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";s:4:"text";s:29473:"Today fifty percent of affected patients live at least three or more years after diagnosis; 20 percent … Nat Rev Neurol 9:617–628. found that IL-35 can also be produced by B cells in mice. Journal of Neurology We used a random-effects model to summarize individual studies and assessed heterogeneity (I2) with the χ2 test on Cochrane’s Q statistic. 86) per 100 000 person-years. https://doi.org/10.1371/journal.pone.0072381, Fogh I, Ratti A, Gellera C, Lin K, Tiloca C, Moskvina V, Corrado L, Soraru G, Cereda C, Corti S, Gentilini D, Calini D, Castellotti B, Mazzini L, Querin G, Gagliardi S, Del Bo R, Conforti FL, Siciliano G, Inghilleri M, Sacca F, Bongioanni P, Penco S, Corbo M, Sorbi S, Filosto M, Ferlini A, Di Blasio AM, Signorini S, Shatunov A, Jones A, Shaw PJ, Morrison KE, Farmer AE, Van Damme P, Robberecht W, Chio A, Traynor BJ, Sendtner M, Melki J, Meininger V, Hardiman O, Andersen PM, Leigh NP, Glass JD, Overste D, Diekstra FP, Veldink JH, van Es MA, Shaw CE, Weale ME, Lewis CM, Williams J, Brown RH, Landers JE, Ticozzi N, Ceroni M, Pegoraro E, Comi GP, D'Alfonso S, van den Berg LH, Taroni F, Al-Chalabi A, Powell J, Silani V (2014) A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis. In the United States, a prevalence of 5.2 … A total of 15,927 persons were identified as having definite ALS across the three national databases and through web portal registration for 2014 ( Table ). Assuring our community by providing high quality, innovative, professional testing services to help our clients make informed decisions. In Europe, the median incidence rate (/100,000 population) was 2.08 (IQR 1.47-2.43), corresponding to an estimated 15,355 (10,852-17,938) cases. Curr Opin Neurol. The estimated prevalence for 2014 was 5.0 per 100,000 population, representing no increase from 2013 (5.0 per 100,000). Background: The findings of recent genetic polymorphism studies in ALS suggest that the influence of genetic risk factors for the disease may vary by ethnicity. J Neurol Neurosurg Psychiatry 83:102–108. The authors would like to thank Xuefeng Lai, Jinlang Lv, Junyou Yu, Wei Zhang, and Huan Yu for retrieving and managing articles as well as extracting data. https://doi.org/10.1002/sim.1186, Egger M, Davey Smith G, Schneider M, Minder C (1997) Bias in meta-analysis detected by a simple, graphical test. Prevalence of amyotrophic lateral sclerosis - United States, 2010-2011. INTRODUCTION. 1 See this image and copyright information in PMC. Abstract. https://doi.org/10.1056/NEJMra1603471, CAS Careers. doi: 10.1136/bmjopen-2014-007359. Global variation in prevalence and incidence of amyotrophic lateral sclerosis: a systematic review and meta-analysis. J Neurol Neurosurg Psychiatry 87:821–830. Lancet Global Health 2013;1:e339-e349 (3) 2014 USRDS annual data report: Epidemiology of kidney disease in the United States. Role of Oxidative Stress in the Pathogenesis of Amyotrophic Lateral Sclerosis: Antioxidant Metalloenzymes and Therapeutic Strategies. © 2021 Springer Nature Switzerland AG. Stat Med 21:1539–1558. MMWR Morb Mortal Wkly Rep 67:1285–1289. https://doi.org/10.1136/jnnp-2015-312751, Chen L, Zhang B, Chen R, Tang L, Liu R, Yang Y, Yang Y, Liu X, Ye S, Zhan S, Fan D (2015) Natural history and clinical features of sporadic amyotrophic lateral sclerosis in China. https://doi.org/10.1136/jnnp-2015-310471, Dorst J, Chen L, Rosenbohm A, Dreyhaupt J, Hubers A, Schuster J, Weishaupt JH, Kassubek J, Gess B, Meyer T, Weyen U, Hermann A, Winkler J, Grehl T, Hagenacker T, Lingor P, Koch JC, Sperfeld A, Petri S, Grosskreutz J, Metelmann M, Wolf J, Winkler AS, Klopstock T, Boentert M, Johannesen S, Storch A, Schrank B, Zeller D, Liu XL, Tang L, Fan DS, Ludolph AC (2019) Prognostic factors in ALS: a comparison between Germany and China. Neurology 88:296–303. [49] not included in this figure (latest year of data collection during study); Country-specific crude prevalence rate of ALS. Barceló MA, Povedano M, Vázquez-Costa JF, Franquet Á, Solans M, Saez M. Sci Rep. 2021 Mar 18;11(1):6207. doi: 10.1038/s41598-021-85395-z. - 104.238.101.238. Soc Sci Med 51:887–895, A Chio G Mora C Moglia U Manera A Canosa S Cammarosano A Ilardi D Bertuzzo E Bersano P Cugnasco M Grassano F Pisano L Mazzini A Calvo VD Piemonte Register for ALS 2017 Secular trends of amyotrophic lateral sclerosis: the piemonte and valle d'aosta register, JAMA Neurol 74: 1097–1104 10.1001/jamaneurol.2017.1387, Arthur KC, Calvo A, Price TR, Geiger JT, Chio A, Traynor BJ (2016) Projected increase in amyotrophic lateral sclerosis from 2015 to 2040. This study was funded by the National Natural Science Foundation (grant number 91646107). volume 267, pages944–953(2020)Cite this article. https://doi.org/10.1136/jnnp-2013-307223, Article J Neurol 212:205–213, Okumiya K, Wada T, Fujisawa M, Ishine M, Garcia Del Saz E, Hirata Y, Kuzuhara S, Kokubo Y, Seguchi H, Sakamoto R, Manuaba I, Watofa P, Rantetampang AL, Matsubayashi K (2014) Amyotrophic lateral sclerosis and parkinsonism in Papua, indonesia: 2001–2012 survey results. *Lighter shaded areas indicate the…, Temporal trends in incidence and prevalence. Lancet Glob Health 6:e998–e1007. https://doi.org/10.1016/s2214-109x(18)30275-4, Noubiap JJ, Nansseu JR, Nyaga UF, Nkeck JR, Endomba FT, Kaze AD, Agbor VN, Bigna JJ (2019) Global prevalence of diabetes in active tuberculosis: a systematic review and meta-analysis of data from 2.3 million patients with tuberculosis. eCollection 2021. Correspondence to 2017 Feb 1;46(1):57-74. doi: 10.1093/ije/dyw061. N Engl J Med 377:162–172. Article In the USA, there are thought to be between 15,000 and 21,000 people living with ALS. 4 The relatively low prevalence is potentially understated due to the rapid progression of ALS. The overall crude worldwide ALS prevalence and incidence were 4.42 (95% CI 3.92–4.96) per 1,00,000 population and 1.59 (95% CI 1.39–1.81) per 1,00,000 person-years, respectively. PubMed Google Scholar. Amyotroph Lateral Scler Frontotemporal Degener 18:284–290. Panel A does not include 2 study…. https://doi.org/10.15585/mmwr.mm6746a1. This article does not contain any studies with human participants or animals performed by any of the authors. ALS is a common neuromuscular disease worldwide. PubMed BMJ 315:629–634, Marin B, Fontana A, Arcuti S, Copetti M, Boumediene F, Couratier P, Beghi E, Preux PM, Logroscino G (2018) Age-specific ALS incidence: a dose-response meta-analysis. https://doi.org/10.14336/ad.2018.0327, Beard JD, Steege AL, Ju J, Lu J, Luckhaupt SE, Schubauer-Berigan MK (2017) Mortality from amyotrophic lateral sclerosis and parkinson's disease among different occupation groups—United States, 1985–2011. Biomolecules. https://doi.org/10.1016/s2214-109x(18)30487-x, Etminan N, Chang HS, Hackenberg K, de Rooij NK, Vergouwen MDI, Rinkel GJE, Algra A (2019) Worldwide incidence of aneurysmal subarachnoid hemorrhage according to region, time period, blood pressure, and smoking prevalence in the population: a systematic review and meta-analysis. Background: https://doi.org/10.1038/nrneurol.2013.203, Korner S, Kammeyer J, Zapf A, Kuzma-Kozakiewicz M, Piotrkiewicz M, Kuraszkiewicz B, Goszczynska H, Gromicho M, Grosskreutz J, Andersen PM, de Carvalho M, Petri S (2019) Influence of environment and lifestyle on incidence and progress of amyotrophic lateral sclerosis in A German ALS population. Nat Genet 41:1083–1087. Immediate online access to all issues from 2019. In all, 37 articles met the inclusion criteria. The global decline in prevalence of lymphatic filariasis has been one of the major successes of the WHO’s NTD programme. https://doi.org/10.1136/jnnp-2011-300188, Logroscino G, Piccininni M, Marin B, Nichols E, Abd-Allah F, Abdelalim A, Alahdab F, Asgedom SW, Awasthi A, Chaiah Y, Daryani A, Do HP, Dubey M, Elbaz A, Eskandarieh S, Farhadi F, Farzadfar F, Fereshtehnejad S-M, Fernandes E, Filip I, Foreman KJ, Gebre AK, Gnedovskaya EV, Hamidi S, Hay SI, Irvani SSN, Ji JS, Kasaeian A, Kim YJ, Mantovani LG, Mashamba-Thompson TP, Mehndiratta MM, Mokdad AH, Nagel G, Nguyen TH, Nixon MR, Olagunju AT, Owolabi MO, Piradov MA, Qorbani M, Radfar A, Reiner RC, Sahraian MA, Sarvi S, Sharif M, Temsah O, Tran BX, Truong NT, Venketasubramanian N, Winkler AS, Yimer EM, Feigin VL, Vos T, Murray CJL (2018) Global, regional, and national burden of motor neuron diseases 1990–2016: a systematic analysis for the global burden of disease study 2016. Amyotroph Lateral Scler Frontotemporal Degener 14:116–123. World Health Organization Coronavirus disease situation dashboard presents official daily counts of COVID-19 cases and deaths worldwide, along with vaccination rates and other vaccination data, while providing a hub to other resources. Summary statistics for all studies and by region. Neuroepidemiology 47:59–66. 2021 Mar 16;11(3):437. doi: 10.3390/biom11030437. ALS has a worldwide occurrence of about 2 per 100,000 population and a prevalence of 4 per 100,000 population to 7 per 100,000 population (Swash, 2001) with an estimated at 1.2–4.0 per 100,000 affected individuals in Caucasian populations and a lower rate in many other ethnic populations (Gordon, 2011).The figures vary considerably in different European and North American populations … No risk factor analysed in GBD showed an association with motor neuron disease incidence. Article https://doi.org/10.1093/oxfordjournals.aje.a113043, Higgins JP, Thompson SG (2002) Quantifying heterogeneity in a meta-analysis. https://doi.org/10.1212/wnl.0000000000003509, Noubiap JJ, Bigna JJ, Nansseu JR, Nyaga UF, Balti EV, Echouffo-Tcheugui JB, Kengne AP (2018) Prevalence of dyslipidaemia among adults in Africa: a systematic review and meta-analysis. https://doi.org/10.1016/j.jfma.2013.01.008, McKenzie JE, Beller EM, Forbes AB (2016) Introduction to systematic reviews and meta-analysis. Respirology 21:626–637. The Association Between Maladaptive Metacognitive Beliefs and Emotional Distress in People Living With Amyotrophic Lateral Sclerosis. https://doi.org/10.1007/s10654-018-0392-x, Taskent RO, Gokcumen O (2017) The Multiple histories of Western Asia: perspectives from ancient and modern genomes. The authors declare that they have no conflict of interest. https://doi.org/10.1159/000477126, Kahana E, Alter M, Feldman S (1976) Amyotrophic lateral sclerosis: a population study. ALS affects more males than females. 2019 Oct;32(5):771-776. doi: 10.1097/WCO.0000000000000730. The pooled Median prevalence (/100,000 population) was 5.40 (IQR 4.06-7.89), or 39,863 (29,971-58,244) prevalent cases. Recent population-based studies reported a prevalence of ALS between 4.1 and 8.4 per 100 000 persons [1▪,2,3,4▪,5,7▪▪,8,11–13]. Epidemiology of amyotrophic lateral sclerosis: an update of recent literature. According to the global estimates, there are around four to six people per 100,000 living wit h ALS at any given point in time. Having accurate incidence and prevalence estimates would facilitate efficient allocation of healthcare resources. Bartoletti-Stella A, Vacchiano V, De Pasqua S, Mengozzi G, De Biase D, Bartolomei I, Avoni P, Rizzo G, Parchi P, Donadio V, Chiò A, Pession A, Oppi F, Salvi F, Liguori R, Capellari S; BoReALS. Currently, it is projected that 4-6 people per 100,000 are living with ALS at any given time. als. Disparity in rates among ALS incidence and prevalence studies may be due to differences in study design or true variations in population demographics such as age and geography, including environmental factors and genetic predisposition. Part of Springer Nature. Using the estimated U.S. population number of 320,000,000, the prevalence of ALS would be 12,800-19,800. Subscription will auto renew annually. Hum Biol 89:107–117, Anne MB, Judith RK, Joanna LM, Joan MH, Luciano C, Kenneth KK, Luca LC (1991) Drift, admixture, and selection in human evolution: a study with DNA polymorphisms. PubMed We identified 124 studies that were eligible for final inclusion, including 110 studies of incidence and 58 studies of prevalence. Results: We included data from 17 studies comprising 137 514 participants. The longest survival time were in Asia (ranging from 3.74 years in South Asia to 9.23 years in West Asia). In 2015, the estimated prevalence of ALS cases was 5.2 per 100,000 population with a total of 16,583 cases identified. Conclusions: The prevalence of disease is defined as the number of people living with a disease at a particular time and varies among geographic areas worldwide. 2016 Aug 5;65(8):1-12. doi: 10.15585/mmwr.ss6508a1. Acta Neurol Scand 83:280–285, CAS Dodd R, Fisher PL, Makin S, Moore P, Cherry MG. Front Psychol. Approximately 6,000 people are diagnosed with ALS each year in the USA, according to the available statistics and around 93% of the patients in the U.S are Caucasian whereas 60 % are men. https://doi.org/10.1159/000448921, Demetriou CA, Hadjivasiliou PM, Kleopa KA, Christou YP, Leonidou E, Kyriakides T, Zamba-Papanicolaou E (2017) Epidemiology of amyotrophic lateral sclerosis in the Republic of Cyprus: a 25-year retrospective study. Conclusions: Disparity in rates among ALS incidence and prevalence studies may be due to differences in study design or true variations in population … *Lighter shaded areas indicate the lowest and highest reported rate; darker shaded area represent the inter-quartile (IQ) range. Variation in worldwide incidence of amyotrophic lateral sclerosis: a meta-analysis. Evid Based Ment Health 1:37–39, Loney PL, Chambers LW, Bennett KJ, Roberts JG, Stratford PW (1998) Critical appraisal of the health research literature: prevalence or incidence of a health problem. We searched Medline, Embase, Web of Science, and Cochrane library to identify articles published until September 9, 2018. Mehta P, Antao V, Kaye W, Sanchez M, Williamson D, Bryan L, Muravov O, Horton K; Division of Toxicology and Human Health Sciences, Agency for Toxic Substances and Disease Registry, Atlanta, Georgia; Centers for Disease Control and Prevention (CDC). Within a population of 100,000 people, there are 2 new ALS cases each year. Temporal trends in incidence and prevalence. This site needs JavaScript to work properly. https://doi.org/10.1093/hmg/ddt587, Du Y, Wen Y, Guo X, Hao J, Wang W, He A, Fan Q, Li P, Liu L, Liang X, Zhang F (2018) A Genome-wide expression association analysis identifies genes and pathways associated with amyotrophic lateral sclerosis. Median prevalence (/100,000 population) was 5.40 (IQR 4.06-7.89), or 39,863 (29,971-58,244) prevalent cases. Currently the cause of ALS is unknown; however, a small proportion of cases are familial . https://doi.org/10.1016/s1474-4422(18)30404-6, Article Mehta P, Kaye W, Bryan L, Larson T, Copeland T, Wu J, Muravov O, Horton K. MMWR Surveill Summ. Proc Natl Acad Sci 94:7719–7724, van Es MA, Veldink JH, Saris CG, Blauw HM, van Vught PW, Birve A, Lemmens R, Schelhaas HJ, Groen EJ, Huisman MH, van der Kooi AJ, de Visser M, Dahlberg C, Estrada K, Rivadeneira F, Hofman A, Zwarts MJ, van Doormaal PT, Rujescu D, Strengman E, Giegling I, Muglia P, Tomik B, Slowik A, Uitterlinden AG, Hendrich C, Waibel S, Meyer T, Ludolph AC, Glass JD, Purcell S, Cichon S, Nothen MM, Wichmann HE, Schreiber S, Vermeulen SH, Kiemeney LA, Wokke JH, Cronin S, McLaughlin RL, Hardiman O, Fumoto K, Pasterkamp RJ, Meininger V, Melki J, Leigh PN, Shaw CE, Landers JE, Al-Chalabi A, Brown RH Jr, Robberecht W, Andersen PM, Ophoff RA, van den Berg LH (2009) Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. Adult-Onset Motor Neuron Disorder 2 An estimated 5000 people in the United States are diagnosed with ALS each year with a prevalence of at least 16,000. https://doi.org/10.1016/s1474-4422(18)30404-6, https://doi.org/10.1371/journal.pone.0178019, https://doi.org/10.1016/j.jfma.2013.01.008, https://doi.org/10.3109/21678421.2016.1140210, https://doi.org/10.1080/21678421.2016.1197942, https://doi.org/10.1080/21678421.2017.1281961, https://doi.org/10.1136/bmjopen-2013-004353, https://doi.org/10.1212/wnl.0000000000003509, https://doi.org/10.1016/s2214-109x(18)30275-4, https://doi.org/10.1016/s2214-109x(18)30487-x, https://doi.org/10.1001/jamaneurol.2019.0006, https://doi.org/10.1016/s0140-6736(17)32448-0, https://doi.org/10.1093/oxfordjournals.aje.a113043, https://doi.org/10.1007/s10654-018-0392-x, https://doi.org/10.1371/journal.pone.0035333, https://doi.org/10.1371/journal.pone.0072381, https://doi.org/10.1007/s10571-017-0512-2, https://doi.org/10.1016/s1474-4422(10)70197-6, https://doi.org/10.1038/s41582-018-0047-2, https://doi.org/10.1007/s00415-019-09290-4, https://doi.org/10.3109/17482968.2012.726226, https://doi.org/10.1212/wnl.0000000000004115, https://doi.org/10.1038/nrneurol.2013.203, https://doi.org/10.1007/s00415-019-09652-y. https://doi.org/10.3109/21678421.2016.1140210, Scialo C, Novi G, Bandettini di Poggio M, Canosa A, Sormani MP, Mandich P, Origone P, Truffelli R, Mancardi GL, Caponnetto C (2016) Clinical epidemiology of amyotrophic lateral sclerosis in Liguria, Italy: an update of LIGALS register. ALS is one of the foremost umpire and party analysis laboratories in the world, providing accurate global inspection and analysis services for metals, minerals, ores, precious metals, ferro-alloys and solid fuels. Article https://doi.org/10.1093/ije/dyw061, Chio A, Logroscino G, Traynor BJ, Collins J, Simeone JC, Goldstein LA, White LA (2013) Global epidemiology of amyotrophic lateral sclerosis: a systematic review of the published literature. Lancet Neurol 17:1083–1097. Google Scholar, Montuschi A, Iazzolino B, Calvo A, Moglia C, Lopiano L, Restagno G, Brunetti M, Ossola I, Lo Presti A, Cammarosano S, Canosa A, Chio A (2015) Cognitive correlates in amyotrophic lateral sclerosis: a population-based study in Italy. https://doi.org/10.1007/s00415-019-09652-y, DOI: https://doi.org/10.1007/s00415-019-09652-y, Over 10 million scientific documents at your fingertips, Not logged in https://doi.org/10.3109/17482968.2012.726226, Floeter MK, Traynor BJ, Farren J, Braun LE, Tierney M, Wiggs EA, Wu T (2017) Disease progression in C9orf72 mutation carriers. J Epidemiol 23:35–40. However, scientific studies reporting that IL-35 is secreted by B cells in humans, specifically in cancer patients, are very rare. Google Scholar, Benjaminsen E, Alstadhaug KB, Baloch F, Gulsvik M, Odeh F (2017) Amyotrophic lateral sclerosis in Nordland County, Norway 2000–2015. Amyotroph Lateral Scler Frontotemporal Degener 17:275–281. https://doi.org/10.1038/ng.442, Diekstra FP, Saris CG, van Rheenen W, Franke L, Jansen RC, van Es MA, van Vught PW, Blauw HM, Groen EJ, Horvath S, Estrada K, Rivadeneira F, Hofman A, Uitterlinden AG, Robberecht W, Andersen PM, Melki J, Meininger V, Hardiman O, Landers JE, Brown RH Jr, Shatunov A, Shaw CE, Leigh PN, Al-Chalabi A, Ophoff RA, van den Berg LH, Veldink JH (2012) Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS. In 2015, the prevalence and incidence and/or prevalence rates average age of 70–79 providing high quality,,! Secreted by B cells in mice via your institution the use of ELISA kits from different manufacturers a! To the electronic supplementary material with age population with a total of 16,583 cases identified having incidence. Include 2 study outliers als global prevalence Govoni et al any given time, Hylton,... 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