Evidence map›Paper›PMID 34161860›Full record

ArticleEuropean journal of medical genetics2021

Facial analysis technology for the detection of Down syndrome in the Democratic Republic of the Congo.

Antonio R Porras, Matthew S Bramble, Kizito Mosema Be Amoti, D'Andre Spencer, Cécile Dakande, Hans Manya, Neerja Vashist, Esther Likuba, Joachim Mukau Ebwel, Céleste Musasa and 7 more

Open access · hybridAbstract read
In one paragraph

Article in European journal of medical genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

7 citing papers in PubMed, 16 citations in OpenAlex.

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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

17 authors at 6 institutions in 3 countries.

Antonio R PorrasSheikh Zayed Institute for Pediatric Surgical Innovation, Children's National Hospital, Washington, DC, USA; Department of Biostatistics and Informatics, Colorado School of Public Health, University of Colorado Anschutz Medical Campus, Aurora, CO, USA. Electronic address: antonio.porras@cuanschutz.edu.
Matthew S BrambleCenter for Genetic Medicine Research, Children's Research Institute, Children's National Hospital, Washington, DC, USA.
Kizito Mosema Be AmotiCenter for Genetic Medicine Research, Children's Research Institute, Children's National Hospital, Washington, DC, USA; Biamba Marie Mutombo Hospital, Kinshasa, Democratic Republic of the Congo; Institut National de Recherche Biomédicale (INRB), Kinshasa, Democratic Republic of the Congo.
D'Andre SpencerCenter for Genetic Medicine Research, Children's Research Institute, Children's National Hospital, Washington, DC, USA.
Cécile DakandeCenter for Genetic Medicine Research, Children's Research Institute, Children's National Hospital, Washington, DC, USA; Institut National de Recherche Biomédicale (INRB), Kinshasa, Democratic Republic of the Congo.
Hans ManyaCenter for Genetic Medicine Research, Children's Research Institute, Children's National Hospital, Washington, DC, USA; Institut National de Recherche Biomédicale (INRB), Kinshasa, Democratic Republic of the Congo.
Neerja VashistCenter for Genetic Medicine Research, Children's Research Institute, Children's National Hospital, Washington, DC, USA; Department of Genomics and Precision Medicine, George Washington University School of Medicine and Health Sciences, Washington, DC, USA.
Esther LikubaInstitut National de Recherche Biomédicale (INRB), Kinshasa, Democratic Republic of the Congo.
Joachim Mukau EbwelUniversité Pédagogique Nationale, Kinshasa, Democratic Republic of the Congo.
Céleste MusasaCenter for Genetic Medicine Research, Children's Research Institute, Children's National Hospital, Washington, DC, USA; Faculty of Medicine, Congo Protestant University, Kinshasa, Université Protestante au Congo.
Helen MalherbeUniversity of KwaZulu Natal, Durban, South Africa.
Bilal MohammedSheikh Zayed Institute for Pediatric Surgical Innovation, Children's National Hospital, Washington, DC, USA.
Carlos Tor-DiezSheikh Zayed Institute for Pediatric Surgical Innovation, Children's National Hospital, Washington, DC, USA.
Dieudonné Mumba NgoyiInstitut National de Recherche Biomédicale (INRB), Kinshasa, Democratic Republic of the Congo; Department of Tropical Medicine, University of Kinshasa, Kinshasa, Democratic Republic of the Congo.
Désiré Tshala KatumbayInstitut National de Recherche Biomédicale (INRB), Kinshasa, Democratic Republic of the Congo; Department of Neurology and School of Public Health, Oregon Health & Science University, Portland, OR, USA.
Marius George LinguraruSheikh Zayed Institute for Pediatric Surgical Innovation, Children's National Hospital, Washington, DC, USA; Departments of Radiology Pediatrics and Biomedical Engineering, George Washington University, Washington, DC, USA. Electronic address: mlingura@childrensnational.org.
Eric VilainCenter for Genetic Medicine Research, Children's Research Institute, Children's National Hospital, Washington, DC, USA; International Research Laboratory of Epigenetics, Data, Politics, Centre National de la Recherche Scientifique, Washington, DC, USA; Department of Genomics and Precision Medicine, George Washington University School of Medicine and Health Sciences, Washington, DC, USA. Electronic address: evilain@childrensnational.org.
Children's National · USNational Institute of Biomedical Research · CDChildren's Hospital Colorado · USUniversité Pédagogique Nationale · CDUniversité Protestante au Congo · CDUniversity of KwaZulu-Natal · ZA

Funding

Clinical and Translational Science Institute at Childrens NationalUL1TR001876 · NCATS · CHILDREN'S RESEARCH INSTITUTE · PI BELL, MICHAEL J · 2016 to 2021
$25.6M
University of California Launching Future Leaders in Global Health Research Training ProgramD43TW009343 · FIC · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CRAIG R COHEN, Sung-Jae Lee · 2017 to 2026
$14.7M
Clinical and Translational Science Institute at Childrens National-Mentored Career Development CoreKL2TR001877 · NCATS · CHILDREN'S RESEARCH INSTITUTE · PI LUBAN, NAOMI L · 2016 to 2020
$2.0M
Mobile Diagnosis of Congenital Genetic Conditions: A Model for Screening and Surveillance in Low-Resource SettingsR21HD102988 · NICHD · CHILDREN'S RESEARCH INSTITUTE · PI LINGURARU, MARIUS GEORGE, MUMBA, NGOYI · 2021 to 2021
$409k
FIC NIH HHS D43 TW009343NCATS NIH HHS UL1 TR001876NICHD NIH HHS R21 HD102988
6 · The paper itself

Abstract

Down syndrome is one of the most common chromosomal anomalies affecting the world's population, with an estimated frequency of 1 in 700 live births. Despite its relatively high prevalence, diagnostic rates based on clinical features have remained under 70% for most of the developed world and even lower in countries with limited resources. While genetic and cytogenetic confirmation greatly increases the diagnostic rate, such resources are often non-existent in many low- and middle-income countries, particularly in Sub-Saharan Africa. To address the needs of countries with limited resources, the implementation of mobile, user-friendly and affordable technologies that aid in diagnosis would greatly increase the odds of success for a child born with a genetic condition. Given that the Democratic Republic of the Congo is estimated to have one of the highest rates of birth defects in the world, our team sought to determine if smartphone-based facial analysis technology could accurately detect Down syndrome in individuals of Congolese descent. Prior to technology training, we confirmed the presence of trisomy 21 using low-cost genomic applications that do not need advanced expertise to utilize and are available in many low-resourced countries. Our software technology trained on 132 Congolese subjects had a significantly improved performance (91.67% accuracy, 95.45% sensitivity, 87.88% specificity) when compared to previous technology trained on individuals who are not of Congolese origin (p < 5%). In addition, we provide the list of most discriminative facial features of Down syndrome and their ranges in the Congolese population. Collectively, our technology provides low-cost and accurate diagnosis of Down syndrome in the local population.

Indexed as

FaciesAutomated Facial RecognitionDemocratic Republic of the CongoDeveloping CountriesDown SyndromeGenetic TestingHumansImage Processing, Computer-AssistedMachine LearningSensitivity and SpecificityCongoDown syndromeDRCFacial analysisMachine learningScreening

Identifiers

PMID34161860
PMCPMC8363515
OpenAlexW3176358524

What OpenQuestion holds

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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.