TY - JOUR
T1 - Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia
AU - Sønderby, Ida E.
AU - Gústafsson, Ómar
AU - Doan, Nhat Trung
AU - Hibar, Derrek P.
AU - Martin-Brevet, Sandra
AU - Abdellaoui, Abdel
AU - Ames, David
AU - Amunts, Katrin
AU - Andersson, Michael
AU - Armstrong, Nicola J.
AU - Bernard, Manon
AU - Blackburn, Nicholas
AU - Blangero, John
AU - Boomsma, Dorret I.
AU - Bralten, Janita
AU - Brattbak, Hans Richard
AU - Brodaty, Henry
AU - Brouwer, Rachel M.
AU - Bülow, Robin
AU - Calhoun, Vince
AU - Caspers, Svenja
AU - Cavalleri, Gianpiero
AU - Chen, Chi Hua
AU - Cichon, Sven
AU - Ciufolini, Simone
AU - Corvin, Aiden
AU - Crespo-Facorro, Benedicto
AU - Curran, Joanne E.
AU - Dale, Anders M.
AU - Dalvie, Shareefa
AU - Dazzan, Paola
AU - de Geus, Eco J.C.
AU - de Zubicaray, Greig I.
AU - de Zwarte, Sonja M.C.
AU - Delanty, Norman
AU - den Braber, Anouk
AU - Desrivières, Sylvane
AU - Donohoe, Gary
AU - Draganski, Bogdan
AU - Ehrlich, Stefan
AU - Espeseth, Thomas
AU - Fisher, Simon E.
AU - Franke, Barbara
AU - Frouin, Vincent
AU - Fukunaga, Masaki
AU - Gareau, Thomas
AU - Glahn, David C.
AU - Grabe, Hans
AU - Groenewold, Nynke A.
AU - Haavik, Jan
AU - Håberg, Asta
AU - Hashimoto, Ryota
AU - Hehir-Kwa, Jayne Y.
AU - Heinz, Andreas
AU - Hillegers, Manon H.J.
AU - Hoffmann, Per
AU - Holleran, Laurena
AU - Hottenga, Jouke Jan
AU - Hulshoff, Hilleke E.
AU - Ikeda, Masashi
AU - Jahanshad, Neda
AU - Jernigan, Terry
AU - Jockwitz, Christiane
AU - Johansson, Stefan
AU - Jonsdottir, Gudrun A.
AU - Jönsson, Erik G.
AU - Kahn, Rene
AU - Kaufmann, Tobias
AU - Kelly, Sinead
AU - Kikuchi, Masataka
AU - Knowles, Emma E.M.
AU - Kolskår, Knut K.
AU - Kwok, John B.
AU - Hellard, Stephanie Le
AU - Leu, Costin
AU - Liu, Jingyu
AU - Lundervold, Astri J.
AU - Lundervold, Arvid
AU - Martin, Nicholas G.
AU - Mather, Karen
AU - Mathias, Samuel R.
AU - McCormack, Mark
AU - McMahon, Katie L.
AU - McRae, Allan
AU - Milaneschi, Yuri
AU - Moreau, Clara
AU - Morris, Derek
AU - Mothersill, David
AU - Mühleisen, Thomas W.
AU - Murray, Robin
AU - Nordvik, Jan E.
AU - Nyberg, Lars
AU - Olde Loohuis, Loes M.
AU - Ophoff, Roel
AU - Paus, Tomas
AU - Pausova, Zdenka
AU - Penninx, Brenda
AU - Peralta, Juan M.
AU - Pike, Bruce
AU - Prieto, Carlos
AU - Pudas, Sara
AU - Quinlan, Erin
AU - Quintana, Daniel S.
AU - Reinbold, Céline S.
AU - Marques, Tiago Reis
AU - Reymond, Alexandre
AU - Richard, Genevieve
AU - Rodriguez-Herreros, Borja
AU - Roiz-Santiañez, Roberto
AU - Rokicki, Jarek
AU - Rucker, James
AU - Sachdev, Perminder
AU - Sanders, Anne Marthe
AU - Sando, Sigrid B.
AU - Schmaal, Lianne
AU - Schofield, Peter R.
AU - Schork, Andrew J.
AU - Schumann, Gunter
AU - Shin, Jean
AU - Shumskaya, Elena
AU - Sisodiya, Sanjay
AU - Steen, Vidar M.
AU - Stein, Dan J.
AU - Steinberg, Stacy
AU - Strike, Lachlan
AU - Teumer, Alexander
AU - Thalamuthu, Anbu
AU - Tordesillas-Gutierrez, Diana
AU - Turner, Jessica
AU - Ueland, Torill
AU - Uhlmann, Anne
AU - Ulfarsson, Magnus O.
AU - van ’t Ent, Dennis
AU - van der Meer, Dennis
AU - van Haren, Neeltje E.M.
AU - Vaskinn, Anja
AU - Vassos, Evangelos
AU - Walters, G. Bragi
AU - Wang, Yunpeng
AU - Wen, Wei
AU - Whelan, Christopher D.
AU - Wittfeld, Katharina
AU - Wright, Margie
AU - Yamamori, Hidenaga
AU - Zayats, Tetyana
AU - Agartz, Ingrid
AU - Westlye, Lars T.
AU - Jacquemont, Sébastien
AU - Djurovic, Srdjan
AU - Stefánsson, Hreinn
AU - Stefánsson, Kári
AU - Thompson, Paul
AU - Andreassen, Ole A.
AU - ENIGMA-CNV working group
PY - 2020/3/1
Y1 - 2020/3/1
N2 - Carriers of large recurrent copy number variants (CNVs) have a higher risk of developing neurodevelopmental disorders. The 16p11.2 distal CNV predisposes carriers to e.g., autism spectrum disorder and schizophrenia. We compared subcortical brain volumes of 12 16p11.2 distal deletion and 12 duplication carriers to 6882 non-carriers from the large-scale brain Magnetic Resonance Imaging collaboration, ENIGMA-CNV. After stringent CNV calling procedures, and standardized FreeSurfer image analysis, we found negative dose-response associations with copy number on intracranial volume and on regional caudate, pallidum and putamen volumes (β = −0.71 to −1.37; P < 0.0005). In an independent sample, consistent results were obtained, with significant effects in the pallidum (β = −0.95, P = 0.0042). The two data sets combined showed significant negative dose-response for the accumbens, caudate, pallidum, putamen and ICV (P = 0.0032, 8.9 × 10−6, 1.7 × 10− 9, 3.5 × 10−12 and 1.0 × 10−4, respectively). Full scale IQ was lower in both deletion and duplication carriers compared to non-carriers. This is the first brain MRI study of the impact of the 16p11.2 distal CNV, and we demonstrate a specific effect on subcortical brain structures, suggesting a neuropathological pattern underlying the neurodevelopmental syndromes.
AB - Carriers of large recurrent copy number variants (CNVs) have a higher risk of developing neurodevelopmental disorders. The 16p11.2 distal CNV predisposes carriers to e.g., autism spectrum disorder and schizophrenia. We compared subcortical brain volumes of 12 16p11.2 distal deletion and 12 duplication carriers to 6882 non-carriers from the large-scale brain Magnetic Resonance Imaging collaboration, ENIGMA-CNV. After stringent CNV calling procedures, and standardized FreeSurfer image analysis, we found negative dose-response associations with copy number on intracranial volume and on regional caudate, pallidum and putamen volumes (β = −0.71 to −1.37; P < 0.0005). In an independent sample, consistent results were obtained, with significant effects in the pallidum (β = −0.95, P = 0.0042). The two data sets combined showed significant negative dose-response for the accumbens, caudate, pallidum, putamen and ICV (P = 0.0032, 8.9 × 10−6, 1.7 × 10− 9, 3.5 × 10−12 and 1.0 × 10−4, respectively). Full scale IQ was lower in both deletion and duplication carriers compared to non-carriers. This is the first brain MRI study of the impact of the 16p11.2 distal CNV, and we demonstrate a specific effect on subcortical brain structures, suggesting a neuropathological pattern underlying the neurodevelopmental syndromes.
UR - http://www.scopus.com/inward/record.url?scp=85054383956&partnerID=8YFLogxK
U2 - 10.1038/s41380-018-0118-1
DO - 10.1038/s41380-018-0118-1
M3 - Article
C2 - 30283035
AN - SCOPUS:85054383956
VL - 25
SP - 584
EP - 602
JO - Molecular Psychiatry
JF - Molecular Psychiatry
SN - 1359-4184
IS - 3
ER -