Methadone maintenance therapy (MMT) has been empirically shown to reduce the risk of suicide for male patients (
6). A further step in minimizing suicidal behavior in this population of methadone patients can be provided by psychologists or social workers trained in Cognitive-Behavior Therapy (
7) for depression and anxiety. Some of our patients were already exposed to at least basic principles of Cognitive Behavior Therapy (CBT) in various counseling centers free of charge or for a fee by private professionals. The participation in methadone treatment and the exposure to elements of CBT have presumably jointly lowered the level of hopelessness in our sample of patients. This perhaps explains why only less than a third of our patients (30.8%) scored in the pathological range on Beck Hopelessness Scale (scores above 3 points).
The main contribution of this study lies in publishing the finding that, in our sample, the hopelessness scores did not statistically correlate with concurrent abuse of opiates, oxycodone, or cocaine. One reason for this may be the adverse impact of restricted or skewed range in the hopelessness scores on Beck’s scale. The adverse impact of restricted range of data on correlation coefficients is explained in more detail in classical textbooks of statistics (
8,
9). The theory of restricted range also applies, by a logical extension, to severely skewed distributions as in our study: only 6 patients in our sample of 52 scored in the categories of moderate and severe hopelessness on Beck scale. Our correlational results are thus predominantly based on a comparison of patients with normal BHS scores to those scoring within the mild range on Beck’s scale. The results might be different on new patients at the time of their entry to methadone treatment, when they are presumably still more depressed and likely to experience higher levels of hopelessness.
The correlation of oxycodone use to Beck’s items “my future seems dark to me” and “things just don’t work out the way I want them” could perhaps be linked to analgesic properties of that substance: future studies would need to include measures of pain (e.g., the Brief Pain Inventory) to examine if those using oxycodone suffer from uncontrolled chronic pain.
A major limitation of our study lies in its cross-sectional nature and in the small number of urine tests over a short time span (none of our patients was tested more than 3 times over the 7 days of this study). A prospective study over at least 6 months on patients entering methadone treatment, with repeated measures of hopelessness and repeated urine tests, could provide valuable information on the changes in hopelessness scores and their relationship, over time, to urine tests for concurrent substance abuse. Various doctoral dissertations in this area could be carried out by focusing on additional variables such as variation in the methadone or suboxone dose, number of past suicide attempts, method of the attempted suicide, scores on measures of pain or measures of sleep quality, or psychopathology measures such as the Millon Clinical Multiaxial Inventory at the onset of methadone treatment and 6 months later. An important step in this direction has been the study by Mokhber, Afshari, and Farhoodi (
6).
The inclusion of data on past or concurrent psychopathology appears to be of particular importance for future studies, especially in studies with longitudinal design, as there is a complex interplay between methadone and pre-existing psychopathology. Antipsychotic effects of methadone were reported by some clinicians and researchers. For example, a placebo-controlled study by Brizer et al., (
10) determined that patients with treatment-resistant chronic paranoid schizophrenia who received methadone plus neuroleptic showed significant improvement.
The study by Maremmani et al., (
11) concluded that stabilization dosages need to be higher in patients with a major psychiatric illness than in those free of such diagnosis and that those with major psychiatric illness take longer to reach stabilization phase in methadone treatment and need an especially cautious attention from clinicians during the tapering of methadone. A recent study by Maremmani et al., (
12) determined that methadone proved to be therapeutically more effective on patients characterized by “sensitivity-psychoticism,” whereas buprenorphine was more effective on patients displaying a “violence-suicide” symptomatology. Case studies led by Khazaal in Switzerland and by Sadek in Canada suggest that methadone reduces the frequency of pre-existing obsessive compulsive symptoms and also may reduce severe depression or anxiety: these symptoms may resurface if methadone is tapered below a certain minimal level (
13-
15).
Concurrent alcoholism may be a severe confounding factor in the studies of hopelessness in methadone patients: future studies in this area would benefit from including laboratory tests such as the carbohydrate deficient transferrin test (
16) to detect intensive ethanol consumption.
It is also of interest in this context that a genetic factor involving the single nucleotide polymorphism (SNP) of the cannabinoid receptor type 1 gene (CNR1) named rs2023239 was recently determined to provide an independent protective effect against lifetime major depressive disorder among opiate dependent outpatients (
17). European studies suggested that potential predictors of suicidal risk among methadone patients include not only depression and alcoholism but also certain somatic comorbidities (
18,
19). For example, positive tests for hepatitis C virus were found to be associated with higher suicidal risk (
19). An inclusion of such somatic variables in future research on methadone patients is worthwhile.