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Cardiovascular And Dementia Risk in diabeTes: the Role of Nox2- Related Oxidative Stress. (CARTESIO)

2026年11月3日 更新者:Daniele Pastori、Neuromed IRCCS

Cardiovascular And Dementia Risk in diabeTes Experimental and Clinical Study: Investigation on Nox2- Related Oxidative Stress (CARTESIO).

The prevalence of dementia and diabetes has increased in recent decades. The WHO forecasts an increase in the all-cause dementia prevalence to 152 million by 2050. Type 2 diabetes (T2D) is a well-known risk factor for dementia. The prevalence of T2D was estimated to be 6.28% (462 million people) worldwide, and 22% among people aged 70 years and older. Even pre-diabetes has been shown to be a risk factor for all-cause dementia, Alzheimer¿s disease (AD) and vascular dementia (VD).

There are various mechanisms by which T2D and dementia are connected. First, there are atherosclerotic consequences of T2D that favour VD. T2D is strongly associated with micro- and macrovascular diseases. This association is essentially determined by diabetes duration. Oxidative stress is the direct result of the imbalance between the production of reactive oxygen species (ROS) and intracellular antioxidant defences. It is involved in the onset of diabetes and neurological pathologies such as AD, Parkinson¿s disease, and amyotrophic lateral sclerosis. Therefore, as oxidative stress is a common pathway in diabetes and dementia, the evaluation of oxidative stress, using specific and direct biomarkers, is necessary to monitor the risk of dementia in patients with diabetes. Furthermore, it is important to study the mechanisms that lead to changes in the oxidative state, in order to define new therapeutic targets that allow delaying the eventual onset of dementia.

This project aims at defining how 1) soluble (s)NOX2-derived peptide(dp), a new direct biomarker of oxidative stress, could be used to stratify the risk of dementia in T2D patients; 2) if p47phox, a key cytosolic subunit that drives NOX2 activation, could be considered a therapeutic target to reduce oxidative stress-mediated dementia in T2D.

A clinical Aim will collect data of a T2D population to evaluate cognitive function, by the Multidimensional geriatric assessment (MGA) and cognitive biomarkers such as brain-derived neurotrophic factor (BDNF) and ß-amyloid 42/40 and oxidative stress by sNOX2dp.

A second Aim will explore the contribution of NOX2 activation in the thrombotic process and cognitive impairment in T2D patients by the evaluation of endothelial dysfunction, as a thrombogenic risk factor, and quantitative analysis of the thrombus formation process.

Finally, a preclinical Aim will test the hypothesis that p47phox could be a therapeutic target to prevent oxidative stress-mediated dementia in T2D. Specifically, we tested the effects of the p47phox inhibitor peptide both in vitro, in human umbilical vein endothelial cells (HUVEC), and in animal models (C57BL/6J) of high-fat diet (HFD)-induced diabetes.

Considering the prevalence of dementia in T2D and the uncertainty in their management, the proposed work is expected to generate results of immediate clinical significance.

調査の概要

研究の種類

観察的

入学 (推定)

250

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究場所

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

50年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

サンプリング方法

非確率サンプル

調査対象母集団

Patients with diabetes attending outpatients clinic

説明

Inclusion Criteria:

  • Established diagnosis of T2D according to the 2019 ESC guidelines
  • Written informed consent obtained from the patient before enrollment
  • Antidiabetic drug-naive, or treated with one or two oral anti-diabetic drugs, or treated with human NPH insulin or longacting insulin analogue or pre-mixed insulin, alone or in combination with one or two oral anti-diabetic drugs
  • Age >50 years

Exclusion Criteria:

  • - Acute decompensation of glycaemic control requiring immediate intensification of treatment to prevent acute complications of diabetes (eg diabetes ketoacidosis) within 90 days prior to screening
  • HbA1c >10%
  • History of chronic pancreatitis or idiopathic acute pancreatitis
  • History of ischemic stroke or transient ischemic attack
  • Acute coronary event within 30 days before enrolment
  • Currently planned coronary, carotid or peripheral artery revascularization
  • Chronic Heart Failure NYHA Class IV
  • End-stage liver disease, defined as the presence of acute or chronic liver disease and recent history of one or more of the following: ascites, encephalopathy, variceal bleeding, bilirubin >2.0 mg/dL, albumin level <3.5 g/dL, prothrombin time >4 seconds prolonged, international normalised ratio (INR) >1.7 or prior liver transplant
  • End-stage chronic kidney disease (eGFR <30 ml/min)
  • Malignant neoplasm requiring chemotherapy, surgery, radiation or palliative therapy in the previous 5 years
  • Life expectancy <2 years (and in any case before the completion of the study)
  • Low adherence to prescribed medications
  • Female of childbearing potential who is pregnant, breast-feeding or intend to become pregnant or is not using adequate contraceptive methods
  • Use of oral anticoagulants (atrial fibrillation of venous thromboembolism)

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 観測モデル:OTHER
  • 時間の展望:OTHER

コホートと介入

グループ/コホート
Study group

Patients with diabetes with cognitive impairment

Control group

Patients with diabetes without cognitive impairment

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Multidimensional geriatric assessment (MGA): MMSE
時間枠:18 months

T2D patients, with or without cognitive impairment will undergo the Mini-Mental State Examination (MMSE)

18 months
Multidimensional geriatric assessment (MGA): MoCA
時間枠:18 months

T2D patients, with or without cognitive impairment will undergo the MoCA (Montreal Cognitive Assessment or The MoCA Test

18 months
Multidimensional geriatric assessment (MGA): SPMSQ
時間枠:18 months

T2D patients, with or without cognitive impairment will undergo the Short Portable Mental State Questionary (SPMSQ)

18 months
Multidimensional geriatric assessment (MGA): SBT
時間枠:18 months

T2D patients, with or without cognitive impairment will undergo the Short Blessed Test (SBT)

18 months
Lifestyle habits: nutritional assessment
時間枠:18 months

T2D patients, with or without cognitive impairment will undergo the Mini Nutritional Assessment (MNA)

18 months
Lifestyle habits: daily activity
時間枠:18 months

T2D patients, with or without cognitive impairment will undergo the Basic Activities of Daily Living (BADL), cognitive biomarker BDNF and ß-amyloid 42/40

18 months
Cognitive function evaluation: biomarker BDNF
時間枠:18 months

T2D patients, with or without cognitive impairment will undergo the dosage of BDNF and ß-amyloid 42/40

18 months
Cognitive function evaluation: biomarker ß-amyloid 42/40
時間枠:18 months

T2D patients, with or without cognitive impairment will undergo the dosage of ß-amyloid 42/40

18 months
NOX2-mediated oxidative stress
時間枠:18 months

soluble sNOX2-dp by ELISA test

18 months

二次結果の測定

結果測定
メジャーの説明
時間枠
Thrombus formation
時間枠:18 months

T2D patients, with or without cognitive impairment will undergo evaluation of thrombus formation process will be assessed by quantitative analysis by "Total Thrombus formation Analysis System (TTAS).

18 months
Experimental mice models: NOX2 pathway
時間枠:18 months

The role of NOX2 will be studied by comparing p47phox-/- mice and wild-type C57BL/6J adult mice. p47phox is the cytosolic subunit of phagocyte NOX2, and is required for its activation and subsequent production of superoxide.

Diabetes in p47phox-/- mice and in wild-type C57BL/6J adult mice will be induced by the administration of a high-fat diet (HFD) for 8 weeks.

18 months
Endothelial dysfunction: FMD
時間枠:18 months

Endothelial function study by flow-mediated dilation (FMD) analysis

18 months
Endothelial dysfunction: VWF
時間枠:18 months

Endothelial function will be evaluated by von Willebrand factor (VWF) levels

18 months
Endothelial dysfunction: ET1
時間枠:18 months

Endothelial function will be evaluated by circulating biomarkers such as endothelin 1, whose enhanced activity and/or levels have been associated to endothelial dysfunction in the insulin-resistant states of obesity and type 2 diabetes

18 months
In vitro study - HUVEC
時間枠:18 months

The effects of p47phox IP will be studied in vitro in human umbilical vein endothelial cells (HUVEC). HUVEC will be challenged with scalar concentrations of glucose or vehicle. Cell viability will be investigated by FACS analysis. Nitric oxide (NO) production will be measured by diaminofluorescein-FM diacetate and nitrite/nitrate assay, and NOX2 activity will be assessed by ELISA test of conditioned media. The effects of p47phox IP angiogenesis will be also tested in HUVEC subjected to high-glucose stimulation

18 months

協力者と研究者

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スポンサー

協力者

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2024年8月31日

一次修了 (推定)

2027年1月1日

研究の完了 (推定)

2027年2月28日

試験登録日

最初に提出

2026年10月26日

QC基準を満たした最初の提出物

2026年11月3日

最初の投稿 (実際)

2026年11月10日

学習記録の更新

投稿された最後の更新 (実際)

2026年11月10日

QC基準を満たした最後の更新が送信されました

2026年11月3日

最終確認日

2026年11月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • PNRR-MCNT1-2023-12377768

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いいえ

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