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GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases.

Hellen LesmannAlexander HustinxShahida MoosaHannah KlinkhammerElaine MarchiPilar CaroIbrahim M AbdelrazekJean Tori PantelMerle Ten HagenMeow-Keong ThongRifhan Azwani Binti MazlanSok Kun TaeTom KamphansWolfgang MeiswinkelJing-Mei LiBehnam JavanmardiAlexej KnausAnnette UwinezaCordula KnoppTinatin TkemaladzeMiriam ElbrachtLarissa MatternRami Abou JamraClara VelmansVincent StrehlowMaureen JacobAngela PeronCristina DiasBeatriz Carvalho NunesThainá VilellaIsabel Furquim PinheiroChong Ae KimMaria Isabel MelaragnoHannah WeilandSophia KaptainKarolina ChwiałkowskaMiroslaw KwasniewskiRamy SaadSarah WiethoffHimanshu GoelClara TangAnna HauTahsin Stefan BarakatPrzemysław PanekAmira NabilJulia SuhFrederik BraunIsrael GomyLuisa AverdunkEkanem EkureGaber BergantBorut PeterlinClaudio GrazianoNagwa GaboonMoisés O Fiesco-RoaAlessandro Mauro SpinelliNina-Maria WilpertPrasit PhowthongkumNergis GüzelTobias B HaackRana BitarAndreas TzschachAgusti Rodriguez-PalmeroTheresa BrunetSabine Rudnik-SchönebornSilvina Noemi Contreras-CapetilloAva OberlackCarole Samango-SprouseTeresa SadeghinMargaret OlayaKonrad PlatzerArtem O BorovikovFranziska SchnabelLara HeuftVera HerrmannRenske OegemaNour ElkhateebSheetal KumarKatalin KomlosiKhoushoua MohamedSilvia KalantariFabio SirchiaAntonio F Martinez-MonsenyMatthias HöllerLouiza ToutounaAmal MohamedAmaia Lasa-AranzastiJohn Andrew SayerNadja EhmkeMagdalena DanyelHenrike SczakielSarina SchwartzmannFelix BoschannMax ZhaoRonja AdamLara EinickeDenise HornKee Seang ChewChoy Chen KamMiray KarakoyunBen Pode-ShakkedAviva EliyahuRachel RockTeresa CarrionOdelia ChorinYuri A ZarateMarcelo Martinez ContiMert KarakayaMoon Ley TungBharatendu ChandraArjan BoumanAimé Z LumakaNaveed WasifMarwan S ShinawiPatrick R BlackburnTianyun WangTim NiehuesAxel SchmidtRegina Rita RothDagmar WieczorekPing HuRebekah L WaikelSuzanna E Ledgister HanchardGehad ElmakkawySylvia SafwatFrédéric EbsteinElke KrügerSébastien KüryStephane BezieauAnnabelle ArltEric OlingerFelix MarbachDong LiLucie DupuisRoberto Mendoza-LondonoSofia Douzgou HougeDenisa WeisBrian Hon-Yin ChungChristopher C Y MakHülya KayseriliNursel ElciogluAyca AykutPeli Özlem Şimşek-KiperNina BögershausenBernd WollnikHeidi Beate BentzenIngo KurthChristian NetzerAleksandra Jezela-StanekKoen DevriendtKaren W GrippMartin MückeAlain VerloesChristian P SchaafChristoffer NellåkerBenjamin D SolomonMarkus M NöthenEbtesam AbdallaGholson J LyonPeter M KrawitzTzung-Chien Hsieh
Published in: Research square (2024)
The most important factor that complicates the work of dysmorphologists is the significant phenotypic variability of the human face. Next-Generation Phenotyping (NGP) tools that assist clinicians with recognizing characteristic syndromic patterns are particularly challenged when confronted with patients from populations different from their training data. To that end, we systematically analyzed the impact of genetic ancestry on facial dysmorphism. For that purpose, we established the GestaltMatcher Database (GMDB) as a reference dataset for medical images of patients with rare genetic disorders from around the world. We collected 10,980 frontal facial images - more than a quarter previously unpublished - from 8,346 patients, representing 581 rare disorders. Although the predominant ancestry is still European (67%), data from underrepresented populations have been increased considerably via global collaborations (19% Asian and 7% African). This includes previously unpublished reports for more than 40% of the African patients. The NGP analysis on this diverse dataset revealed characteristic performance differences depending on the composition of training and test sets corresponding to genetic relatedness. For clinical use of NGP, incorporating non-European patients resulted in a profound enhancement of GestaltMatcher performance. The top-5 accuracy rate increased by +11.29%. Importantly, this improvement in delineating the correct disorder from a facial portrait was achieved without decreasing the performance on European patients. By design, GMDB complies with the FAIR principles by rendering the curated medical data findable, accessible, interoperable, and reusable. This means GMDB can also serve as data for training and benchmarking. In summary, our study on facial dysmorphism on a global sample revealed a considerable cross ancestral phenotypic variability confounding NGP that should be counteracted by international efforts for increasing data diversity. GMDB will serve as a vital reference database for clinicians and a transparent training set for advancing NGP technology.
Keyphrases
  • end stage renal disease
  • newly diagnosed
  • chronic kidney disease
  • ejection fraction
  • prognostic factors
  • endothelial cells
  • electronic health record
  • healthcare
  • big data
  • gene expression
  • single cell
  • machine learning