Insulin Resistance and Mild Cognitive Impairment (IRMCI) Study (IRMCI)
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|ClinicalTrials.gov Identifier: NCT02409238|
Recruitment Status : Unknown
Verified March 2016 by Andrew Wee Kien Han, SingHealth Polyclinics.
Recruitment status was: Recruiting
First Posted : April 6, 2015
Last Update Posted : March 31, 2016
|First Submitted Date ICMJE||March 26, 2015|
|First Posted Date ICMJE||April 6, 2015|
|Last Update Posted Date||March 31, 2016|
|Study Start Date ICMJE||April 2015|
|Estimated Primary Completion Date||December 2017 (Final data collection date for primary outcome measure)|
|Current Primary Outcome Measures ICMJE
|Original Primary Outcome Measures ICMJE
|Change History||Complete list of historical versions of study NCT02409238 on ClinicalTrials.gov Archive Site|
|Current Secondary Outcome Measures ICMJE
|Original Secondary Outcome Measures ICMJE||Same as current|
|Current Other Pre-specified Outcome Measures||Not Provided|
|Original Other Pre-specified Outcome Measures||Not Provided|
|Brief Title ICMJE||Insulin Resistance and Mild Cognitive Impairment (IRMCI) Study|
|Official Title ICMJE||Insulin Resistance and Mild Cognitive Impairment (MCI) in Older Chinese Adults With Pre-Diabetes and Diabetes: Cognitive Effects of Lifestyle Intervention and Metformin Treatment in a Randomized Controlled Trial|
Dementia (Alzheimer's Disease) is sometimes called "Type 3 Diabetes" because of the strong connection between Type 2 diabetes (a function of insulin resistance) with Dementia.
The investigators therefore hypothesize that Reducing Insulin Resistance using Intensive Lifestyle Intervention (Exercise and Weight loss) + Metformin Treatment in Prediabetic & diet-control-only Diabetic overweight and mildly cognitively impaired individuals 55 years or older would lead to better Cognitive Function (compared to standard care) after 2 years.
Subjects will be monitored and assessed using a battery of Cognitive and psychological tests and PET scans to demonstrate glucose utilization in the relevant areas of the brain.
This 3-year open-label study aims to recruit 360 subjects with 50% (180 subjects) randomized to receiving Intensive lifestyle intervention with Metformin (if diabetic) vs the other 50% who would receive only the usual standard level of care in the primary care setting.
General Introduction In this trial, the drug to be studied is Metformin. It is an insulin-sensitizing biguanide which has long been used safely as an effective antidiabetic drug for patients with type II diabetes.
Rationale for the Study Purpose Dementia is a clinical syndrome due to multiple aetiologies, of which Alzheimer disease (AD) and Vascular Dementia (VaD) are the two most common. Dementia represents the advanced stage of a syndrome spectrum of cognitive impairment, an age-associated neurodegenerative condition that includes ageing related cognitive disorder (aka age-associated memory impairment or subject memory impairment, i.e. memory loss without other cognitive problems and are within normal limits given the person's age), and Mild Cognitive Impairment (MCI), a clinical entity that includes memory and cognitive impairment but no significant functional disability to meet threshold criteria for diagnosis of dementia. Of note, MCI is considered a prodromal state of dementia that increases the risk of subsequently developing dementia.
MCI can be classified into two main categories: (1) amnestic MCI and (2) non-amnestic MCI. Each MCI subtype can be further classified according to the presumed aetiology: degenerative; vascular; psychiatric; or traumatic.
Currently available drugs approved for AD (anticholinesterases and Memantine) have limited efficacy and do not alter the pathophysiological basis of disease nor disease progression. No drugs are currently approved by regulatory authorities specifically for the treatment of MCI. Because treatments are less effective when the disease is far advanced, individuals with MCI at earlier stages of their illness are likely better candidates for clinical trials. Neuropathology-based studies of "clinically non-demented" individuals show high burdens of vascular and AD types of pathology. MCI may therefore be a pathologically-based preclinical or early clinical phase of dementia that is likely to progress to AD or VaD, and is hence an appropriate predementia syndrome for therapeutic intervention.
Vascular-related Risk Factors. Prior research up to date amply supports the hugely important role of vascular-related risk factors in the aetiology of both AD and VaD. Because vascular-related risk factors are treatable, it should be possible to prevent, postpone or mitigate VaD as well as AD (to the extent due to the vascular contribution of its aetiology). The vascular and related factors that have been associated with dementia and cognitive decline include diabetes and insulin resistance, high blood pressure (BP) and hypertension, total cholesterol and other lipid parameters, body mass index (BMI) and obesity, and the metabolic syndrome (MetS). MetS is a clustering of cardiovascular risk factors related to central obesity including impaired glucose metabolism, dyslipidaemia, and high BP that is associated with increased risk for both Type 2 Diabetes Mellitus (T2DM) and coronary artery disease (CAD). MetS has been shown to be associated with an increased risk of predementia syndromes including age-related cognitive decline, MCI and VaD, albeit with mixed findings of associations with AD. Insulin resistance is widely considered to play the central role in the pathophysiological mechanism of MetS. Hence, lifestyle and therapeutic interventions targeted at lowering insulin resistance is a promising MCI treatment option with the aim to slow cognitive decline and prevent or delay progression to dementia due to AD and/or VaD).
The role of insulin resistance in MCI and dementia Insulin and insulin resistance play important roles and functions in the central nervous system and the development of age-related neurodegenerative diseases, including glucose metabolism, vascular function, synaptic maintenance, beta-amyloid regulation, and tau phosphorylation. Insulin is transported across the blood-brain barrier, and brain insulin receptors are selectively localized in key brain regions, such as hippocampus, entorhinal cortex, and frontal cortex, where it plays a direct role in modulating levels of important neurotransmitters, synaptic plasticity, learning and memory. Insulin has also been shown to regulate the metabolism of beta-amyloid and tau, the building blocks of amyloid plaques and neurofibrillary tangles which are the neuropathological hallmarks of AD. Peripheral hyperinsulinemia promotes oxidative stress, protein glycosylation and cerebral ischemia and impairs the clearance of amyloid beta in the brain through competition for insulin degrading enzyme (IDE).
Diabetic patients are more likely to manifest impaired cognitive function, cognitive decline and a significantly higher risk of developing Alzheimer's disease or vascular dementia. Both hyperglycaemia and insulin resistance (IR) have also been shown in population-based studies to be associated with poor cognitive function in older persons. Hippocampal volumes were smaller in diabetic patients and in those with increased insulin resistance than in normal healthy controls. Several mechanisms are likely to explain the increased risk of cognitive impairment in T2D. Insulin resistance as mentioned above has been shown to play a direct role in cognitive impairment in individuals with type 2 diabetes (T2D). Additionally, chronic hyperglycaemia has been shown to be associated with decreased cerebral blood flow, decreased glucose transport across the blood brain barrier, reduced cerebral glucose metabolism and microvascular changes from endothelial damage. Finally, metabolic and vascular risk factors such as dyslipidaemia and hypertension which are closely linked to IR and T2D have been shown to predict cerebrovascular disease, cognitive decline and dementia.
Lowering Insulin Resistance Recent data support the development of therapeutics that target insulin pathways and particularly the lowering of insulin resistance as potential treatments for AD. Insulin administration reduces neuronal accumulation of beta-amyloid peptides and synaptic binding of toxic beta-amyloid derived diffusible ligands in cell culture; it improves cognitive performance in rodents and reportedly in patients with early AD. Insulin-sensitizers like peroxisome proliferator-activated receptor-gamma (PPAR- gamma) have been reported to improve insulin sensitivity, decrease inflammation and inhibit A-beta-stimulated secretion of pro-inflammatory products.
Rosiglitazone is a thiazolidinedione that stimulate PPAR-gamma and has been shown to inhibit beta-amyloid production. This insulin sensitizer is used as an oral drug (Avandia) effective in the treatment and prevention of diabetes. However, recent concerns about increased cardiovascular mortality has restricted its use in diabetic patients.
Initial reports suggest that Rosiglitazone is a promising drug in the treatment of AD. Positive effects on cognitive function have been reported in preclinical animal studies and a handful of preliminary clinical studies. However, these findings have not been confirmed subsequently by Phase III trials of patients with mild to moderate AD.
A growing consensus about treatment trials of AD is that they may be conducted at too late in the disease process for them to be effective.
Nevertheless an abundance of data strongly supports the central role of underlying metabolic pathogenesis in AD and VaD. Agents which modify insulin sensitivity remain as therapeutic options highly worthy of further inquiry. As rosiglitazone is a substrate for the multidrug-resistant gene product permeability glycoprotein, it may not have high penetration through the blood-brain barrier.
Metformin, however, is an insulin-sensitizing biguanide has long been used safely as an effective antidiabetic drug for patients with T2D and is the only antidiabetic drug that has been conclusively shown to prevent cardiovascular complications of diabetes. It has been shown that metformin evidently crosses the blood-brain barrier, accumulates in the brain and acts directly on the central nervous system.
A major mechanism of metformin action is activation of AMP-activated protein kinase (AMPK), which plays a key role in cellular energy homeostasis, insulin signalling, and the metabolism of glucose and fats. The activation of AMP-activated protein kinase and anti-inflammatory actions of metformin has been shown to occur not only in peripheral tissues but also in the brain.
There is hitherto no published report of the effect of metformin treatment on cognitive outcomes in diabetic patients. Recently, the investigators have completed a 4 year follow-up study of older diabetic patients and have found that long term metformin use of ≥6 years was prospectively associated with lower risk of cognitive impairment.
Metformin is an oral antidiabetic drug in the biguanide class. It is the first-line drug of choice for the treatment of type 2 diabetes, in particular, in overweight and obese people.
In this trial, the dosage schedule of metformin is only 250 mg thrice a day, (up-titrated weekly from a starting dose of 250 mg once a day). Despite its well-documented tolerability, this proposed weekly incremental dosage is designed to further reduce possible side-effects to drug-naive diabetic subjects taking Metformin for the 1st time.
Hypothesis The novel strategy of lowering insulin resistance with dietary modification and exercise in combination with a commonly used safe anti-diabetic medication, metformin could help to slow down cognitive decline and dementia.
Study Population Chinese patients are used as this proposed clinical trial builds upon and also uses the patients of our on-going Singapore Longitudinal Ageing Studies (SLAS) Study, where only Chinese Patients are used.
360 Chinese patients with prediabetes or diabetes with MCI will be identified and recruited from the community and primary care clinics in:
Study Design Summary 24-month randomized controlled parallel-group study (IRMCI Study) of overweight-or-obese pre-diabetes older patients (IRMCI-1) or untreated type 2 diabetes (IRMCI-2) older patients, all with amnestic MCI or non-amnestic multi-domain MCI, will be randomly assigned within Apolipoprotein E4 (ApoE4) positive and ApoE4 negative strata to:
Cognitive screening and diagnostic assessments are performed using the Mini mental State Examination (MMSE) and Montreal Cognitive Assessment scale (MoCA), and a comprehensive Neuropsychological Test Battery that will assess performance on multiple cognitive domains (Memory, Story Memory, Language, Executive function, Visual-Spatial and Constructional ability and Attention.)
The Subjects with age-and education-adjusted MMSE<26 or MOCA<26 or memory and non-memory domains test score that is 1.0 Standard Deviation (SD) or more below age-education adjusted norms are evaluated by Clinical Dementia Rating (CDR) scale. Subjects with a CDR global score of 0.5 together with Sum of Boxes of ≥3 or global score of ≥1 denoting dementia undergo a structured clinical assessment including neurologic examination, laboratory tests and final review by an expert panel of neurologists and psychiatrists, for final diagnosis and sub-classification of MCI, according to an standard SLAS protocol already established for the assessment and diagnosis of MCI and dementia.
Randomization:Subjects will be split into 2 Groups namely (1) Pre-Diabetic and (2) Diabetic. Each of these 2 groups will be stratified with APOE 4 allele as a stratification factor. .
The Prediabetic group will thus be similarly stratified into (B) Prediabetic-APOE4+ and (A) Prediabetic-APOE4-.
The Diabetic group will thus be stratified into (D) Diabetic-APOE4+ and (C) Diabetic-APOE4-.
Each of these four groups (A), (B), (C), & (D) will have their individual list of 360 randomization numbers generated by NUS Research Fellow using SAS computer programme. Each of these 360 x 4 numbers will be individually sealed in envelopes that will be numbered and used serially (from 0001st to 0360th for each group).
Subjects will have their Diabetic/Prediabetic status and APOE4+or- status determined using existing and baseline laboratory tests. They will then be assigned accordingly to the appropriate group [ ie (A), (B), (C), & (D)]. Trained nurses will then assign subjects to treatment vs control arm using the treatment allocation determined within the serially allotted sealed envelopes. .
There will not be any blinding as this is an open-labelled randomised controlled trial.
|Study Type ICMJE||Interventional|
|Study Phase ICMJE||Phase 4|
|Study Design ICMJE||Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
|Study Arms ICMJE||
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
|Recruitment Status ICMJE||Unknown status|
|Estimated Enrollment ICMJE
|Original Estimated Enrollment ICMJE||Same as current|
|Study Completion Date ICMJE||Not Provided|
|Estimated Primary Completion Date||December 2017 (Final data collection date for primary outcome measure)|
|Eligibility Criteria ICMJE||
|Ages ICMJE||55 Years and older (Adult, Older Adult)|
|Accepts Healthy Volunteers ICMJE||No|
|Contacts ICMJE||Contact information is only displayed when the study is recruiting subjects|
|Listed Location Countries ICMJE||Singapore|
|Removed Location Countries|
|NCT Number ICMJE||NCT02409238|
|Other Study ID Numbers ICMJE||MCI-LM 3|
|Has Data Monitoring Committee||No|
|U.S. FDA-regulated Product||Not Provided|
|IPD Sharing Statement ICMJE||Not Provided|
|Responsible Party||Andrew Wee Kien Han, SingHealth Polyclinics|
|Study Sponsor ICMJE||SingHealth Polyclinics|
|PRS Account||SingHealth Polyclinics|
|Verification Date||March 2016|
ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP