Disentangling mechanisms behind the pleiotropic effects of proximal 16p11.2 BP4-5 CNVs

被引:1
|
作者
Auwerx, Chiara [1 ,2 ,3 ,4 ]
Moix, Samuel [2 ,3 ,4 ]
Kutalik, Zoltan [2 ,3 ,4 ]
Reymond, Alexandre [1 ]
机构
[1] Univ Lausanne, Ctr Integrat Genom, Lausanne, Switzerland
[2] Univ Lausanne, Dept Computat Biol, Lausanne, Switzerland
[3] Swiss Inst Bioinformat, Lausanne, Switzerland
[4] Univ Ctr Primary Care & Publ Hlth, Lausanne, Switzerland
基金
瑞士国家科学基金会;
关键词
COPY-NUMBER VARIATION; DELETIONS; DISORDER; AUTISM; MICRODELETION; PHENOTYPES; VARIANTS; COMPLEX; DOSAGE; KIDNEY;
D O I
10.1016/j.ajhg.2024.08.014
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Whereas 16p11.2 BP4-5 copy-number variants (CNVs) represent one of the most pleiotropic etiologies of genomic syndromes in both clinical and population cohorts, the mechanisms leading to such pleiotropy remain understudied. Identifying 73 deletion and 89 duplication carrier individuals among unrelated White British UK Biobank participants, we performed a phenome-wide association study (PheWAS) between the region's copy number and 117 complex traits and diseases, mimicking four dosage models. Forty-six phenotypes (39%) were affected by 16p11.2 BP4-5 CNVs, with the deletion-only, mirror, U-shape, and duplication-only models being the best fit for 30, 10, 4, and 2 phenotypes, respectively, aligning with the stronger deleteriousness of the deletion. Upon individually adjusting CNV effects for either body mass index (BMI), height, or educational attainment (EA), we found that sixteen testable deletion-driven associations-primarily with cardiovascular and metabolic traits-were BMI dependent, with EA playing a more subtle role and no association depending on height. Bidirectional Mendelian randomization supported that 13 out of these 16 associations were secondary consequences of the CNV's impact on BMI. For the 23 traits that remained significantly associated upon individual adjustment for mediators, matched-control analyses found that 10 phenotypes, including musculoskeletal traits, liver enzymes, fluid intelligence, platelet count, and pneumonia and acute kidney injury risk, remained associated under strict Bonferroni correction, with 10 additional nominally significant associations. These results paint a complex picture of 16p11.2 BP4-5's pleiotropic pattern that involves direct effects on multiple physiological systems and indirect co-morbidities consequential to the CNV's impact on BMI and EA, acting through trait-specific dosage mechanisms.
引用
收藏
页数:16
相关论文
共 7 条
  • [1] DISENTANGLING MECHANISMS BEHIND THE PLEIOTROPIC EFFECTS OF PROXIMAL 16P11.2 BP4-5 COPY-NUMBER VARIANTS
    Auwerx, Chiara
    Moix, Samuel
    Kutalik, Zoltan
    Reymond, Alexandre
    EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2024, 87 : 85 - 85
  • [2] The pleiotropic spectrum of proximal 16p11.2 CNVs
    Auwerx, Chiara
    Kutalik, Zoltan
    Reymond, Alexandre
    AMERICAN JOURNAL OF HUMAN GENETICS, 2024, 111 (11) : 2309 - 2346
  • [3] The Immune Signaling Adaptor LAT Contributes to the Neuroanatomical Phenotype of 16p11.2 BP2-BP3 CNVs
    Loviglio, Maria Nicla
    Arbogast, Thomas
    Jonch, Aia Elise
    Collins, Stephan C.
    Popadin, Konstantin
    Bonnet, Camille S.
    Giannuzzi, Giuliana
    Maillard, Anne M.
    Jacquemont, Sebastien
    Yalcin, Binnaz
    Katsanis, Nicholas
    Golzio, Christelle
    Reymond, Alexandre
    AMERICAN JOURNAL OF HUMAN GENETICS, 2017, 101 (04) : 564 - 577
  • [4] A Potential Contributory Role for Ciliary Dysfunction in the 16p11.2 600 kb BP4-BP5 Pathology
    Migliavacca, Eugenia
    Golzio, Christelle
    Maennik, Katrin
    Blumenthal, Ian
    Oh, Edwin C.
    Harewood, Louise
    Kosmicki, Jack A.
    Loviglio, Maria Nicla
    Giannuzzi, Giuliana
    Hippolyte, Loyse
    Maillard, Anne M.
    Alfaiz, Ali Abdullah
    van Haelst, Mieke M.
    Andrieux, Joris
    Gusella, James F.
    Daly, Mark J.
    Beckmann, Jacques S.
    Jacquemont, Sebastien
    Talkowski, Michael E.
    Katsanis, Nicholas
    Reymond, Alexandre
    AMERICAN JOURNAL OF HUMAN GENETICS, 2015, 96 (05) : 784 - 796
  • [5] Phenotypic spectrum in four cases presenting 16p11.2 reciprocal CNVs associated with additional rare gene variants - pleiotropic clinical outcomes
    Barbarii, Teodora
    Barca, Diana
    Tudorache, Raluca
    Nedelea, Florina Mihaela
    Cardos, Georgeta
    Craiu, Dana
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 : 472 - 472
  • [6] QUANTIFYING THE EFFECTS OF 16P11.2 CNVs ON BRAIN STRUCTURE, A MULTI-SITE 'GENETIC-FIRST'MRI STUDY
    Martin-Brevet, Sandra
    Rodriguez-Herreros, Borja
    Nielsen, Jared A.
    Moreau, Clara
    Modenato, Claudia
    Maillard, Anne M.
    Chung, Wendy K.
    Sherr, Elliott H.
    Spiro, John E.
    Beckmann, Jacques S.
    Hadjikhani, Nouchine
    Reymond, Alexandre
    Buckner, Randy L.
    Draganski, Bogdan
    Jacquemont, Sebastien
    EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2019, 29 : S859 - S860
  • [7] Rare Pathogenic Copy Number Variation in the 16p11.2 (BP4-BP5) Region Associated with Neurodevelopmental and Neuropsychiatric Disorders: A Review of the Literature
    Oliva-Teles, Natalia
    de Stefano, Maria Chiara
    Gallagher, Louise
    Rakic, Severin
    Jorge, Paula
    Cuturilo, Goran
    Markovska-Simoska, Silvana
    Borg, Isabella
    Wolstencroft, Jeanne
    Tumer, Zeynep
    Harwood, Adrian J.
    Kodra, Yllka
    Skuse, David
    INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH, 2020, 17 (24) : 1 - 16