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Erratum: WITHDRAWN: The Role of Intercostal Nerve Block Combined with Puncture Surgery Robot Controlled by Fuzzy Proportion Integral Differential Algorithm under the Guidance of MRI Image in the Treatment of Lung Cancer (Neuroscience letters PII: S0304-3940(20)30474-2)

Chao, D; Li, Q; Hu, G
This article has been withdrawn at the request of the Editor-in-Chief. The Publisher apologizes for any inconvenience this may cause. The full Elsevier Policy on Article Withdrawal can be found at https://urldefense.proofpoint.com/v2/url?u=https-3A__www.elsevier.com_about_our-2Dbusiness_policies_article-2Dwithdra&d=DwIBAg&c=j5oPpO0eBH1iio48DtsedeElZfc04rx3ExJHeIIZuCs&r=CY_mkeBghQnUPnp2mckgsNSbUXISJaiBQUhM-Uz9W58&m=6Uq_rgJBKU9aAjc3bVqy_J2muSz0KuapQJUNLMRrNMc&s=vwLGr-ZQKkvqPTXOfH3kp2XeSnZEs3sCNDiFY6qa7DQ&e= wal.
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EMBASE:632204469
ISSN: 1872-7972
CID: 4557632

Neurotoxic Reactive Astrocytes Drive Neuronal Death after Retinal Injury

Guttenplan, Kevin A; Stafford, Benjamin K; El-Danaf, Rana N; Adler, Drew I; Münch, Alexandra E; Weigel, Maya K; Huberman, Andrew D; Liddelow, Shane A
Glaucoma is a neurodegenerative disease that features the death of retinal ganglion cells (RGCs) in the retina, often as a result of prolonged increases in intraocular pressure. We show that preventing the formation of neuroinflammatory reactive astrocytes prevents the death of RGCs normally seen in a mouse model of glaucoma. Furthermore, we show that these spared RGCs are electrophysiologically functional and thus still have potential value for the function and regeneration of the retina. Finally, we demonstrate that the death of RGCs depends on a combination of both an injury to the neurons and the presence of reactive astrocytes, suggesting a model that may explain why reactive astrocytes are toxic only in some circumstances. Altogether, these findings highlight reactive astrocytes as drivers of RGC death in a chronic neurodegenerative disease of the eye.
PMID: 32579912
ISSN: 2211-1247
CID: 4514532

Manipulating synthetic optogenetic odors reveals the coding logic of olfactory perception

Chong, Edmund; Moroni, Monica; Wilson, Christopher; Shoham, Shy; Panzeri, Stefano; Rinberg, Dmitry
How does neural activity generate perception? Finding the combinations of spatial or temporal activity features (such as neuron identity or latency) that are consequential for perception remains challenging. We trained mice to recognize synthetic odors constructed from parametrically defined patterns of optogenetic activation, then measured perceptual changes during extensive and controlled perturbations across spatiotemporal dimensions. We modeled recognition as the matching of patterns to learned templates. The templates that best predicted recognition were sequences of spatially identified units, ordered by latencies relative to each other (with minimal effects of sniff). Within templates, individual units contributed additively, with larger contributions from earlier-activated units. Our synthetic approach reveals the fundamental logic of the olfactory code and provides a general framework for testing links between sensory activity and perception.
PMID: 32554567
ISSN: 1095-9203
CID: 4486312

Author Correction: Dissociating task acquisition from expression during learning reveals latent knowledge

Kuchibhotla, Kishore V; Sten, Tom Hindmarsh; Papadoyannis, Eleni S; Elnozahy, Sarah; Fogelson, Kelly A; Kumar, Rupesh; Boubenec, Yves; Holland, Peter C; Ostojic, Srdjan; Froemke, Robert C
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
PMID: 32555158
ISSN: 2041-1723
CID: 4494632

ST-Segment Elevation in Patients with Covid-19 - A Case Series [Letter]

Bangalore, Sripal; Sharma, Atul; Slotwiner, Alexander; Yatskar, Leonid; Harari, Rafael; Shah, Binita; Ibrahim, Homam; Friedman, Gary H; Thompson, Craig; Alviar, Carlos L; Chadow, Hal L; Fishman, Glenn I; Reynolds, Harmony R; Keller, Norma; Hochman, Judith S
PMID: 32302081
ISSN: 1533-4406
CID: 4383882

Renin-Angiotensin-Aldosterone System Inhibitors and Risk of Covid-19

Reynolds, Harmony R; Adhikari, Samrachana; Pulgarin, Claudia; Troxel, Andrea B; Iturrate, Eduardo; Johnson, Stephen B; Hausvater, Anaïs; Newman, Jonathan D; Berger, Jeffrey S; Bangalore, Sripal; Katz, Stuart D; Fishman, Glenn I; Kunichoff, Dennis; Chen, Yu; Ogedegbe, Gbenga; Hochman, Judith S
BACKGROUND:There is concern about the potential of an increased risk related to medications that act on the renin-angiotensin-aldosterone system in patients exposed to coronavirus disease 2019 (Covid-19), because the viral receptor is angiotensin-converting enzyme 2 (ACE2). METHODS:We assessed the relation between previous treatment with ACE inhibitors, angiotensin-receptor blockers, beta-blockers, calcium-channel blockers, or thiazide diuretics and the likelihood of a positive or negative result on Covid-19 testing as well as the likelihood of severe illness (defined as intensive care, mechanical ventilation, or death) among patients who tested positive. Using Bayesian methods, we compared outcomes in patients who had been treated with these medications and in untreated patients, overall and in those with hypertension, after propensity-score matching for receipt of each medication class. A difference of at least 10 percentage points was prespecified as a substantial difference. RESULTS:Among 12,594 patients who were tested for Covid-19, a total of 5894 (46.8%) were positive; 1002 of these patients (17.0%) had severe illness. A history of hypertension was present in 4357 patients (34.6%), among whom 2573 (59.1%) had a positive test; 634 of these patients (24.6%) had severe illness. There was no association between any single medication class and an increased likelihood of a positive test. None of the medications examined was associated with a substantial increase in the risk of severe illness among patients who tested positive. CONCLUSIONS:We found no substantial increase in the likelihood of a positive test for Covid-19 or in the risk of severe Covid-19 among patients who tested positive in association with five common classes of antihypertensive medications.
PMID: 32356628
ISSN: 1533-4406
CID: 4412912

Optical Control of Lysophosphatidic Acid Signaling

Morstein, Johannes; Dacheux, Mélanie A; Norman, Derek D; Shemet, Andrej; Donthamsetti, Prashant C; Citir, Mevlut; Frank, James A; Schultz, Carsten; Isacoff, Ehud Y; Parrill, Abby L; Tigyi, Gabor J; Trauner, Dirk
Lysophosphatidic acid (LPA) is a phospholipid that acts as an extracellular signaling molecule and activates the family of lysophosphatidic acid receptors (LPA1-6). These G protein-coupled receptors (GPCRs) are broadly expressed and are particularly important in development as well as in the nervous, cardiovascular, reproductive, gastrointestinal, and pulmonary systems. Here, we report on a photoswitchable analogue of LPA, termed AzoLPA, which contains an azobenzene photoswitch embedded in the acyl chain. AzoLPA enables optical control of LPA receptor activation, shown through its ability to rapidly control LPA-evoked increases in intracellular Ca2+ levels. AzoLPA shows greater activation of LPA receptors in its light-induced cis-form than its dark-adapted (or 460 nm light-induced) trans-form. AzoLPA enabled the optical control of neurite retraction through its activation of the LPA2 receptor.
PMID: 32469525
ISSN: 1520-5126
CID: 4481992

Diffusion MRI detects early brain microstructure abnormalities in 2-month-old 3×Tg-AD mice

Falangola, Maria Fatima; Nie, Xingju; Ward, Ralph; McKinnon, Emilie T; Dhiman, Siddhartha; Nietert, Paul J; Helpern, Joseph A; Jensen, Jens H
The 3×Tg-AD mouse is one of the most studied animal models of Alzheimer's disease (AD), and develops both amyloid beta deposits and neurofibrillary tangles in a temporal and spatial pattern that is similar to human AD pathology. Additionally, abnormal myelination patterns with changes in oligodendrocyte and myelin marker expression are reported to be an early pathological feature in this model. Only few diffusion MRI (dMRI) studies have investigated white matter abnormalities in 3×Tg-AD mice, with inconsistent results. Thus, the goal of this study was to investigate the sensitivity of dMRI to capture brain microstructural alterations in 2-month-old 3×Tg-AD mice. In the fimbria, the fractional anisotropy (FA), kurtosis fractional anisotropy (KFA), and radial kurtosis (K┴ ) were found to be significantly lower in 3×Tg-AD mice than in controls, while the mean diffusivity (MD) and radial diffusivity (D┴ ) were found to be elevated. In the fornix, K┴ was lower for 3×Tg-AD mice; in the dorsal hippocampus MD and D┴ were elevated, as were FA, MD, and D┴ in the ventral hippocampus. These results indicate, for the first time, dMRI changes associated with myelin abnormalities in young 3×Tg-AD mice, before they develop AD pathology. Morphological quantification of myelin basic protein immunoreactivity in the fimbria was significantly lower in the 3×Tg-AD mice compared with the age-matched controls. Our results demonstrate that dMRI is able to detect widespread, significant early brain morphological abnormalities in 2-month-old 3×Tg-AD mice.
PMID: 32557874
ISSN: 1099-1492
CID: 4485302

Subcortical Brain Volume, Regional Cortical Thickness, and Cortical Surface Area Across Disorders: Findings From the ENIGMA ADHD, ASD, and OCD Working Groups

Boedhoe, Premika S W; van Rooij, Daan; Hoogman, Martine; Twisk, Jos W R; Schmaal, Lianne; Abe, Yoshinari; Alonso, Pino; Ameis, Stephanie H; Anikin, Anatoly; Anticevic, Alan; Arango, Celso; Arnold, Paul D; Asherson, Philip; Assogna, Francesca; Auzias, Guillaume; Banaschewski, Tobias; Baranov, Alexander; Batistuzzo, Marcelo C; Baumeister, Sarah; Baur-Streubel, Ramona; Behrmann, Marlene; Bellgrove, Mark A; Benedetti, Francesco; Beucke, Jan C; Biederman, Joseph; Bollettini, Irene; Bose, Anushree; Bralten, Janita; Bramati, Ivanei E; Brandeis, Daniel; Brem, Silvia; Brennan, Brian P; Busatto, Geraldo F; Calderoni, Sara; Calvo, Anna; Calvo, Rosa; Castellanos, Francisco X; Cercignani, Mara; Chaim-Avancini, Tiffany M; Chantiluke, Kaylita C; Cheng, Yuqi; Cho, Kang Ik K; Christakou, Anastasia; Coghill, David; Conzelmann, Annette; Cubillo, Ana I; Dale, Anders M; Dallaspezia, Sara; Daly, Eileen; Denys, Damiaan; Deruelle, Christine; Di Martino, Adriana; Dinstein, Ilan; Doyle, Alysa E; Durston, Sarah; Earl, Eric A; Ecker, Christine; Ehrlich, Stefan; Ely, Benjamin A; Epstein, Jeffrey N; Ethofer, Thomas; Fair, Damien A; Fallgatter, Andreas J; Faraone, Stephen V; Fedor, Jennifer; Feng, Xin; Feusner, Jamie D; Fitzgerald, Jackie; Fitzgerald, Kate D; Fouche, Jean-Paul; Freitag, Christine M; Fridgeirsson, Egill A; Frodl, Thomas; Gabel, Matt C; Gallagher, Louise; Gogberashvili, Tinatin; Gori, Ilaria; Gruner, Patricia; Gürsel, Deniz A; Haar, Shlomi; Haavik, Jan; Hall, Geoffrey B; Harrison, Neil A; Hartman, Catharina A; Heslenfeld, Dirk J; Hirano, Yoshiyuki; Hoekstra, Pieter J; Hoexter, Marcelo Q; Hohmann, Sarah; Høvik, Marie F; Hu, Hao; Huyser, Chaim; Jahanshad, Neda; Jalbrzikowski, Maria; James, Anthony; Janssen, Joost; Jaspers-Fayer, Fern; Jernigan, Terry L; Kapilushniy, Dmitry; Kardatzki, Bernd; Karkashadze, Georgii; Kathmann, Norbert; Kaufmann, Christian; Kelly, Clare; Khadka, Sabin; King, Joseph A; Koch, Kathrin; Kohls, Gregor; Kohls, Kerstin; Kuno, Masaru; Kuntsi, Jonna; Kvale, Gerd; Kwon, Jun Soo; Lázaro, Luisa; Lera-Miguel, Sara; Lesch, Klaus-Peter; Hoekstra, Liesbeth; Liu, Yanni; Lochner, Christine; Louza, Mario R; Luna, Beatriz; Lundervold, Astri J; Malpas, Charles B; Marques, Paulo; Marsh, Rachel; Martínez-Zalacaín, Ignacio; Mataix-Cols, David; Mattos, Paulo; McCarthy, Hazel; McGrath, Jane; Mehta, Mitul A; Menchón, José M; Mennes, Maarten; Martinho, Mauricio Moller; Moreira, Pedro S; Morer, Astrid; Morgado, Pedro; Muratori, Filippo; Murphy, Clodagh M; Murphy, Declan G M; Nakagawa, Akiko; Nakamae, Takashi; Nakao, Tomohiro; Namazova-Baranova, Leyla; Narayanaswamy, Janardhanan C; Nicolau, Rosa; Nigg, Joel T; Novotny, Stephanie E; Nurmi, Erika L; Weiss, Eileen Oberwelland; O'Gorman Tuura, Ruth L; O'Hearn, Kirsten; O'Neill, Joseph; Oosterlaan, Jaap; Oranje, Bob; Paloyelis, Yannis; Parellada, Mara; Pauli, Paul; Perriello, Chris; Piacentini, John; Piras, Fabrizio; Piras, Federica; Plessen, Kerstin J; Puig, Olga; Ramos-Quiroga, J Antoni; Reddy, Y C Janardhan; Reif, Andreas; Reneman, Liesbeth; Retico, Alessandra; Rosa, Pedro G P; Rubia, Katya; Rus, Oana Georgiana; Sakai, Yuki; Schrantee, Anouk; Schwarz, Lena; Schweren, Lizanne J S; Seitz, Jochen; Shaw, Philip; Shook, Devon; Silk, Tim J; Simpson, H Blair; Skokauskas, Norbert; Soliva Vila, Juan Carlos; Solovieva, Anastasia; Soreni, Noam; Soriano-Mas, Carles; Spalletta, Gianfranco; Stern, Emily R; Stevens, Michael C; Stewart, S Evelyn; Sudre, Gustavo; Szeszko, Philip R; Tamm, Leanne; Taylor, Margot J; Tolin, David F; Tosetti, Michela; Tovar-Moll, Fernanda; Tsuchiyagaito, Aki; van Erp, Theo G M; van Wingen, Guido A; Vance, Alasdair; Venkatasubramanian, Ganesan; Vilarroya, Oscar; Vives-Gilabert, Yolanda; von Polier, Georg G; Walitza, Susanne; Wallace, Gregory L; Wang, Zhen; Wolfers, Thomas; Yoncheva, Yuliya N; Yun, Je-Yeon; Zanetti, Marcus V; Zhou, Fengfeng; Ziegler, Georg C; Zierhut, Kathrin C; Zwiers, Marcel P; Thompson, Paul M; Stein, Dan J; Buitelaar, Jan; Franke, Barbara; van den Heuvel, Odile A
OBJECTIVE:Attention deficit hyperactivity disorder (ADHD), autism spectrum disorder (ASD), and obsessive-compulsive disorder (OCD) are common neurodevelopmental disorders that frequently co-occur. The authors sought to directly compare these disorders using structural brain imaging data from ENIGMA consortium data. METHODS:-weighted whole-brain MRI data from healthy control subjects (N=5,827) and from patients with ADHD (N=2,271), ASD (N=1,777), and OCD (N=2,323) from 151 cohorts worldwide were analyzed using standardized processing protocols. The authors examined subcortical volume, cortical thickness, and cortical surface area differences within a mega-analytical framework, pooling measures extracted from each cohort. Analyses were performed separately for children, adolescents, and adults, using linear mixed-effects models adjusting for age, sex, and site (and intracranial volume for subcortical and surface area measures). RESULTS:No shared differences were found among all three disorders, and shared differences between any two disorders did not survive correction for multiple comparisons. Children with ADHD compared with those with OCD had smaller hippocampal volumes, possibly influenced by IQ. Children and adolescents with ADHD also had smaller intracranial volume than control subjects and those with OCD or ASD. Adults with ASD showed thicker frontal cortices compared with adult control subjects and other clinical groups. No OCD-specific differences were observed across different age groups and surface area differences among all disorders in childhood and adulthood. CONCLUSIONS:The study findings suggest robust but subtle differences across different age groups among ADHD, ASD, and OCD. ADHD-specific intracranial volume and hippocampal differences in children and adolescents, and ASD-specific cortical thickness differences in the frontal cortex in adults, support previous work emphasizing structural brain differences in these disorders.
PMID: 32539527
ISSN: 1535-7228
CID: 4484542

Impending Shortages of Kidney Replacement Therapy for COVID-19 Patients

Goldfarb, David S; Benstein, Judith A; Zhdanova, Olga; Hammer, Elizabeth; Block, Clay A; Caplin, Nina J; Thompson, Nathan; Charytan, David M
PMID: 32345750
ISSN: 1555-905x
CID: 4412262