Abstract


Odds ratios for high altitude and neuropsychiatric symptoms. (
The recent retrospective study by Brenner et al. (2011) involving most U.S. counties, which spanned 20 years, reported a dramatic increase of suicide in high altitude populations. This finding was independent of demographic factors usually associated with suicide such as age, race, gender, or income. The higher suicide rate at high altitude is not explained by increased overall mortality since there is a negative correlation between altitude and overall mortality. Previous findings from our group may shed some light on this finding (Arregui 1995; Arregui et al 1995). Using epidemiological surveys we described an increased prevalence of depression in men living at high altitude compared with those living at sea level (see Fig 1A). Moreover, migraines and CMS occur more frequently at high altitude. In addition, depression is associated with the presence of migraines and CMS at high altitude (Arregui et al 1995) (see Fig 1B). Depression is responsible for the majority of suicide cases worldwide (Henriksson et al. 1993). Therefore, increased depression prevalence at high altitude populations may explain the association of increased suicide rate at high altitude (Brenner et al. 2011). Currently, the contribution of migraine in the association between suicide and high altitude is not entirely clear. However, migraine is also a risk factor for psychiatric disorders, including depression (Pompili et al. 2010). Both, depression and migraine are associated with serotonin related abnormalities, and both are part of the chronic mountain sickness symptomatology. However, further research is warranted. Another potential explanation for the association between suicide and high altitude is that people who are depressed preferentially migrate to the highlands. Due to the higher prevalence of depression at high altitude we will expect a measurable migration rate from sea level to the high altitude. Nevertheless, at least in Peru, there is an opposite trend, people from high altitude migrate to coastline cities (Instituto Nacional de Estadistica e Informatica, 1995).
Noteworthy, chronic hypoxia is associated with changes in monoamine systems including dopamine and serotonin (Arregui et al. 1994; Davis and Carlsson 1973). For instance, striatum dopamine uptake sites are increased in mice exposed to 14 days of hypoxia (Arregui et al. 1994). Additionally, concentrations of the serotonin metabolite 5-hydroxy indolacetic acid (5-HIAA) are reduced in the striatum and hypothalamus (Saligout et al. 1986), frontal cortex, pons and medulla of rats exposed to chronic hypoxia (Ray et al. 2011). Dopamine and serotonin are known to play a central role in the pathophysiology and treatment of depression (Dunlop and Nemeroff 2007; Carr and Lucki 2010). It is possible that these neurotransmitter alterations might be related to changes in neuronal energetic metabolism, particularly, reduction of mitochondrial respiration, as previously described in chronic hypoxia (Hochachka et al. 1994; Chavez et al. 1995; Caceda et al. 2001). Interestingly, it has been recently suggested that mitochondrial dysfunction may play role in depression (Burroughs and French 2007; Lucca et al. 2009).
The coexistence of depression, migraine and CMS does not appear to be a random association (Arregui et al. 1995). Hypobaric hypoxia increases the hematocrit, but may also be the cause of neurologic symptoms and mood disorders. Depression is responsible for most suicide cases and it is reasonable to suggest that the correlation between suicide and altitude found by Brenner et al. (2011) is due to a high prevalence of depression. Prospective studies are required to establish the relation between depression, high altitude and suicide. These studies are also relevant at sea level in conditions such as sleep apnea and chronic pulmonary diseases, where hypoxia play a major pathogenic role.
