A pilot study on the use of interferon beta-1a in early Alzheimer’s disease subjects
Despite the fact that multiple sclerosis (MS) and Alzheimer's disease (AD) share common neuroimmunological features, interferon beta 1a (IFNβ1a), the well-established treatment for the prevention of disease progression and cognitive decline in MS patients, has never been used in AD. We evaluate...
Saved in:
Published in | Journal of neuroinflammation Vol. 11; no. 1; p. 30 |
---|---|
Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
BioMed Central Ltd
13.02.2014
BioMed Central |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Despite the fact that multiple sclerosis (MS) and Alzheimer's disease (AD) share common neuroimmunological features, interferon beta 1a (IFNβ1a), the well-established treatment for the prevention of disease progression and cognitive decline in MS patients, has never been used in AD. We evaluated the safety and efficacy of IFNβ1a in subjects affected by mild-to-moderate AD in a double-blind, randomized, placebo-controlled, multicenter pilot study. Forty-two early Alzheimer's patients were randomized to receive either a 22 mcg subcutaneous injection of IFNβ1a or placebo three times per week. A treatment period of 28 weeks was followed by 24 weeks of observation. IFNβ1a was well tolerated and adverse events were infrequent and mild to moderate. Although not statistically significant, a reduction in disease progression during follow-up was measured in IFNβ1a-treated patients by the Alzheimer's Disease Assessment Scale cognitive subscale. Interestingly, the treatment group showed significant improvements in the Instrumental Activities of Daily Living and Physical Self-maintenance Scale. This study suggests that IFNβ1a is safe and well tolerated in early AD patients, and its possible beneficial role should be further investigated in larger studies. |
---|---|
AbstractList | Despite the fact that multiple sclerosis (MS) and Alzheimer's disease (AD) share common neuroimmunological features, interferon beta 1a (IFNβ1a), the well-established treatment for the prevention of disease progression and cognitive decline in MS patients, has never been used in AD. We evaluated the safety and efficacy of IFNβ1a in subjects affected by mild-to-moderate AD in a double-blind, randomized, placebo-controlled, multicenter pilot study. Forty-two early Alzheimer's patients were randomized to receive either a 22 mcg subcutaneous injection of IFNβ1a or placebo three times per week. A treatment period of 28 weeks was followed by 24 weeks of observation. IFNβ1a was well tolerated and adverse events were infrequent and mild to moderate. Although not statistically significant, a reduction in disease progression during follow-up was measured in IFNβ1a-treated patients by the Alzheimer's Disease Assessment Scale cognitive subscale. Interestingly, the treatment group showed significant improvements in the Instrumental Activities of Daily Living and Physical Self-maintenance Scale. This study suggests that IFNβ1a is safe and well tolerated in early AD patients, and its possible beneficial role should be further investigated in larger studies.Despite the fact that multiple sclerosis (MS) and Alzheimer's disease (AD) share common neuroimmunological features, interferon beta 1a (IFNβ1a), the well-established treatment for the prevention of disease progression and cognitive decline in MS patients, has never been used in AD. We evaluated the safety and efficacy of IFNβ1a in subjects affected by mild-to-moderate AD in a double-blind, randomized, placebo-controlled, multicenter pilot study. Forty-two early Alzheimer's patients were randomized to receive either a 22 mcg subcutaneous injection of IFNβ1a or placebo three times per week. A treatment period of 28 weeks was followed by 24 weeks of observation. IFNβ1a was well tolerated and adverse events were infrequent and mild to moderate. Although not statistically significant, a reduction in disease progression during follow-up was measured in IFNβ1a-treated patients by the Alzheimer's Disease Assessment Scale cognitive subscale. Interestingly, the treatment group showed significant improvements in the Instrumental Activities of Daily Living and Physical Self-maintenance Scale. This study suggests that IFNβ1a is safe and well tolerated in early AD patients, and its possible beneficial role should be further investigated in larger studies. Despite the fact that multiple sclerosis (MS) and Alzheimer's disease (AD) share common neuroimmunological features, interferon beta 1a (IFNβ1a), the well-established treatment for the prevention of disease progression and cognitive decline in MS patients, has never been used in AD. We evaluated the safety and efficacy of IFNβ1a in subjects affected by mild-to-moderate AD in a double-blind, randomized, placebo-controlled, multicenter pilot study. Forty-two early Alzheimer's patients were randomized to receive either a 22 mcg subcutaneous injection of IFNβ1a or placebo three times per week. A treatment period of 28 weeks was followed by 24 weeks of observation. IFNβ1a was well tolerated and adverse events were infrequent and mild to moderate. Although not statistically significant, a reduction in disease progression during follow-up was measured in IFNβ1a-treated patients by the Alzheimer's Disease Assessment Scale cognitive subscale. Interestingly, the treatment group showed significant improvements in the Instrumental Activities of Daily Living and Physical Self-maintenance Scale. This study suggests that IFNβ1a is safe and well tolerated in early AD patients, and its possible beneficial role should be further investigated in larger studies. Despite the fact that multiple sclerosis (MS) and Alzheimer's disease (AD) share common neuroimmunological features, interferon beta 1a (IFN[beta]1a), the well-established treatment for the prevention of disease progression and cognitive decline in MS patients, has never been used in AD. We evaluated the safety and efficacy of IFN[beta]1a in subjects affected by mild-to-moderate AD in a double-blind, randomized, placebo-controlled, multicenter pilot study. Forty-two early Alzheimer's patients were randomized to receive either a 22 mcg subcutaneous injection of IFN[beta]1a or placebo three times per week. A treatment period of 28 weeks was followed by 24 weeks of observation. IFN[beta]1a was well tolerated and adverse events were infrequent and mild to moderate. Although not statistically significant, a reduction in disease progression during follow-up was measured in IFN[beta]1a-treated patients by the Alzheimer's Disease Assessment Scale cognitive subscale. Interestingly, the treatment group showed significant improvements in the Instrumental Activities of Daily Living and Physical Self-maintenance Scale. This study suggests that IFN[beta]1a is safe and well tolerated in early AD patients, and its possible beneficial role should be further investigated in larger studies. Despite the fact that multiple sclerosis (MS) and Alzheimer's disease (AD) share common neuroimmunological features, interferon beta 1a (IFNβ1a), the well-established treatment for the prevention of disease progression and cognitive decline in MS patients, has never been used in AD. We evaluated the safety and efficacy of IFNβ1a in subjects affected by mild-to-moderate AD in a double-blind, randomized, placebo-controlled, multicenter pilot study. Forty-two early Alzheimer's patients were randomized to receive either a 22 mcg subcutaneous injection of IFNβ1a or placebo three times per week. A treatment period of 28 weeks was followed by 24 weeks of observation. IFNβ1a was well tolerated and adverse events were infrequent and mild to moderate. Although not statistically significant, a reduction in disease progression during follow-up was measured in IFNβ1a-treated patients by the Alzheimer's Disease Assessment Scale cognitive subscale. Interestingly, the treatment group showed significant improvements in the Instrumental Activities of Daily Living and Physical Self-maintenance Scale. This study suggests that IFNβ1a is safe and well tolerated in early AD patients, and its possible beneficial role should be further investigated in larger studies. Doc number: 30 Abstract: Despite the fact that multiple sclerosis (MS) and Alzheimer's disease (AD) share common neuroimmunological features, interferon beta 1a (IFNβ1a), the well-established treatment for the prevention of disease progression and cognitive decline in MS patients, has never been used in AD. We evaluated the safety and efficacy of IFNβ1a in subjects affected by mild-to-moderate AD in a double-blind, randomized, placebo-controlled, multicenter pilot study. Forty-two early Alzheimer's patients were randomized to receive either a 22 mcg subcutaneous injection of IFNβ1a or placebo three times per week. A treatment period of 28 weeks was followed by 24 weeks of observation. IFNβ1a was well tolerated and adverse events were infrequent and mild to moderate. Although not statistically significant, a reduction in disease progression during follow-up was measured in IFNβ1a-treated patients by the Alzheimer's Disease Assessment Scale cognitive subscale. Interestingly, the treatment group showed significant improvements in the Instrumental Activities of Daily Living and Physical Self-maintenance Scale. This study suggests that IFNβ1a is safe and well tolerated in early AD patients, and its possible beneficial role should be further investigated in larger studies. Despite the fact that multiple sclerosis (MS) and Alzheimer's disease (AD) share common neuroimmunological features, interferon beta 1a (IFN[beta]1a), the well-established treatment for the prevention of disease progression and cognitive decline in MS patients, has never been used in AD. We evaluated the safety and efficacy of IFN[beta]1a in subjects affected by mild-to-moderate AD in a double-blind, randomized, placebo-controlled, multicenter pilot study. Forty-two early Alzheimer's patients were randomized to receive either a 22 mcg subcutaneous injection of IFN[beta]1a or placebo three times per week. A treatment period of 28 weeks was followed by 24 weeks of observation. IFN[beta]1a was well tolerated and adverse events were infrequent and mild to moderate. Although not statistically significant, a reduction in disease progression during follow-up was measured in IFN[beta]1a-treated patients by the Alzheimer's Disease Assessment Scale cognitive subscale. Interestingly, the treatment group showed significant improvements in the Instrumental Activities of Daily Living and Physical Self-maintenance Scale. This study suggests that IFN[beta]1a is safe and well tolerated in early AD patients, and its possible beneficial role should be further investigated in larger studies. Keywords: Alzheimer's disease, clinical trials, randomized, controlled, multiple sclerosis, interferon |
Audience | Academic |
Author | Iemolo, Francesco Paolillo, Andrea Zappalà, Giuseppe Bruno, Giuseppe Ruggieri, Stefano Castellano, Anna Grimaldi, Luigi Maria |
AuthorAffiliation | 2 U.V.A. Neurologia, Azienda Ospedaliera Garibaldi-Nesima, Via Palermo 135, 95122 Catania, Italy 6 MerckSerono S.A., Merck Serono-Italy An affiliate of Merck KGA, Darmsdadt, Germany, Via Casilina 125, 00176 Roma, Italy 3 U.O.C. Provinciale di Neurologia, Via Papa Giovanni XIII, 97019 Vittoria, RG, Italy 1 U.O. di Neurologia, Fondazione Istituto San Raffaele “G. Giglio” di Cefalù, Contrada Pietrapollastra, 90015 Cefalù, PA, Italy 4 Clinica Neurologica, IRCCS Neuromed, Via Atinense, 18, 86077 Pozzilli, IS, Italy 5 Centro U.V.A., Dipartimento di Scienze Neurologiche, Università degli Studi di Roma “La Sapienza”, Viale dell’Università, 30, 00185 Roma, Italy |
AuthorAffiliation_xml | – name: 5 Centro U.V.A., Dipartimento di Scienze Neurologiche, Università degli Studi di Roma “La Sapienza”, Viale dell’Università, 30, 00185 Roma, Italy – name: 6 MerckSerono S.A., Merck Serono-Italy An affiliate of Merck KGA, Darmsdadt, Germany, Via Casilina 125, 00176 Roma, Italy – name: 3 U.O.C. Provinciale di Neurologia, Via Papa Giovanni XIII, 97019 Vittoria, RG, Italy – name: 1 U.O. di Neurologia, Fondazione Istituto San Raffaele “G. Giglio” di Cefalù, Contrada Pietrapollastra, 90015 Cefalù, PA, Italy – name: 2 U.V.A. Neurologia, Azienda Ospedaliera Garibaldi-Nesima, Via Palermo 135, 95122 Catania, Italy – name: 4 Clinica Neurologica, IRCCS Neuromed, Via Atinense, 18, 86077 Pozzilli, IS, Italy |
Author_xml | – sequence: 1 givenname: Luigi Maria surname: Grimaldi fullname: Grimaldi, Luigi Maria – sequence: 2 givenname: Giuseppe surname: Zappalà fullname: Zappalà, Giuseppe – sequence: 3 givenname: Francesco surname: Iemolo fullname: Iemolo, Francesco – sequence: 4 givenname: Anna surname: Castellano fullname: Castellano, Anna – sequence: 5 givenname: Stefano surname: Ruggieri fullname: Ruggieri, Stefano – sequence: 6 givenname: Giuseppe surname: Bruno fullname: Bruno, Giuseppe – sequence: 7 givenname: Andrea surname: Paolillo fullname: Paolillo, Andrea |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/24524367$$D View this record in MEDLINE/PubMed |
BookMark | eNqNkk9rFDEYxoNU7B89e5MBL71Mmz8zyeQirMWqUPCiXkMmeaebZWayJhlhe_Jr-PX8JM2wde2WFiSHhCe_5-Hl4T1GB6MfAaHXBJ8R0vBzIipaUiyrkpCS4WfoaKcc3HsfouMYVxgzWnP6Ah3SqqYV4-IIfV8Ua9f7VMQ02U3hxyItoZgiFL4r3JggdBCy2kLSJdFZKkCHflMs-psluAHCn1-_Y2FdBJ1NcWpXYFJ8iZ53uo_w6u4-Qd8uP3y9-FReffn4-WJxVbZ1g1NZWdta4LbmlmJMOXAsjRGys13TApfS1BUIwMJgEFYQbKvWamYpMULTTrMT9G6bu57aAayBMQXdq3Vwgw4b5bVT-z-jW6pr_1MxyUhuIwe83wa0zj8RsP9j_KDmXtXcqyJEMZxDTu-mCP7HBDGpwUUDfa9H8FNUpMY1qxpZNf-DkoaJWsiMvn2ArvwUxlznTGHJMZXkH3Wte1Bu7Hwe08yhalEzyXkjRJWps0eofCwMzuSd6lzW9wxv7he7K-Tv5mTgfAuY4GMM0O0QgtW8m4-0VD9wGJd0cn4u1vVP-m4BQeHm6g |
CitedBy_id | crossref_primary_10_1136_jnnp_2017_316201 crossref_primary_10_1590_1980_57642018dn13_010002 crossref_primary_10_3390_cancers14225495 crossref_primary_10_3390_ijms232214394 crossref_primary_10_1186_s12974_024_03298_y crossref_primary_10_3310_hta21260 crossref_primary_10_3390_jpm11111116 crossref_primary_10_3389_fimmu_2021_738511 crossref_primary_10_1016_j_jneuroim_2023_578031 crossref_primary_10_1016_j_jns_2017_03_031 crossref_primary_10_2174_1874467213666200422090135 crossref_primary_10_1038_s41582_020_00435_y crossref_primary_10_1111_cen3_12518 crossref_primary_10_3233_JAD_200607 crossref_primary_10_1016_j_brainresbull_2019_06_015 crossref_primary_10_1186_s12974_019_1417_4 crossref_primary_10_1016_j_drudis_2022_01_004 crossref_primary_10_1517_14728222_2014_989834 crossref_primary_10_3233_JAD_171131 crossref_primary_10_1016_j_ebiom_2022_104175 crossref_primary_10_1016_j_jaut_2014_08_002 crossref_primary_10_1186_s12974_020_01877_3 crossref_primary_10_1093_brain_awv408 crossref_primary_10_1016_j_drudis_2019_05_009 crossref_primary_10_1016_j_ejphar_2024_176882 crossref_primary_10_1002_glia_23460 crossref_primary_10_1016_j_bbadis_2022_166430 crossref_primary_10_3389_fnagi_2022_968444 crossref_primary_10_18632_oncoscience_309 crossref_primary_10_1097_WNR_0000000000001132 crossref_primary_10_1186_s12859_016_1065_y crossref_primary_10_3389_fneur_2021_658695 crossref_primary_10_1016_j_pnpbp_2019_109661 crossref_primary_10_1038_s41398_018_0355_8 crossref_primary_10_1007_s12031_018_1249_1 crossref_primary_10_1080_1744666X_2023_2248391 crossref_primary_10_1016_j_coph_2015_09_015 crossref_primary_10_1016_j_mehy_2022_110996 crossref_primary_10_1177_1179573517722512 crossref_primary_10_1002_alz_13076 crossref_primary_10_3233_JAD_215125 |
Cites_doi | 10.1001/archneur.62.4.563 10.1038/nature08983 10.1191/1352458505ms1144oa 10.1089/rej.2009.0993 10.1111/j.1749-6632.1999.tb07821.x 10.1001/archneur.60.8.1119 10.1212/WNL.51.3.682 10.1016/S0165-5728(99)00029-6 10.1136/jnnp-2012-304740 10.1097/00062752-199901000-00004 10.1016/0165-0173(95)00011-9 10.1146/annurev.neuro.30.051606.094313 10.1016/S0165-5728(99)00106-X 10.1177/1352458509350309 10.1016/j.expneurol.2006.04.015 10.1016/j.mcn.2010.08.001 10.1073/pnas.86.19.7611 10.1002/ana.1218 10.1152/physrev.00023.2009 |
ContentType | Journal Article |
Copyright | COPYRIGHT 2014 BioMed Central Ltd. 2014 Grimaldi et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. Copyright © 2014 Grimaldi et al.; licensee BioMed Central Ltd. 2014 Grimaldi et al.; licensee BioMed Central Ltd. |
Copyright_xml | – notice: COPYRIGHT 2014 BioMed Central Ltd. – notice: 2014 Grimaldi et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. – notice: Copyright © 2014 Grimaldi et al.; licensee BioMed Central Ltd. 2014 Grimaldi et al.; licensee BioMed Central Ltd. |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 3V. 7T5 7TK 7X7 7XB 88E 8FI 8FJ 8FK ABUWG AFKRA AZQEC BENPR CCPQU DWQXO FYUFA GHDGH H94 K9. M0S M1P PHGZM PHGZT PIMPY PJZUB PKEHL PPXIY PQEST PQQKQ PQUKI PRINS 7X8 5PM |
DOI | 10.1186/1742-2094-11-30 |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed ProQuest Central (Corporate) Immunology Abstracts Neurosciences Abstracts Health & Medical Collection ProQuest Central (purchase pre-March 2016) Medical Database (Alumni Edition) ProQuest Hospital Collection Hospital Premium Collection (Alumni Edition) ProQuest Central (Alumni) (purchase pre-March 2016) ProQuest Central (Alumni) ProQuest Central UK/Ireland ProQuest Central Essentials - QC ProQuest Central ProQuest One ProQuest Central Korea Health Research Premium Collection Health Research Premium Collection (Alumni) AIDS and Cancer Research Abstracts ProQuest Health & Medical Complete (Alumni) ProQuest Health & Medical Collection Medical Database ProQuest Central Premium ProQuest One Academic (New) Publicly Available Content Database ProQuest Health & Medical Research Collection ProQuest One Academic Middle East (New) ProQuest One Health & Nursing ProQuest One Academic Eastern Edition (DO NOT USE) ProQuest One Academic ProQuest One Academic UKI Edition ProQuest Central China MEDLINE - Academic PubMed Central (Full Participant titles) |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) Publicly Available Content Database ProQuest One Academic Middle East (New) ProQuest Central Essentials ProQuest Health & Medical Complete (Alumni) ProQuest Central (Alumni Edition) ProQuest One Community College ProQuest One Health & Nursing ProQuest Central China ProQuest Central Health Research Premium Collection Health and Medicine Complete (Alumni Edition) ProQuest Central Korea Health & Medical Research Collection AIDS and Cancer Research Abstracts ProQuest Central (New) ProQuest Medical Library (Alumni) ProQuest One Academic Eastern Edition ProQuest Hospital Collection Health Research Premium Collection (Alumni) Neurosciences Abstracts ProQuest Hospital Collection (Alumni) ProQuest Health & Medical Complete ProQuest Medical Library ProQuest One Academic UKI Edition Immunology Abstracts ProQuest One Academic ProQuest One Academic (New) ProQuest Central (Alumni) MEDLINE - Academic |
DatabaseTitleList | MEDLINE - Academic AIDS and Cancer Research Abstracts MEDLINE Publicly Available Content Database |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database – sequence: 3 dbid: BENPR name: ProQuest Central url: https://www.proquest.com/central sourceTypes: Aggregation Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 1742-2094 |
EndPage | 30 |
ExternalDocumentID | PMC3931325 oai_biomedcentral_com_1742_2094_11_30 3226274671 A539668774 24524367 10_1186_1742_2094_11_30 |
Genre | Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't Journal Article |
GeographicLocations | Italy Germany |
GeographicLocations_xml | – name: Germany – name: Italy |
GroupedDBID | --- 0R~ 29L 2VQ 2WC 4.4 53G 5GY 5VS 7X7 88E 8FI 8FJ AAFWJ AAJSJ AASML AAWTL AAYXX ABDBF ABUWG ACGFO ACGFS ACIHN ACPRK ACUHS ADBBV ADRAZ ADUKV AEAQA AENEX AFKRA AFPKN AHBYD AHMBA AHSBF AHYZX ALIPV ALMA_UNASSIGNED_HOLDINGS AMKLP AMTXH AOIJS BAPOH BAWUL BCNDV BENPR BFQNJ BMC BPHCQ BVXVI C6C CCPQU CITATION CS3 DIK DU5 E3Z EBD EBLON EBS EJD ESX F5P FYUFA GROUPED_DOAJ GX1 H13 HMCUK HYE IAO IHR INH INR IPNFZ ITC KQ8 M1P M48 M~E O5R O5S OK1 OVT P2P PGMZT PHGZM PHGZT PIMPY PQQKQ PROAC PSQYO RBZ RIG RNS ROL RPM RSV SBL SOJ TR2 TUS UKHRP WOQ WOW XSB ~8M CGR CUY CVF ECM EIF NPM PJZUB PPXIY PMFND 3V. 7T5 7TK 7XB 8FK AZQEC DWQXO H94 K9. PKEHL PQEST PQUKI PRINS 7X8 PUEGO -A0 ABVAZ ACRMQ ADINQ AFGXO AFNRJ C24 5PM |
ID | FETCH-LOGICAL-b580t-4ddbde6d56d20026e609cc79fdf8be699c54e7e07c0e7d710d4bda3d21c7a2fa3 |
IEDL.DBID | RBZ |
ISSN | 1742-2094 |
IngestDate | Thu Aug 21 14:21:46 EDT 2025 Wed May 22 07:13:25 EDT 2024 Fri Jul 11 00:50:51 EDT 2025 Sun Aug 24 03:24:59 EDT 2025 Fri Jul 25 02:43:47 EDT 2025 Tue Jun 17 22:05:28 EDT 2025 Tue Jun 10 21:03:04 EDT 2025 Mon Jul 21 05:35:18 EDT 2025 Tue Jul 01 02:54:23 EDT 2025 Thu Apr 24 23:10:16 EDT 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 1 |
Language | English |
License | This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-b580t-4ddbde6d56d20026e609cc79fdf8be699c54e7e07c0e7d710d4bda3d21c7a2fa3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 ObjectType-Undefined-3 ObjectType-Article-2 ObjectType-Feature-1 |
OpenAccessLink | http://dx.doi.org/10.1186/1742-2094-11-30 |
PMID | 24524367 |
PQID | 1500960291 |
PQPubID | 55345 |
PageCount | 1 |
ParticipantIDs | pubmedcentral_primary_oai_pubmedcentral_nih_gov_3931325 biomedcentral_primary_oai_biomedcentral_com_1742_2094_11_30 proquest_miscellaneous_1505348948 proquest_miscellaneous_1501837579 proquest_journals_1500960291 gale_infotracmisc_A539668774 gale_infotracacademiconefile_A539668774 pubmed_primary_24524367 crossref_primary_10_1186_1742_2094_11_30 crossref_citationtrail_10_1186_1742_2094_11_30 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2014-02-13 |
PublicationDateYYYYMMDD | 2014-02-13 |
PublicationDate_xml | – month: 02 year: 2014 text: 2014-02-13 day: 13 |
PublicationDecade | 2010 |
PublicationPlace | England |
PublicationPlace_xml | – name: England – name: London |
PublicationTitle | Journal of neuroinflammation |
PublicationTitleAlternate | J Neuroinflammation |
PublicationYear | 2014 |
Publisher | BioMed Central Ltd BioMed Central |
Publisher_xml | – name: BioMed Central Ltd – name: BioMed Central |
References | 10.1186/1742-2094-11-30-B14 10.1186/1742-2094-11-30-B25 10.1186/1742-2094-11-30-B13 10.1186/1742-2094-11-30-B24 10.1186/1742-2094-11-30-B16 10.1186/1742-2094-11-30-B26 10.1186/1742-2094-11-30-B10 10.1186/1742-2094-11-30-B23 10.1186/1742-2094-11-30-B2 10.1186/1742-2094-11-30-B3 10.1186/1742-2094-11-30-B4 10.1186/1742-2094-11-30-B5 10.1186/1742-2094-11-30-B6 10.1186/1742-2094-11-30-B18 10.1186/1742-2094-11-30-B7 10.1186/1742-2094-11-30-B17 10.1186/1742-2094-11-30-B9 10.1186/1742-2094-11-30-B19 10.1186/1742-2094-11-30-B1 15824253 - Arch Neurol. 2005 Apr;62(4):563-8 20393191 - Physiol Rev. 2010 Apr;90(2):465-94 23544717 - Am J Manag Care. 2013 Feb2013;19(2 Suppl):S21-7 19995846 - Mult Scler. 2010 Jan;16(1):68-77 11601495 - Ann Neurol. 2001 Oct;50(4):443-51 18558855 - Annu Rev Neurosci. 2008;31:247-69 20336135 - Nature. 2010 Mar 25;464(7288):529-35 20182045 - J Alzheimers Dis. 2010;21(1):1-14 23595944 - J Neurol Neurosurg Psychiatry. 2013 Nov;84(11):1186-91 20462385 - Rejuvenation Res. 2010 Apr-Jun;13(2-3):301-13 8866675 - Brain Res Brain Res Rev. 1995 Sep;21(2):195-218 2529544 - Proc Natl Acad Sci U S A. 1989 Oct;86(19):7611-5 16764858 - Exp Neurol. 2006 Sep;201(1):172-81 12925369 - Arch Neurol. 2003 Aug;60(8):1119-22 10496186 - J Neuroimmunol. 1999 Sep 1;99(1):131-41 20696249 - Mol Cell Neurosci. 2010 Dec;45(4):408-17 9551903 - J Immunol. 1998 Jan 15;160(2):681-90 15794391 - Mult Scler. 2005 Apr;11(2):175-81 23001712 - J Alzheimers Dis. 2013;33(2):297-312 9915549 - Curr Opin Hematol. 1999 Jan;6(1):15-24 9126051 - Brain. 1997 Mar;120 ( Pt 3):393-9 10672233 - Ann N Y Acad Sci. 1999;893:113-25 10496180 - J Neuroimmunol. 1999 Sep 1;99(1):82-90 11971121 - Neurology. 2002 Apr 23;58(8 Suppl 4):S3-9 18728744 - Neuropsychiatr Dis Treat. 2008 Apr;4(2):321-36 9748010 - Neurology. 1998 Sep;51(3):682-9 |
References_xml | – ident: 10.1186/1742-2094-11-30-B17 doi: 10.1001/archneur.62.4.563 – ident: 10.1186/1742-2094-11-30-B1 doi: 10.1038/nature08983 – ident: 10.1186/1742-2094-11-30-B23 doi: 10.1191/1352458505ms1144oa – ident: 10.1186/1742-2094-11-30-B24 doi: 10.1089/rej.2009.0993 – ident: 10.1186/1742-2094-11-30-B7 doi: 10.1111/j.1749-6632.1999.tb07821.x – ident: 10.1186/1742-2094-11-30-B2 doi: 10.1001/archneur.60.8.1119 – ident: 10.1186/1742-2094-11-30-B14 doi: 10.1212/WNL.51.3.682 – ident: 10.1186/1742-2094-11-30-B13 doi: 10.1016/S0165-5728(99)00029-6 – ident: 10.1186/1742-2094-11-30-B26 doi: 10.1136/jnnp-2012-304740 – ident: 10.1186/1742-2094-11-30-B4 doi: 10.1097/00062752-199901000-00004 – ident: 10.1186/1742-2094-11-30-B5 doi: 10.1016/0165-0173(95)00011-9 – ident: 10.1186/1742-2094-11-30-B10 doi: 10.1146/annurev.neuro.30.051606.094313 – ident: 10.1186/1742-2094-11-30-B9 doi: 10.1016/S0165-5728(99)00106-X – ident: 10.1186/1742-2094-11-30-B19 doi: 10.1177/1352458509350309 – ident: 10.1186/1742-2094-11-30-B18 doi: 10.1016/j.expneurol.2006.04.015 – ident: 10.1186/1742-2094-11-30-B25 doi: 10.1016/j.mcn.2010.08.001 – ident: 10.1186/1742-2094-11-30-B6 doi: 10.1073/pnas.86.19.7611 – ident: 10.1186/1742-2094-11-30-B16 doi: 10.1002/ana.1218 – ident: 10.1186/1742-2094-11-30-B3 doi: 10.1152/physrev.00023.2009 – reference: 20696249 - Mol Cell Neurosci. 2010 Dec;45(4):408-17 – reference: 18728744 - Neuropsychiatr Dis Treat. 2008 Apr;4(2):321-36 – reference: 10672233 - Ann N Y Acad Sci. 1999;893:113-25 – reference: 16764858 - Exp Neurol. 2006 Sep;201(1):172-81 – reference: 23001712 - J Alzheimers Dis. 2013;33(2):297-312 – reference: 20393191 - Physiol Rev. 2010 Apr;90(2):465-94 – reference: 11971121 - Neurology. 2002 Apr 23;58(8 Suppl 4):S3-9 – reference: 23544717 - Am J Manag Care. 2013 Feb2013;19(2 Suppl):S21-7 – reference: 8866675 - Brain Res Brain Res Rev. 1995 Sep;21(2):195-218 – reference: 19995846 - Mult Scler. 2010 Jan;16(1):68-77 – reference: 9748010 - Neurology. 1998 Sep;51(3):682-9 – reference: 9551903 - J Immunol. 1998 Jan 15;160(2):681-90 – reference: 12925369 - Arch Neurol. 2003 Aug;60(8):1119-22 – reference: 15824253 - Arch Neurol. 2005 Apr;62(4):563-8 – reference: 9126051 - Brain. 1997 Mar;120 ( Pt 3):393-9 – reference: 23595944 - J Neurol Neurosurg Psychiatry. 2013 Nov;84(11):1186-91 – reference: 11601495 - Ann Neurol. 2001 Oct;50(4):443-51 – reference: 20182045 - J Alzheimers Dis. 2010;21(1):1-14 – reference: 2529544 - Proc Natl Acad Sci U S A. 1989 Oct;86(19):7611-5 – reference: 18558855 - Annu Rev Neurosci. 2008;31:247-69 – reference: 15794391 - Mult Scler. 2005 Apr;11(2):175-81 – reference: 20462385 - Rejuvenation Res. 2010 Apr-Jun;13(2-3):301-13 – reference: 20336135 - Nature. 2010 Mar 25;464(7288):529-35 – reference: 10496186 - J Neuroimmunol. 1999 Sep 1;99(1):131-41 – reference: 9915549 - Curr Opin Hematol. 1999 Jan;6(1):15-24 – reference: 10496180 - J Neuroimmunol. 1999 Sep 1;99(1):82-90 |
SSID | ssj0032562 |
Score | 2.2620912 |
Snippet | Despite the fact that multiple sclerosis (MS) and Alzheimer's disease (AD) share common neuroimmunological features, interferon beta 1a (IFNβ1a), the... Despite the fact that multiple sclerosis (MS) and Alzheimer's disease (AD) share common neuroimmunological features, interferon beta 1a (IFN[beta]1a), the... Doc number: 30 Abstract: Despite the fact that multiple sclerosis (MS) and Alzheimer's disease (AD) share common neuroimmunological features, interferon beta... Despite the fact that multiple sclerosis (MS) and Alzheimer’s disease (AD) share common neuroimmunological features, interferon beta 1a (IFNβ1a), the... |
SourceID | pubmedcentral biomedcentral proquest gale pubmed crossref |
SourceType | Open Access Repository Aggregation Database Index Database Enrichment Source |
StartPage | 30 |
SubjectTerms | Activities of daily living Adjuvants, Immunologic - therapeutic use Advertising executives Aged Alzheimer Disease - drug therapy Alzheimer's disease Analysis of Variance Antidepressants Antilipemic agents Blood-brain barrier Cholesterol Double-Blind Method Family medical history Female Free radicals Hematology Humans Interferon beta-1a Interferon-beta - therapeutic use Male Mental Status Schedule Middle Aged Neuropsychological Tests Older people Pathogenesis Physiological aspects Pilot Projects Proteins Retrospective Studies Statins Time Factors Treatment Outcome |
SummonAdditionalLinks | – databaseName: Health & Medical Collection dbid: 7X7 link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1Lb9QwELagSIgL4k1KQUZCKpfQJHbsWBzQClFVSOXUSnuzHD_UlbbJssle-PWdyXqXuoheYzuJPTP2N_b4G0I-CXABgvFlXmFYDVdFgWleyrwVxvLAXFVwvCh8_kucXfKf83oeN9yGGFa5mxOnidr1FvfITwC4INquVPlt9TvHrFF4uhpTaDwkj5C6DEO65HzvcDFYzqtI51M24gTAdwVaofiWuu_OFfdlsjLdnZ9vLVBp8OSt1ej0GXkaYSSdbeX-nDzw3Qvy-DwelL8kFzO6Wiz7kU70sbTvKAA9uhk87QNFioh18Gt42vrR5KWBR9Qj1TGdLf9c-cW1Xx8PNB7e0GHT4m7N8Ipcnv64-H6WxwQKeVs3xZhz51rnhauFw1gM4UWhrJUquNC0Xihla-6lL6QtvHSANRxvnQEBlVaaKhj2mhx0feffEioqJxteBy5N4AAaWiErxsC4VWG9KE1GviaDqVdbsgyN9NVpCUhVoyg0igI8EM2KjHzZDb22kZscU2Qs9eSjNOLfBp_3DXZf-m_VY5SlRoOFd1oT7x1Av5D6Ss9qBi5fAzA4I0dJTTA0mxbvtEFHQx_0X7XMyMd9MbbE4LXO95upDkycspbq3jo1443iTUbebBVs3zE8HOdMyIzIRPWSMU5LusXVRBXOFFJz1of3__o78gREyjEYvWRH5GBcb_x7wFpj-2EyqBty3yfO priority: 102 providerName: ProQuest – databaseName: Scholars Portal Journals: Open Access dbid: M48 link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1bi9UwEA66gvgi3q2uEkHQl65tc2sQkYO4LMLxySP7FtIkZQ_Udm17QH3yb_j3_CXOtD3H7bqKr8mkJXPpzDSTbwh5KiEFKG1I4wzLarhOEmzzksaFtI6XzGcJx4vCy_fyaMXfHYvj3-2AJgZ2F6Z22E9q1VYHXz5_fQ0G_2ow-Fy-gKA6A2lrPkLyXSZXwC0ptNIl3x0pMPDt2Xg7ciSecH4ueMC5u-_VzGWd_3Cf8VzzqsozburwBrk-xZd0MSrETXIp1LfI1eV0gn6bfFzQ03XV9HTAlaVNTSECpJsu0KakiB3RlqGF0SL0Nk4tDNGAGMh0UX07CetPof35_UdHp3Md2m0K_JHT3SGrw7cf3hzFU2-FuBB50sfc-8IH6YX0WKYhg0y0c0qXvsyLILV2ggcVEuWSoDyEIZ4X3oLsUqdsVlp2l-zVTR3uEyozr3IuSq5sySGeKKTKGAO714kLMrUReTljpzkdcTQMIlvPZ8DIDArDoDAgOTEsicjBlvnGTbDl2D2jMkP6kss_FzzfLdi-6a-kz1CaBrULnunsdCUB9oWoWGYhGGSDOUTIEdmfUYINuvn0Vh_MVoUNhNqYH2Y6jciT3TSuxLq2OjSbgQa-qUoo_U8awXiueR6Re6OK7TaG5-acSRURNVO-GY_nM_X6ZEARZxpRO8WD_2fXQ3INxMuxZj1l-2SvbzfhEYRkffF4MLVfCJ4wvw priority: 102 providerName: Scholars Portal |
Title | A pilot study on the use of interferon beta-1a in early Alzheimer’s disease subjects |
URI | https://www.ncbi.nlm.nih.gov/pubmed/24524367 https://www.proquest.com/docview/1500960291 https://www.proquest.com/docview/1501837579 https://www.proquest.com/docview/1505348948 http://dx.doi.org/10.1186/1742-2094-11-30 https://pubmed.ncbi.nlm.nih.gov/PMC3931325 |
Volume | 11 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1La9wwEB6aBEovpe-6SRcVCunFrW3JkkVPm5IQChtKSWDpRciWTBY2dlh7L_31mbG923j7uPTigzSSkUajmdGMPgG8l-gClNbHYUJpNUJHET3zEoe5tIUouUsiQReFZxfy_Ep8nafzX2DROxH8OJOf0GROkJda9IB7e3CQCFSD5Jif_Nhsuhw1d9LffeyJBxSfP3Swc7N9OVJIu9vyPb00zpm8p4TOnsDjwXpk057dT-GBr57Bw9kQH38Ol1N2u1jWLetQY1ldMbTv2LrxrC4ZIUOsSr_C0ty3NowtFjFPCMdsuvx57Rc3fnXcsCFmw5p1Toc0zQu4Oju9_HIeDu8mhHmaRW0onMudly6VjlIwpJeRLgqlS1dmuZdaF6nwykeqiLxyaGI4kTuLfIkLZZPS8pewX9WVfw1MJk5lIi2FsqVAWyGXKuEcZVpHhZexDeDzaDLNbY-RYQi1elyDAmSIFYZYgY6H4VEAHzdTb4oBkpxexliazjXJ5O8NPmwbbP70V9Jj4qUhOcU-CztcN8BxEeKVmaYcPb0Mrd8AjkaUKF_FuHqzGswg341BM5p8v0THAbzbVlNLylmrfL3uaHC_VKnS_6RJuci0yAJ41S-w7cAoJi64VAGo0dIbzfG4plpcdwjhXBMiZ_rmv7hzCI-Q44JS1GN-BPvtau3fogXW5hPYU3M1gYOT04tv3yfdOQZ-ZyKbdFJ5B4RJLrA |
linkProvider | BioMedCentral |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3db9MwED-NTgJeEN8EBhgJNF6y5cOxYyGECmzq2FohtEl7M4ntaJVKUppWCP4o_kbu2qQsQ-xtr7GdD9_57nfx-XcALwWGAEXmQj-itBqugoDKvIR-LjLDi9hGAaeDwsORGJzwT6fJ6Qb8bs_CUFplaxOXhtpWhv6R7yJwIbQdqfDd9LtPVaNod7UtobFSi0P38weGbPXbg48o31dRtL93_GHgN1UF_DxJg7nPrc2tEzYRlhIUhBOBMkaqwhZp7oRSJuFOukCawEmLDtjy3Gb41qGRWVRkMd73GmzyGEOZHmy-3xt9_tLa_hgBRNQQCIWp2EW4H6EeKr4iC7xwqH7S8YUXPcI5l9hN1zzn__Zvw60GuLL-StPuwIYr78L1YbM1fw-O-2w6nlRztiSsZVXJEFqyRe1YVTAipZgVboZXczfP_DDDS8wRuTLrT36dufE3N9uuWbNdxOpFTv-H6vtwciWT-wB6ZVW6R8BEZGXKk4LLrOAIU3IhozhGc6IC40SYefCmM5l6uqLn0ESY3W1BPdIkCk2iwJhHx4EHO-3Ua9OwoVNRjoleRkWp-HfA6_WA9kn_7bpNstRkIvCeJmtOOuB3EdmW7icxBpkpAm8Ptjo9cWmbbnOrDboxLbX-uxA8eLFuppGULle6arHsg6ZaJlJd2ieJeap46sHDlYKtP4y241HBpQeyo3qdOe62lOOzJTl5rIgMNHl8-as_hxuD4-GRPjoYHT6BmyheTqnwYbwFvfls4Z4i0pvnz5rlxeDrVa_oP6a-aBc |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1Zb9QwELZKkSpeEDeBAkZCKi9pk_iKxdNyrMrRCqEWVbxYSWyrK0Ky2mRf-PXM5FhtyvHCWxSPE2Uuz8Qznwl5ISEF8JmLwwTLariOIjzmJQ5zmRXcM5tEHBuFT07l8Tn_cCEudsjXsRdm4GDtOzhHYDLwpe_hO9zuRy87Jw4XxfejpfW97afyCOLrBASveY_Od41cV0IoNNgvr7-NHprBMp_0jZI98QD584cHXGmDLyer11UfvrWITQsst1as-S1ycwg16azXjdtkx1V3yN7JsJl-l5zN6HJR1i3tIGZpXVEIBum6cbT2FGEkVt6t4G7u2iyMM7hFHcIh01n589ItfrjVQUOHDR7arHP8o9PcI-fzd2dvjsPhkIUwF2nUhtza3DpphbRYryGdjHRRKO2tT3MntS4Ed8pFqoicshCPWJ7bDIQYFypLfMbuk92qrtxDQmViVcqF5yrzHAKLXKqEMXAAOiqcjLOAvJow0yx7QA2DENfTEZCuQVEYFAVkKYZFATkcWW-KAb8cj9EoTZfHpPL3CS83E8Y3_ZX0AGVp0KhRqbKhNwG-C-GxzEwwSAtTCJUDsj-hBGMspsOjNphBlRsDMTcmiomOA_J8M4wzscCtcvW6owHnqoTS_6QRjKeapwF50CvY5sNwA50zqQKiJqo34fF0pFpcdnDiTCN8p3j0X9J5RvY-v52bT-9PPz4mN0D4HEvbY7ZPdtvV2j2ByK3Nn3Zm-Av9uj9y |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=A+pilot+study+on+the+use+of+interferon+beta-1a+in+early+Alzheimer%E2%80%99s+disease+subjects&rft.jtitle=Journal+of+neuroinflammation&rft.au=Grimaldi%2C+Luigi+Maria&rft.au=Zappal%C3%A0%2C+Giuseppe&rft.au=Iemolo%2C+Francesco&rft.au=Castellano%2C+Anna&rft.date=2014-02-13&rft.issn=1742-2094&rft.eissn=1742-2094&rft.volume=11&rft.issue=1&rft.spage=30&rft_id=info:doi/10.1186%2F1742-2094-11-30&rft.externalDBID=n%2Fa&rft.externalDocID=10_1186_1742_2094_11_30 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1742-2094&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1742-2094&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1742-2094&client=summon |