Evidence map›Paper›PMID 30019097›Full record

ArticleFamilial cancer2019

Modified capture-recapture estimates of the number of families with Lynch syndrome in Central Ohio.

John Michael O Ranola, Rachel Pearlman, Heather Hampel, Brian H Shirts

Abstract read
In one paragraph

Article in Familial cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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0cells of the map it votes in
3citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

John Michael O RanolaDepartment of Laboratory Medicine, University of Washington, 1959 NE Pacific Street, NW120, Box 357110, Seattle, WA, 98195-7110, USA.ORCID http://orcid.org/0000-0001-6177-4227
Rachel PearlmanDepartment of Internal Medicine and the Comprehensive Cancer Center, The Ohio State University, Columbus, OH, USA.
Heather HampelDepartment of Internal Medicine and the Comprehensive Cancer Center, The Ohio State University, Columbus, OH, USA.
Brian H ShirtsDepartment of Laboratory Medicine, University of Washington, 1959 NE Pacific Street, NW120, Box 357110, Seattle, WA, 98195-7110, USA. shirtsb@uw.edu.

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Marian Esvelt · 1985 to 2026
$296.4M
Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
Damon Runyon Cancer Research Foundation DRR-33-15NCI NIH HHS NCI 5P30 CA015704-39NCI NIH HHS P30 CA015704NCI NIH HHS P30 CA016058
6 · The paper itself

Abstract

Past methods for estimating the population frequency of familial cancer syndromes have used cases and controls ignoring the familial nature of genetic disease. In this study we modified the capture-recapture method from ecology to estimate the number of families in central Ohio with Lynch syndrome (LS). We screened 1566 colorectal cancer cases and 545 endometrial cancer cases in central Ohio from 1999 to 2005 and identified 58 with LS. We screened an additional 3346 colorectal and 342 endometrial cancer cases from 2013 to 2016 and identified 149 with LS. We found 12 LS mutations shared between families observed in the first and second studies. We identified three individuals between studies who were closely related and eight who were more distantly related. We used identified family relationships and genetic test results to estimate family size and structure. Applying a modified capture-recapture method we estimate 1693 3-generation families in the area who have 288 unique LS causing mutations. Comprehensive colorectal and endometrial cancer screening will take about 20 years to identify 50% of families with LS. This is the first time that the capture-recapture method has been applied to estimate the burden of families with a specific heritable disease. Family structure reveals the potential extent of prevention and the time necessary to identify a proportion of families with LS.

Indexed as

Colorectal Neoplasms, Hereditary NonpolyposisCost of IllnessEarly Detection of CancerEndometrial NeoplasmsFemaleGenetic TestingHumansMedical History TakingMutationOhioCapture–recaptureCascade testingGenetic counselingLynch syndromeMark–recapturePopulation geneticsPopulation structurePrevalence

Identifiers

PMID30019097
PMCPMC6324998

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.