The Limitations of Psychiatric Diagnoses

1983 ◽  
Vol 51 (4) ◽  
pp. 231-235 ◽  
Author(s):  
Malcolm P.I. Weller

Psychiatric disorders are not always easy to incorporate within the medical model, neuropathological changes are seldom demonstrable and, when they are, they are irrelevant to functional illnesses. The meaning of the term illness in this group is not the same as in medicine generally and the validity of each illness category depends on the internal consistency and homegeneity of the category, the lack of overlap with other categories and the inter-rate reliability, but these desiderata are not adequately met for neurotic and personality problems or alchoholism. The major division between schizophrenia and manic depressive psychosis is not as sharply delineated as might be imagined and trans-Atlantic diagnostic practices have swung from one type of divergence to another. Nevertheless an increasing number of physical findings in these disorders suggest that they are frequently underpinned by organic factors. By definition this is certainly the case for organic psychoses, including epileptic psychosis and dementia. On the other hand, alchoholism, drug addiction, psychopathy and neuroses may be better incorporated within a psychological model, although here too weaker, but still apparent, physical and genetic factors remain intriguing features for medical consideration. Nevertheless life expectancy, fertility and socioeconomic circumstances are adversely affected by most psychiatric disorders, making them genuine illnesses by such criteria.

CNS Spectrums ◽  
1997 ◽  
Vol 2 (9) ◽  
pp. 42-44
Author(s):  
Giovanni P. A. Placidi ◽  
Maura Boldrini

AbstractDuring the last 30 years, several studies in psychiatric genetics have been conducted. These include a series of clinical and family-oriented studies on genetic factors in schizophrenia, alcoholism, and manic-depressive disorder. Since these trials have taken place, great emphasis has been placed on the hypothesis that psychiatric disorders could have a genetic vulnerability. This hypothesis is supported by significant advancements in biological and mathematical analysis methods, as well as by the large number of epidemiological and diagnostic studies on the prevalence of psychiatric disorders in patients' families. This article provides on overview of this research.Many other hypotheses have been raised by the optimism of research, but are often followed by experimental failures. There are several pitfalls in methods, ranging from sample selection to genotyping to statistical analysis methods. Finally, the interpretations of the results often have been misunderstood. Nonetheless, this body of research contributes to future genetic perspectives in psychiatry.


1991 ◽  
Vol 158 (4) ◽  
pp. 549-553 ◽  
Author(s):  
M. Soyka ◽  
G. Naber ◽  
A. Völcker

The prevalence of delusional jealousy in 8134 psychiatric in-patients was 1.1%. Delusions of jealousy were most frequent in organic psychoses (7.0%), paranoid disorders (6.7%), alcohol psychosis (5.6%) and schizophrenia (2.5%), while in affective disorder delusions of jealousy could be found in only 0.1%. Because schizophrenia and affective disorder were the most common diagnoses, most patients with delusions of jealousy were schizophrenics. In schizophrenia, women were more likely to suffer from delusional jealousy, while in alcohol psychosis, men were more likely than women to suffer from delusional jealousy.


1990 ◽  
Vol 20 (2) ◽  
pp. 311-319 ◽  
Author(s):  
Kenneth S. Kendler

SynopsisAll major psychiatric disorders aggregate in families. For most disorders, both genes and environmental factors play an important role in this aggregation. While recent work has tended to concentrate on the importance of genetic factors, this report focuses on the potential importance of environmental risk factors which themselves aggregate in families. In particular, this article examines how much of the familial aggregation of a psychiatric disorder may result from the familial aggregation of a risk factor. The model is illustrated and then applied to putative familial risk factors for schizophrenia and depression. The results of the model suggest that if parental loss and exposure to pathogenic rearing practices are true risk factors for depression, then they could account for a significant proportion of the familial aggregation of depression. By contrast, the model predicts that even if obstetric injury and low social class are true risk factors for schizophrenia, they together would account for only a very small proportion of the tendency for schizophrenia to aggregate in families.


2019 ◽  
pp. 304-323
Author(s):  
Joan Kaufman ◽  
Janitza L Montalvo-Ortiz ◽  
Richard S Lee

Individuals with a history of child abuse are at high risk for a broad range of psychiatric and substance use disorders. This chapter reviews key findings from research on the genetics of child abuse-related psychiatric disorders, neuroimaging investigations with maltreated youth, and resiliency studies. Relevant empirical work in the field was reviewed, with an emphasis on prior reviews, meta-analytic studies, and recent publications. Genetic factors are not associated with distinct psychiatric disorders but rather diverse clinical phenotypes, and a history of abuse is frequently associated with alterations in structural and functional brain changes across multiple brain regions and circuits that mediate a wide variety of emotional and cognitive processes. Heterogeneity in clinical outcome and brain measures varies as a function of a wide range of factors, and emerging findings on genetic and neural plasticity offers significant promise in understanding risk and resilience in maltreated youth. Child maltreatment is a strong predictor of early onset of psychiatric illness, increased comorbidity, and poor treatment response; however, a history of abuse need not lead to the development of psychiatric problems. Risk is altered by genetic factors, and can be ameliorated by positive factors in the environment—including the availability of positive support, enrichment experiences, and the delivery of evidence-based psychotherapeutic clinical interventions. Future multidisciplinary and translational studies will help to further delineate the mechanisms by which experiences of maltreatment confers risk for psychopathology, as well as help to further delineate factors associated with resiliency.


Author(s):  
Ravi Gupta

Sleep-related movement disorders include disorders that manifest as simple and mostly stereotyped movements occurring at sleep–wake interface or during sleep. Restless legs syndrome (RLS), the most common sleep-related movement disorder. RLS is a treatable condition that psychiatrists must be familiar with due to its common comorbidity with a broad range of psychiatric disorders. In addition, commonly used psychotropic medications are known to induce or worsen RLS symptoms in predisposed individuals, and these symptoms may be mistaken for akathisia or sleep-initiation insomnia and lead to mismanagement. This chapter discusses, among other RLS-related topics, the diagnosis, epidemiology, predisposing factors, genetic factors, and the role of iron metabolism.


2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Diana C. Dima ◽  
Rachael Adams ◽  
Stefanie C. Linden ◽  
Alister Baird ◽  
Jacqueline Smith ◽  
...  

Abstract Rare copy number variants associated with increased risk for neurodevelopmental and psychiatric disorders (referred to as ND-CNVs) are characterized by heterogeneous phenotypes thought to share a considerable degree of overlap. Altered neural integration has often been linked to psychopathology and is a candidate marker for potential convergent mechanisms through which ND-CNVs modify risk; however, the rarity of ND-CNVs means that few studies have assessed their neural correlates. Here, we used magnetoencephalography (MEG) to investigate resting-state oscillatory connectivity in a cohort of 42 adults with ND-CNVs, including deletions or duplications at 22q11.2, 15q11.2, 15q13.3, 16p11.2, 17q12, 1q21.1, 3q29, and 2p16.3, and 42 controls. We observed decreased connectivity between occipital, temporal, and parietal areas in participants with ND-CNVs. This pattern was common across genotypes and not exclusively characteristic of 22q11.2 deletions, which were present in a third of our cohort. Furthermore, a data-driven graph theory framework enabled us to successfully distinguish participants with ND-CNVs from unaffected controls using differences in node centrality and network segregation. Together, our results point to alterations in electrophysiological connectivity as a putative common mechanism through which genetic factors confer increased risk for neurodevelopmental and psychiatric disorders.


2019 ◽  
Vol 273 ◽  
pp. 575-577
Author(s):  
Carolina Muniz Carvalho ◽  
Pedro M. Pan ◽  
Vanessa K. Ota ◽  
Letícia M. Spindola ◽  
Gabriela Xavier ◽  
...  

1996 ◽  
Vol 168 (2) ◽  
pp. 139-142 ◽  
Author(s):  
Kieran C. Murphy ◽  
Michael J. Owen

BackgroundPrevious reports have suggested an increased prevalence of minor physical anomalies (MPAs) in schizophrenia.MethodA review of the literature was performed to examine the relationship between MPAs, schizophrenia and other disorders.ResultsPrevious studies demonstrate a number of methodological shortcomings. Moreover, MPAs are found in several other psychiatric disorders. Proponents of the neurodevelopmental model of schizophrenia have focused on an environmental explanation for the increased prevalence of MPAs. We argue that this may be overly simplistic and propose various ways in which genetic factors may also be involved.ConclusionsBetter studies should be performed to examine more precisely the nature of MPAs in schizophrenia and other disorders and also the relationship between MPAs and other developmental abnormalities. At present, it is unclear if MPAs are directly related to the pathogenesis of the disorder or even if they are related to the timing of critical events.


1978 ◽  
Vol 133 (5) ◽  
pp. 436-444 ◽  
Author(s):  
Julien Mendlewicz ◽  
Paul Verbanck ◽  
Paul Linkowski ◽  
Jean Wilmotte

SummaryGenetic factors play an important role in drug metabolism and drug response. In order to investigate genetic variables in lithium prophylaxis and lithium distribution across the erythrocyte in manic-depression, we have examined forty-two pairs of twins monozygotic (n = 25) and dizygotic (n = 17) with manic-depression. Concordant twins as a group show better lithium prophylaxis than do discordant twins. These results are consistent with previously published family studies of affective illness suggesting a positive relationship between genetic background and success of lithium prophylaxis.Lithium distribution across the red blood cell (RBC) was assessed by estimating lithium RBC/plasma ratios. The lithium ratio's intrapair differences in both groups of twins were minimal with a high heritability index suggesting that genetic factors play a role in lithium ion distribution. A high linear correlation was found between lithium ratio and plasma lithium and there was no difference in lithium ratios according to sex, affective state and response to lithium. The distribution of lithium ratios was homogenous in the lithium responders' population but this was not the case in the non-responders, suggesting biological heterogeneity of lithium distribution in lithium failures. The implications of these results are discussed as they relate to the genetic determinates of lithium prophylaxis in manic-depressive illness.These results indicate that lithium ratios are of limited value in lithium maintenance therapy. Our lithium kinetic data, however, are consistent with the concept of a lithium extrusion mechanism from red blood cells.


2013 ◽  
Vol 25 (3) ◽  
pp. 187-190
Author(s):  
Ghaffari Nejad Alireza ◽  
Fariborz Estilaee ◽  
Mohammad M. Sadeghi

ObjectivesTrichotillomania (TTM) is a psychiatric syndrome characterised by the inability to control repetitive hair pulling. Psychiatric data reveal that TTM is not usually prevalent among all family members of patients, and so far only one case of familial TTM has been reported.MethodsIn this study, we report a case of familial TTM that afflicted four sisters and discuss the importance of genetic factors in this disorder.ResultsThis report suggests that, similar to many other psychiatric disorders, TTM can be detected in other family members and that genetic factors not only have a significant role in the development of such disorders but also in determination of the disorder subtype. This report also shows that the comorbidities in one member of the family might predict the existence of comorbidities in other members. On the basis of response to medication.Conclusionthe authors suggest that a genetic disorder like polymorphism in serotonin receptors or dopamine can cause such a disorder.


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