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Disease-modifying Properties of Lithium in the Neurobiology of Alzheimer's Disease

Primary Purpose

Cognitive Impairment, Alzheimer Disease

Status
Unknown status
Phase
Phase 2
Locations
Brazil
Study Type
Interventional
Intervention
Lithium Carbonate
Placebo
Sponsored by
University of Sao Paulo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cognitive Impairment focused on measuring mild cognitive impairment, Alzheimer's disease, Lithium, disease-modification, cognition, early Alzheimer's disease

Eligibility Criteria

60 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • patients with amnestic mild cognitive impairment;
  • age: 60 to 80 years-old;

Exclusion Criteria:

  • sensory deficiencies that might preclude the administration of cognitive tests;
  • active major psychiatry disorder;
  • unstable clinical conditions such as cardiac insufficiency, uncontrolled diabetes mellitus, renal failure;
  • previous use of lithium salts;
  • concurrent participation in other clinical trial or intervention studies;

Sites / Locations

  • Institute of Psychiatry, Faculty of Medicine - University of Sao Paulo

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Lithium

Placebo

Arm Description

Patients received low doses of lithium salts (from 150 mg to 450 mg of lithium salts daily) to achieve sub-therapeutic lithium levels (target serum lithium level of 0,25 - 0,5 mEq/L). Lithium doses were administered twice a day. Lithium doses were titrated to achieve the target serum lithium levels within the first two weeks after study recruitment. After achieving the target serum lithium level, lithium salts doses remained stable until the end of the study.

Identical placebo tablets were administered twice-a-day for two years.

Outcomes

Primary Outcome Measures

effect of lithium to delay progression of cognitive deficits in patients with amnestic MCI

Secondary Outcome Measures

effect of lithium on CSF levels of Total Tau, Phosphorylated Tau and Amyloid-beta42
the effect of lithium on the activity of GSK3β in platelets and leukocytes drawn from peripheral blood.

Full Information

First Posted
January 22, 2010
Last Updated
January 22, 2010
Sponsor
University of Sao Paulo
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1. Study Identification

Unique Protocol Identification Number
NCT01055392
Brief Title
Disease-modifying Properties of Lithium in the Neurobiology of Alzheimer's Disease
Official Title
Disease-modifying Properties of Lithium in the Neurobiology of Alzheimer's Disease: a Double-blind, Placebo-controlled Prevention Study in Elderly Patients With Mild Cognitive Impairment
Study Type
Interventional

2. Study Status

Record Verification Date
December 2009
Overall Recruitment Status
Unknown status
Study Start Date
March 2007 (undefined)
Primary Completion Date
March 2009 (Actual)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
University of Sao Paulo

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Lithium salts have been used for the treatment of psychiatric disorders for over five decades, mostly as a mood-stabilizing drug. Recent evidence points to the inhibition of the enzyme glycogen synthase kinase-3beta (GSK3) as one of its mechanisms of action. The overactivity of this enzyme has been implicated in the pathogenesis of Alzheimer's disease (AD), given its involvement in mechanisms related to the hyperphosphorylation of Tau protein and the production of beta-amyloid peptide. These are key events leading respectively to the formation of neurofibrillary tangles and senile plaques, which are the neuropathological hallmarks of the disease. Several in vitro and animal studies have shown that the inhibition of GSK3 by lithium and other agents attenuates these pathological processes, reinforcing the notion that GSK3 is a likely target for future disease-modifying therapies for AD. Indeed, a recent study published by our group showed that chronic lithium use is associated with a decrement in the expected prevalence of dementia, in a sample of elderly individuals with bipolar disorder. To investigate this putative neuroprotective effect in a prospective way, the investigators started 24-month randomized, double-blinded controlled trial of lithium for the prevention of dementia in a sample of elderly individuals with amnestic mild cognitive impairment (MCI), a condition associated with increased risk for the development of AD. The clinical and biological outcomes of this trial include the attenuation of cognitive deficits, and the modification of certain biological markers of the disease (as measured in the cerebrospinal fluid, leukocytes and platelets). The objective of the present application is to enable the extension of this ongoing trial to an additional 2-year follow-up. A longer follow-up (48 months) will increase the statistical power to ascertain the primary outcome variables of this study, particularly the con-version from MCI to Alzheimer's disease. This will warrant a more consistent conclusion about the potential of lithium treatment in the prevention of dementia, in addition to a better evaluation of safety and tolerability profiles of the long-term use of lithium in older individuals.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cognitive Impairment, Alzheimer Disease
Keywords
mild cognitive impairment, Alzheimer's disease, Lithium, disease-modification, cognition, early Alzheimer's disease

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Lithium
Arm Type
Experimental
Arm Description
Patients received low doses of lithium salts (from 150 mg to 450 mg of lithium salts daily) to achieve sub-therapeutic lithium levels (target serum lithium level of 0,25 - 0,5 mEq/L). Lithium doses were administered twice a day. Lithium doses were titrated to achieve the target serum lithium levels within the first two weeks after study recruitment. After achieving the target serum lithium level, lithium salts doses remained stable until the end of the study.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Identical placebo tablets were administered twice-a-day for two years.
Intervention Type
Drug
Intervention Name(s)
Lithium Carbonate
Intervention Description
lithium carbonate tablets, 150 mg to 450 mg (target serum lithium level 0.25 mEq/L - 0.5 mEq/L), divided in two doses, two years.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Identical placebo tablets were administered twice-a-day for two years.
Primary Outcome Measure Information:
Title
effect of lithium to delay progression of cognitive deficits in patients with amnestic MCI
Time Frame
two year
Secondary Outcome Measure Information:
Title
effect of lithium on CSF levels of Total Tau, Phosphorylated Tau and Amyloid-beta42
Time Frame
one year
Title
the effect of lithium on the activity of GSK3β in platelets and leukocytes drawn from peripheral blood.
Time Frame
one year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients with amnestic mild cognitive impairment; age: 60 to 80 years-old; Exclusion Criteria: sensory deficiencies that might preclude the administration of cognitive tests; active major psychiatry disorder; unstable clinical conditions such as cardiac insufficiency, uncontrolled diabetes mellitus, renal failure; previous use of lithium salts; concurrent participation in other clinical trial or intervention studies;
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Orestes V Forlenza, Ph.D.
Organizational Affiliation
Department and Institute of Psychiatry, Faculty of Medicine - University of Sao Paulo
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Wagner F Gattaz, Ph.D.
Organizational Affiliation
Department and Institute of Psychiatry, Faculty of Medicine - University of Sao Paulo
Official's Role
Study Director
Facility Information:
Facility Name
Institute of Psychiatry, Faculty of Medicine - University of Sao Paulo
City
Sao Paulo
State/Province
SP
ZIP/Postal Code
05403-010
Country
Brazil

12. IPD Sharing Statement

Citations:
PubMed Identifier
30947755
Citation
Forlenza OV, Radanovic M, Talib LL, Gattaz WF. Clinical and biological effects of long-term lithium treatment in older adults with amnestic mild cognitive impairment: randomised clinical trial. Br J Psychiatry. 2019 Nov;215(5):668-674. doi: 10.1192/bjp.2019.76.
Results Reference
derived
PubMed Identifier
25093483
Citation
Aprahamian I, Santos FS, dos Santos B, Talib L, Diniz BS, Radanovic M, Gattaz WF, Forlenza OV. Long-term, low-dose lithium treatment does not impair renal function in the elderly: a 2-year randomized, placebo-controlled trial followed by single-blind extension. J Clin Psychiatry. 2014 Jul;75(7):e672-8. doi: 10.4088/JCP.13m08741.
Results Reference
derived
PubMed Identifier
21525519
Citation
Forlenza OV, Diniz BS, Radanovic M, Santos FS, Talib LL, Gattaz WF. Disease-modifying properties of long-term lithium treatment for amnestic mild cognitive impairment: randomised controlled trial. Br J Psychiatry. 2011 May;198(5):351-6. doi: 10.1192/bjp.bp.110.080044.
Results Reference
derived

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Disease-modifying Properties of Lithium in the Neurobiology of Alzheimer's Disease

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