IFMA Preventive Health Management Inc.

Institute for Medical Advancement

New York, NY 10005, USA

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Affective Disorders

About one in every eight women can expect to develop clinical depression during their lifetime, while prevalences in males are only slightly less. Schizophrenia and bipolar illness each affects about one percent of the general population, causing the loss of the ability to work, to have close relationships, and to have a fulfilling life. Available treatments, though effective, are incomplete and there is no cure for a considerable proportion of patients.

Incomplete Treatments

Pharmacological treatment is unsatisfactory in the sense that (1) a large proportion of patients (35%-45%) exhibit a refractory clinical picture which is resistant to all treatment modalities, and (2) treatment response cannot predicted for the individual patient for any of the currently available antipsychotics and antidepressants. In tandem with the benefits of pharmacological medications are significant risks associated with their use ("unwanted side effects").

Etiology of Major Psychiatric Disorders

Evidence from twin, family and adoption studies suggests that there is a genetic predisposition to major psychiatric disorders which varies across patients and may "explain" some 25%-60% of causality. Genetic predisposition acts nonspecifically, by elevating a subject's "vulnerability" (or "sensitivity") to environmental or endogenous challenges. Vulnerability is neither necessary nor sufficient for the development of psychiatric disorders.

Mechanisms that Support and Maintain Health

A subject's vulnerability is compensated by resilience factors. The term "resilience" denotes all those endogenous mechanisms that support and maintain health. Strengthening resilience combined with the early detection of impending mental health problems are a much better strategy than passively waiting until clinical symptoms develop. In fact, "vulnerable" subjects can significantly benefit from early interventions that strengthen resilience and general health.

More to Explore

Stassen HH, Angst J, Hell D, Scharfetter C, Szegedi A: Is there a common resilience mechanism underlying antidepressant drug response? Evidence from 2848 patients. J Clin Psychiatry 2007; 68(8): 1195-1205
Lötscher K, Stassen HH, Hell D, Bridler R: Community-based crisis home programme — cost-efficient alternative to psychiatric hospitalization. Nervenarzt 2009; 80(7): 818-826
Stassen HH, Anghelescu IG, Angst J, Böker H, Lötscher K, Rujescu D, Szegedi A, Scharfetter C: Predicting Response to Psychopharmacological Treatment. Survey of Recent Results. Pharmacopsychiatry 2011; 44: 263-272
Mohr C, Braun S, Bridler R, Chmetz F, Delfino JP, Kluckner VJ, Lott P, Schrag Y, Seifritz E, Stassen HH: Insufficient Coping Behavior under Chronic Stress and Vulnerability to Psychiatric Disorders. Psychopathology 2014; 47: 235-243
Trithemius
Recovery from Depression under Antidepressants: 35-40% Placebo Responders
Fig. 3: Under antidepressants, we typically find 35-40% of patients to be placebo responders, another 40% exhibit either no or incomplete improvement. In consequence, no more than 20% of patients benefit from antidepressant drug treatment. An especially puzzling point is the observation that some 25-35% of patients under antidepressants show incomplete response to treatment after initial improvement.
Study of 2,673 patients: (1) patients showing early improvement (first 2 weeks of treatment) are at least 3 times more likely to become responders compared to patients with a late onset; (2) patients showing late onset of improvement are more likely to get "stuck" in their recovery; (3) the probability to become a treatment responder drops below 15% if there are no signs of improvement during the first 2 weeks of treatment.
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