Abstract:Aim: Multiomics delivers more biological insight than targeted investigations. We applied multiomics to patients with heart failure (HF) and reduced ejection fraction (HFrEF), with machine learning applied to advanced ECG (AECG) and echocardiography artificial intelligence (Echo AI). Patients & methods: In total, 46 patients with HFrEF and 20 controls underwent metabolomic profiling, including liquid/gas chromatography–mass spectrometry and solid-phase microextraction volatilomics in plasma and urine. HFrE… Show more
“…Similarly, AI-based biomarker discovery using deep phenotyping with multiomics and analysis of digital electrocardiogram and data from wearable devices shows promising results in HF ( 50 ), left ventricular systolic dysfunction ( 51 , 52 ), and arrhythmia ( 53 ). Although reviewing specific applications of AI in cardiovascular contexts exceeds the scope of this review, several interesting review articles address this area ( 54 – 58 ). Giordano and colleagues discuss the efficacy and application of machine learning and AI in clinical decision making when developing personalized models of patient care ( 59 ).…”
Section: Network Medicine: a Tool For Cardiovascular Disease Researchmentioning
Cardiovascular diseases (CVD) are diverse disorders affecting the heart and vasculature in millions of people worldwide. Like other fields, CVD research has benefitted from the deluge of multiomics biomedical data. Current CVD research focuses on disease etiologies and mechanisms, identifying disease biomarkers, developing appropriate therapies and drugs, and stratifying patients into correct disease endotypes. Systems biology offers an alternative to traditional reductionist approaches and provides impetus for a comprehensive outlook toward diseases. As a focus area, network medicine specifically aids the translational aspect of in silico research. This review discusses the approach of network medicine and its application to CVD research.
“…Similarly, AI-based biomarker discovery using deep phenotyping with multiomics and analysis of digital electrocardiogram and data from wearable devices shows promising results in HF ( 50 ), left ventricular systolic dysfunction ( 51 , 52 ), and arrhythmia ( 53 ). Although reviewing specific applications of AI in cardiovascular contexts exceeds the scope of this review, several interesting review articles address this area ( 54 – 58 ). Giordano and colleagues discuss the efficacy and application of machine learning and AI in clinical decision making when developing personalized models of patient care ( 59 ).…”
Section: Network Medicine: a Tool For Cardiovascular Disease Researchmentioning
Cardiovascular diseases (CVD) are diverse disorders affecting the heart and vasculature in millions of people worldwide. Like other fields, CVD research has benefitted from the deluge of multiomics biomedical data. Current CVD research focuses on disease etiologies and mechanisms, identifying disease biomarkers, developing appropriate therapies and drugs, and stratifying patients into correct disease endotypes. Systems biology offers an alternative to traditional reductionist approaches and provides impetus for a comprehensive outlook toward diseases. As a focus area, network medicine specifically aids the translational aspect of in silico research. This review discusses the approach of network medicine and its application to CVD research.
“…10 Department of Cardiovascular Medicine, Fukushima Medical University, Fukushima, Japan. 11 Department of Cardiovascular Medicine, Nagoya City University East Medical Center, Nagoya, Japan. 12 Department of Community Medicine for Cardiology, Tokushima University Graduate School of Biomedical Sciences, Tokushima, Japan.…”
Section: Abbreviationsmentioning
confidence: 99%
“…Recently, several researchers reported that advanced imaging can identify subtypes in which treatment was effective [8,9]. An advancing area in this research field is the application of artificial intelligence to carry out detailed phenotyping using multi-omics data, which enables stratification of early-stage diseases and assessment of prognosis [10,11]. Identification of effective subtypes of HF treatment is therefore an essential research topic for optimizing treatment of HF [12].…”
Background
Identification of the effective subtypes of treatment for heart failure (HF) is an essential topic for optimizing treatment of the disorder. We hypothesized that the beneficial effect of SGLT2 inhibitors (SGLT2i) on the levels of N-terminal pro-brain natriuretic peptide (NT-proBNP) might depend on baseline diastolic function. To elucidate the effects of SGLT2i in type 2 diabetes mellitus (T2DM) and chronic HF we investigated, as a post-hoc sub-study of the CANDLE trial, the effects of canagliflozin on NT-proBNP levels from baseline to 24 weeks, with the data stratified by left ventricular (LV) diastolic function at baseline.
Methods
Patients (n = 233) in the CANDLE trial were assigned randomly to either an add-on canagliflozin (n = 113) or glimepiride treatment groups (n = 120). The primary endpoint was a comparison between the two groups of the changes from baseline to 24 weeks in NT-pro BNP levels, stratified according to baseline ventricular diastolic function.
Results
The change in the geometric mean of NT-proBNP level from baseline to 24 weeks was 0.98 (95% CI 0.89–1.08) in the canagliflozin group and 1.07 (95% CI 0.97–1.18) in the glimepiride group. The ratio of change with canagliflozin/glimepiride was 0.93 (95% CI 0.82–1.05). Responder analyses were used to investigate the response of an improvement in NT-proBNP levels. Although the subgroup analyses for septal annular velocity (SEP-e′) showed no marked heterogeneity in treatment effect, the subgroup with an SEP-e′ < 4.7 cm/s indicated there was an association with lower NT-proBNP levels in the canagliflozin group compared with that in the glimepiride group (ratio of change with canagliflozin/glimepiride (0.83, 95% CI 0.66–1.04).
Conclusions
In the subgroup with a lower LV diastolic function, canagliflozin showed a trend of reduced NT-pro BNP levels compared to that observed with glimepiride. This study suggests that the beneficial effects of canagliflozin treatment may be different in subgroups classified by the severity of LV diastolic dysfunction.
“…Metabolomics refer to global analyses of small molecule metabolites in a biological system ( Nicholson and Lindon, 2008 ). High-throughput metabolomics-based methods have been widely employed for screening novel biomarkers and elucidating the multiple targets and metabolic pathways of heart disease ( Jiang et al, 2020 ; Deidda et al, 2021 ; Gladding et al, 2021 ). Further, metabolic profiling provides integrative information on physiological as well as pathological changes ( Mamas et al, 2011 ; Johnson and Gonzalez, 2012 ).…”
Coronary heart disease (CHD) is one of the leading causes of deaths globally. Identification of serum metabolic biomarkers for its early diagnosis is thus much desirable. Serum samples were collected from healthy controls (n = 86) and patients with CHD (n = 166) and subjected to untargeted and targeted metabolomics analyses. Subsequently, potential biomarkers were detected and screened, and a clinical model was developed for diagnosing CHD. Four dysregulated metabolites, namely PC(17:0/0:0), oxyneurine, acetylcarnitine, and isoundecylic acid, were identified. Isoundecylic acid was not found in Human Metabolome Database, so we could not validate differences in its relative abundance levels. Further, the clinical model combining serum oxyneurine, triglyceride, and weight was found to be more robust than that based on PC(17:0/0:0), oxyneurine, and acetylcarnitine (AUC = 0.731 vs. 0.579, sensitivity = 83.0 vs. 75.5%, and specificity = 64.0 vs. 46.5%). Our findings indicated that serum metabolomics is an effective method to identify differential metabolites and that serum oxyneurine, triglyceride, and weight appear to be promising biomarkers for the early diagnosis of CHD.
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