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Singleton, Andrew

https://orcid.org/0000-0001-5606-700X

Mayo Clinic

Global Parkinson's Genetics Program (GP2) Chevy Chase Maryland USA

Citations 24

Fine‐Mapping of SNCA in Rapid Eye Movement Sleep Behavior Disorder and Overt Synucleinopathies
Krohn, Lynne , Wu, Richard Y. J. , Heilbron, Karl , Ruskey, Jennifer A. , Laurent, Sandra B., Blauwendraat, Cornelis , Alam, Armaghan , Arnulf, Isabelle , Hu, Michele T.M., Dauvilliers, Yves , Högl, Birgit , Toft, Mathias , Bjørnarå, Kari Anne , Stefani, Ambra , Holzknecht, Evi , Monaca, Christelle, Abril, Beatriz, Young, Peter , Heidbreder, Anna , Mollenhauer, Brit , Sixel‐Döring, Friederike , Trenkwalder, Claudia , Šonka, Karel , Figorilli, Michela , Puligheddu, Monica , Dijkstra, Femke , Viaene, Mineke , Oertel, Wolfang, Toffoli, Marco , Gagnon, Jean‐François , Nalls, Mike A., Singleton, Andrew B., Désautels, Alex , Montplaisir, Jacques , Ross, Owen A. , Dupré, Nicolas , Postuma, Ronald B., Antelmi, Elena , Cochen De Cock, Valérie , Rouleau, Guy Armand , Gan-Or, Ziv , Ross, Owen A , Dauvilliers, Yves , Stefani, Ambra , Toft, Mathias , Arnulf, Isabelle , Högl, Birgit , Sonka, Karel , Figorilli, Michela , Puligheddu, Monica , Heidbreder, Anna , Plazzi, Giuseppe , Antelmi, Elena , Ferini-Strambi, Luigi , Kemlink, David , Gigli, Gian Luigi , Valente, Mariarosaria , Singleton, Andrew , Cannon, Paul, Boeve, Bradley F. , Fon, Edward A , Postuma, Ronald B. , Pihlstrøm, Lasse , Gan‐Or, Ziv

Annals of Neurology | January 24, 2020 | Volume: 87 | Issue: 4 | Pages: 584-598

10.1002/ana.25687 Get It

Objective Rapid eye movement sleep behavior disorder (RBD) is a prodromal synucleinopathy, as >80% will eventually convert to overt synucleinopathy. We performed an in‐depth analysis of the SNCA locus to identify RBD‐specific risk variants. Methods Full sequencing and genotyping of SNCA was performed in isolated/idiopathic RBD (iRBD, n = 1,076), Parkinson disease (PD, n = 1,013), dementia with Lewy bodies (DLB, n = 415), and control subjects (n = 6,155). The iRBD cases were diagnosed with RBD prior to neurodegeneration, although some have since converted. A replication cohort from 23andMe of PD patients with probable RBD (pRBD) was also analyzed (n = 1,782 cases; n = 131,250 controls). Adjusted logistic regression models and meta‐analyses were performed. Effects on conversion rate were analyzed in 432 RBD patients with available data using Kaplan–Meier survival analysis. Results A 5′‐region SNCA variant (rs10005233) was associated with iRBD (odds ratio [OR] = 1.43, p = 1.1E‐08), which was replicated in pRBD. This variant is in linkage disequilibrium (LD) with other 5′ risk variants across the different synucleinopathies. An independent iRBD‐specific suggestive association (rs11732740) was detected at the 3′ of SNCA (OR = 1.32, p = 4.7E‐04, not statistically significant after Bonferroni correction). Homozygous carriers of both iRBD‐specific SNPs were at highly increased risk for iRBD (OR = 5.74, p = 2E‐06). The known top PD‐associated variant (3′ variant rs356182) had an opposite direction of effect in iRBD compared to PD. Interpretation There is a distinct pattern of association at the SNCA locus in RBD as compared to PD, with an opposite direction of effect at the 3′ of SNCA . Several 5′ SNCA variants are associated with iRBD and with pRBD in overt synucleinopathies. ANN NEUROL 2020;87:584–598
Arguing against the proposed definition changes of PD
Duda, John E., Ferman, Tanis J. , Goldman, Jennifer G. , Growdon, John H., Hurtig, Howard I., Kaufer, Daniel , Kantarci, Kejal , Leverenz, James B. , Lippa, Carol F. , McKeith, Ian G. , Singleton, Andrew , Taylor, Angela , Tsuang, Debby W. , Zabetian, Cyrus P. , Boeve, Bradley F. , Dickson, Dennis W. , Galasko, Douglas , Galvin, James E. , López, Oscar L. , Weintraub, Daniel , Goldman, Jennifer G , Leverenz, James B , Kantarci, Kejal , Zabetian, Cyrus P , Ferman, Tanis J

Movement Disorders | August 5, 2016 | Volume: 31 | Issue: 11 | Pages: 1619-1622

10.1002/mds.26721 Get It

ABSTRACT As members of the Lewy Body Dementia Association Scientific Advisory Council, we aim to address some of the issues raised in the article titled “Time to Redefine PD? Introductory Statement of the MDS Task Force on the Definition of Parkinson's Disease.” In particular, we suggest that the 1‐year rule distinguishing Parkinson's disease dementia from dementia with Lewy bodies is worth maintaining because it serves an important purpose in clinical practice and clinical and basic science research and when helping the lay community understand the complexity of these different clinical phenotypes. Furthermore, we believe that adding an additional diagnostic label, “PD (dementia with Lewy bodies subtype),” will confuse rather than clarify the distinction between dementia with Lewy bodies and PD or PD dementia, and will not improve management or expedite therapeutic development. We present arguments supporting our contentions. © 2016 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society.
Identical twins with the C9orf72 repeat expansion are discordant for ALS
Xi, Zhengrui, Yunusova, Yana , Blitterswijk, Marka van , Dib, Samar, Ghani, Mahdi , Moreno, Danielle , Sato, Christine , Liang, Yan , Singleton, Andrew , Rademakers, Rosa , Zinman, Lorne , van Blitterswijk, Marka, Robertson, Janice, Robertson, Janice , Rogaeva, Ekaterina A. , van Blitterswijk, Marka

Neurology | September 11, 2014 | Volume: 83 | Issue: 16 | Pages: 1476-1478

10.1212/wnl.0000000000000886 Get It

Does trans size matter in Huntington disease?
Ross, Owen A. , Singleton, Andrew , Ross, Owen A

Neurology | February 9, 2012 | Volume: 78 | Issue: 10 | Pages: 686-687

10.1212/wnl.0b013e3182494d77 Get It

Siblings With Ischemic Stroke Study
Nalls, Michael A., Matarín, Mar, Brott, Thomas G. , Brown, Robert D. , Hardy, John , Kissela, Brett , Rich, Stephen S. , Singleton, Andrew , Hernandez, Dena G., Ferrucci, Luigi , Pearce, Kerra, Keller, M., Worrall, Bradford B. , Investigators*, for the Siblings With Ischemic Stroke Study, Burgin, W. Scott , Meschia, James F. , Investigators*, for the Siblings With Ischemic Stroke Study, Rich, Stephen S , Hardy, John , Ferrucci, Luigi

Stroke | September 23, 2011 | Volume: 42 | Issue: 10 | Pages: 2726-2732

10.1161/strokeaha.111.620484 Get It

Background and Purpose— Ischemic stroke has a strong familial component to risk. The Siblings With Ischemic Stroke Study (SWISS) is a genome-wide, family-based analysis that included use of imputed genotypes. The Siblings With Ischemic Stroke Study was conducted to examine the associations between single-nucleotide polymorphisms (SNPs) and risk of stroke and stroke subtypes within pairs. Methods— The Siblings With Ischemic Stroke Study enrolled 312 probands with ischemic stroke from 70 US and Canadian centers. Affected siblings were ascertained by centers and confirmed by central record review; unaffected siblings were ascertained by telephone contact. Ischemic stroke was subtyped according to Trial of Org 10172 in Acute Stroke Treatment criteria. Genotyping was performed with an Illumina 610 quad array (probands) and an Illumina linkage V array (affected siblings). SNPs were imputed by using 1000 Genomes Project data and MACH software. Family-based association analyses were conducted by using the sibling transmission-disequilibrium test. Results— For all pairs, the correlation of age at stroke within pairs of affected siblings was r =0.83 (95% CI, 0.78–0.86; P <2.2×10 −16 ). The correlation did not differ substantially by subtype. The concordance of stroke subtypes among affected pairs was 33.8% (kappa=0.13; P =5.06×10 −4 ) and did not differ by age at stroke in the proband. Although no SNP achieved genome-wide significance for risk of ischemic stroke, there was clustering of the most associated SNPs on chromosomes 3p and 6p. Conclusions— Stroke subtype and age at stroke in affected sibling pairs exhibit significant clustering. No individual SNP reached genome-wide significance. However, 2 promising candidate loci were, although these risk loci warrant further examination in larger sample collections.
Candidate Gene Polymorphisms for Ischemic Stroke
Matarín, Mar, Brown, W. Mark , Dena, Hernandez, Britton, Angela, Vrieze, Fabienne Wavrant De, Brott, Thomas G. , Brown, Robert D., Worrall, Bradford B. , Case, L. Douglas, Metter, E. Jeffrey , Gamble, Dale M., Hardy, John , Rich, Stephen S. , Singleton, Andrew , Chanock, Stephen Jacob , Ferrucci, Luigi , Meschia, James F. , Rich, Stephen S , Hardy, John

Stroke | September 4, 2009 | Volume: 40 | Issue: 11 | Pages: 3436-3442

10.1161/strokeaha.109.558015 Get It

Background and Purpose— Ischemic stroke (IS) is a multifactorial disorder with strong evidence from twin, family, and animal model studies suggesting a genetic influence on risk and prognosis. Several candidate genes for IS have been proposed, but few have been replicated. We investigated the contribution of 67 candidate genes (369 single nucleotide polymorphisms [SNPs]) on the risk of IS in a North American population of European descent. Methods— Two independent studies were performed. In the first, 342 SNPs from 52 candidate genes were genotyped in 307 IS cases and 324 control subjects. The SNPs significantly associated with IS were tested for replication in another cohort of 583 IS cases and 270 control subjects. In the second study, 212 SNPs from 62 candidate genes were analyzed in 710 IS cases with subtyping available and 3751 control subjects. Results— None of the candidate genes (SNPs) were significantly associated with IS risk independent of known stroke risk factors after correction for multiple hypotheses testing. Conclusion— These results are consistent with previous meta-analyses that demonstrate an absence of genetic association of variants in plausible candidate genes with IS risk. Our study suggests that the effect of the investigated SNPs may be weak or restricted to specific populations or IS subtypes.
Meeting Report: Consensus Statement—Parkinson’s Disease and the Environment: Collaborative on Health and the Environment and Parkinson’s Action Network (CHE PAN) Conference 26–28 June 2007
Bronstein, Jeff M. , Carvey, Paul M., Chen, Honglei , Cory‐Slechta, Deborah A. , Monte, Donato A. Di , Duda, John E. , English, Paul , Goldman, Samuel M. , Grate, Stephen J., Hoppin, Jane A. , Jewell, Sarah A. , Kamel, Freya , Langston, J. William, Logroscino, Giancarlo , Nelson, Lorene M. , Ravina, Bernard, Rocca, Walter A. , Ross, G. Webster, Schettler, Ted, Schwarzschild, Michael A. , Scott, Bill, Seegal, Richard F., Singleton, Andrew , Steenland, Kyle , Eeden, Stephen Van Den, Weisskopf, Marc G. , Hansen, Johnni , Koroshetz, Walter J. , Tanner, Caroline M. , Logroscino, Giancarlo

Environmental Health Perspectives | August 25, 2008 | Volume: 117 | Issue: 1 | Pages: 117-121

10.1289/ehp.11702 Get It

Abstract Background Parkinson’s disease (PD) is the second most common neurodegenerative disorder. People with PD, their families, scientists, health care providers, and the general public are increasingly interested in identifying environmental contributors to PD risk. Methods In June 2007, a multidisciplinary group of experts gathered in Sunnyvale, California, USA, to assess what is known about the contribution of environmental factors to PD. Results We describe the conclusions around which they came to consensus with respect to environmental contributors to PD risk. We conclude with a brief summary of research needs. Conclusions PD is a complex disorder, and multiple different pathogenic pathways and mechanisms can ultimately lead to PD. Within the individual there are many determinants of PD risk, and within populations, the causes of PD are heterogeneous. Although rare recognized genetic mutations are sufficient to cause PD, these account for &lt; 10% of PD in the U.S. population, and incomplete penetrance suggests that environmental factors may be involved. Indeed, interplay among environmental factors and genetic makeup likely influences the risk of developing PD. There is a need for further understanding of how risk factors interact, and studying PD is likely to increase understanding of other neurodegenerative disorders.
Whole Genome Analyses Suggest Ischemic Stroke and Heart Disease Share an Association With Polymorphisms on Chromosome 9p21
Matarín, Mar, Brown, W. Mark , Singleton, Andrew , Hardy, John , Meschia, James F. , Hardy, John

Stroke | March 15, 2008 | Volume: 39 | Issue: 5 | Pages: 1586-1589

10.1161/strokeaha.107.502963 Get It

Background and Purpose— Recently independent studies reported an association between coronary heart disease and single-nucleotide polymorphisms (SNPs) located at chromosome 9p21, near CDKN2A and CDKN2B genes. Given that stroke is a common complication after myocardial infarction, we investigated if the same SNPs were associated with ischemic stroke in our population. Methods— We recently initiated a whole genome analysis of ischemic stroke and published the first stage of a case control study using >400 000 SNPs from Illumina Infinium Human-1 and HumanHap300 assays. We focused on SNPs recently associated with heart disease by Helgadottir and colleagues and SNPs from the same haplotype block. Results— In analyses both unadjusted and adjusted for stroke risk factors, significant associations with ischemic stroke were observed for SNPs from the same haplotype block previously associated with myocardial infarction. Significant association was also seen between disease and haplotypes involving these SNPs, both with and without adjustment for stroke risk factors (odd ratios: 1.01 to 2.65). Conclusions— These data are important for 3 reasons: first, they suggest a genetic association for stroke; second, they suggest that this association shares pathogenic mechanisms with heart disease and diabetes; and third, they illustrate, that public release of data can facilitate rapid risk locus discovery.