Sergio Luis Schmidt

Prof. Sergio Luis Schmidt

orcid

Research Focus & Metrics

Academic Career Length

41Years (1986-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
2 October 2018 in Frontiers in Psychiatry
Verified
Journal Article
Open access
PDF file
JTJulio C. Tolentino
Julio C. Tolentino
SSSergio Luis Schmidt
Sergio Luis Schmidt
Background: Depression diagnosis requires five or more symptoms (Diagnostic and Statistical Manual of Mental Disorders-DSM-5). One of them must be either Depressed mood or Anhedonia, named main criteria. Although the secondary symptoms can be divided into somatic and non-somatic clusters, the DSM-5 identify depression in all or none fashion. In contrast, depression severity is a continuous variable. Therefore, it is commonly assessed with scales such as the Hamilton Depression Rating Scale (HAMD). Previously, we reported that patients with moderate depression (MD) exhibit greater impairments in cardiac-autonomic modulation than severely depressed (SD) patients. However, clinicians usually do not use scales. Objective: To verify whether the DSM-5 symptoms would be able to discriminate SD from MD and MD from non-depressed (ND) subjects. Material and Methods: Depression was diagnosed based on the Structured Clinical Interview for DSM-5® Disorders. The HAMD evaluated depression severity. In depressed subjects, MD and SD were defined considering the HAMD scores. ND was defined considering both the absence of DSM-5 criteria for depression and the HAMD score. Among 782 outpatients, 46 SD were found. MD and ND subjects were randomly sampled to match the demographic variables of the SD group. Results: Discriminant analysis showed that Depressed Mood was the most reliable symptom to discriminate ND from MD. Anhedonia discriminated SD from MD. Among the secondary DSM-5 criteria, the somatic cluster discriminated ND from MD and the non-somatic cluster SD from MD patients. Discussion: The presence of the somatic cluster in MD may indicate decreased vagal tone and/or increased sympathetic tone, leading to higher cardiovascular risk. As SD is associated with the non-somatic cluster, these patients are at risk of committing suicide. The DSM-5 symptoms exhibited by the patient may help the choice of adequate pharmacological treatment. This would avoid the use of antidepressants that unnecessarily increase cardiac risk in MD. When the symptom cluster suggests SD, the treatment must focus on the prevention of suicide. Conclusions: Depression severity may be inferred based on the DSM-5 criteria. The presence of the Anhedonia main criterium accompanied by non-somatic criteria indicate SD. The Depressive Mood criterium followed by somatic criteria suggest MD.

4 June 2003 in Environmental Health
Verified
Journal Article
Open access
PDF file
EYEdna M Yokoo
Edna M Yokoo
JVJoaquim G Valente
Joaquim G Valente
LGLynn Grattan
Lynn Grattan
SSSergio Luis Schmidt
Sergio Luis Schmidt
IPIlleane Platt
Illeane Platt
ESEllen K Silbergeld
Ellen K Silbergeld
The neurotoxic effects of methylmercury (MeHg) have been demonstrated in both human and animal studies. Both adult and fetal brains are susceptible to the effects of MeHg toxicity. However, the specific effects of adult exposures have been less well-documented than those of children with prenatal exposures. This is largely because few studies of MeHg exposures in adults have used sensitive neurological endpoints. The present study reports on the results of neuropsychological testing and hair mercury concentrations in adults (>17 yrs) living in fishing communities of Baixada Cuiabana (Mato Grosso) in the Pantanal region of Brazil. A cross-sectional study was conducted in six villages on the Cuiaba River. Participants included 129 men and women older than 17 years of age. They were randomly selected in proportion to the age range and number of inhabitants in each village. Questionnaire information was collected on demographic variables, including education, occupation, and residence history. Mercury exposure was determined by analysis of hair using flameless atomic absorption spectrophotometry. The neurocognitive screening battery included tests from the Wechsler Memory Scale and the Wechsler Adult Intelligence Scale, Concentrated Attention Test of the Toulouse-Pierron Factorial Battery, the Manual Ability Subtests of the Tests of Mechanical Ability, and the Profile of Mood States. Mercury exposures in this population were associated with fish consumption. The hair mercury concentration in the 129 subjects ranged from 0.56 to 13.6 μg/g; the mean concentration was 4.2 ± 2.4 micrograms/g and the median was 3.7 μg/g. Hair mercury levels were associated with detectable alterations in performance on tests of fine motor speed and dexterity, and concentration. Some aspects of verbal learning and memory were also disrupted by mercury exposure. The magnitude of the effects increased with hair mercury concentration, consistent with a dose-dependent effect. This study suggests that adults exposed to MeHg may be at risk for deficits in neurocognitive function. The functions disrupted in adults, namely attention, fine-motor function and verbal memory, are similar to some of those previously reported in children with prenatal exposures.

1 December 2000 in Brain and Cognition
Verified
Journal Article
Closed access
SSSergio Luis Schmidt
Sergio Luis Schmidt
RORosinda Martins Oliveira
Rosinda Martins Oliveira
FRFabı́ola Ribeiro Rocha
Fabı́ola Ribeiro Rocha
YAYael Abreu-Villaça
Yael Abreu-Villaça

1 May 2000 in Neuropsychologia
Verified
Journal Article
Closed access
SSSergio Luis Schmidt
Sergio Luis Schmidt
RORosinda M. Oliveira
Rosinda M. Oliveira
TKThomas Eichenberg Krahe
Thomas Eichenberg Krahe
CFCláudio Carneiro Filgueiras
Cláudio Carneiro Filgueiras

1 March 2001 in Pharmacology Biochemistry and Behavior
Verified
Journal Article
Closed access
AMAlexandre E Medina
Alexandre E Medina
AMAlex C. Manhães
Alex C. Manhães
SSSergio Luis Schmidt
Sergio Luis Schmidt

1 December 1991 in Experimental Brain Research
Verified
Journal Article
Closed access
PDF file
EDE. C. Dias
E. C. Dias
CRC. E. Rocha-Miranda
C. E. Rocha-Miranda
RBR. F. Bernardes
R. F. Bernardes
SSSergio Luis Schmidt
Sergio Luis Schmidt