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Blood Clotting Markers and Heart Ultrasound in People With Device-Detected Atrial Fibrillation (DDAF-HEV)

2026年7月14日 更新者:Andreas Sjøholm-Christensen

Device-Detected Atrial Fibrillation - Haemostatic Profile and Echocardiographic Variables

The purpose of this observational study is to investigate whether blood tests related to blood clotting are associated with established clinical stroke risk scores, the total amount of device-detected atrial fibrillation recorded by an implanted cardiac device, and ultrasound measurements of the heart in people with device-detected atrial fibrillation. The study will also evaluate whether these baseline measurements are associated with future clinical outcomes and may improve future stroke risk assessment.

Device-detected atrial fibrillation is an irregular heart rhythm detected by implanted cardiac devices such as pacemakers, implantable cardiac monitors, and implantable defibrillators. It is often brief and does not cause symptoms. Although it increases the risk of stroke and systemic embolism, the risk is lower than in people with clinically diagnosed atrial fibrillation. As a result, it remains difficult to identify which patients are most likely to benefit from blood-thinning medication, which reduces the risk of stroke but also increases the risk of bleeding.

The study will include 222 participants with implanted cardiac devices, including 111 participants with device-detected atrial fibrillation and 111 age-, sex-, and cardiac device indication-matched control participants without device-detected atrial fibrillation. At baseline, participants will undergo blood sampling, ultrasound examination of the heart, and routine device interrogation. Information on medical history and established clinical stroke risk factors will also be collected. The implanted cardiac device will be used to determine the total amount of device-detected atrial fibrillation recorded during the year before study inclusion.

The baseline analyses will investigate whether established clinical stroke risk scores, the total amount of device-detected atrial fibrillation, and heart ultrasound findings are associated with changes in blood clotting that may indicate an increased tendency to form blood clots. The study will evaluate both primary and additional blood clotting markers to improve the understanding of the biological mechanisms underlying thromboembolic risk in device-detected atrial fibrillation.

Participants will subsequently be followed for 10 years to determine whether baseline blood clotting markers, the total amount of device-detected atrial fibrillation, heart ultrasound findings, and clinical stroke risk scores are associated with future clinical outcomes, including stroke, systemic embolism, hospitalization, death, progression to clinically diagnosed atrial fibrillation, and initiation of oral anticoagulant therapy.

The findings may improve the understanding of thromboembolic risk in people with device-detected atrial fibrillation and support the development of more individualized approaches to future stroke risk assessment and treatment.

調査の概要

詳細な説明

Scientific Rationale Device-detected atrial fibrillation (DDAF) is associated with an increased risk of stroke and systemic embolism, although the risk is lower than in patients with clinically diagnosed atrial fibrillation. Consequently, it remains challenging to identify which patients are most likely to benefit from oral anticoagulant therapy while minimizing the risk of bleeding. Current stroke risk assessment in patients with device-detected atrial fibrillation relies primarily on clinical risk scores and does not incorporate haemostatic biomarkers, the burden of device-detected atrial fibrillation, or echocardiographic markers of atrial remodeling that may contribute to thromboembolic risk. This study aims to improve the understanding of thromboembolic risk in patients with DDAF and to evaluate whether integrating clinical stroke risk scores, DDAF burden, advanced echocardiographic variables, and haemostatic biomarkers may improve future stroke risk assessment.

Study Design This is a prospective, single-center observational cohort study conducted at the Department of Cardiology, Esbjerg and Grindsted Hospital, University Hospital of Southern Denmark, in collaboration with the Unit for Thrombosis Research, Department of Clinical Diagnostics.

The study consists of a single prospective observational cohort with three prespecified baseline analyses followed by a prospective 10-year longitudinal follow-up. A total of 222 participants will be enrolled, including 111 participants with device-detected atrial fibrillation and 111 control participants matched for age, sex, and indication for cardiac device implantation.

Baseline Assessments At baseline, all participants will undergo standardized blood sampling, comprehensive transthoracic echocardiography, and collection of demographic and clinical information. Device interrogation will be performed to quantify the burden of device-detected atrial fibrillation. Clinical thromboembolic risk will be assessed using the CHA₂DS₂-VASc score. In addition, the ABC-stroke score will be calculated to evaluate its associations with haemostatic biomarkers and subsequent clinical outcomes in participants with device-detected atrial fibrillation.

Independent variables in the prespecified baseline analyses include the CHA₂DS₂-VASc score, the ABC-stroke score, burden of device-detected atrial fibrillation, and advanced echocardiographic variables.

The baseline analyses are designed to address three prespecified objectives. Together, these analyses are intended to determine whether established clinical stroke risk scores, burden of device-detected atrial fibrillation, and cardiac structural and functional abnormalities are associated with a more prothrombotic haemostatic profile.

  1. To investigate whether the primary haemostatic biomarkers, endogenous thrombin potential (ETP) and von Willebrand factor antigen, differ between participants with device-detected atrial fibrillation and matched controls and whether they are associated with the CHA₂DS₂-VASc and ABC-stroke risk scores. Secondary analyses will evaluate associations between additional haemostatic biomarkers and the clinical stroke risk scores.
  2. To investigate whether the primary haemostatic biomarkers are associated with the burden of device-detected atrial fibrillation. Secondary analyses will evaluate associations between DDAF burden and additional haemostatic biomarkers.
  3. To investigate whether the primary haemostatic biomarkers are associated with advanced echocardiographic variables, including left atrial size and function. Secondary analyses will evaluate associations between echocardiographic variables and additional haemostatic biomarkers.

The primary cross-sectional outcome measures are endogenous thrombin potential (ETP) and von Willebrand factor antigen. Secondary cross-sectional outcome measures comprise additional biomarkers of coagulation and fibrinolysis.

Longitudinal Follow-up Participants will subsequently be followed for 10 years through electronic health records, routine device interrogation reports, and Danish national health registries. Follow-up data will be collected every second year to evaluate whether baseline primary and secondary haemostatic biomarkers, DDAF burden, clinical stroke risk scores, and echocardiographic findings are associated with subsequent stroke, systemic embolism, hospitalization, death, progression to clinically diagnosed atrial fibrillation, and initiation of oral anticoagulant therapy.

Statistical Analysis The sample size was calculated to provide 80% statistical power at a two-sided significance level of 5% to detect the expected differences in endogenous thrombin potential and von Willebrand factor antigen between predefined CHA₂DS₂-VASc stroke risk groups, based on previously published effect sizes.

Continuous variables will be assessed for normality using histograms and Q-Q plots. Variables with skewed distributions will be logarithmically transformed where appropriate. Homogeneity of variances will be assessed before parametric analyses. Continuous variables will be summarized as mean ± standard deviation or median with interquartile range according to data distribution, whereas categorical variables will be summarized as frequencies and percentages.

Baseline comparisons between participants with device-detected atrial fibrillation and matched controls will be performed using appropriate parametric or non-parametric statistical methods according to data distribution. Multivariable regression models will be adjusted for predefined confounding variables as appropriate.

The prespecified baseline analyses will primarily be performed using multivariable linear regression models with endogenous thrombin potential and von Willebrand factor antigen as the primary dependent variables. Secondary analyses will evaluate associations with additional haemostatic biomarkers. Regression models will be adjusted for prespecified confounding variables. Continuous predictors will be assessed for approximate linearity, and the assumptions underlying the linear regression models will be evaluated before interpretation of the results. Sensitivity analyses will be performed to evaluate the robustness of the primary findings. Adjustment for multiple testing will be performed using the Holm-Bonferroni procedure.

Longitudinal analyses will evaluate whether baseline haemostatic biomarkers, burden of device-detected atrial fibrillation, clinical stroke risk scores, and echocardiographic findings are associated with subsequent clinical outcomes. Time-to-event analyses will be performed using Cox proportional hazards regression models when appropriate. Hazard ratios with 95% confidence intervals will be reported. Statistical significance will be defined as a two-sided p-value <0.05.

研究の種類

観察的

入学 (推定)

222

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

      • Esbjerg、デンマーク、6700
        • 募集
        • Department of Cardiology, Esbjerg and Grindsted Hospital, Southwest Denmark
        • コンタクト:
        • 主任研究者:
          • Andreas Sjøholm-Christensen, MD

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

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

サンプリング方法

確率サンプル

調査対象母集団

Participants will be recruited from the Department of Cardiology, Esbjerg and Grindsted Hospital, University Hospital of Southern Denmark. The study population comprises adults with implanted cardiac devices undergoing routine outpatient device interrogation. The device-detected atrial fibrillation cohort will include participants with at least one episode of device-detected atrial fibrillation lasting ≥1 minute identified during routine device interrogation within the previous 12 months. The control cohort will comprise participants without device-detected atrial fibrillation during the previous 4 years, recruited from the same outpatient population and matched on age, sex, and indication for cardiac device implantation. All participants will be enrolled consecutively from a single-center cardiology outpatient clinic.

説明

Inclusion Criteria:

  • Age > 50 years at inclusion
  • Implanted cardiac device with an atrial electrode
  • ≥1 episode of device-detected atrial fibrillation lasting ≥1 minute, detected at routine cardiac device interrogation within the last 12 months
  • Written informed consent obtained prior to inclusion

Exclusion Criteria:

  • History of ECG-documented atrial fibrillation at any time prior to inclusion
  • Use of oral anticoagulation or dual antiplatelet therapy within 6 months prior to inclusion, irrespective of indication
  • Current treatment with oral contraceptives or hormone replacement therapy
  • Pregnancy or breastfeeding
  • End-stage renal disease (creatinine clearance <15 mL/min, calculated using the Cockcroft-Gault equation)
  • Active malignancy, defined as cancer diagnosis not followed by curative treatment within 6 months of diagnosis
  • Major surgery within the last 3 months
  • Connective tissue disease requiring treatment
  • Acute coronary syndrome, stroke/transient ischemic attack, or venous thromboembolism within 3 months prior to inclusion
  • Known thrombophilia
  • Clinically significant hepatic or hematological disease requiring treatment and/or specialist follow-up
  • Mechanical heart valve, moderate-to-severe mitral stenosis, or other valvular disease requiring intervention

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

コホートと介入

グループ/コホート
Device-detected atrial fibrillation
Patients with implanted cardiac devices with at least one episode of device-detected atrial fibrillation lasting ≥ 1 minute within the preceding year, identified during routine device interrogation visits.
Matched controls without device-detected atrial fibrillation
Patients with implanted cardiac devices without device-detected atrial fibrillation in the preceding four years, matched 1:1 to cases on age, sex, and indication for device implantation, identified during routine device follow-up visits.

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
Thrombin generation assessed by endogenous thrombin potential
時間枠:Baseline
Thrombin generation plays a pivotal role in blood clotting and thus serve as primary outcome measure. Thrombin generation will be assessed through measurement of endogenous thrombin potential (nmol/L x min), using the calibrated automated thrombography (CAT) method.
Baseline
Levels of von Willebrand factor (vWF) antigen
時間枠:Baseline
von Willebrand factor plays an important role in platelet plug formation. von Willebrand factor antigen (%) will be measured using an in-house immunoassay.
Baseline

二次結果の測定

結果測定
メジャーの説明
時間枠
Plasma P-selectin Concentration
時間枠:Baseline
Plasma concentration of soluble P-selectin antigen (ng/ml) measured using an enzyme-linked immunosorbent assay (ELISA). P-selectin will only be measured in participants with elevated von Willebrand factor antigen concentrations.
Baseline
Thrombin generation assessed by lag time
時間枠:Baseline.
Thrombin generation plays a pivotal role in blood clotting. Thrombin generation will be assessed through measurement of lag time (min), using the calibrated automated thrombography (CAT) method.
Baseline.
Thrombin generation assessed by peak thrombin concentration
時間枠:Baseline
Thrombin generation plays a pivotal role in blood clotting. Thrombin generation will be assessed through measurement of peak thrombin concentration (nmol/L), using the calibrated automated thrombography (CAT) method.
Baseline
Thrombin generation assessed by time to peak
時間枠:Baseline
Thrombin generation plays a pivotal role in blood clotting. Thrombin generation will be assessed through measurement of time to peak (min), using the calibrated automated thrombography (CAT) method.
Baseline
Kallikrein generation assessed by lag time
時間枠:Baseline
Kallikrein generation plays an important role in the contact activation system of the secondary hemostasis. Kallikrein generation will be assessed through measurement of lag time (min), using the calibrated automated thrombography (CAT) method.
Baseline
High-sensitivity Cardiac Troponin T (hs-cTnT) Concentration
時間枠:Baseline
Plasma concentration of high-sensitivity cardiac troponin T (hs-cTnT) in ng/L measured at baseline
Baseline
Kallikrein generation assessed by peak kallikrein concentration
時間枠:Baseline
Kallikrein generation plays an important role in the contact activation system of the secondary hemostasis. Kallikrein generation will be assessed through measurement of peak kallikrein concentration (nmol/L), using the calibrated automated thrombography (CAT) method.
Baseline
Kallikrein generation assessed by time to peak
時間枠:Baseline
Kallikrein generation plays an important role in the contact activation system of the secondary hemostasis. Kallikrein generation will be assessed through measurement of time to peak (min), using the calibrated automated thrombography (CAT) method.
Baseline
Kallikrein generation assessed by endogenous kallikrein potential
時間枠:Baseline
Kallikrein generation plays an important role in the contact activation system of the secondary hemostasis. Kallikrein generation will be assessed through measurement of endogenous kallikrein potential (nmol/L*min), using the calibrated automated thrombography (CAT) method.
Baseline
Concentrations of prothrombin fragment 1 + 2
時間枠:Baseline
Activation of the inactive prothrombin to the active thrombin will be estimated from concentrations of prothrombin fragment 1 + 2 (pmol/L), using a commercial enzyme-linked immunosorbent assay (ELISA).
Baseline
Concentration of cleaved high-molecular weight kininogen (cHK)
時間枠:Baseline
cHK is an essential component of the contact activation system of the coagulation cascade. cHK (µg/ml) will be measured with the help of enzyme-linked immunosorbent assay (ELISA).
Baseline
Concentration of coagulation factor XII (FXII)
時間枠:Baseline
FXII is an essential component of the contact activation system of the coagulation cascade. FXII (µg/ml) will be measured with the help of enzyme-linked immunosorbent assay (ELISA).
Baseline
Concentration of prekallikrein
時間枠:Baseline
Prekallikrein is an essential component of the contact activation system of the coagulation cascade. Prekallikrein (µg/ml) will be measured with the help of enzyme-linked immunosorbent assay (ELISA).
Baseline
Concentration of high-molecular weight kininogen (HK)
時間枠:Baseline
HK plays a key role in the contact activation system of the coagulation cascade. HK (%) will be measured using enzyme-linked immunosorbent assay (ELISA).
Baseline
Concentration of C1-inhibitor
時間枠:Baseline
C1-inhibitor is the main regulator of the contact activation system. Concentration of C1-inhibitor (g/L) will be measured using nephelometry.
Baseline
Concentration of coagulation factor VII (FVII)
時間枠:Baseline
FVII plays an important role in the secondary hemostasis. Concentration of FVII (%) will be measured using clot assay.
Baseline
Concentration of coagulation factor X (FX)
時間枠:Baseline
FX plays an important role in the secondary hemostasis. Concentration of FX (%) will be measured using clot assay.
Baseline
Concentration of coagulation factor II (FII)
時間枠:Baseline
FII plays an important role in the secondary hemostasis. Concentration of FII (%) will be measured using clot assay.
Baseline
Concentration of protein C
時間枠:Baseline
Protein C is essential for the regulation of the blood coagulation cascade. Concentration of protein C (%) will be measured using chromogenic assay.
Baseline
Concentration of protein S
時間枠:Baseline
Protein S is essential for the regulation of the blood coagulation cascade. Concentration of protein S (%) will be measured using turbidity.
Baseline
Concentration of antithrombin (AT)
時間枠:Baseline
Antithrombin is essential for the regulation of the blood coagulation cascade. Concentration of antithrombin (%) will be measured using chromogenic assay.
Baseline
Concentration of tissue factor pathway inhibitor (TFPI)
時間枠:Baseline
TFPI is important in the regulation of the blood coagulation system. TFPI (pg/ml) will be measured using enzyme-linked immunosorbent assay (ELISA).
Baseline
Fibrin turnover assessed by maximum lysis velocity (Vmax)
時間枠:Baseline
Fibrin turnover will be assessed through fibrin clot lysis, where measurement of Vmax (optical density (OD)/min) will be conducted.
Baseline
Fibrin turnover assessed by peak optical density (OD)
時間枠:Baseline
Fibrin turnover will be assessed through fibrin clot lysis, where measurement of peak OD (OD) will be conducted.
Baseline
Fibrin turnover assessed by clot lysis
時間枠:Baseline
Fibrin turnover will be assessed through fibrin clot lysis, where measurement of clot lysis (%) will be conducted.
Baseline
Fibrin turnover assessed by overall hemostatic potential (OHP)
時間枠:Baseline
Fibrin turnover will be assessed through fibrin clot lysis, where measurement of OHP (OD x min) will be conducted.
Baseline
Fibrin turnover assessed by fiber diameter
時間枠:Baseline
Fibrin turnover will be assessed through fibrin clot lysis, where measurement of fiber diameter (µm) will be conducted.
Baseline
Fibrin turnover assessed by fiber density
時間枠:Baseline
Fibrin turnover will be assessed through fibrin clot lysis, where measurement of fiber density (x 10^6 Da/cm^3) will be conducted.
Baseline
Concentration of fibrinogen
時間枠:Baseline
Conversion of fibrinogen to fibrin, in which thrombin plays a key role, is essential for blood coagulation. Concentrations of fibrinogen (µmol/L) will be measured using nephelometry.
Baseline
Concentration of D-dimer
時間枠:Baseline
D-dimer is a fibrin degradation product that reflects the fibrinolysis process (the breakdown of fibrin network), which plays a crucial role in preventing blood clots from causing complications. D-dimer (mg/L) will be measured using immunoassay.
Baseline
Concentration of tissue-type plasminogen activator (t-PA)
時間枠:Baseline
t-PA is a protein that stimulates the breakdown of blood clots. It helps convert plasminogen into its active form, plasmin, the major enzyme responsible for the breakdown of blood clots. Concentration of t-PA (ng/ml) will be measured using enzyme-linked immunosorbent assay (ELISA).
Baseline
Concentration of plasminogen activator inhibitor 1 (PAI-1)
時間枠:Baseline
PAI-1 functions as the inhibitor of t-PA, which will stimulate the formation of blood clots. Concentration of PAI-1 (ng/ml) will be measured using enzyme-linked immunosorbent assay (ELISA).
Baseline
Levels of plasminogen
時間枠:Baseline
Plasminogen is the inactive form of plasmin, the major enzyme that breaks down blood clots. Levels of plasminogen (%) will be measured using chromogenic assay.
Baseline
Levels of coagulation factor XIII (FXIII)
時間枠:Baseline
FXIII plays a key role in stabilizing the blood clots. Levels of FXIII will be measured using immunoassay.
Baseline
Levels of plasmin inhibitor (PI)
時間枠:Baseline
PI is the major inhibitor of plasmin. Levels of PI (%) will be measured using chromogenic assay.
Baseline
Levels of thrombin activatable fibrinolysis inhibitor (TAFI)
時間枠:Baseline
TAFI is an enzyme that is activated by thrombin, which downregulates fibrinolysis, stimulating blood clot formation. Levels TAFI will be measured using enzyme-linked immunosorbent assay (ELISA).
Baseline
ADAMTS13 Antigen Concentration
時間枠:Baseline
Plasma concentration of ADAMTS13 antigen (ng/mL) measured using an enzyme-linked immunosorbent assay (ELISA). ADAMTS13 will only be measured in participants with elevated von Willebrand factor antigen concentrations.
Baseline
N-terminal Pro-B-type Natriuretic Peptide (NT-proBNP) Concentration
時間枠:Baseline
Plasma concentration of N-terminal pro-B-type natriuretic peptide (NT-proBNP) in ng/L measured at baseline.
Baseline
Stroke
時間枠:Up to 10 years.
Clinical stroke verified with imaging e.g. CT or MR.
Up to 10 years.
Transient Ischemic Attack
時間枠:Up to 10 years
Transient Ischemic Attack verified with imaging e.g. CT or MR
Up to 10 years
Systemic embolism
時間枠:Up to 10 years
Systemic embolism verified with imaging e.g. CT, MR or ultrasound
Up to 10 years
Hospitalizations
時間枠:Up to 10 years
All cause hospitalizations
Up to 10 years
Heart failure hospitalizations
時間枠:Up to 10 years
New onset or worsening of heart failure leading to hospitalization or urgent visit heart failure clinic
Up to 10 years
All-cause mortality
時間枠:Up to 10 years
All-cause mortality
Up to 10 years
Cardiovascular death
時間枠:Up to 10 years
Cardiovascular death
Up to 10 years
Progression to clinically diagnosed atrial fibrillation or atrial flutter
時間枠:Up to 10 years
Atrial fibrillation or flutter verified by a 12-lead ECG or ambulatory ECG monitoring
Up to 10 years
Progression to >24 hours device-detected atrial fibrillation
時間枠:Up to 10 years.
Progression to >24 hours device-detected atrial fibrillation at a scheduled out-of hospital or acute cardiac device interrogation
Up to 10 years.
Initiation of oral anticoagulant therapy
時間枠:Up to 10 years
Initiation of oral anticoagulant therapy with minimum 3 months treatment duration.
Up to 10 years
Pulmonary embolism
時間枠:Up to 10 years
Pulmonary embolism verified with imaging e.g. CT or V/Q scan
Up to 10 years
Deep venous thrombosis
時間枠:Up to 10 years
Deep venous thrombosis verified with radiology e.g. ultrasound or CT
Up to 10 years

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出版物と役立つリンク

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一般刊行物

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)

2026年2月27日

一次修了 (推定)

2029年2月1日

研究の完了 (推定)

2037年9月1日

試験登録日

最初に提出

2026年7月8日

QC基準を満たした最初の提出物

2026年7月14日

最初の投稿 (実際)

2026年7月20日

学習記録の更新

投稿された最後の更新 (実際)

2026年7月20日

QC基準を満たした最後の更新が送信されました

2026年7月14日

最終確認日

2026年7月1日

詳しくは

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個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

IPD プランの説明

Individual participant data will not be shared publicly due to privacy regulations and ethical restrictions. Aggregated data will be reported in publications.

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いいえ

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