Ignite Creation Date:
2024-05-06 @ 8:13 PM
Last Modification Date:
2024-10-26 @ 3:23 PM
Study NCT ID:
NCT06299436
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-05-28
First Post:
2024-03-01
Brief Title:
Hemodynamic Assessment of underLying myocyTe Function in Right Heart Failure
Sponsor:
Johns Hopkins University
Organization:
Johns Hopkins University
Study Overview
Official Title:
Hemodynamic Assessment of underLying myocyTe Function in Right Heart Failure
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
HALT-RHF
Brief Summary:
Right ventricular RV failure is recognized to worsen patient outcomes in the setting of heart failure with reduced ejection fraction HFrEF-related pulmonary hypertension PH yet the investigators fall short in trying to identify and treat it The current proposal will 1 determine the best clinical indicators of intrinsic RV myocyte contractile failure in humans with HFrEF-PH 2 clarify underlying mechanisms and 3 test novel treatments on RV myocytes The long-term goal of this proposal will be to better identify and treat RV failure in humans suffering from HFrEF-PH
Detailed Description:
This proposal aims to improve diagnosis and mechanistic understanding of right ventricular RV myocyte dysfunction in heart failure patients with reduced ejection fraction and pulmonary hypertension HFrEF-PH RV dysfunction is common and hastens poor outcomes in HFrEF-PH Despite its importance clinical ability to characterize it remains imprecise This frustrates prognostic and therapeutic efforts in many scenarios such as the prediction of RV failure following left ventricular assist device In 2023 the investigators reported that RV myocyte contractile reserve indices such as calcium-activated isometric tension and length-dependent active tension are reduced in RV tissue of explanted end-stage human HFrEF-PH hearts Notably clinical indices correlated modestly with calcium-activated tension but completely failed to capture depression of length-dependent tension the latter a key contributor to RV Frank-Starling reserve This deficiency highlights one possible reason why clinical indices fail to identify RV failure A shortcoming of this work was its study of end-stage disease and the investigators believe better clinical correlates of myocyte dysfunction from earlier-stage disease may provide more insight at a time point when interventions would still be helpful The investigators central hypothesis is that clinical identification of RV myocyte disease in HFrEF-PH requires measuring RV contractile reserve as is elicited during exercise The investigators prior study of primary PH patients supports this and new preliminary data in patients with PH secondary to heart failure does so as well Delving deeper the investigators recently reported a novel deficiency of the sarcomere thick filament in HFrEF-PH RV myocytes driven by an excess of myosin in the inactive super-relaxed state that hinders its recruitment to form cross-bridges by either calcium- or stretch-activation The latter is important as it is not seen in small rodents and only recently reported in pigs thus newly linking super-relaxed myosin to RV myocyte and chamber reserve in humans The investigators new phospho-proteomic data shows less myosin binding protein-C phosphorylation yet more phosphorylation of several sarcomere Z-disc proteins and supports the potential role based on kinase and phosphatase modifications
This proposal was spawned by these recent findings The investigators objectives are to 1 identify clinical indices that capture RV myocyte reserve failure in earlier-to-mid stage HFrEF-PH 2 uncover mechanisms of myocyte length-dependent contractile depression and 3 test sarcomere-activating drugs that might prove useful for HFrEF-PH RV failure The investigators combine state-of-the-art pressure-volume loop and clinical assessments of RV chamber function with phenotyping of the myocyte contractile apparatus The investigators further explore a new role of super-relaxed myosin in depressed myocyte reserve The proposal leverages my translational and basic muscle expertise developed over the past several years with K23 support and a stellar collaborative team Its objectives align with NHLBI strategic visions for the RV and advanced HF There are three Specific Aims
Aim 1 Test whether clinical measures of RV exercise reserve better reflect RV myocyte contractile dysfunction in earlier-stage HFrEF-PH HFrEF patients referred for right heart cath undergo a well-established protocol at Johns Hopkins to assess clinical hemodynamic and echocardiographic RV indices alongside RV pressure-volume loop parameters at rest and with supine bicycle exercise RV endomyocardial biopsies are obtained and isolated myocytes permeabilized to assess contractile mechanics and calcium- and length-activated tension The investigators then test whether clinical RV exercise reserve parameters will more sensitively reflect RV myocyte contractile reserve limitations than commonly used resting measures of RV function
Aim 2 Determine roles and identities of phosphorylation mediators of reduced HFrEF-PH RV myocyte length-dependent reserve New phospho-proteomic data finds protein kinase A PKA-hypophosphorylation of thick filament proteins and hyperphosphorylation of Z-disc scaffold proteins in HFrEF-PH RV myocardium PKA incubation increases myocyte length-dependent tension while protein phosphatase 2a which does not reverse PKA changes improves calcium-activated tension The investigators test the relevance to myocyte contractile reserve failure in HFrEF-PH in permeabilized RV myocytes by selective kinase and phosphatase incubation then selectively mutate high-value phospho-modified sites to test the role in length-dependent activation
Aim 3 Determine whether newer sarcomere-activating drugs restore HFrEF RV myocyte length-dependent tension Two sarcomere-activating drugs are tested in HFrEF-PH RV myocytes danicamtiv and CK-136 which should augment length-dependent tension better than similar previously tested drugs The investigators determine impact on skinned myocyte contractile reserve then test if the clinical RV reserve indices identified in Aim 1 can predict impact on individual HFrEF-PH RV myocytes from the same patient
Expected outcomes the investigators will identify optimal clinical indices of RV reserve failure in HFrEF-PH clarify myocyte mechanisms of length-dependent reserve and test novel RV drugs Findings will impact RV failure due to HFrEF-PH and should apply to its other causes as well The investigators research team has exceptional expertise in translational RV phenotyping and muscle biophysics and is uniquely poised to deliver on this proposal
This proposal was spawned by these recent findings The investigators objectives are to 1 identify clinical indices that capture RV myocyte reserve failure in earlier-to-mid stage HFrEF-PH 2 uncover mechanisms of myocyte length-dependent contractile depression and 3 test sarcomere-activating drugs that might prove useful for HFrEF-PH RV failure The investigators combine state-of-the-art pressure-volume loop and clinical assessments of RV chamber function with phenotyping of the myocyte contractile apparatus The investigators further explore a new role of super-relaxed myosin in depressed myocyte reserve The proposal leverages my translational and basic muscle expertise developed over the past several years with K23 support and a stellar collaborative team Its objectives align with NHLBI strategic visions for the RV and advanced HF There are three Specific Aims
Aim 1 Test whether clinical measures of RV exercise reserve better reflect RV myocyte contractile dysfunction in earlier-stage HFrEF-PH HFrEF patients referred for right heart cath undergo a well-established protocol at Johns Hopkins to assess clinical hemodynamic and echocardiographic RV indices alongside RV pressure-volume loop parameters at rest and with supine bicycle exercise RV endomyocardial biopsies are obtained and isolated myocytes permeabilized to assess contractile mechanics and calcium- and length-activated tension The investigators then test whether clinical RV exercise reserve parameters will more sensitively reflect RV myocyte contractile reserve limitations than commonly used resting measures of RV function
Aim 2 Determine roles and identities of phosphorylation mediators of reduced HFrEF-PH RV myocyte length-dependent reserve New phospho-proteomic data finds protein kinase A PKA-hypophosphorylation of thick filament proteins and hyperphosphorylation of Z-disc scaffold proteins in HFrEF-PH RV myocardium PKA incubation increases myocyte length-dependent tension while protein phosphatase 2a which does not reverse PKA changes improves calcium-activated tension The investigators test the relevance to myocyte contractile reserve failure in HFrEF-PH in permeabilized RV myocytes by selective kinase and phosphatase incubation then selectively mutate high-value phospho-modified sites to test the role in length-dependent activation
Aim 3 Determine whether newer sarcomere-activating drugs restore HFrEF RV myocyte length-dependent tension Two sarcomere-activating drugs are tested in HFrEF-PH RV myocytes danicamtiv and CK-136 which should augment length-dependent tension better than similar previously tested drugs The investigators determine impact on skinned myocyte contractile reserve then test if the clinical RV reserve indices identified in Aim 1 can predict impact on individual HFrEF-PH RV myocytes from the same patient
Expected outcomes the investigators will identify optimal clinical indices of RV reserve failure in HFrEF-PH clarify myocyte mechanisms of length-dependent reserve and test novel RV drugs Findings will impact RV failure due to HFrEF-PH and should apply to its other causes as well The investigators research team has exceptional expertise in translational RV phenotyping and muscle biophysics and is uniquely poised to deliver on this proposal
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| R01HL172830 | NIH | NHLBINIH | httpsreporternihgovquickSearchR01HL172830 |