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Myelofibrosis - Epidemiology Forecast - 2034

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    Report

  • 131 Pages
  • April 2024
  • Region: Global
  • DelveInsight
  • ID: 5524904
UP TO OFF until Dec 31st 2024

Key Highlights

  • In the 7MM, the total prevalent cases of ALS was around 67,000 in 2023, which is expected to grow during the study period (2020-2034).
  • The United States contributed to the largest diagnosed prevalent population of ALS, acquiring ~40% of the 7MM in 2023.
  • Amongst EU4 and the UK, the age group of 70-79 accounted for the highest cases in 2023, followed by 60-69 and 50-59 years.
  • The major sites of onset of ALS are the bulbar, and spinal, along with other uncertain regions. In 2023, the patients with the spinal as a site of onset accounted highest cases in the US, i.e., 15,000, followed by the bulbar site of onset.
  • In 2023, the patients with the spinal as a site of onset accounted for around 7,000 cases in Japan
This report delivers an in-depth understanding of ALS, historical and forecasted epidemiology in the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan.

Geography Covered

  • The United States
  • EU4 (Germany, France, Italy, and Spain) and the United Kingdom
  • Japan

Study Period: 2020-2034

Amyotrophic Lateral Sclerosis Disease Understanding

Amyotrophic Lateral Sclerosis Overview

ALS, often referred to as Lou Gehrig's disease, is a progressive neurodegenerative disorder affecting the nerve cells in the brain and spinal cord, leading to muscle weakness, paralysis, and ultimately respiratory failure. While the exact cause remains unclear, a combination of genetic and environmental factors likely contributes to its onset. Diagnosis relies on neurological examination and various tests to rule out other conditions.

Amyotrophic Lateral Sclerosis Diagnosis

Diagnosing ALS involves a thorough neurological examination, medical history review, and various tests to exclude other possible conditions. Electromyography (EMG) and nerve conduction studies evaluate nerve and muscle function, while imaging scans like MRI rule out alternative causes of symptoms. Despite these efforts, ALS diagnosis remains challenging without a definitive test. Early and accurate diagnosis is crucial for initiating symptom management and support services. Biomarkers, like cerebrospinal fluid neurofilament levels, though not yet integrated into clinical practice, show promise for diagnosis and monitoring effects. They could aid in patient stratification and research studies, particularly in cases where symptoms are ambiguous or overlap with other conditions.

Amyotrophic Lateral Sclerosis Epidemiology

The ALS epidemiology chapter in the report provides historical as well as forecasted epidemiology segmented by the Total Prevalent Population of ALS, Diagnosed Prevalence of ALS, Type-specific Distribution of ALS, Gender-specific Distribution of ALS, Mutation-specific Distribution of ALS, Distribution Based on Site of Onset of ALS, and Age-specific Distribution of ALS in the 7MM market covering the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan from 2020 to 2034.
  • Among the 7MM, the US accounted for the highest prevalent cases of ALS in 2023, with around 24,000 cases; these cases are expected to increase during the forecast period.
  • Amongst EU4 and the UK, the diagnosed prevalent cases of ALS were highest in Germany, while the lowest number of cases was in Spain in 2023.
  • The major sites of onset of ALS are the bulbar, and spinal, along with other uncertain regions. In 2023, the patients with the spinal as a site of onset accounted highest cases in the US, i.e., 15,000, followed by the bulbar site of onset.
  • According to the estimates, in Japan, it is observed that ALS was most prevalent in the 70-79 years age group, followed by 60-69 years, and 50-59 years.

Scope of the Report

  • The report covers a segment of key events, an executive summary, descriptive overview of ALS, explaining its causes, signs and symptoms, and pathogenesis.
  • Comprehensive insight into the epidemiology segments and forecasts, and disease progression has been provided.
  • The report provides an edge while developing business strategies, understanding trends, expert insights/KOL views, and patient journey in the 7MM.
  • A detailed review of current challenges in establishing the diagnosis.

Amyotrophic Lateral Sclerosis Report Insights

  • Patient Population
  • Country-wise Epidemiology Distribution
  • Age-wise cases of Amyotrophic Lateral Sclerosis

Amyotrophic Lateral Sclerosis Report Key Strengths

  • Eleven Years Forecast
  • The 7MM Coverage
  • Amyotrophic Lateral Sclerosis Epidemiology Segmentation

Amyotrophic Lateral Sclerosis Report Assessment

  • Current Diagnostic Practices

Epidemiology Insights

  • What are the disease risk, burdens, and unmet needs of Amyotrophic Lateral Sclerosis? What will be the growth opportunities across the 7MM concerning the patient population with Amyotrophic Lateral Sclerosis?
  • What is the historical and forecasted Amyotrophic Lateral Sclerosis patient pool in the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan?
  • Which age group of Amyotrophic Lateral Sclerosis has a high patient share?

Reasons to Buy

  • Insights on patient burden/disease, evolution in diagnosis, and factors contributing to the change in the epidemiology of the disease during the forecast years.
  • To understand the age-specific Amyotrophic Lateral Sclerosis prevalence cases in varying geographies over the coming years.
  • To understand the perspective of key opinion leaders around the current challenges with establishing the diagnosis.
  • Detailed insights on various factors hampering disease diagnosis and other existing diagnostic challenges.

Table of Contents

1. Key Insights2. Report Introduction3. Executive Summary of Myelofibrosis4. Epidemiology Methodology
5. Myelofibrosis Epidemiology Overview at a Glance
5.1. Patient Share (%) of Myelofibrosis in 2020
5.2. Patient Share (%) of Myelofibrosis in 2034
6. Disease Background and Overview
6.1. Introduction
6.2. Subtypes
6.3. Signs and Symptoms
6.4. Causes
6.5. Pathogenesis
6.6. Prognosis
6.7. Risk Factor
6.8. Diagnosis
6.8.1. Blood Test
6.8.2. Bone Marrow Tests
6.8.3. Molecular Testing
6.8.4. Mutation-Enhanced Morphologic Diagnosis
6.9. Risk-based Scoring in Myelofibrosis
7. Epidemiology and Patient Population
7.1. Key Findings
7.2. Assumptions and Rationale
7.3. Total Prevalent Cases of Myelofibrosis in the 7MM
7.4. the United States
7.4.1. Total Prevalent Cases of Myelofibrosis in the United States
7.4.2. Type-Specific Cases of Myelofibrosis in the United States
7.4.3. Myelofibrosis Cases Based on Risk Stratification in the United States
7.4.4. Age-Specific Cases of Myelofibrosis in the United States
7.4.5. Myelofibrosis Cases Based on Molecular Alterations in the United States
7.5. EU4 and the UK
7.5.1. Total Prevalent Cases of Myelofibrosis in EU4 and the UK
7.5.2. Type-Specific Cases of Myelofibrosis in EU4 and the UK
7.5.3. Myelofibrosis Cases Based on Risk Stratification in EU4 and the UK
7.5.4. Age-Specific Cases of Myelofibrosis in EU4 and the UK
7.5.5. Myelofibrosis Cases Based on Molecular Alterations in EU4 and the UK
7.6. Japan
7.6.1. Total Prevalent Cases of Myelofibrosis in Japan
7.6.2. Type-Specific Cases of Myelofibrosis in Japan
7.6.3. Myelofibrosis Cases Based on Risk Stratification in Japan
7.6.4. Age-Specific Cases of Myelofibrosis in Japan
7.6.5. Myelofibrosis Cases Based on Molecular Alterations in Japan
8. Kol Views
9. Appendix
9.1. Bibliography
9.2. Report Methodology
10. Publisher Capabilities11. Disclaimer12. About the Publisher
List of Tables
Table 1: Summary of Myelofibrosis Epidemiology (2020-2034)
Table 2: List of the Available Risk Score for Myelofibrosis and Their Prognostic Relevance
Table 3: Mutation and Karyotype-enhanced IPSS (MIPSS-70+ VERSION 2.0) for Patients With Primary Myelofibrosis
Table 4: Total Prevalent Cases of Myelofibrosis in the 7MM (2020-2034)
Table 5: Total Prevalent Cases of Myelofibrosis in the US (2020-2034)
Table 6: Type-specific Cases of Myelofibrosis in the US (2020-2034)
Table 7: Myelofibrosis Cases Based on Risk Stratification in the US (2020-2034)
Table 8: Age-specific Cases of Myelofibrosis in the US (2020-2034)
Table 9: Myelofibrosis Cases Based on Molecular Alterations in the US (2020-2034)
Table 10: Total Prevalent Cases of Myelofibrosis in EU4 and the UK (2020-2034)
Table 11: Type-specific Cases of Myelofibrosis in EU4 and the UK (2020-2034)
Table 12: Myelofibrosis cases Based on Risk Stratification in EU4 and the UK (2020-2034)
Table 13: Age-specific Cases of Myelofibrosis in EU4 and the UK (2020-2034)
Table 14: Myelofibrosis Cases Based on Molecular Alterations in EU4 and the UK (2020-2034)
Table 15: Total Prevalent Cases of Myelofibrosis in Japan (2020-2034)
Table 16: Type-specific Cases of Myelofibrosis in Japan (2020-2034)
Table 17: Myelofibrosis Cases Based on Risk Stratification in Japan (2020-2034)
Table 18: Age-specific Cases of Myelofibrosis in Japan (2020-2034)
Table 19: Myelofibrosis Cases Based on Molecular Alterations in the Japan (2020-2034)
List of Figures
Figure 1: Risk Factors Associated with Postherpetic Neuralgia
Figure 2: Sensory Alterations Experienced During Postherpetic Neuralgia
Figure 3: Total Incident Cases of Herpes Zoster in the 7MM (2020-2034)
Figure 4: Total Incident Cases of PHN in the 7MM (2020-2034)
Figure 5: Total Incident Cases of PHN in the United States (2020-2034)
Figure 6: Gender-specific Cases of PHN in the United States (2020-2034)
Figure 7: Age-specific Cases of PHN in the United States (2020-2034)
Figure 8: Total Treated Cases of PHN in the United States (2020-2034)
Figure 9: Total Incident Cases of PHN in EU4 and the UK (2020-2034)
Figure 10: Gender-specific Cases of PHN in EU4 and the UK (2020-2034)
Figure 11: Age-specific Cases of PHN in EU4 and the UK (2020-2034)
Figure 12: Total Treated Cases of PHN in EU4 and the UK (2020-2034)
Figure 13: Total Incident Cases of PHN in Japan (2020-2034)
Figure 14: Gender-specific Cases of PHN in Japan (2020-2034)
Figure 15: Age-specific Cases of PHN in Japan (2020-2034)
Figure 16: Total Treated Cases of PHN in Japan (2020-2034)