1/9
Looks like no tags are added yet.
Name | Mastery | Learn | Test | Matching | Spaced | Call with Kai |
|---|
No study sessions yet.
Research into genes causing schizophrenia
Ripke et al reported 108 genetic variations that could mediate a vulnerability to the disorder, including variations on chromosomes 8 and 11, and the C4 gene
Hong et al found a variation on the gene TPH was far more common in Chinese patients with schizophrenia (this codes for serotonin production)
Genetic inheritance
Some people may have a predisposition to schizophrenia, and hence the condition is at least partly inherited, meaning it runs in families through faulty genes
Having certain genes increases a person’s vulnerability to developing schizophrenia, inheriting biochemical imbalances or brain structure abnormalities
C4 gene function
C4 is found at synapses in the CNS and mediates the pruning of synapses that normally takes place in development
A faulty variant of C4 is a risk factor for schizophrenia as this can lead to hyper-pruning
Research supports the idea that excessive hyper-pruning can lead to symptoms of schizophrenia
This may help to understand the mystery of why brains from people with schizophrenia tend to have a thinner cerebral cortex with fewer synapses than unaffected individuals
Gottesman & Shields findings
Children of 2 schizophrenic patients who share 100% genetic similarity, have a 46% chance of developing the disorder
MZ twins who share 100% genetic similarity have a 48% chance of developing the disorder if one twin is diagnosed
First degree relatives share 50% genetic similarity have a 13% chance of developing the disorder if a parent is diagnosed
In second degree relatives, like grandchildren, share 25% genetic similarity and have a 5% chance of developing schizophrenia, if a grandparent is diagnosed.
MacDonald & Schultz (2009) - Twin study
Suggested among MZ twins, if one twin is diagnosed with schizophrenia then the other is 99x more likely to suffer from the condition
This implies that genetics are involved in the development of schizophrenia
Tienari et al (2000) - adoption study
164 adoptees whose biological mothers were diagnosed with schizophrenia, matched with children whose biological mothers did not suffer from schizophrenia
Found 7% of the sample whose biological mothers had schizophrenia had also been diagnosed with the condition compared to just 4 from the control group
Validates the idea that schiz has a genetic component as adoptees do not share environmental influences with their biological mothers and provides concurrent validity for the role of genes in schiz
Research Support (+)
Joseph et al - 40% concordance rate for MZ twins and a 7% concordance rate for DZ twins. The higher concordance rate for schizophrenia for MZ twins suggests genes have some influence of the development of schizophrenia
Implies schizophrenia may be caused by genetic inheritance, possibly through a faulty C4 gene
Incomplete explanation (-)
Faulty genetics cannot be the sole cause of schiz, as if this was the case MZ twins would have a concordance rate of 100% as they share the same genotype.
Nurturing influences must therefore play a role in developing schizophrenia, e.g. stress, drugs, alcohol and a difficult childhood (i.e. deprivation and/or abuse)
Biological determinism (-)
Although psychology is seeking in general laws to explain all behaviours, this genetic theory into schizophrenia overlooks many aspects
This implies that the account neglects to consider the role of environmental factors as well as free will in the development and recovery from schizophrenia
Applications (+)
Vulnerable groups in society who have relatives suffering from schizophrenia are often advised by clinicians on their risk of developing the disorder
Individuals with schizophrenia would be made aware of the risk of their biological children developing the disorder, so they can think about alternative options like adoption or using surrogates.