PKP2-Arrhythmogenic Cardiomyopathy (PKP2-ACM) – Market Outlook, Epidemiology, Competitive Landscape, and Market Forecast Report – 2022 To 2032
Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is a hereditary cardiac disorder characterized by impaired function of the right ventricle (RV) and the occurrence of ventricular arrhythmias, which can ultimately lead to sudden cardiac death. The condition is characterized by the replacement of cardiomyocytes with fibrofatty tissue. ARVD/C is typically inherited in an autosomal dominant manner, but it exhibits incomplete penetrance, and the expression of the disease varies significantly with age. In rare cases, autosomal recessive inheritance can occur with or without cutaneous involvement. The progressive fibrotic replacement process leads to electrical instability, increasing the risk of syncope and sudden cardiac death, or causing alterations in cardiac function, resembling dilated cardiomyopathy, which may result in right- or bi-ventricular heart failure. The diagnosis of ARVD/C is challenging and relies on applying the 2010 Task Force criteria, which consider family history, distinctive electrocardiographic findings, arrhythmic events, and structural and histological abnormalities. Mutations in the PKP2 gene are responsible for 9-43% of ARVC cases and are considered the most common genetic cause of the condition. However, it should be noted that a single pathogenic variant in PKP2 may not be sufficient to cause the full manifestation of the disease. The PKP2 gene encodes a protein that belongs to the Armadillo (ARM) repeat family. Plakophilin proteins, including Plakophilin-2, contain multiple ARM repeats and are localized in cell desmosomes and nuclei. They play a crucial role in linking cadherins to intermediate filaments in the cytoskeleton. Plakophilin-2 is essential for the assembly of junctional proteins and serves as a vital morphogenic factor and architectural component in the heart. ARVC often exhibits familial clustering, with a family history of the condition present in 30-50% of cases.
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Additionally,
men tend to have a higher incidence and greater severity of ARVC than women.
ARVC has an estimated prevalence of 1 per 5000 individuals in the general
population
Thelansis’s “PKP2-Arrhythmogenic
Cardiomyopathy (PKP2-ACM) Market Outlook, Epidemiology, Competitive Landscape,
and Market Forecast Report – 2022 To 2032" covers disease overview,
epidemiology, drug utilization, prescription share analysis, competitive
landscape, clinical practice, regulatory landscape, patient share, market
uptake, market forecast, and key market insights under the potential PKP2-Arrhythmogenic
Cardiomyopathy (PKP2-ACM) treatment modalities options for eight major markets
(USA, Germany, France, Italy, Spain, UK, Japan, and China).
KOLs insights
of PKP2-Arrhythmogenic Cardiomyopathy (PKP2-ACM) across 8 MM market from the
centre of Excellence/ Public/ Private hospitals participated in the study.
Insights around current treatment landscape, epidemiology, clinical
characteristics, future treatment paradigm, and Unmet needs.
PKP2-Arrhythmogenic Cardiomyopathy
(PKP2-ACM) Market
Forecast Patient Based Forecast Model (MS. Excel Based Automated
Dashboard), which Data Inputs with sourcing, Market Event, and Product Event,
Country specific Forecast Model, Market uptake and patient share uptake,
Attribute Analysis, Analog Analysis, Disease burden, and pricing scenario,
Summary, and Insights.
Thelansis Competitive Intelligence (CI) practice
has been established based on a deep understanding of the pharma/biotech
business environment to provide an optimized support system to all levels of
the decision-making process. It enables business leaders in forward-thinking
and proactive decision-making. Thelansis supports scientific and commercial
teams in seamless CI support by creating an AI/ ML-based technology-driven
platform that manages the data flow from primary and secondary sources.
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