1988
DOI: 10.1001/archpsyc.1988.01800300049005
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Dopamine Metabolism and Disposition in Schizophrenic Patients

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Cited by 79 publications
(29 citation statements)
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References 44 publications
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“…Samples were stored at 溪 80 袏 C until the time of the assay. Patients were not treated with debrisoquin, which has been shown to decrease the peripheral contribution to plasma HVA (Maas et al 1988(Maas et al , 1993Swann et al 1980;Davidson et al 1987a;Kopin et al 1988;Duncan et al 1993). However, the low-monoamine diet, minimization of physical activity, and fasting prior to the blood draw used in this study has been shown to reduce statistical effects on plasma HVA levels (Davidson et al 1987b).…”
Section: Blood Drawsmentioning
confidence: 94%
See 1 more Smart Citation
“…Samples were stored at 溪 80 袏 C until the time of the assay. Patients were not treated with debrisoquin, which has been shown to decrease the peripheral contribution to plasma HVA (Maas et al 1988(Maas et al , 1993Swann et al 1980;Davidson et al 1987a;Kopin et al 1988;Duncan et al 1993). However, the low-monoamine diet, minimization of physical activity, and fasting prior to the blood draw used in this study has been shown to reduce statistical effects on plasma HVA levels (Davidson et al 1987b).…”
Section: Blood Drawsmentioning
confidence: 94%
“…Davidson et al (1991b) observed no significant differences in baseline values of plasma HVA, but did observe a difference in change in plasma HVA from baseline in exacerbated patients, and a correlation between peak psychosis and peak plasma HVA during withdrawal. Studies of drugfree exacerbated patients have also reported positive associations between plasma HVA and positive symptoms (Maas et al 1988). Studies examining both metabolites have shown differing results.…”
mentioning
confidence: 99%
“…Despite some argument (Kopin et al 1988;Lambert et al 1993;Maas et al 1988), several lines of investigations have focused on plasma levels of homovanillic acid (pHVA), a major metabolite of DA, for the study of DA-related mental disorders such as schizophrenia based on the assumption that dysfunction in central dopaminergic activity is, to some extent, reflected in this peripheral measure (see Friedhoff and Amin 1997 for review). While conflicting results have been reported regarding differences in pHVA levels between patients with schizophrenia and control subjects (Doran et al 1985;Koreen et al 1994;Maas et al 1993;Pickar et al 1984;Steinberg et al 1993;Sumiyoshi et al 1997a;Whelton et al 1993), there has been accumulated evidence for the association between pHVA levels in schizophrenia and the outcome of neuroleptic treatment (Akiyama et al 1995;Chang et al 1993;Davis et al 1985;Garver et al 1997;Green et al 1993;Nagaoka et al 1997;Sumiyoshi et al 1997b).…”
mentioning
confidence: 99%
“…However, we recently ex amined the relationship of cerebrospinal fluid (CSF) homovanillic acid (HV A) to a complex component of schizophrenia (psychosis) and found a strong correla tion between the two (n = 24, r = 0.70, P = .00(1) (Maas et al unpublished observation). Several other groups have also found this strong correlation and have reported signiftcant correlations between plasma HV A and severity of psychosis (Davis et al 1991;Maas et al 1988;Pickar et al 1986). …”
Section: Although This Model In Which Psychopathologicmentioning
confidence: 73%