Book contents
- Frontmatter
- Contents
- Foreword
- Acknowledgements
- Chapter 1 Introduction
- Keynote Essay 1: Defining Who We Are: DNA in Forensics, Genealogy and Human Origins
- Section 1 Principles Of Cellular And Molecular Biology
- SECTION 2 MOLECULAR PATHOLOGY
- Chapter 8 Genomes and the Environment: An Overview of Molecular Pathology
- Chapter 9 Genetics, Genomics, Health and Disease: General Considerations
- Chapter 10 Chromosome Disorders
- Chapter 11 Mendelian Inheritance
- Chapter 12 Unusual Molecular Processes that Impact on Disease
- Chapter 13 Population Genetics
- Chapter 14 Complex Multifactorial Inheritance
- Chapter 15 Molecular Basis for Phenotypic Variation
- Chapter 16 Medical Genetics
- Keynote Essay 3: Human Cloning: Should We Go There?
- Chapter 17 Neoplasia: General Considerations
- Chapter 18 Oncogenes
- Chapter 19 Mammalian DNA Repair
- Chapter 20 Tumour Suppressor Genes and Inherited Susceptibility to Cancer
- Chapter 21 Carcinoma
- Chapter 22 Leukaemias and Lymphomas
- Chapter 23 Molecular Approaches to the Diagnosis, Prognostication and Monitoring of Cancer
- Keynote Essay 4: Microbes, Molecules, Maladies and Man
- Chapter 24 Molecular Basis of Infectious Diseases: General Considerations
- Chapter 25 Immunology
- Chapter 26 Human Immunodeficiency Virus
- Chapter 27 Tuberculosis
- Chapter 28 Malaria
- Chapter 29 Influenza
- Chapter 30 Oncogenic Viruses
- Chapter 31 Vaccines and Immunisation
- Keynote Essay 5: Drugs and the 21st Century
- SECTION 3 MOLECULAR THERAPEUTICS
- SECTION 4 RESEARCH AND THE CONTINUING EVOLUTION OF MOLECULAR MEDICINE
- Glossary
- Contributors’ Biographies
- Source Material And Recommended Reading
- Permissions And Credits
- Index
Chapter 14 - Complex Multifactorial Inheritance
from SECTION 2 - MOLECULAR PATHOLOGY
Published online by Cambridge University Press: 04 June 2019
- Frontmatter
- Contents
- Foreword
- Acknowledgements
- Chapter 1 Introduction
- Keynote Essay 1: Defining Who We Are: DNA in Forensics, Genealogy and Human Origins
- Section 1 Principles Of Cellular And Molecular Biology
- SECTION 2 MOLECULAR PATHOLOGY
- Chapter 8 Genomes and the Environment: An Overview of Molecular Pathology
- Chapter 9 Genetics, Genomics, Health and Disease: General Considerations
- Chapter 10 Chromosome Disorders
- Chapter 11 Mendelian Inheritance
- Chapter 12 Unusual Molecular Processes that Impact on Disease
- Chapter 13 Population Genetics
- Chapter 14 Complex Multifactorial Inheritance
- Chapter 15 Molecular Basis for Phenotypic Variation
- Chapter 16 Medical Genetics
- Keynote Essay 3: Human Cloning: Should We Go There?
- Chapter 17 Neoplasia: General Considerations
- Chapter 18 Oncogenes
- Chapter 19 Mammalian DNA Repair
- Chapter 20 Tumour Suppressor Genes and Inherited Susceptibility to Cancer
- Chapter 21 Carcinoma
- Chapter 22 Leukaemias and Lymphomas
- Chapter 23 Molecular Approaches to the Diagnosis, Prognostication and Monitoring of Cancer
- Keynote Essay 4: Microbes, Molecules, Maladies and Man
- Chapter 24 Molecular Basis of Infectious Diseases: General Considerations
- Chapter 25 Immunology
- Chapter 26 Human Immunodeficiency Virus
- Chapter 27 Tuberculosis
- Chapter 28 Malaria
- Chapter 29 Influenza
- Chapter 30 Oncogenic Viruses
- Chapter 31 Vaccines and Immunisation
- Keynote Essay 5: Drugs and the 21st Century
- SECTION 3 MOLECULAR THERAPEUTICS
- SECTION 4 RESEARCH AND THE CONTINUING EVOLUTION OF MOLECULAR MEDICINE
- Glossary
- Contributors’ Biographies
- Source Material And Recommended Reading
- Permissions And Credits
- Index
Summary
INTRODUCTION
Many disorders with a Mendelian pattern of inheritance have been well characterised and many of the genes controlling these disorders have been identified. There are, however, many common diseases with an inherited component that do not follow a specific pattern of inheritance. These diseases are conventionally known as complex multi factorial traits and include conditions such as asthma, diabetes and many of the cardio vascular disorders. The term multifactorial indicates that there are multiple causative agents – both genetic and environmental. These traits therefore have a complex molecular mechanism that involves many processes such as physiological mechanisms, development and homeostasis, to name but a few.
This chapter will review basic concepts of multifactorial inheritance and illustrate what a complex disease is, and how it differs from Mendelian disorders. Furthermore, the design and implementation of complex disease gene discovery, and the strengths and pitfalls of these approaches, will be discussed. Finally, the impact of the knowledge of complex disease genetics on clinical medicine and its relevance to future disease treatment will be discussed.
HOW DO COMPLEX DISEASES DIFFER FROM MENDELIAN DISORDERS?
Complex diseases differ in very distinct ways from Mendelian disorders, and the key differences are summarised in Table 1. The single most important difference is related to the impact of the genetic factors on the disease. For most Mendelian diseases, the inheritance of a pathogenic gene variant or mutation is associated with that disease because it has such a debilitating impact on the gene product that it almost always results in disease. This is not the case with complex diseases, where the presence of a specific genetic factor is not causal but may increase or decrease the risk of developing disease. Risk is defined as the probability of an adverse event and its value in clinical medicine is primarily to predict outcome. The goal of complex disease prediction is therefore to identify an individual or a population in which an intervention could prevent adverse outcome. Complex diseases are usually not influenced by only one gene but by many genes that contribute to disease outcome and may have an additive, multiplicative or interactive effect.
- Type
- Chapter
- Information
- Molecular Medicine for Clinicians , pp. 177 - 186Publisher: Wits University PressPrint publication year: 2008