[50] Genomic Medicine and Personalized Medicine Flashcards

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1
Q

What is Genomic Medicine?

A

The medical discipline that involves using genomic information about an individual for clinical care.

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2
Q

What is Personalized Medicine?

A

The tailoring of medical treatment to the individual characteristics of each patient.

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3
Q

How does Genomic Medicine contribute to Personalized Medicine?

A

By providing information about a person’s genetic makeup to guide decisions made in regard to the prevention, diagnosis, and treatment of disease.

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4
Q

What are the potential benefits of Personalized Medicine?

A
  • Increased effectiveness of treatment
  • Reduced side effects
  • Prevention strategies tailored to individual risk
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5
Q

What is the Human Genome Project?

A

An international research project with the goal of determining the sequence of human DNA and identifying the genes that it contains.

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6
Q

How has the Human Genome Project contributed to Genomic Medicine?

A

It provided a reference sequence of the human genome and identified genes associated with various diseases, which are used in genomic medicine.

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7
Q

What is Genomic Sequencing?

A

The process of determining the complete DNA sequence of an organism’s genome at a single time.

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8
Q

How does Genomic Sequencing contribute to Personalized Medicine?

A

By identifying genetic variants in individuals, which can inform personalized treatment strategies.

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9
Q

What are Single Nucleotide Polymorphisms (SNPs)?

A

Variations at single positions in a DNA sequence among individuals.

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10
Q

How do SNPs contribute to Personalized Medicine?

A

Certain SNPs are associated with response to certain drugs or risk of disease, which can guide personalized medical decisions.

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11
Q

Define the term “Pharmacogenomics”.

A

The study of how genes affect a person’s response to drugs.

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12
Q

How does Pharmacogenomics contribute to Personalized Medicine?

A

By understanding how a person’s genetic make-up affects their response to drugs, it can guide the choice of drugs and doses for each individual.

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13
Q

What is a Genetic Marker?

A

A DNA sequence with a known physical location on a chromosome and associated with a particular gene or trait.

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14
Q

How can Genetic Markers contribute to Genomic Medicine?

A

Genetic markers can be used to identify genetic variants associated with diseases, which can inform diagnosis and treatment decisions in genomic medicine.

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15
Q

What is Genome-Wide Association Studies (GWAS)?

A

An observational study of a genome-wide set of genetic variants in different individuals to see if any variant is associated with a trait.

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16
Q

How do GWAS contribute to Genomic Medicine?

A

They can identify genetic variants associated with diseases, which can inform diagnosis and treatment decisions in genomic medicine.

17
Q

What is the main challenge in Personalized Medicine?

A

The main challenge is translating genomic research into clinical practice, including ethical, legal, and social issues.

18
Q

How can Genomic Medicine impact disease prevention?

A

It can identify individuals with genetic predispositions to certain diseases, allowing for personalized prevention strategies.

19
Q

How can Genomic Medicine contribute to diagnosis?

A

By identifying genetic variants associated with diseases, it can provide a precise diagnosis.

20
Q

How can Genomic Medicine contribute to treatment?

A

By identifying how an individual’s genetic makeup can affect their response to drugs, it can guide the choice of drugs and doses for each individual.