CMR derived left ventricular septal convexity in carriers of the hypertrophic cardiomyopathy-causing MYBPC3-Q1061X mutation

This manuscript has not been published before and is not currently being considered for publication elsewhere. Increased septal convexity of left ventricle has been described in subjects with hypertrophic cardiomyopathy (HCM)-causing mutations without left ventricular hypertrophy (LVH). Our objective was to study septal convexity by cardiac magnetic resonance (CMR) in subjects with the Finnish founder mutation Q1016X in the myosin-binding protein C gene (MYBPC3). Septal convexity was measured in end-diastolic 4-chamber CMR image in 67 study subjects (47 subjects with the MYBPC3-Q1061X mutation and 20 healthy relatives without the mutation). Septal convexity was significantly increased in subjects with the MYBPC3-Q1061X mutation and LVH (n = 32) compared to controls (11.4 +/- 4.3 vs 2.7 +/- 3.2 mm, P <0.001). In mutation carriers without LVH, there was a trend for increased septal convexity compared to controls (4.9 +/- 2.5 vs 2.7 +/- 3.2 mm, P = 0.074). When indexed for BSA, septal convexity in mutation carriers without LVH was 2.8 +/- 1.4 mm/m(2) and 1.5 +/- 1.6 mm/m(2) in controls (P = 0.036). In all mutation carriers, septal convexity correlated significantly with body surface area, age, maximal LV wall thickness, LV mass, and late gadolinium enhancement. Subjects with the MYBPC3-Q10961X mutation have increased septal convexity irrespective of the presence of LVH. Septal convexity appears to reflect septal remodeling, and could be useful in recognizing LVH negative mutation carriers.Peer reviewe

Novel electrocardiographic features in carriers of hypertrophic cardiomyopathy causing sarcomeric mutations

Objectives: The sensitivity and specificity of the conventional 12-lead ECG to identify carriers of hypertrophic cardiomyopathy (HCM) - causing mutations without left ventricular hypertrophy (LVH) has been limited. We assessed the ability of novel electrocardiographic parameters to improve the detection of HCM mutation carriers. Methods: We studied 140 carriers (G+) of the TPM7-Asp175Asn or MYBPC3-Glnl 061X pathogenic variants for HCM: The G+/LVH+ group (n = 98) consisted of mutation carriers with LVH and the G+/LVH- group (n = 42) without LVH. The control group consisted of 30 subjects. The standard 12-lead ECG was comprehensively analyzed and two novel ECG variables were introduced: RVlRV3 and septal remodeling. A subset of 65 individuals underwent cardiac magnetic resonance imaging and 2D strain echocardiography. Results: Conventional major ECG criteria were sensitive (90%) and specific (97%) in identifying G+/LVH+ subjects. RV1RV3 and septal remodeling were more prevalent in the G+/LVH- subjects compared to the control group (33% vs 3%, p = 0.005 and 45% vs 3%, p <0.001, respectively). The combination of RVlRV3 and Q waves and repolarization abnormalities (QR) differentiated between the G+/LVH- subjects and the control group with a sensitivity of 52% and specificity of 97%. The combination of septa] remodeling and QR differentiated between G+/LVH- subjects and the control group with a sensitivity of 64% and specificity of 97%. Conclusions: The novel ECG-parameters RVlRV3 and septal remodeling were effective in identifying G+/LVH-subjects and could be useful in the diagnostics of new suspected HCM patients and in the screening and follow-up of HCM families. (C) 2018 Elsevier Inc. All rights reserved.Peer reviewe

Very High Spatial Resolution Soil Moisture Observation of Heterogeneous Subarctic Catchment Using Nonlocal Averaging and Multitemporal SAR Data

A soil moisture estimation method was developed for Sentinel-1 synthetic aperture radar (SAR) ground range detected high resolution (GRDH) data to analyze moisture conditions in a gently undulating and heterogeneous subarctic area containing forests, wetlands, and open orographic tundra. In order to preserve the original 10-m pixel spacing, PIMSAR (pixel-based multitemporal nonlocal averaging) nonlocal mean filtering was applied. It was guided by multitemporal statistics of SAR images in the area. The gradient boosted trees (GBT) machine learning method was used for the soil moisture algorithm development. Discrete and continuous in situ soil moisture values were used for training and validation of the algorithm. For surface soil moisture, the root mean square error (RMSE) of the method was 6.5% and 8.8% for morning and evening images, respectively. The corresponding maximum errors were 34.1% and 33.8%. The pixelwise sensitivity to the training set and method choice was estimated as the variance of the soil moisture values derived using the algorithms for the three best methods with respect to the criteria: the smallest maximum error, the smallest RMSE value, and the highest coefficient of determination (R-2) value. It was, on average, 6.3% with a standard deviation of 5.7%. Our approach successfully produced instantaneous high-resolution soil moisture estimates on daily basis for the subarctic landscape and can further be applied to various hydrological, biogeochemical, and management purposes.Peer reviewe

Very High Spatial Resolution Soil Moisture Observation of Heterogeneous Subarctic Catchment Using Nonlocal Averaging and Multitemporal SAR Data

A soil moisture estimation method was developed for Sentinel-1 synthetic aperture radar (SAR) ground range detected high resolution (GRDH) data to analyze moisture conditions in a gently undulating and heterogeneous subarctic area containing forests, wetlands, and open orographic tundra. In order to preserve the original 10-m pixel spacing, PIMSAR (pixel-based multitemporal nonlocal averaging) nonlocal mean filtering was applied. It was guided by multitemporal statistics of SAR images in the area. The gradient boosted trees (GBT) machine learning method was used for the soil moisture algorithm development. Discrete and continuous in situ soil moisture values were used for training and validation of the algorithm. For surface soil moisture, the root mean square error (RMSE) of the method was 6.5% and 8.8% for morning and evening images, respectively. The corresponding maximum errors were 34.1% and 33.8%. The pixelwise sensitivity to the training set and method choice was estimated as the variance of the soil moisture values derived using the algorithms for the three best methods with respect to the criteria: the smallest maximum error, the smallest RMSE value, and the highest coefficient of determination (R-2) value. It was, on average, 6.3% with a standard deviation of 5.7%. Our approach successfully produced instantaneous high-resolution soil moisture estimates on daily basis for the subarctic landscape and can further be applied to various hydrological, biogeochemical, and management purposes.Peer reviewe

Fibrosis and wall thickness affect ventricular repolarization dynamics in hypertrophic cardiomyopathy

Background Hypertrophic cardiomyopathy (HCM) is characterized by ventricular repolarization abnormalities and risk of ventricular arrhythmias. Our aim was to study the association between the phenotype and ventricular repolarization dynamics in HCM patients. Methods Results HCM patients with either the MYBPC3-Q1061X or TPM1-D175N mutation (n = 46) and control subjects without mutation and hypertrophy (n = 35) were studied with 24-hr ambulatory ECG recordings by measuring time intervals of rate-adapted QT (QTe), maximal QT, and T-wave apex to wave end (TPE) intervals and the QTe/RR slope. Findings were correlated to specified echocardiographic and cardiac magnetic resonance imaging (CMRI) findings. Rate-adapted QTe interval was progressively longer in HCM patients with decreasing heart rates compared to control subjects (p = 0.020). The degree of hypertrophy correlated with measured QTe values. HCM patients with maximal wall thickness higher than the mean (20.6 mm) had longer maximum QTe and median TPE intervals compared to control subjects and HCM patients with milder hypertrophy (p p = 0.014, respectively). HCM patients with late gadolinium enhancement (LGE) on CMRI had steeper QTe/RR slopes compared to HCM patients without LGE and control subjects (p = 0.044 and p = 0.001, respectively). LGE was an independent predictor of QTe/RR slope (p = 0.023, B = 0.043). Conclusion Dynamics of ventricular repolarization in HCM are affected by hypertrophy and fibrosis. LGE may confer an independent effect on QT dynamics which may increase the arrhythmogenic potential in HCM.Peer reviewe

Genetic basis and outcome in a nationwide study of Finnish patients with hypertrophic cardiomyopathy

Aims Nationwide large-scale genetic and outcome studies in cohorts with hypertrophic cardiomyopathy (HCM) have not been previously published. Methods and results We sequenced 59 cardiomyopathy-associated genes in 382 unrelated Finnish patients with HCM and found 24 pathogenic or likely pathogenic mutations in six genes in 38.2% of patients. Most mutations were located in sarcomere genes (MYBPC3, MYH7, TPM1, and MYL2). Previously reported mutations by our study group (MYBPC3-Gln1061Ter, MYH7-Arg1053Gln, and TPM1-Asp175Asn) and a fourth major mutation MYH7-Val606Met accounted for 28.0% of cases. Mutations in GLA and PRKAG2 were found in three patients. Furthermore, we found 49 variants of unknown significance in 31 genes in 20.4% of cases. During a 6.7 +/- 4.2 year follow-up, annual all-cause mortality in 482 index patients and their relatives with HCM was higher than that in the matched Finnish population (1.70 vs. 0.87%; P <0.001). Sudden cardiac deaths were rare (n = 8). Systolic heart failure (hazard ratio 17.256, 95% confidence interval 3.266-91.170, P = 0.001) and maximal left ventricular wall thickness (hazard ratio 1.223, 95% confidence interval 1.098-1.363, P <0.001) were independent predictors of HCM-related mortality and life-threatening cardiac events. The patients with a pathogenic or likely pathogenic mutation underwent an implantable cardioverter defibrillator implantation more often than patients without a pathogenic or likely pathogenic mutation (12.9 vs. 3.5%, P <0.001), but there was no difference in all-cause or HCM-related mortality between the two groups. Mortality due to HCM during 10 year follow-up among the 5.2 million population of Finland was studied from death certificates of the National Registry, showing 269 HCM-related deaths, of which 32% were sudden. Conclusions We identified pathogenic and likely pathogenic mutations in 38% of Finnish patients with HCM. Four major sarcomere mutations accounted for 28% of HCM cases, whereas HCM-related mutations in non-sarcomeric genes were rare. Mortality in patients with HCM exceeded that of the general population. Finally, among 5.2 million Finns, there were at least 27 HCM-related deaths annually.Peer reviewe