The Clinical Genome Resource (ClinGen) Familial
Hypercholesterolemia Variant Curation Expert Panel consensus
guidelines for LDLR variant classification

J 2022

The Clinical Genome Resource (ClinGen) Familial Hypercholesterolemia Variant Curation Expert Panel consensus guidelines for LDLR variant classification

CHORA, J. R., M. A. IACOCCA, Lukas TICHÝ, H. WAND, C. L. KURTZ et. al.

Základní údaje

Originální název

The Clinical Genome Resource (ClinGen) Familial Hypercholesterolemia Variant Curation Expert Panel consensus guidelines for LDLR variant classification

Autoři

CHORA, J. R., M. A. IACOCCA, Lukas TICHÝ (203 Česká republika), H. WAND, C. L. KURTZ, H. ZIMMERMANN, A. LEON, M. WILLIAMS, C. L. HUMPHRIES, A. J. HOOPER, M. TRINDER, L. R. BRUNHAM, A. COSTA PEREIRA, C. E. JANNES, M. CHEN, J. CHONIS, J. WANG, S. KIM, T. JOHNSTON, Přemysl SOUČEK (203 Česká republika, domácí), Michal KRAMÁREK (703 Slovensko, domácí), S. E LEIGH., A. CARRIÉ, E. J. SIJBRANDS, R. A HEGELE., Tomáš FREIBERGER (203 Česká republika, domácí), J. W. KNOWLES a M. BOURBON

Vydání

Genetics In Medicine, United States, Lippincott, Williams & Wilkins, 2022, 1098-3600

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

30101 Human genetics

Stát vydavatele

Spojené státy

Utajení

není předmětem státního či obchodního tajemství

Odkazy

URL

Impakt faktor

Impact factor: 8.800

Kód RIV

RIV/00216224:14110/22:00126147

Organizační jednotka

Lékařská fakulta

DOI

http://dx.doi.org/10.1016/j.gim.2021.09.012

UT WoS

000797597400004

Klíčová slova anglicky

ACMG/AMP; ClinGen; Familial hypercholesterolemia; LDLR; Variant classification

Štítky

14110114, rivok

Příznaky

Mezinárodní význam, Recenzováno

Změněno: 28. 6. 2022 09:22, Mgr. Tereza Miškechová

Anotace

V originále

Purpose: In 2015, the American College of Medical Genetics and Genomics (ACMG) and the Association for Molecular Pathology (AMP) published consensus standardized guidelines for sequence-level variant classification in Mendelian disorders. To increase accuracy and consistency, the Clinical Genome Resource Familial Hypercholesterolemia (FH) Variant Curation Expert Panel was tasked with optimizing the existing ACMG/AMP framework for disease-specific classification in FH. In this study, we provide consensus recommendations for the most common FH-associated gene, LDLR, where >2300 unique FH-associated variants have been identified. Methods: The multidisciplinary FH Variant Curation Expert Panel met in person and through frequent emails and conference calls to develop LDLR-specific modifications of ACMG/AMP guidelines. Through iteration, pilot testing, debate, and commentary, consensus among experts was reached. Results: The consensus LDLR variant modifications to existing ACMG/AMP guidelines include (1) alteration of population frequency thresholds, (2) delineation of loss-of-function variant types, (3) functional study criteria specifications, (4) cosegregation criteria specifications, and (5) specific use and thresholds for in silico prediction tools, among others. Conclusion: Establishment of these guidelines as the new standard in the clinical laboratory setting will result in a more evidence-based, harmonized method for LDLR variant classification worldwide, thereby improving the care of patients with FH. (C) 2021 American College of Medical Genetics and Genomics.

Citovat

CHORA, J. R., M. A. IACOCCA, Lukas TICHÝ, H. WAND, C. L. KURTZ, H. ZIMMERMANN, A. LEON, M. WILLIAMS, C. L. HUMPHRIES, A. J. HOOPER, M. TRINDER, L. R. BRUNHAM, A. COSTA PEREIRA, C. E. JANNES, M. CHEN, J. CHONIS, J. WANG, S. KIM, T. JOHNSTON, Přemysl SOUČEK, Michal KRAMÁREK, S. E LEIGH., A. CARRIÉ, E. J. SIJBRANDS, R. A HEGELE., Tomáš FREIBERGER, J. W. KNOWLES a M. BOURBON. The Clinical Genome Resource (ClinGen) Familial Hypercholesterolemia Variant Curation Expert Panel consensus guidelines for LDLR variant classification. Genetics In Medicine. United States: Lippincott, Williams & Wilkins, 2022, roč. 24, č. 2, s. 293-306. ISSN 1098-3600. Dostupné z: https://dx.doi.org/10.1016/j.gim.2021.09.012.

@article{1863070,
   author = {Chora, J. R. and Iacocca, M. A. and Tichý, Lukas and Wand, H. and Kurtz, C. L. and Zimmermann, H. and Leon, A. and Williams, M. and Humphries, C. L. and Hooper, A. J. and Trinder, M. and Brunham, L. R. and Costa Pereira, A. and Jannes, C. E. and Chen, M. and Chonis, J. and Wang, J. and Kim, S. and Johnston, T. and Souček, Přemysl and Kramárek, Michal and Leigh., S. E and Carrié, A. and Sijbrands, E. J. and Hegele., R. A and Freiberger, Tomáš and Knowles, J. W. and Bourbon, M.},
   article_location = {United States},
   article_number = {2},
   doi = {http://dx.doi.org/10.1016/j.gim.2021.09.012},
   keywords = {ACMG/AMP; ClinGen; Familial hypercholesterolemia; LDLR; Variant classification},
   language = {eng},
   issn = {1098-3600},
   journal = {Genetics In Medicine},
   title = {The Clinical Genome Resource (ClinGen) Familial Hypercholesterolemia Variant Curation Expert Panel consensus guidelines for LDLR variant classification},
   url = {https://www.sciencedirect.com/science/article/pii/S109836002104140X?via%3Dihub},
   volume = {24},
   year = {2022}
}

TY  - JOUR
ID  - 1863070
AU  - Chora, J. R. - Iacocca, M. A. - Tichý, Lukas - Wand, H. - Kurtz, C. L. - Zimmermann, H. - Leon, A. - Williams, M. - Humphries, C. L. - Hooper, A. J. - Trinder, M. - Brunham, L. R. - Costa Pereira, A. - Jannes, C. E. - Chen, M. - Chonis, J. - Wang, J. - Kim, S. - Johnston, T. - Souček, Přemysl - Kramárek, Michal - Leigh., S. E - Carrié, A. - Sijbrands, E. J. - Hegele., R. A - Freiberger, Tomáš - Knowles, J. W. - Bourbon, M.
PY  - 2022
TI  - The Clinical Genome Resource (ClinGen) Familial Hypercholesterolemia Variant Curation Expert Panel consensus guidelines for LDLR variant classification
JF  - Genetics In Medicine
VL  - 24
IS  - 2
SP  - 293-306
EP  - 293-306
PB  - Lippincott, Williams & Wilkins
SN  - 10983600
KW  - ACMG/AMP
KW  - ClinGen
KW  - Familial hypercholesterolemia
KW  - LDLR
KW  - Variant classification
UR  - https://www.sciencedirect.com/science/article/pii/S109836002104140X?via%3Dihub
N2  - Purpose: In 2015, the American College of Medical Genetics and Genomics (ACMG) and the Association for Molecular Pathology (AMP) published consensus standardized guidelines for sequence-level variant classification in Mendelian disorders. To increase accuracy and consistency, the Clinical Genome Resource Familial Hypercholesterolemia (FH) Variant Curation Expert Panel was tasked with optimizing the existing ACMG/AMP framework for disease-specific classification in FH. In this study, we provide consensus recommendations for the most common FH-associated gene, LDLR, where >2300 unique FH-associated variants have been identified. Methods: The multidisciplinary FH Variant Curation Expert Panel met in person and through frequent emails and conference calls to develop LDLR-specific modifications of ACMG/AMP guidelines. Through iteration, pilot testing, debate, and commentary, consensus among experts was reached. Results: The consensus LDLR variant modifications to existing ACMG/AMP guidelines include (1) alteration of population frequency thresholds, (2) delineation of loss-of-function variant types, (3) functional study criteria specifications, (4) cosegregation criteria specifications, and (5) specific use and thresholds for in silico prediction tools, among others. Conclusion: Establishment of these guidelines as the new standard in the clinical laboratory setting will result in a more evidence-based, harmonized method for LDLR variant classification worldwide, thereby improving the care of patients with FH. (C) 2021 American College of Medical Genetics and Genomics.
ER  -

CHORA, J. R., M. A. IACOCCA, Lukas TICHÝ, H. WAND, C. L. KURTZ, H. ZIMMERMANN, A. LEON, M. WILLIAMS, C. L. HUMPHRIES, A. J. HOOPER, M. TRINDER, L. R. BRUNHAM, A. COSTA PEREIRA, C. E. JANNES, M. CHEN, J. CHONIS, J. WANG, S. KIM, T. JOHNSTON, Přemysl SOUČEK, Michal KRAMÁREK, S. E LEIGH., A. CARRIÉ, E. J. SIJBRANDS, R. A HEGELE., Tomáš FREIBERGER, J. W. KNOWLES a M. BOURBON. The Clinical Genome Resource (ClinGen) Familial Hypercholesterolemia Variant Curation Expert Panel consensus guidelines for LDLR variant classification. \textit{Genetics In Medicine}. United States: Lippincott, Williams \&{} Wilkins, 2022, roč.~24, č.~2, s.~293-306. ISSN~1098-3600. Dostupné z: https://dx.doi.org/10.1016/j.gim.2021.09.012.

Podrobný výpis o publikaci