Evidence map›Paper›PMID 29862559›Full record

ArticleGenetic epidemiology2018

Analysis of pedigree data in populations with multiple ancestries: Strategies for dealing with admixture in Caribbean Hispanic families from the ADSP.

Rafael A Nafikov, Alejandro Q Nato, Harkirat Sohi, Bowen Wang, Lisa Brown, Andrea R Horimoto, Badri N Vardarajan, Sandra M Barral, Giuseppe Tosto, Richard P Mayeux and 3 more

Abstract read
In one paragraph

Article in Genetic epidemiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
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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

13 authors.

Rafael A NafikovDivision of Medical Genetics, Department of Medicine, University of Washington, Seattle, Washington.ORCID 0000-0002-5248-1059
Alejandro Q NatoDivision of Medical Genetics, Department of Medicine, University of Washington, Seattle, Washington.
Harkirat SohiDivision of Medical Genetics, Department of Medicine, University of Washington, Seattle, Washington.
Bowen WangDepartment of Statistics, University of Washington, Seattle, Washington.
Lisa BrownDepartment of Biostatistics, University of Washington, Seattle, Washington.
Andrea R HorimotoDivision of Medical Genetics, Department of Medicine, University of Washington, Seattle, Washington.
Badri N VardarajanDepartment of Neurology, Columbia University, New York, Washington.
Sandra M BarralDepartment of Neurology, Columbia University, New York, Washington.
Giuseppe TostoDepartment of Neurology, Columbia University, New York, Washington.
Richard P MayeuxDepartment of Neurology, Columbia University, New York, Washington.
Timothy A ThorntonDepartment of Biostatistics, University of Washington, Seattle, Washington.
Elizabeth BlueDivision of Medical Genetics, Department of Medicine, University of Washington, Seattle, Washington.
Ellen M WijsmanDivision of Medical Genetics, Department of Medicine, University of Washington, Seattle, Washington.ORCID 0000-0002-2725-6669

Funding

National Centralized Repository for Alzheimer's Disease and Related Dementias (NCRAD)U24AG021886 · NIA · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI TATIANA M. FOROUD · 2002 to 2026
$119.8M
THERAPEUTIC EFFECTS OF INTRA-NASAL INSULIN DETEMIRP50AG005136 · NIA · UNIVERSITY OF WASHINGTON · PI GRABOWSKI, THOMAS J. · 1985 to 2019
$57.2M
The National Institute on Aging (NIA) Late Onset of Alzheimer's Disease (LOAD) Family-Based Study (FBS)U24AG056270 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Gary Wayne Beecham, TATIANA M. FOROUD · 2017 to 2026
$31.4M
Neurobehavior, Neuropathology, and Risk Factors in Alzheimer's DiseaseT32AG052354 · NIA · UNIVERSITY OF WASHINGTON · PI Brian C. Kraemer, ELAINE R. PESKIND · 2016 to 2026
$6.7M
Collaborative GWAS of Dementia, AD and related MRI and Cognitive EndophenotypesR01AG033193 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI SESHADRI, SUDHA · 2009 to 2016
$4.4M
Methods for the Genetic Epidemiology of Complex TraitsR37GM046255 · NIGMS · UNIVERSITY OF WASHINGTON · PI THOMPSON, ELIZABETH ALISON · 2008 to 2017
$4.2M
Sequence-based Discovery of AD Risk & Protective AllelesU01AG049506 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI BOERWINKLE, ERIC A., SALERNO, WILLIAM JAMES · 2014 to 2017
$3.8M
Genetic Studies of Alzheimer's Disease in Caribbean HispanicsRF1AG015473 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MAYEUX, RICHARD P · 2015 to 2018
$3.3M
CHARGE: Identifying Risk & Protective SNV for AD in ADSP Case-control SampleU01AG049505 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI SESHADRI, SUDHA · 2014 to 2017
$3.0M
Sequence-based Discovery of AD Risk & Protective AllelesU01AG049507 · NIA · UNIVERSITY OF WASHINGTON · PI WIJSMAN, ELLEN M · 2014 to 2017
$2.9M
ADSP Follow-up in Multi-Ethnic Cohorts via Endophenotypes, Omics & Model SystemsU01AG052409 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI FORNAGE, MYRIAM, SESHADRI, SUDHA · 2016 to 2020
$1.6M
NIA NIH HHS P50 AG005136NIA NIH HHS R01 AG033193NIA NIH HHS RF1 AG015473NIA NIH HHS T32 AG052354NIA NIH HHS U01 AG049505NIA NIH HHS U01 AG049506NIA NIH HHS U01 AG049507NIA NIH HHS U01 AG052409NIA NIH HHS U24 AG021886NIA NIH HHS U24 AG056270NIGMS NIH HHS R37 GM046255NIH HHS 5P50AG005136-34NIH HHS 5U01AG049505-04NIH HHS 5U01AG049506-04NIH HHS 5U01AG049507-04U.S. Department of Health and Human Services
6 · The paper itself

Abstract

Multipoint linkage analysis is an important approach for localizing disease-associated loci in pedigrees. Linkage analysis, however, is sensitive to misspecification of marker allele frequencies. Pedigrees from recently admixed populations are particularly susceptible to this problem because of the challenge of accurately accounting for population structure. Therefore, increasing emphasis on use of multiethnic samples in genetic studies requires reevaluation of best practices, given data currently available. Typical strategies have been to compute allele frequencies from the sample, or to use marker allele frequencies determined by admixture proportions averaged over the entire sample. However, admixture proportions vary among pedigrees and throughout the genome in a family-specific manner. Here, we evaluate several approaches to model admixture in linkage analysis, providing different levels of detail about ancestral origin. To perform our evaluations, for specification of marker allele frequencies, we used data on 67 Caribbean Hispanic admixed families from the Alzheimer's Disease Sequencing Project. Our results show that choice of admixture model has an effect on the linkage analysis results. Variant-specific admixture proportions, computed for individual families, provide the most detailed regional admixture estimates, and, as such, are the most appropriate allele frequencies for linkage analysis. This likely decreases the number of false-positive results, and is straightforward to implement.

Indexed as

Gene PoolPedigreePhylogenySequence Analysis, DNAAlzheimer DiseaseCaribbean RegionEthnicityFamilyFemaleGene FrequencyGenetic LinkageGenetics, PopulationHispanic or LatinoHumansLod ScoreMalecomplex traitlarge pedigreeslate-onset diseaseMarkov Chain Monte Carlomissing data

Identifiers

PMID29862559
PMCPMC6160322

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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.