| H00058 | |
| H番号 | H00058 |
| 名称 | 筋萎縮性側索硬化症 (ALS) |
| 概要 | Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder characterized by a progressive degeneration of motor neurons in the brain and spinal cord. In 90% of patients, ALS is sporadic, with no clear genetic linkage. On the other hand, the remaining 10% of cases show familial inheritance, with mutations in SOD1, TDP43(TARDBP), FUS, or C9orf72 genes being the most frequent causes. In spite of such difference, familial ALS and sporadic ALS have similarities in their pathological features. Proposed disease mechanisms contributing to motor neuron degeneration in ALS are: impaired proteostasis, aberrant RNA processing, mitochondrial disfunction and oxidative stress, microglia activation, and axonal dysfunction. |
| カテゴリ | 神経変性疾患 疾患パスウェイ hsa05014 筋萎縮性側索硬化症 |
| ネットワーク | nt06410(H00058) Calcium signaling nt06412(H00058) Unfolded protein response (UPR) signaling nt06413(H00058) Autophagy nt06414(H00058) Apoptosis nt06415(H00058) PI3K signaling nt06418(H00058) Oxidative phosphorylation nt06419(H00058) Microtubule-based transport nt06420(H00058) Ubiquitin-proteasome system nt06421(H00058) Mitophagy nt06423(H00058) Cytoskeletal regulation nt06424(H00058) RNA processing nt06464 Amyotrophic lateral sclerosis nt06515(H00058) Regulation of kinetochore-microtubule interactions nt06530(H00058) PI3K signaling |
| 病因遺伝子 | (ALS1) SOD1 [HSA:6647] [KO:K04565] (ALS1) NEFH [HSA:4744] [KO:K04574] (ALS1) PRPH [HSA:5630] [KO:K07607] (ALS1) DCTN1 [HSA:1639] [KO:K04648] (ALS2) ALS2 [HSA:57679] [KO:K04575] (ALS4) SETX [HSA:23064] [KO:K10706] (ALS5) SPG11 [HSA:80208] [KO:K19026] (ALS6) FUS [HSA:2521] [KO:K13098] (ALS8) VAPB [HSA:9217] [KO:K10707] (ALS9) ANG [HSA:283] [KO:K16631] (ALS10) TARDBP [HSA:23435] [KO:K23600] (ALS11) FIG4 [HSA:9896] [KO:K22913] (ALS12) OPTN [HSA:10133] [KO:K19946] (ALS15) UBQLN2 [HSA:29978] [KO:K04523] (ALS16) SIGMAR1 [HSA:10280] [KO:K20719] (ALS18) PFN1 [HSA:5216] [KO:K05759] (ALS19) ERBB4 [HSA:2066] [KO:K05085] (ALS20) HNRNPA1 [HSA:3178] [KO:K12741] (ALS21) MATR3 [HSA:9782] [KO:K13213] (ALS22) TUBA4A [HSA:7277] [KO:K07374] (ALS23) ANXA11 [HSA:311] [KO:K17095] (ALS24) NEK1 [HSA:4750] [KO:K08857] (ALS25) KIF5A [HSA:3798] [KO:K10396] (ALS26) TIA1 [HSA:7072] [KO:K13201] (ALS27) SPTLC1 [HSA:10558] [KO:K00654] (ALS28) LRP12 [HSA:29967] [KO:K20050] (ALSPDC) TRPM7 [HSA:54822] [KO:K04982] (ALSPDC) MAPT [HSA:4137] [KO:K04380] |
| 病原体 | - |
| 環境要因 | - |
| 発癌物質 | - |
| 治療薬 | リルゾール [DR:D00775] エダラボン [DR:D01552] ダントロレンナトリウム水和物 [DR:D02274] バクロフェン [DR:D00241] チザニジン塩酸塩 [DR:D00776] エペリゾン塩酸塩 [DR:D01671] アフロクアロン [DR:D01638] |
| コメント | Affected region: motor cortex, brain stem, spinal cord Microscopic lesion: hyaline inclusions |
| リンク | ICD-11: 8B60.0 ICD-10: G12.2 MeSH: D000690 OMIM: 105400 205100 602433 602099 608030 608627 611895 612069 612577 613435 300857 614373 614808 615515 615426 606070 617839 616208 617839 617892 617921 619133 620285 620452 105500 |
| 文献 | PMID:28980624 著者 Hardiman O, Al-Chalabi A, Chio A, Corr EM, Logroscino G, Robberecht W, Shaw PJ, Simmons Z, van den Berg LH タイトル Amyotrophic lateral sclerosis. 雑誌 Nat Rev Dis Primers 3:17071 (2017) DOI:10.1038/nrdp.2017.71 PMID:26213621 著者 Yamashita S, Ando Y タイトル Genotype-phenotype relationship in hereditary amyotrophic lateral sclerosis. 雑誌 Transl Neurodegener 4:13 (2015) DOI:10.1186/s40035-015-0036-y PMID:15952898 (ALS1) 著者 Valentine JS, Doucette PA, Zittin Potter S タイトル Copper-zinc superoxide dismutase and amyotrophic lateral sclerosis. 雑誌 Annu Rev Biochem 74:563-93 (2005) DOI:10.1146/annurev.biochem.72.121801.161647 PMID:15106121 (ALS4) 著者 Chen YZ, Bennett CL, Huynh HM, Blair IP, Puls I, Irobi J, Dierick I, Abel A, Kennerson ML, Rabin BA, Nicholson GA, Auer-Grumbach M, Wagner K, De Jonghe P, Griffin JW, Fischbeck KH, Timmerman V, Cornblath DR, Chance PF タイトル DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4). 雑誌 Am J Hum Genet 74:1128-35 (2004) DOI:10.1086/421054 PMID:19251628 (ALS6) 著者 Vance C, Rogelj B, Hortobagyi T, De Vos KJ, Nishimura AL, Sreedharan J, Hu X, Smith B, Ruddy D, Wright P, Ganesalingam J, Williams KL, Tripathi V, Al-Saraj S, Al-Chalabi A, Leigh PN, Blair IP, Nicholson G, de Belleroche J, Gallo JM, Miller CC, Shaw CE タイトル Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. 雑誌 Science 323:1208-11 (2009) DOI:10.1126/science.1165942 PMID:16501576 (ALS9) 著者 Greenway MJ, Andersen PM, Russ C, Ennis S, Cashman S, Donaghy C, Patterson V, Swingler R, Kieran D, Prehn J, Morrison KE, Green A, Acharya KR, Brown RH Jr, Hardiman O タイトル ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis. 雑誌 Nat Genet 38:411-3 (2006) DOI:10.1038/ng1742 PMID:18802454 (ALS10) 著者 Rutherford NJ, Zhang YJ, Baker M, Gass JM, Finch NA, Xu YF, Stewart H, Kelley BJ, Kuntz K, Crook RJ, Sreedharan J, Vance C, Sorenson E, Lippa C, Bigio EH, Geschwind DH, Knopman DS, Mitsumoto H, Petersen RC, Cashman NR, Hutton M, Shaw CE, Boylan KB, Boeve B, Graff-Radford NR, Wszolek ZK, Caselli RJ, Dickson DW, Mackenzie IR, Petrucelli L, Rademakers R タイトル Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis. 雑誌 PLoS Genet 4:e1000193 (2008) DOI:10.1371/journal.pgen.1000193 PMID:19118816 (ALS11) 著者 Chow CY, Landers JE, Bergren SK, Sapp PC, Grant AE, Jones JM, Everett L, Lenk GM, McKenna-Yasek DM, Weisman LS, Figlewicz D, Brown RH, Meisler MH タイトル Deleterious variants of FIG4, a phosphoinositide phosphatase, in patients with ALS. 雑誌 Am J Hum Genet 84:85-8 (2009) DOI:10.1016/j.ajhg.2008.12.010 PMID:20428114 (ALS12) 著者 Maruyama H, Morino H, Ito H, Izumi Y, Kato H, Watanabe Y, Kinoshita Y, Kamada M, Nodera H, Suzuki H, Komure O, Matsuura S, Kobatake K, Morimoto N, Abe K, Suzuki N, Aoki M, Kawata A, Hirai T, Kato T, Ogasawara K, Hirano A, Takumi T, Kusaka H, Hagiwara K, Kaji R, Kawakami H タイトル Mutations of optineurin in amyotrophic lateral sclerosis. 雑誌 Nature 465:223-6 (2010) DOI:10.1038/nature08971 PMID:30870681 (ALS1-ALS23) 著者 Mathis S, Goizet C, Soulages A, Vallat JM, Masson GL タイトル Genetics of amyotrophic lateral sclerosis: A review. 雑誌 J Neurol Sci 399:217-226 (2019) DOI:10.1016/j.jns.2019.02.030 PMID:26945885 (ALS24) 著者 Brenner D, Muller K, Wieland T, Weydt P, Bohm S, Lule D, Hubers A, Neuwirth C, Weber M, Borck G, Wahlqvist M, Danzer KM, Volk AE, Meitinger T, Strom TM, Otto M, Kassubek J, Ludolph AC, Andersen PM, Weishaupt JH タイトル NEK1 mutations in familial amyotrophic lateral sclerosis. 雑誌 Brain 139:e28 (2016) DOI:10.1093/brain/aww033 PMID:29566793 (ALS25) 著者 Nicolas A, Kenna KP, Renton AE, Ticozzi N, Faghri F, Chia R, Dominov JA, Kenna BJ, Nalls MA, Keagle P, Rivera AM, van Rheenen W, Murphy NA, van Vugt JJFA, Geiger JT, Van der Spek RA, Pliner HA, Shankaracharya, Smith BN, Marangi G, Topp SD, Abramzon Y, Gkazi AS, Eicher JD, Kenna A, Mora G, Calvo A, Mazzini L, Riva N, Mandrioli J, Caponnetto C, Battistini S, Volanti P, La Bella V, Conforti FL, Borghero G, Messina S, Simone IL, Trojsi F, Salvi F, Logullo FO, D'Alfonso S, Corrado L, Capasso M, Ferrucci L, Moreno CAM, Kamalakaran S, Goldstein DB, Gitler AD, Harris T, Myers RM, Phatnani H, Musunuri RL, Evani US, Abhyankar A, Zody MC, Kaye J, Finkbeiner S, Wyman SK, LeNail A, Lima L, Fraenkel E, Svendsen CN, Thompson LM, Van Eyk JE, Berry JD, Miller TM, Kolb SJ, Cudkowicz M, Baxi E, Benatar M, Taylor JP, Rampersaud E, Wu G, Wuu J, Lauria G, Verde F, Fogh I, Tiloca C, Comi GP, Soraru G, Cereda C, Corcia P, Laaksovirta H, Myllykangas L, Jansson L, Valori M, Ealing J, Hamdalla H, Rollinson S, Pickering-Brown S, Orrell RW, Sidle KC, Malaspina A, Hardy J, Singleton AB, Johnson JO, Arepalli S, Sapp PC, McKenna-Yasek D, Polak M, Asress S, Al-Sarraj S, King A, Troakes C, Vance C, de Belleroche J, Baas F, Ten Asbroek ALMA, Munoz-Blanco JL, Hernandez DG, Ding J, Gibbs JR, Scholz SW, Floeter MK, Campbell RH, Landi F, Bowser R, Pulst SM, Ravits JM, MacGowan DJL, Kirby J, Pioro EP, Pamphlett R, Broach J, Gerhard G, Dunckley TL, Brady CB, Kowall NW, Troncoso JC, Le Ber I, Mouzat K, Lumbroso S, Heiman-Patterson TD, Kamel F, Van Den Bosch L, Baloh RH, Strom TM, Meitinger T, Shatunov A, Van Eijk KR, de Carvalho M, Kooyman M, Middelkoop B, Moisse M, McLaughlin RL, Van Es MA, Weber M, Boylan KB, Van Blitterswijk M, Rademakers R, Morrison KE, Basak AN, Mora JS, Drory VE, Shaw PJ, Turner MR, Talbot K, Hardiman O, Williams KL, Fifita JA, Nicholson GA, Blair IP, Rouleau GA, Esteban-Perez J, Garcia-Redondo A, Al-Chalabi A, Rogaeva E, Zinman L, Ostrow LW, Maragakis NJ, Rothstein JD, Simmons Z, Cooper-Knock J, Brice A, Goutman SA, Feldman EL, Gibson SB, Taroni F, Ratti A, Gellera C, Van Damme P, Robberecht W, Fratta P, Sabatelli M, Lunetta C, Ludolph AC, Andersen PM, Weishaupt JH, Camu W, Trojanowski JQ, Van Deerlin VM, Brown RH Jr, van den Berg LH, Veldink JH, Harms MB, Glass JD, Stone DJ, Tienari P, Silani V, Chio A, Shaw CE, Traynor BJ, Landers JE タイトル Genome-wide Analyses Identify KIF5A as a Novel ALS Gene. 雑誌 Neuron 97:1268-1283.e6 (2018) DOI:10.1016/j.neuron.2018.02.027 PMID:28817800 (ALS26) 著者 Mackenzie IR, Nicholson AM, Sarkar M, Messing J, Purice MD, Pottier C, Annu K, Baker M, Perkerson RB, Kurti A, Matchett BJ, Mittag T, Temirov J, Hsiung GR, Krieger C, Murray ME, Kato M, Fryer JD, Petrucelli L, Zinman L, Weintraub S, Mesulam M, Keith J, Zivkovic SA, Hirsch-Reinshagen V, Roos RP, Zuchner S, Graff-Radford NR, Petersen RC, Caselli RJ, Wszolek ZK, Finger E, Lippa C, Lacomis D, Stewart H, Dickson DW, Kim HJ, Rogaeva E, Bigio E, Boylan KB, Taylor JP, Rademakers R タイトル TIA1 Mutations in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Promote Phase Separation and Alter Stress Granule Dynamics. 雑誌 Neuron 95:808-816.e9 (2017) DOI:10.1016/j.neuron.2017.07.025 PMID:34059824 (ALS27) 著者 Mohassel P, Donkervoort S, Lone MA, Nalls M, Gable K, Gupta SD, Foley AR, Hu Y, Saute JAM, Moreira AL, Kok F, Introna A, Logroscino G, Grunseich C, Nickolls AR, Pourshafie N, Neuhaus SB, Saade D, Gangfuss A, Kolbel H, Piccus Z, Le Pichon CE, Fiorillo C, Ly CV, Topf A, Brady L, Specht S, Zidell A, Pedro H, Mittelmann E, Thomas FP, Chao KR, Konersman CG, Cho MT, Brandt T, Straub V, Connolly AM, Schara U, Roos A, Tarnopolsky M, Hoke A, Brown RH, Lee CH, Hornemann T, Dunn TM, Bonnemann CG タイトル Childhood amyotrophic lateral sclerosis caused by excess sphingolipid synthesis. 雑誌 Nat Med 27:1197-1204 (2021) DOI:10.1038/s41591-021-01346-1 PMID:37339631 (ALS28) 著者 Kume K, Kurashige T, Muguruma K, Morino H, Tada Y, Kikumoto M, Miyamoto T, Akutsu SN, Matsuda Y, Matsuura S, Nakamori M, Nishiyama A, Izumi R, Niihori T, Ogasawara M, Eura N, Kato T, Yokomura M, Nakayama Y, Ito H, Nakamura M, Saito K, Riku Y, Iwasaki Y, Maruyama H, Aoki Y, Nishino I, Izumi Y, Aoki M, Kawakami H タイトル CGG repeat expansion in LRP12 in amyotrophic lateral sclerosis. 雑誌 Am J Hum Genet 110:1086-1097 (2023) DOI:10.1016/j.ajhg.2023.05.014 PMID:16051700 (ALSPDC) 著者 Hermosura MC, Nayakanti H, Dorovkov MV, Calderon FR, Ryazanov AG, Haymer DS, Garruto RM タイトル A TRPM7 variant shows altered sensitivity to magnesium that may contribute to the pathogenesis of two Guamanian neurodegenerative disorders. 雑誌 Proc Natl Acad Sci U S A 102:11510-5 (2005) DOI:10.1073/pnas.0505149102 PMID:17185385 (ALSPDC) 著者 Sundar PD, Yu CE, Sieh W, Steinbart E, Garruto RM, Oyanagi K, Craig UK, Bird TD, Wijsman EM, Galasko DR, Schellenberg GD タイトル Two sites in the MAPT region confer genetic risk for Guam ALS/PDC and dementia. 雑誌 Hum Mol Genet 16:295-306 (2007) DOI:10.1093/hmg/ddl463 PMID:29403345 (ALSPDC) 著者 Hata Y, Ma N, Yoneda M, Morimoto S, Okano H, Murayama S, Kawanishi S, Kuzuhara S, Kokubo Y タイトル Nitrative Stress and Tau Accumulation in Amyotrophic Lateral Sclerosis/Parkinsonism-Dementia Complex (ALS/PDC) in the Kii Peninsula, Japan. 雑誌 Front Neurosci 11:751 (2017) DOI:10.3389/fnins.2017.00751 |