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Concentration-Dependent Activity of Hydromethylthionine on Cognitive Decline and Brain Atrophy in Mild to Moderate Alzheimer’s Disease
Journal of Alzheimer's Disease, Volume: 72, Issue: 3, Pages: 931 - 946
Swansea University Author: Vesna Vuksanovic
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DOI (Published version): 10.3233/jad-190772
Abstract
Background:Although hydromethylthionine is a potent tau aggregation inhibitor, no difference was found in either of two Phase III trials in mild to moderate Alzheimer’s disease (AD) comparing doses in the range 150–250 mg/day with 8 mg/day intended as a control.Objective:To determine how drug exposu...
Published in: | Journal of Alzheimer's Disease |
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ISSN: | 1387-2877 1875-8908 |
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IOS Press
2019
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<?xml version="1.0"?><rfc1807><datestamp>2022-07-21T14:19:28.4616275</datestamp><bib-version>v2</bib-version><id>60500</id><entry>2022-07-14</entry><title>Concentration-Dependent Activity of Hydromethylthionine on Cognitive Decline and Brain Atrophy in Mild to Moderate Alzheimer’s Disease</title><swanseaauthors><author><sid>a1a6e2bd0b6ee99f648abb6201dea474</sid><ORCID>0000-0003-4655-698X</ORCID><firstname>Vesna</firstname><surname>Vuksanovic</surname><name>Vesna Vuksanovic</name><active>true</active><ethesisStudent>false</ethesisStudent></author></swanseaauthors><date>2022-07-14</date><deptcode>HDAT</deptcode><abstract>Background:Although hydromethylthionine is a potent tau aggregation inhibitor, no difference was found in either of two Phase III trials in mild to moderate Alzheimer’s disease (AD) comparing doses in the range 150–250 mg/day with 8 mg/day intended as a control.Objective:To determine how drug exposure is related to treatment response.Methods:A sensitive plasma assay for the drug was used in a population pharmacokinetic analysis of samples from 1,162 of the 1,686 patients who participated in either of the Phase III trials with available samples and efficacy outcome data.Results:There are steep concentration-response relationships for steady state plasma levels in the range 0.3–0.8 ng/ml at the 8 mg/day dose. Using a threshold based on the lower limit of quantitation of the assay on Day 1, there are highly significant differences in cognitive decline and brain atrophy in patients with above threshold plasma levels, both for monotherapy and add-on therapy, but with effect sizes reduced by half as add-on. Plasma concentrations in the range 4–21 ng/ml produced by the high doses are not associated with any additional benefit.Conclusions:Hydromethylthionine has pharmacological activity on brain structure and function at the 8 mg/day dose as monotherapy or as add-on to symptomatic treatments. This combined with a plateau at higher doses is consistent with the lack of dose-response seen in the Phase III trials. Treatment benefit is predicted to be maximal at 16 mg/day as monotherapy. A placebo-controlled trial in mild/moderate AD is now ongoing to confirm efficacy at this dose.</abstract><type>Journal Article</type><journal>Journal of Alzheimer's Disease</journal><volume>72</volume><journalNumber>3</journalNumber><paginationStart>931</paginationStart><paginationEnd>946</paginationEnd><publisher>IOS Press</publisher><placeOfPublication/><isbnPrint/><isbnElectronic/><issnPrint>1387-2877</issnPrint><issnElectronic>1875-8908</issnElectronic><keywords>Acetylcholinesterase inhibitor, Alzheimer’s disease, clinical trials, drug interaction, leucomethylthioninium, population pharmacokinetics, hydromethylthionine</keywords><publishedDay>26</publishedDay><publishedMonth>11</publishedMonth><publishedYear>2019</publishedYear><publishedDate>2019-11-26</publishedDate><doi>10.3233/jad-190772</doi><url/><notes/><college>COLLEGE NANME</college><department>Health Data Science</department><CollegeCode>COLLEGE CODE</CollegeCode><DepartmentCode>HDAT</DepartmentCode><institution>Swansea University</institution><apcterm/><funders/><projectreference/><lastEdited>2022-07-21T14:19:28.4616275</lastEdited><Created>2022-07-14T10:29:53.5246961</Created><path><level id="1">Faculty of Medicine, Health and Life Sciences</level><level id="2">Swansea University Medical School - Medicine</level></path><authors><author><firstname>Bjoern O.</firstname><surname>Schelter</surname><order>1</order></author><author><firstname>Helen</firstname><surname>Shiells</surname><order>2</order></author><author><firstname>Thomas C.</firstname><surname>Baddeley</surname><order>3</order></author><author><firstname>Christopher M.</firstname><surname>Rubino</surname><order>4</order></author><author><firstname>Harish</firstname><surname>Ganesan</surname><order>5</order></author><author><firstname>Jeffrey</firstname><surname>Hammel</surname><order>6</order></author><author><firstname>Vesna</firstname><surname>Vuksanovic</surname><orcid>0000-0003-4655-698X</orcid><order>7</order></author><author><firstname>Roger T.</firstname><surname>Staff</surname><order>8</order></author><author><firstname>Alison D.</firstname><surname>Murray</surname><order>9</order></author><author><firstname>Luc</firstname><surname>Bracoud</surname><order>10</order></author><author><firstname>Gernot</firstname><surname>Riedel</surname><order>11</order></author><author><firstname>Serge</firstname><surname>Gauthier</surname><order>12</order></author><author><firstname>Jianping</firstname><surname>Jia</surname><order>13</order></author><author><firstname>Peter</firstname><surname>Bentham</surname><order>14</order></author><author><firstname>Karin</firstname><surname>Kook</surname><order>15</order></author><author><firstname>John M.D.</firstname><surname>Storey</surname><order>16</order></author><author><firstname>Charles R.</firstname><surname>Harrington</surname><order>17</order></author><author><firstname>Claude M.</firstname><surname>Wischik</surname><order>18</order></author></authors><documents><document><filename>60500__24688__6402ee34bd9e4be1981a4aa2425d0b8d.pdf</filename><originalFilename>60500_VoR.pdf</originalFilename><uploaded>2022-07-21T14:18:20.6693375</uploaded><type>Output</type><contentLength>762527</contentLength><contentType>application/pdf</contentType><version>Version of Record</version><cronfaStatus>true</cronfaStatus><documentNotes>This article is published online with Open Access and distributed under the terms of the Creative Commons Attribution License (CC-BY 4.0).</documentNotes><copyrightCorrect>true</copyrightCorrect><language>eng</language><licence>https://creativecommons.org/licenses/by/4.0/</licence></document></documents><OutputDurs/></rfc1807> |
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2022-07-21T14:19:28.4616275 v2 60500 2022-07-14 Concentration-Dependent Activity of Hydromethylthionine on Cognitive Decline and Brain Atrophy in Mild to Moderate Alzheimer’s Disease a1a6e2bd0b6ee99f648abb6201dea474 0000-0003-4655-698X Vesna Vuksanovic Vesna Vuksanovic true false 2022-07-14 HDAT Background:Although hydromethylthionine is a potent tau aggregation inhibitor, no difference was found in either of two Phase III trials in mild to moderate Alzheimer’s disease (AD) comparing doses in the range 150–250 mg/day with 8 mg/day intended as a control.Objective:To determine how drug exposure is related to treatment response.Methods:A sensitive plasma assay for the drug was used in a population pharmacokinetic analysis of samples from 1,162 of the 1,686 patients who participated in either of the Phase III trials with available samples and efficacy outcome data.Results:There are steep concentration-response relationships for steady state plasma levels in the range 0.3–0.8 ng/ml at the 8 mg/day dose. Using a threshold based on the lower limit of quantitation of the assay on Day 1, there are highly significant differences in cognitive decline and brain atrophy in patients with above threshold plasma levels, both for monotherapy and add-on therapy, but with effect sizes reduced by half as add-on. Plasma concentrations in the range 4–21 ng/ml produced by the high doses are not associated with any additional benefit.Conclusions:Hydromethylthionine has pharmacological activity on brain structure and function at the 8 mg/day dose as monotherapy or as add-on to symptomatic treatments. This combined with a plateau at higher doses is consistent with the lack of dose-response seen in the Phase III trials. Treatment benefit is predicted to be maximal at 16 mg/day as monotherapy. A placebo-controlled trial in mild/moderate AD is now ongoing to confirm efficacy at this dose. Journal Article Journal of Alzheimer's Disease 72 3 931 946 IOS Press 1387-2877 1875-8908 Acetylcholinesterase inhibitor, Alzheimer’s disease, clinical trials, drug interaction, leucomethylthioninium, population pharmacokinetics, hydromethylthionine 26 11 2019 2019-11-26 10.3233/jad-190772 COLLEGE NANME Health Data Science COLLEGE CODE HDAT Swansea University 2022-07-21T14:19:28.4616275 2022-07-14T10:29:53.5246961 Faculty of Medicine, Health and Life Sciences Swansea University Medical School - Medicine Bjoern O. Schelter 1 Helen Shiells 2 Thomas C. Baddeley 3 Christopher M. Rubino 4 Harish Ganesan 5 Jeffrey Hammel 6 Vesna Vuksanovic 0000-0003-4655-698X 7 Roger T. Staff 8 Alison D. Murray 9 Luc Bracoud 10 Gernot Riedel 11 Serge Gauthier 12 Jianping Jia 13 Peter Bentham 14 Karin Kook 15 John M.D. Storey 16 Charles R. Harrington 17 Claude M. Wischik 18 60500__24688__6402ee34bd9e4be1981a4aa2425d0b8d.pdf 60500_VoR.pdf 2022-07-21T14:18:20.6693375 Output 762527 application/pdf Version of Record true This article is published online with Open Access and distributed under the terms of the Creative Commons Attribution License (CC-BY 4.0). true eng https://creativecommons.org/licenses/by/4.0/ |
title |
Concentration-Dependent Activity of Hydromethylthionine on Cognitive Decline and Brain Atrophy in Mild to Moderate Alzheimer’s Disease |
spellingShingle |
Concentration-Dependent Activity of Hydromethylthionine on Cognitive Decline and Brain Atrophy in Mild to Moderate Alzheimer’s Disease Vesna Vuksanovic |
title_short |
Concentration-Dependent Activity of Hydromethylthionine on Cognitive Decline and Brain Atrophy in Mild to Moderate Alzheimer’s Disease |
title_full |
Concentration-Dependent Activity of Hydromethylthionine on Cognitive Decline and Brain Atrophy in Mild to Moderate Alzheimer’s Disease |
title_fullStr |
Concentration-Dependent Activity of Hydromethylthionine on Cognitive Decline and Brain Atrophy in Mild to Moderate Alzheimer’s Disease |
title_full_unstemmed |
Concentration-Dependent Activity of Hydromethylthionine on Cognitive Decline and Brain Atrophy in Mild to Moderate Alzheimer’s Disease |
title_sort |
Concentration-Dependent Activity of Hydromethylthionine on Cognitive Decline and Brain Atrophy in Mild to Moderate Alzheimer’s Disease |
author_id_str_mv |
a1a6e2bd0b6ee99f648abb6201dea474 |
author_id_fullname_str_mv |
a1a6e2bd0b6ee99f648abb6201dea474_***_Vesna Vuksanovic |
author |
Vesna Vuksanovic |
author2 |
Bjoern O. Schelter Helen Shiells Thomas C. Baddeley Christopher M. Rubino Harish Ganesan Jeffrey Hammel Vesna Vuksanovic Roger T. Staff Alison D. Murray Luc Bracoud Gernot Riedel Serge Gauthier Jianping Jia Peter Bentham Karin Kook John M.D. Storey Charles R. Harrington Claude M. Wischik |
format |
Journal article |
container_title |
Journal of Alzheimer's Disease |
container_volume |
72 |
container_issue |
3 |
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931 |
publishDate |
2019 |
institution |
Swansea University |
issn |
1387-2877 1875-8908 |
doi_str_mv |
10.3233/jad-190772 |
publisher |
IOS Press |
college_str |
Faculty of Medicine, Health and Life Sciences |
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|
hierarchy_top_id |
facultyofmedicinehealthandlifesciences |
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Faculty of Medicine, Health and Life Sciences |
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facultyofmedicinehealthandlifesciences |
hierarchy_parent_title |
Faculty of Medicine, Health and Life Sciences |
department_str |
Swansea University Medical School - Medicine{{{_:::_}}}Faculty of Medicine, Health and Life Sciences{{{_:::_}}}Swansea University Medical School - Medicine |
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description |
Background:Although hydromethylthionine is a potent tau aggregation inhibitor, no difference was found in either of two Phase III trials in mild to moderate Alzheimer’s disease (AD) comparing doses in the range 150–250 mg/day with 8 mg/day intended as a control.Objective:To determine how drug exposure is related to treatment response.Methods:A sensitive plasma assay for the drug was used in a population pharmacokinetic analysis of samples from 1,162 of the 1,686 patients who participated in either of the Phase III trials with available samples and efficacy outcome data.Results:There are steep concentration-response relationships for steady state plasma levels in the range 0.3–0.8 ng/ml at the 8 mg/day dose. Using a threshold based on the lower limit of quantitation of the assay on Day 1, there are highly significant differences in cognitive decline and brain atrophy in patients with above threshold plasma levels, both for monotherapy and add-on therapy, but with effect sizes reduced by half as add-on. Plasma concentrations in the range 4–21 ng/ml produced by the high doses are not associated with any additional benefit.Conclusions:Hydromethylthionine has pharmacological activity on brain structure and function at the 8 mg/day dose as monotherapy or as add-on to symptomatic treatments. This combined with a plateau at higher doses is consistent with the lack of dose-response seen in the Phase III trials. Treatment benefit is predicted to be maximal at 16 mg/day as monotherapy. A placebo-controlled trial in mild/moderate AD is now ongoing to confirm efficacy at this dose. |
published_date |
2019-11-26T04:18:39Z |
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1763754240734396416 |
score |
11.037056 |