Depression is associated with impairments in brain function (
1). Numerous researchers, neuroscientists, and neuropsychologists have focused on studying the relationship between normal brain functions, brain dysfunctions, and behavior. In line with this growing field, recent studies highlight the importance of neuroanatomy and neurofunction-encompassing both neurology and neuropsychology-in examining psychological phenomena (
2-
5). Particularly in the context of mood disorders and depression, the role of neurological factors is increasingly recognized (
1-
3,
6,
7). The hippocampus, a crucial brain region involved in learning and memory, plays a pivotal role in significant cognitive and executive functions, notably in both short-term and long-term memory retention (
8-
10). It is particularly engaged in tasks (
11) requiring delayed recall, and damage to it is linked to increased problems with declarative memory (
12). Magnetic resonance imaging (MRI) studies have revealed that individuals with severe depression often have a reduced hippocampal volume (
13-
15). Other critical areas implicated in the physiological impact of depressive disorders include the basal ganglia, which are essential for learning, declarative memory, and short-term memory retention (
16-
18). The thalamus is another brain region identified as being involved in depression through brain imaging studies (
19,
20). Research using MRI to measure volume (
21) and studies on post-mortem brains (
22) have found that the thalamic volume in depressed individuals, compared to a healthy control group, is reduced. Furthermore, patients with thalamic lesions are more prone to experiencing memory function issues, including difficulties in encoding and recall (
23).
These studies highlight the connection between neurological and neuropsychological impairments and depression. As noted, many of these impairments are associated with deficits in cognitive executive functions, including learning and memory. The findings from most studies in this area suggest that depressed patients experience more memory problems than the general population (
3,
24,
25). Indeed, some research indicates that these issues are more pronounced in depressed patients with suicidal thoughts (
7,
26,
27).
Depression is characterized by reduced pleasure, feelings of guilt, thoughts of death, and suicide (
26). Neuropsychological dysfunction in the realm of depression, particularly regarding executive thinking functions, plays a significant role as a risk factor for suicide (
7). Neurochemical research reveals a relative overlap between individuals prone to violence and impulsivity and those who commit suicide, including a low level of Serotonin (5-HT) and its primary metabolite, 5-hydroxyindoleacetic acid (5-HIAA), in the brain anatomy of individuals who have committed suicide (
7). Various studies on the cognitive functions of suicidal individuals have been conducted. Using standard neuropsychological tools, it has been found that suicidal individuals, compared to those with chronic pain and the general population, exhibit reduced fluency (verbal and non-verbal) and reasoning (
7). However, other studies have not found such neuropsychological differences (
28). It has been observed that poorer decision-making, as another cognitive function, is evident in suicidal patients compared to the general population, with a negative correlation between the inclination for suicide and decision-making ability (
12).
The information presented above demonstrates the presence of structural and biochemical brain damage and dysfunction in depressed and suicidal individuals. Moreover, it has been established that these damages and dysfunctions are related to cognitive functions, including memory.