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
Hauptverfasser: 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.
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container_end_page 2096
container_issue 10
container_start_page 2089
container_title Cancer
container_volume 57
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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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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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. 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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. 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source MEDLINE; Alma/SFX Local Collection
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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