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Biomedical subjects

D G Shen

Publications and source records attributed to D G Shen.

16 recordsLinked to original sources

Classifying spatial patterns of brain activity with machine learning methods: application to lie detection.

Patterns of brain activity during deception have recently been characterized with fMRI on the multi-subject average group level. The clinical value of fMRI in lie detection will be determined by the ability to detect deception in individual subjects, rather than group averages. High-dimensional non-linear pattern classification methods applied to functional magnetic resonance (fMRI) images were used to discriminate between the spatial patterns of brain activity associated with lie and truth. In 22 participants performing a forced-choice deception task, 99% of the true and false responses were discriminated correctly. Predictive accuracy, assessed by cross-validation in participants not included in training, was 88%. The results demonstrate the potential of non-linear machine learning techniques in lie detection and other possible clinical applications of fMRI in individual subjects, and indicate that accurate clinical tests could be based on measurements of brain function with fMRI.

Adult↗

[A study of superoxide dismutase in erythrocytes in Duchenne muscular dystrophy].

In orders to search for possible events in the pathogenesis of Duchenne muscular dystrophy (DMD), the activity of erythrocyte superoxide dismutase has been determined in thirty-seven patients and fifteen carriers of DMD, comparison to fourty-five age-matched normal controls, seventeen cases of infantile, Kugelberg-Welander type spinal muscle atrophy. The results showed that superoxide dismutase activity were elevated especially in early periods of disease in DMD but not in other groups of patients. These findings suggest that alterations of SOD do not constitute the primary mechanism of inducing membrane damage. A considerable increased SOD activity in DMD patients may be a compensatory phenomenon secondary to muscle degeneration.

Adult↗

[Congenital myopathy without specific features (minimal change myopathy)].

A case of Congenital myopathy without specific features was reported. The main clinical findings were generalized muscle weakness and delayed developmental milestones. Histological and histochemical examination on the biopsied muscles demonstrated minimal nonspecific changes, mild variation in fiber size without structure and enzyme abnormality. No prominent necrotic changes were found and Ulrich and Fukuyama type of congenital myopathy were excluded. The abnormal muscle pathology was assumed to have resulted from delayed muscle fiber growth due to defective neural influence.

Child↗

The effect of DDB on dystrophic hamsters: an in vivo and in vitro study.

Dimethyl-4, 4'-dimethoxy-5, 6, 5'-6'-dimethylenedioxybiphenyl-2, 2'-dicarboxylate (DDB) is a synthetic analogue of Schizandrin C, an active compound isolated from a Chinese herb, Fructus schizandrae. We administered this compound to dystrophic hamsters in vivo for 31 days. This led to a 61% reduction of the calcium content, an 86% reduction of the area of calcium deposits, and a 52% reduction of the area of necrosis of cardiac muscle. However, skeletal muscle necrosis was not significantly improved. No clear change in plasma creatine kinase (CK) was observed. In an in vitro incubation study, the rate of CK release and tetanus tension of the extensor digitorum longus muscle of dystrophic hamsters were not substantially changed by the addition of DDB. This study suggests that DDB has some effect on cardiac necrosis, and that it might be useful for treatment of the cardiac involvement in patients with muscular dystrophy or other conditions with accompaning Ca accumulation.

Animals↗

ATPase activity of erythrocyte membrane in patients with trisomy 21 (Down's syndrome).

ATPase activity of crythroyte membranes was determined in 25 cases of Down's syndrome verified by cytological and psychological examinations. The age range of the patients was 8-25 years; 16 males and 9 females. Thirty health male volunteers were selected as the control group. There was a marked reduction of total ATPase, Na+, K+-ATPase, Mg++ATPase activities and rate of ouabain inhibition in the patients with Down's syndrome. The authors suggest that there might exist transport defects in the red cell membranes in such patients.

Adenosine Triphosphatases↗