Multifactorial And Polygenic (Complex) Genetic Disorder

In an age when the majority of monogenic human disease genes have been identified, one of the challenges for the coming generation of human geneticists will be to resolve complex polygenic and multifactorial disorders. This is particularly true due to the fact that human diseases are often caused by a multitude of genetic and environmental factors acting in concert.

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Distinguishing polygenic and multifactorial disorders

The term polygenic can have different meanings, including genetic effects that arise from the interaction of multiple genes. It can be said that polygenic inheritance involves complex traits that are determined by many genes at different loci, without the influence of the environment. Effects of those genes are cumulative, in that no single gene is considered to be dominant or recessive to one another.

On the other hand, multifactorial inheritance describes a trait whose manifestations are determined by two or more genes, accompanied by environmental factors. These conditions show a definite familial tendency, although the incidence in close relatives of affected individuals is usually within the range of 2 to 4%. This is comparable to the conditions caused by mutations in single genes, which has an incidence range in close relatives of affected individuals to be between 25 and 50%.

Since there is seldom a clear distinction between the two, both of these entities are often considered together. Some geneticists tend to use the term polygenic for any trait whose inheritance is complex, whereas others apply the term multifactorial equally indiscriminately.

Multifactorial and polygenic diseases

A number of single-gene disorders are relatively rare when compared to multifactorial and polygenic diseases. Congenital malformations that are thought to have complex multiple interacting causes include congenital heart defects, neural tube defects, pyloric stenosis, cleft palate, and congenital hip dysplasia.

Many of these congenital birth defects are explained by a multifactorial threshold model. This assumes that the gene defects for multifactorial traits are normally distributed within the population, with most individuals having too few of them to cause disease. Thus, the pathological condition will not arise unless there is a genetic liability present that is significant enough to push them past the threshold and into the affected range.

Polygenic and environmental factors contribute significantly to chronic, non-communicable diseases such as coronary heart disease, cancer, diabetes mellitus, asthma, gout, schizophrenia, and osteoporosis. A genetic component to the disease contributes a certain percent (in schizophrenia, for example, it is estimated to be approximately 70%), but no single gene is responsible.

An important concept in multifactorial genetic disorders is the quantitative trait locus, which is used to map polygenic traits measurable in some quantitative manner. Therefore, complex characteristics such as height (normal trait) or diabetes (abnormal trait) are contributed to by a myriad of different genes found on different chromosomes, with additional effects from the environment.

Counseling for multifactorial disorders

A number of factors can influence the recurrence risk in multifactorial disorders, which should be taken into account during genetic counseling. In general, the recurrence risk is slightly greater for consanguineous parents when compared to those who are unrelated. In other words, multifactorial disorders show a slightly increased incidence in the offspring of consanguineous parents, although this incidence is not nearly as striking as autosomal recessive disorders.

If the proband, which is defined as the first affected family member, is severely affected, then the risks to close relatives are greater than if the proband is only mildly affected. If there is more than one affected close relative, the risks for other relatives are significantly increased.

When the disorder in question is more commonly found in one sex, there is a tendency for recurrence risks to be greater for relatives of the less commonly affected sex. The threshold is often different for men and women for some diseases. For example, pyloric stenosis affects boys five times more often than girls, whereas congenital dislocation of the hip is about seven times more frequent in women than in men.

In conclusion, the carriage of certain combinations of genes is responsible for the occurrence of clinically heterogeneous forms of the disease and treatment effectiveness. Population screening for rare genetic disorders with high penetrance will continue to be a mainstay for genetic screening.

References

Further Reading

Last Updated: May 20, 2021

Dr. Tomislav Meštrović

Written by

Dr. Tomislav Meštrović

Dr. Tomislav Meštrović is a medical doctor (MD) with a Ph.D. in biomedical and health sciences, specialist in the field of clinical microbiology, and an Assistant Professor at Croatia's youngest university - University North. In addition to his interest in clinical, research and lecturing activities, his immense passion for medical writing and scientific communication goes back to his student days. He enjoys contributing back to the community. In his spare time, Tomislav is a movie buff and an avid traveler.

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