lynch, Jane F.</creatorcontrib><creatorcontrib>Wagner, Cindy A.</creatorcontrib><creatorcontrib>Brennan, Kathleen</creatorcontrib><creatorcontrib>Mailliard, James A.</creatorcontrib><creatorcontrib>Johnson, P. Steven</creatorcontrib><creatorcontrib>Soori, Janet S.</creatorcontrib><creatorcontrib>McKenna, Patrick J.</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>Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lynch, Henry T.</au><au>Kimberling, William J.</au><au>Biscone, Karen A.</au><au>Lynch, Jane F.</au><au>Wagner, Cindy A.</au><au>Brennan, Kathleen</au><au>Mailliard, James A.</au><au>Johnson, P. Steven</au><au>Soori, Janet S.</au><au>McKenna, Patrick J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Familial heterogeneity of colon cancer risk</atitle><jtitle>Cancer</jtitle><addtitle>Cancer</addtitle><date>1986-05-15</date><risdate>1986</risdate><volume>57</volume><issue>10</issue><spage>2089</spage><epage>2096</epage><pages>2089-2096</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><coden>CANCAR</coden><abstract>The authors have assembled detailed family histories of cancer on 857 cancer probands, of whom 180 manifested colorectal carcinoma. This study determines if some families had a greater risk for colorectal cancer than others, and if so, what factors were associated with an increase in risk. To test for the possibility of heterogeneity of risk, a parameter called the Z‐score, was calculated for each family. The Z‐score is a measure of the number of cancer cases in the family adjusted for the number of expected cases. A permutation test was employed to test whether or not the variance of Z‐scores from the sample was greater then expected by random chance. The variance for families ascertained through colon cancer probands, but not in any of the other groups, was significantly increased. Of the colon group, 10.6% fell into a high‐risk category, as did 5.56% of the rectal cancer families, but only 3.95% of the other groups combined were at high risk. Anatomic sites (in the proband) with the highest Z‐score variances were sigmoid and transverse colon, whereas lower variances were seen for cecum and descending colon. Risk status therefore may be partially dependent upon exact anatomic sites within the colon. 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subjects | Age Factors Analysis of Variance Biological and medical sciences Colonic Neoplasms - genetics Female Gastroenterology. Liver. Pancreas. Abdomen Humans Male Medical sciences Middle Aged Rectal Neoplasms - genetics Risk Sex Factors Statistics as Topic Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Tumors |
title | Familial heterogeneity of colon cancer risk |
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