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Genome-wide Association Studies-GWAS01:11

Genome-wide Association Studies-GWAS

Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...
The JAK-STAT Signaling Pathway01:20

The JAK-STAT Signaling Pathway

Several cytokine receptors have tightly bound Janus kinase or JAK proteins attached at their cytosolic tail. Small signaling molecules such as cytokines, growth hormones, or prolactins bind to the cytokine receptors and initiate their dimerization. The dimerization brings the cytosolic JAKs together that trans-phosphorylate and activates each other. The activated JAKs now phosphorylate cytosolic tails of the cytokine receptors, which serve as binding sites for adaptor proteins such as  SH2...
Rheumatic Heart Disease I: Introduction01:23

Rheumatic Heart Disease I: Introduction

Rheumatic heart disease or RHD is a chronic condition that results from rheumatic fever, causing permanent damage to the heart valves.Etiology and Risk FactorsIt primarily arises from rheumatic fever, an inflammatory disease that can develop after untreated or inadequately treated group A streptococcal (GAS) pharyngitis. Streptococcus spreads through direct contact with oral or respiratory secretions. While the bacteria are the causative agents, factors like malnutrition, overcrowding, poor...
Rheumatic Heart Disease II: Clinical Manifestations and Diagnostic Studies01:22

Rheumatic Heart Disease II: Clinical Manifestations and Diagnostic Studies

The key clinical manifestations of Rheumatic heart disease (RHD) include several distinct cardiac symptoms.Carditis, a hallmark of acute rheumatic fever, involves inflammation of the heart's endocardium, myocardium, and pericardium. Chronic RHD often results from recurrent episodes of carditis. Its symptoms include the following:Murmurs are caused by valvular damage, especially to the mitral and aortic valves. Mitral stenosis or regurgitation is common, with characteristic heart murmurs...
Rheumatic Heart Disease III: Medical Management01:21

Rheumatic Heart Disease III: Medical Management

Rheumatic heart disease (RHD) management can be divided into two main strategies: prevention and long-term management.Primary PreventionPrimary prevention focuses on timely diagnosis and management of group A streptococcal pharyngitis to prevent acute rheumatic fever. The most widely used antibiotic for treating this condition is intramuscular benzathine penicillin G.Acute Rheumatic Fever TreatmentThe primary treatment goal for a patient diagnosed with acute rheumatic fever is to suppress the...
Degenerative Disc Disease ll: Pathophysiology01:23

Degenerative Disc Disease ll: Pathophysiology

The symptoms of degenerative disc disease arise from a combination of mechanical compression, vascular compromise, and biochemical inflammation, which together disrupt nerve function and produce pain.Mechanical CompressionDisc degeneration reduces height and elasticity, predisposing to herniation of the nucleus pulposus, a major cause of radicular pain. Herniations may be protrusion (bulging with intact annulus), extrusion (nucleus extends beyond disc but remains connected), or sequestration...

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Related Experiment Video

Updated: Jul 5, 2026

Flow Cytometry Analysis of Immune Cell Subsets within the Murine Spleen, Bone Marrow, Lymph Nodes and Synovial Tissue in an Osteoarthritis Model
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Flow Cytometry Analysis of Immune Cell Subsets within the Murine Spleen, Bone Marrow, Lymph Nodes and Synovial Tissue in an Osteoarthritis Model

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Update on spondyloarthropathies.

Muhammad Asim Khan1

  • 1Case Western Reserve University, MetroHealth Medical Center, Division of Rheumatology, Cleveland, Ohio 44109, USA.

Annals of Internal Medicine
|June 19, 2002
PubMed
Summary
This summary is machine-generated.

Spondyloarthropathies are chronic inflammatory diseases like ankylosing spondylitis, linked to HLA-B27 and environmental triggers. Research reviews anti-tumor necrosis factor-alpha therapy and other advances for managing these rheumatic conditions.

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Area of Science:

  • Rheumatology and Immunology
  • Genetics and Molecular Biology

Background:

  • Spondyloarthropathies encompass chronic inflammatory rheumatic diseases including ankylosing spondylitis, reactive arthritis, and arthritis linked to psoriasis and inflammatory bowel diseases.
  • Pathologic sites include entheses, axial skeleton, limb joints, and nonarticular structures like the gut, skin, and eye.
  • These conditions are associated with HLA-B27 but not rheumatoid factor, with varying prevalence across ethnic groups.

Purpose of the Study:

  • To review the efficacy of anti-tumor necrosis factor-alpha (anti-TNFα) therapy.
  • To discuss other therapeutic advances in managing spondyloarthropathies.
  • To explore the genetic and environmental factors contributing to these diseases.

Main Methods:

  • Review of existing literature on spondyloarthropathies.
  • Analysis of classification criteria, such as the European Spondyloarthropathy Study Group criteria.
  • Examination of genetic associations, including HLA-B27 and susceptibility genes for related conditions.

Main Results:

  • Spondyloarthropathies occur in genetically predisposed individuals, triggered by environmental factors.
  • Infectious agents like Chlamydia and enterobacteria can trigger reactive arthritis, but triggers for ankylosing spondylitis remain unclear.
  • Genetic susceptibility involves HLA-B27 and other genes linked to Crohn disease, ulcerative colitis, and psoriasis.

Conclusions:

  • Understanding the cellular and molecular mechanisms of inflammation in spondyloarthropathies is ongoing.
  • Anti-tumor necrosis factor-alpha therapy represents a significant therapeutic advance.
  • Further research is needed to fully elucidate the pathogenesis and identify novel therapeutic targets.