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In 1957 all inhabitants (2,612) in a delimited geographical area, Lundby, were examined by a psychiatrist. Personality traits were scored for each individual. During the following 15 years 58 men became alcoholics (44 who had been 15 years or over in 1957). Among the men who in 1957 were scored 'subsolid in combination with symptom neurosis' the risk of becoming an alcoholic was increased 13.5 to 15.8 times. Protective against alcoholism was 'subvalidity in combination with psychosomatic symptoms'. The men with this combination had their risk decreased 12 times. The prediction of alcoholism depended on which factors and which combinations were used. With a sensitivity of 50% a specificity of almost 90% was reached; with a sensitivity of 60% specificities between 70% and 80% were reached.

In 1957 all inhabitants (2,612) in a delimited geographical area, Lundby, were examined by a psychiatrist, and social factors were evaluated for each individual. During the following 15 years 58 men became alcoholics. Among the men who in 1957 were in the age group 0-14 years and belonged to a 'gang', the risk of becoming an alcoholic was 100-fold increased. 'Gang' was also an important factor in the age group 15-24 years. 'Crisis' was an important factor among those over 14, and 'disintegrated environment' in the age group 25-59 years. In the latter age group occupations such as 'entrepreneur', became important as a precipitating factor. 'Married' was the only protective factor found.

In this prospective longitudinal study over 15 years (1957 to 1972) the background factors for those who became alcoholics and those who did not were registered before anybody knew what the outcome would be. The population (2,612 inhabitants) lived in 1957 in a delimited area in the South of Sweden, Lundby. In 1957 nearby everyone (98%) was examined by a single psychiatrist, and again in 1972, irrespective of domicile, by two psychiatrists. Among the men who at the outset did not misuse alcohol, 58 became alcoholics. These alcoholics were compared with the non-alcoholics regarding e.g. personality traits, social factors and interactions between factors.

A method has been developed for the quantitative determination of haloperidol in brain and other tissues. Such determinations have been made after acute and chronic administration of haloperidol to Sprague-Dawley rats. Different regions of the brain including the striatum, the limbic forebrain and the cerebellum have been analyzed separately. The haloperidol effects on Dopa formation have been studied in the same tissue samples. The stimulation of prolactin secretion via blockade of hypothalamic dopaminergic mechanisms and behavioural effects of the drug have been evaluated in parallel experiments. The elimination of haloperidol from brain tissue is a multiphasic process. The fourth phase of elimination is the slowest with a half life of 4 days. No strict correlation was found between serum and brain concentrations of haloperidol. Both after acute and chronic administration there exists apparently a saturating dose above which the brain concentration of the drug increases very little. The dose seems to coincide with that beyond which little increase in Dopa formation is observed. A pharmacokinetic analysis suggests an element of saturable binding or transfer of haloperidol to brain tissue. This mechanism is not preferentially localized to areas of brain rich in dopaminergic synapses. A good correlation was found between the haloperidol concentration in the brain on the one hand and its effects on behaviour, on serum prolactin values and on Dopa formation on the other.

The objective of the present study on cycloid psychosis was to describe the incidence and risk in a defined population sample. We therefore re-evaluated specific diagnostic groups in the 1947 cohort of the Lundby Study. Three female cases were identified as cycloid psychosis according to the diagnostic criteria of Leonhard, Perris and Brockington. No men were found. The incidence rate (per 100 observation years) was found to be 0.016% for women. The cumulative probability i.e. risk, up to 60 years of age was calculated to be 0.7%. Incidence rate and risk for cycloid psychosis in women was thus about half of the corresponding values for schizophrenia as described for the same population in a parallel study. We conclude that cases of cycloid psychosis constitute a substantial proportion of female psychotic patients.