Evidence map›Paper›PMID 36497357›Full record

ArticleCancers2022

Ashkenazi Jewish and Other White

Esther Forkosh, Michael Bergel, Kathryn E Hatchell, Sarah M Nielsen, Brandie Heald, Ariel A Benson, Eitan Friedman, Edward D Esplin, Lior H Katz

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Journal of medical genetics · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Esther ForkoshDepartment of Gastroenterology, Hadassah Medical Center, Jerusalem 91120, Israel.
Michael BergelFaculty of Medicine, Hebrew University of Jerusalem, Jerusalem 91121, Israel.ORCID 0000-0001-6239-8729
Kathryn E HatchellMedical Affairs, Invitae, San Francisco, CA 94103, USA.ORCID 0000-0003-0849-7018
Sarah M NielsenMedical Affairs, Invitae, San Francisco, CA 94103, USA.
Brandie HealdMedical Affairs, Invitae, San Francisco, CA 94103, USA.ORCID 0000-0003-4227-3675
Ariel A BensonDepartment of Gastroenterology, Hadassah Medical Center, Jerusalem 91120, Israel.ORCID 0000-0002-3138-8568
Eitan FriedmanThe Meirav Center High Risk Clinic, Sheba Medical Center, Ramat-Gan 52621, Israel.
Edward D EsplinMedical Affairs, Invitae, San Francisco, CA 94103, USA.ORCID 0000-0001-9205-3756
Lior H KatzDepartment of Gastroenterology, Hadassah Medical Center, Jerusalem 91120, Israel.
Hebrew University of Jerusalem · ILInvitae (United States) · USSheba Medical Center · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: APC I1307K has a higher prevalence among Ashkenazi Jews (AJ), and a two-fold increased risk for colorectal cancer (CRC) compared to non-Jewish populations. We assessed CRC and extracolonic malignancies among I1307K carriers from AJ and non-AJ whites (NAW). Methods: We compared the rate of I1307K in cancer patients who underwent germline genetic testing via a multi-gene panel with healthy subjects retrieved from the gnomAD database. Cases undergoing testing were not selected and testing was undertaken through a commercial laboratory. Results: Overall, 586/7624 (7.6%) AJ with cancer carried I1307K compared to 342/4918 (6.9%) in the AJ control group (p = NS). In the NAW, 318/141,673 (0.2%) cancer patients and 73/58,918 (0.1%) controls carried the variant [OR = 1.8, (95% CI 1.41−2.35), p < 0.001]. I1307K in NAW was associated with an increased risk of CRC [OR = 1.95, (95% CI 1.39−2.73), p < 0.01], melanoma [OR = 2.54, (95% CI 1.57−3.98)], breast [females, OR = 1.73, (95% CI 1.18−2.65), p < 0.01], and prostate cancer [males, OR = 2.42, (95% CI 1.45−3.94), p < 0.01]. Among AJ, the variant increased the risk for CRC [OR = 1.67, (95% CI 1.36−2.05), p < 0.001] and renal cancer [OR = 1.64, (95% CI 1.04−2.47)]. AJ men had a higher risk for any cancer [OR = 1.32, (95% CI 1.05−1.66), p < 0.05] and melanoma [OR = 2.04, (95% CI 1.24−3.22); p < 0.05]. Conclusions: This is the most extensive study to date conducted on I1307K carriers, although it is amenable to selection bias. NAW carrying I1307K had a higher risk of any cancer and several specific cancer types, whereas AJ carrying the variant had a risk for only a few select cancers. Our data add to the research base on I1307 carriers concerning future risk management.

Indexed as

APC I1307KAshkenazi jewscancerCRC

Identifiers

PMID36497357
PMCPMC9740723
OpenAlexW4310363571

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.