Hodgkin's lymphoma: everything you need to know about its genetic predisposition

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Hodgkin's lymphoma represents one of the most studied hematological cancers in the field of medical genetics. With a worldwide incidence of 0.001%, this disease of the lymphatic system has gained special relevance due to recent advances in the understanding of its genetic and hereditary basis.

What is Hodgkin's lymphoma?

Hodgkin's lymphoma is a specific type of cancer that affects the lymphatic system, a critical part of our immune system. Also known as Hodgkin's carcinoma or Hodgkin's disease, this disease is characterized by the presence of distinctive abnormal cells called Hodgkin's lymphoma. Reed-Sternberg cellsformerly known as Hodgkin cells.

The lymphatic system is made up of a network of lymph nodes, lymph vessels and organs that work together to fight infection and disease. When Hodgkin's lymphoma develops, these cancer cells typically originate from B lymphocytes, a type of white blood cell that produces antibodies.

Symptoms and clinical manifestations

Main symptoms of Hodgkin's lymphoma

The first and most characteristic sign of Hodgkin's lymphoma is the painless swelling of the lymph nodesespecially in the neck, armpits or groin. This neck abnormality is often the initial reason for consultation.

Systemic symptoms (Symptoms B)

Patients may experience what is medically referred to as a "B symptoms":

  • Persistent fever without apparent cause
  • Night sweats profuse soaking of bed linens
  • Unexplained weight loss greater than 10% of body weight in 6 months
Other associated symptoms
  • Fatigue extreme and persistent
  • Pruritus generalized (itching) without visible rash
  • Dyspnea (difficulty breathing)
  • Persistent cough
  • Pain in the lymph nodes after alcohol consumption
  • Edema in extremities
  • Abnormal bleeding and appearance of purple
  • Epistaxis (frequent nosebleeds)
  • Recurrent infections

Genetics and Hodgkin's lymphoma

Heritability and genetic predisposition

Recent research has uncovered crucial information about the genetic predisposition Hodgkin's lymphoma. Scientific studies indicate that the estimated heritability (a statistical concept that describes how much of the variation in a given trait can be attributed to variation in genetic factors) of this disease is of the 28,4%, while the heritability explained (a statistical concept that determines how much of the variation in a given trait can be explained by the genetic variants that we know about and can therefore analyze) currently identified is of 24%.

Genes involved

Genetic research has identified a number of key genes associated with the predisposition Hodgkin's lymphoma:

  • TCF3Transcription factor crucial for the development of B cells.
  • CLEC16ARelated to the function of the immune system.
  • GATA3Important regulator of cell differentiation
  • LPPInvolved in cell adhesion and migration.
  • AHI1Associated with neural development and ciliary function.
  • PTPRKProtein tyrosine phosphatase with a role in cell signaling.

Genetic health test with Hodgkin's Lymphoma

PREMIUM DNA

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An genetic health test including Hodgkin's lymphoma represents a significant advance in preventive medicine. By means of a genetic test, and simply with a saliva sample, it is possible to assess the genetic protection Hodgkin's lymphoma or individual predisposition to develop this disease.

How does the test work?

Genetic testing examines specific variants in the genes associated with Hodgkin's lymphoma. The results can indicate whether a person has Hodgkin's lymphoma:

  • Increased protection than the population mean
  • Average risk similar to the general population
  • Greater predisposition requiring specialized medical follow-up

Interpretation of your ADNTRO results

The Hodking's Lymphoma result that you can find in the ADNTRO genetic test, is based on 3,077 cases and 13,680 controls of European descent, providing a solid basis for the interpretation of results.

Differences between Hodgkin's and Non-Hodgkin's disease

A crucial distinction in the diagnosis is to understand the differences between Hodgkin and non-Hodgkin:

Hodgkin's lymphoma:

  • Presence of Reed-Sternberg cells
  • Orderly dissemination from node to adjacent node
  • Better overall prognosis
  • More common in young adults and older adults

Non-Hodgkin's lymphoma:

  • Absence of Reed-Sternberg cells
  • Random dissemination, can skip lymph nodes
  • Most diverse group of diseases
  • Can occur at any age

World Hodgkin's Lymphoma Day

The world Hodgkin's lymphoma dayThe date, celebrated every September 15, is commemorated to raise awareness of this disease, promote research and support affected patients and families. This date highlights the importance of early diagnosis and advances in treatment.

Evolution and prognosis

Dissemination patterns

Hodgkin's lymphoma typically:

  1. Start in one group of lymph nodes
  2. Disseminates in an orderly fashion to nearby lymph nodes
  3. Can be extended to organs such as the lungs, liver or bone marrow

Prognostic factors

The prognosis depends on multiple factors:

  • Stage of disease at diagnosis
  • Patient's age
  • Presence of B symptoms
  • Levels of certain proteins in the blood
  • Individual genetic profile

Implications of personalized medicine

The understanding of the genetic predisposition Hodgkin's lymphoma allows:

  • Targeted screening in high-risk individuals
  • Preventive strategies recommendations
  • Specialized monitoring for early detection

Benefits of genetic analysis

An genetic test with information about Hodgkin's lymphoma offers significant advantages:

  1. Early identification of individuals at risk
  2. Medical planning proactive
  3. Peace of mind for people with low predisposition
  4. Valuable information for reproductive decisions

Advances in the genetic understanding of Hodgkin's lymphoma mark a new era in preventive medicine. The possibility of knowing our genetic protection for Hodgkin's lymphoma through specialized analysis represents a powerful tool for informed medical decision making.

Research continues to reveal new genes and mechanisms involved in this disease, promising increasingly personalized prevention and treatment strategies.

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