Caspi Et Al (2003)

Download as docx, pdf, or txt
Download as docx, pdf, or txt
You are on page 1of 2

Caspi et al (2003)

Caspi et al (2003) carried out a study on the role that gene mutation and epigenetics may
play in major depressive disorder. You can use this study for the following content in the
biological approach:
Research methods used in the biological approach.
To what extent does genetic inheritance influence behaviour?
Procedure and results
Diathesis-stress theories of depression predict that an individual's reaction to stressful events
depends on their genetic make-up. If an individual has a specific genetic predisposition
toward a disorder (genotype), then interaction with stressors in the environment may cause
these genes to be expressed. The aim of this study was to determine whether there is
evidence for a gene-environment interaction (G x E) for a mutation of the serotonin
transporter gene - 5-HTT. The serotonin transporter is involved in the reuptake of serotonin
in brain synapses.
Caspi and his team looked at a sample of 847 New Zealand 26-year-olds. All were members
of a cohort that had been assessed for mental health on an every-other-year basis until they
were 21. They were divided into three groups based on their 5-HTT alleles: Group 1 had two
short alleles; Group 2 had one short and one long allele; Group 3 had two long alleles. The
mutation of the 5-HTT gene has the shorter alleles. Roughly 43% of people have the shorter
alleles.
The participants were asked to fill in a "Stressful life events" questionnaire which asked them
about the frequency of 14 different events - including financial, employment, health, and
relationship stressors - between the ages of 21 and 26. They were also assessed for
depression.
People who had inherited one or more short versions of the allele demonstrated more
symptoms of depression and suicidal ideation in response to stressful life events. The effect
was strongest for those with three or more stressful life events. Simply inheriting the gene
was not enough to lead to depression, but the genes' interaction with stressful life events
increased one's likelihood of developing depression.
In a later study by Wilhelm et al (2006), the researchers looked at DNA samples from 127
people who are part of a longitudinal prospective study looking at mental health. The sample
had been monitored for over 25 years. At five-year intervals, scientists recorded any major
life events and signs of depression. They found that 80 percent of those with two short 5-HTT
genes became depressed after three or more negative life events in a year, whereas those with
two long genes appeared resilient - only 30 percent developed the illness in similar
situations. They also found that childhood maltreatment predicted adult depression only
among individuals carrying a short allele and not among those carrying the longer allele.
However, much more research is needed before a clear relationship between a gene and a
depression can be established.
Evaluation

 The study is correlational, so no cause-effect relationship can be determined.


 The study makes the assumption that serotonin causes depression.
 Information about life-events was self-reported. It may be the salience of the
negative life events which plays a role in depression - that is, those that recalled
them more easily may have a tendency towards depression. Those who are more
resilient, may not recall negative life events as easily.
 The theory acknowledges the interaction between both biological and
environmental factors in depression. This is a more holistic approach, not
reductionist.
 Later studies have not been able to show similar results. Risch et al (2009) carried
out a meta-analysis of attempted replications and found that the results were not
able to be replicated. It appears that the study has low reliability.
 There were some participants who did not carry the gene mutation who became
depressed; therefore, we cannot say that gene expression alone can cause
depression.

You might also like