Evidence map›Paper›PMID 29859674›Full record

ArticlePancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.]2018

Known genetic susceptibility factors for chronic pancreatitis in patients of European ancestry are rare in patients of African ancestry.

Anna Evans Phillips, Jessica LaRusch, Phil Greer, Judah Abberbock, Samer Alkaade, Stephen T Amann, Michelle A Anderson, John Baillie, Peter A Banks, Randall E Brand and 17 more

Open access · greenAbstract read
In one paragraph

Article in Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.], 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 2 pooled it
2.6field-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

16 citing papers in PubMed, 2 syntheses or guidelines pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Health Inequities in Pancreatic Disorders in the Black/African American Community.Journal of racial and ethnic health disparities · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. Acute pancreatitis precedes chronic pancreatitis in the majority of patients: Results from the NAPS2 consortium.Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] · 2022
    Article
  9. Article
  10. Differences in Age at Onset of Symptoms, and Effects of Genetic Variants, in Patients With Early vs Late-Onset Idiopathic Chronic Pancreatitis in a North American Cohort.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2021
    Article
  11. Divergent trends in lifetime drinking and smoking between Black and White Americans diagnosed with chronic pancreatitis.Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] · 2020
    Article
  12. Article
  13. Article
  14. Review
  15. Lifetime Drinking History of Persons With Chronic Pancreatitis.Alcohol and alcoholism (Oxford, Oxfordshire) · 2019
    Article
  16. Article
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

27 authors at 18 institutions in 1 country.

Anna Evans PhillipsDepartment of Medicine, University of Pittsburgh, Pittsburgh, PA, United States.
Jessica LaRuschDepartment of Medicine, University of Pittsburgh, Pittsburgh, PA, United States; Ariel Precision Medicine, Pittsburgh PA, United States.
Phil GreerDepartment of Medicine, University of Pittsburgh, Pittsburgh, PA, United States.
Judah AbberbockDepartment of Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, United States.
Samer AlkaadeDepartment of Medicine, Saint Louis University, St. Louis, MO, United States.
Stephen T AmannDigestive Health Specialists, Tupelo, MS, United States.
Michelle A AndersonDepartment of Medicine, University of Michigan, Ann Arbor, MI, United States.
John BaillieDepartment of Medicine, Virginia Commonwealth University, Richmond, VA, United States.
Peter A BanksDepartment of Medicine, Brigham and Women's Hospital, Boston, MA, United States.
Randall E BrandDepartment of Medicine, University of Pittsburgh, Pittsburgh, PA, United States.
Darwin ConwellDepartment of Medicine, Ohio State University, Columbus, OH, United States.
Gregory A CotéDepartment of Medicine, Medical University of South Carolina, Charleston, SC, United States.
Christopher E ForsmarkDepartment of Medicine, University of Florida, Gainesville, FL, United States.
Timothy B GardnerDepartment of Medicine, Dartmouth Hitchcock Medical Center, Lebanon, NH, United States.
Andres GelrudDepartment of Medicine, University of Chicago, Chicago, IL, United States.
Nalini GudaGI Associates LLC, Aurora Health Care, St. Luke's Medical Center, Milwaukee, WI, United States.
Michele LewisDepartment of Medicine, Mayo Clinic, Jacksonville, FL, United States.
Mary E MoneyWashington County Hospital, Hagerstown, MD, United States.
Thiruvengadam MunirajDepartment of Medicine, Griffin Hospital, Yale Affiliate, New Haven, CT, United States.
Bimaljit S SandhuRichmond Gastroenterology Associates, St. Mary's Hospital, Richmond, VA, United States.
Stuart ShermanDepartment of Medicine, Indiana University, Indianapolis, IN, United States.
Vikesh K SinghDepartment of Medicine, Johns Hopkins Medical Institutions, Baltimore, MD, United States.
Adam SlivkaDepartment of Medicine, University of Pittsburgh, Pittsburgh, PA, United States.
Gong TangDepartment of Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, United States.
C Mel WilcoxDepartment of Medicine, University of Alabama Birmingham, Birmingham, AL, United States.
David C WhitcombDepartment of Medicine, University of Pittsburgh, Pittsburgh, PA, United States; Department of Cell Biology & Physiology, University of Pittsburgh, Pittsburgh, PA, United States; Department of Human Genetics, University of Pittsburgh, Pittsburgh, PA, United States.
Dhiraj YadavDepartment of Medicine, University of Pittsburgh, Pittsburgh, PA, United States. Electronic address: yadavd@upmc.edu.
University of Pittsburgh · USAurora Health Care · USBrigham and Women's Hospital · USDartmouth–Hitchcock Medical Center · USFlorida Digestive Health Specialists · USGriffin Hospital · USIndiana University – Purdue University Indianapolis · USJohns Hopkins University · USMedical University of South Carolina · USSaint Louis University · USSt. Mary's Hospital · USThe Ohio State University · USUniversity of Alabama at Birmingham · USUniversity of Chicago · USUniversity of Florida · USUniversity of Michigan · USVirginia Commonwealth University · USWinnMed · US

Funding

UNIVERSITY OF PITTSBURGH CLINICAL AND TRANSLATIONAL SCIENCE INSTITUTE: BPCAUL1RR024153 · NCRR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REIS, STEVEN E · 2006 to 2011
$73.9M
University of Pittsburgh Clinical and Translational Science InstituteUL1TR000005 · NCATS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REIS, STEVEN E · 2012 to 2015
$50.8M
UPMC Clinical Center for the Study of Chronic Pancreatitis and DiabetesU01DK108306 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Frederico G. S. Toledo, Dhiraj Yadav · 2015 to 2026
$6.4M
The Ohio State University Pancreatic Disorders Network (OSU-PDN)U01DK108327 · NIDDK · OHIO STATE UNIVERSITY · PI CONWELL, DARWIN LEWIS, HART, PHILIP A. · 2015 to 2024
$5.5M
Digestive Diseases Training ProgramT32DK063922 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ARTEEL, GAVIN E, YADAV, DHIRAJ · 2003 to 2022
$5.2M
North American Pancreatitis Study 2 (NAPS2)R01DK061451 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WHITCOMB, DAVID CLEMENT · 2002 to 2010
$4.9M
U-01 CONSORTIUM FOR THE STUDY OF CHRONIC PANCREATITIS,DIABETES AND PANCREATIC CANCER CLINICAL CENTERSU01DK108320 · NIDDK · UNIVERSITY OF FLORIDA · PI CUSI, KENNETH, FORSMARK, CHRISTOPHER E · 2015 to 2024
$4.6M
NAPS2-AS: Race Dependent Risk for PancreatitisR01DK077906 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI YADAV, DHIRAJ · 2010 to 2013
$2.3M
NAPS2 Continuation Genome Wide Association Study of PancreatitisR56DK061451 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WHITCOMB, DAVID CLEMENT · 2011 to 2011
$1.3M
NCATS NIH HHS UL1 TR000005NCRR NIH HHS UL1 RR024153NIDDK NIH HHS R01 DK061451NIDDK NIH HHS R01 DK077906NIDDK NIH HHS R56 DK061451NIDDK NIH HHS T32 DK063922NIDDK NIH HHS U01 DK108306NIDDK NIH HHS U01 DK108320NIDDK NIH HHS U01 DK108327
6 · The paper itself

Abstract

backgroundMultiple pathogenic genetic variants are associated with pancreatitis in patients of European (EA) and Asian ancestries, but studies on patients of African ancestry (AA) are lacking. We evaluated the prevalence of known genetic variations in African-American subjects in the US.

methodsWe studied prospectively enrolled controls (n = 238) and patients with chronic (CP) (n = 232) or recurrent acute pancreatitis (RAP) (n = 45) in the NAPS2 studies from 2000-2014 of self-identified AA. Demographic and phenotypic information was obtained from structured questionnaires. Ancestry and admixture were evaluated by principal component analysis (PCA). Genotyping was performed for pathogenic genetic variants in PRSS1, SPINK1, CFTR and CTRC. Prevalence of disease-associated variants in NAPS2 subjects of AA and EA was compared.

resultsWhen compared with CP subjects of EA (n = 862), prevalence of established pathogenic genetic variants was infrequent in AA patients with CP, overall (29 vs. 8.19%, OR 4.60, 95% CI 2.74-7.74, p < 0.001), and after stratification by alcohol etiology (p < 0.001). On PCA, AA cases were more heterogeneous but distinct from EA subjects; no difference was observed between AA subjects with and without CP-associated variants. Of 19 A A patients with CP who had pathogenic genetic variants, 2 had variants in PRSS1 (R122H, R122C), 4 in SPINK1 (all N34S heterozygotes), 12 in CFTR (2 CFTR

conclusionPathogenic genetic variants reported in EA patients are significantly less common in AA patients. Further studies are needed to determine the complex risk factors for AA subjects with pancreatitis.

Indexed as

African-AmericanAfrican ancestryAlcoholBlacksGeneticsPancreatitis

Identifiers

PMID29859674
PMCPMC8715541
OpenAlexW2803702975

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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.