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1.
Prostate Cancer Prostatic Dis ; 13(3): 248-51, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20514082

ABSTRACT

The objective of this study was to preoperatively predict non-organ-confined disease in patients considering radical prostatectomy. To account for the stage migration seen in prostate cancer, we included only those patients who underwent prostatectomy after the year 2000. Information on a cohort of 1895 patients who underwent radical prostatectomy from 2000 to 2008 was retrieved from the Duke Prostate Center database. Race (African American, non-African American), body mass index, age at surgery, PSA, biopsy Gleason sum (<7, 7 and >7) and clinical tumor stage (cT1, cT2/3) were analyzed by univariate analysis followed by logistic regression analysis. The Duke Interactive Clinical Equation for staging (DICE-S score) was calculated from the logistic regression model. The model was then internally validated using a bootstrapping technique. Biopsy Gleason sums 7 and >7 were more likely to have non-organ-confined disease compared with <7 (OR=2.97, Gleason sum=7; OR=3.25, Gleason sum>7). Clinical tumor stage, cT2/3, predicted non-organ-confined disease (OR=1.58). Older age was associated with non-organ-confined disease (OR=1.02), as was greater PSA (OR=1.12). DICE-S equation x=ln (p/1-p)=-3.627+0.019 (age)+0.109 (PSA)+1.087 (bGleason=7)+1.180 (bGleason >7)+0.459 (clinical T stage >T1), where p=(e(x))/(1+e(x)). A concordance index (prediction accuracy) of 0.73 was reached on internal validation. Using the DICE-S score, age, PSA, biopsy Gleason sum and clinical tumor stage, we can predict non-organ-confined disease in radical prostatectomy at an acceptable accuracy. Preoperative information on disease stage may aid in treatment decisions and surgical approach.


Subject(s)
Prostatectomy , Prostatic Neoplasms/diagnosis , Prostatic Neoplasms/surgery , Aged , Humans , Male , Middle Aged , Neoplasm Staging , Prognosis , Prostate-Specific Antigen/blood , Survival Rate
2.
J Pineal Res ; 31(2): 102-8, 2001 Sep.
Article in English | MEDLINE | ID: mdl-11555164

ABSTRACT

In the present study, we investigated the ability of serotonin and melatonin to bind metals that occur naturally in the brain. An electrochemical technique called adsorptive cathodic stripping voltammetry (AdCSV) was employed to study the metal-serotonin or metal melatonin interactions. The results show that both serotonin and melatonin form stable complexes with lithium and potassium, with serotonin favouring lithium over potassium, and melatonin favouring potassium over lithium. Coordination between either serotonin or melatonin and calcium was not favoured. The stability of the complexes formed between serotonin and the metals decreased with the metals as follows: Li+ > K+ > Al3+ > Na+ > Ca2-. The trend for melatonin-metal complexes was K+ > Li+ > Na+ > Al3+ > Ca2+ The binding and stable complex formation between both ligands, serotonin and melatonin with lithium, potassium and sodium is of biological importance. The binding of serotonin to lithium could provide an explanation for the therapeutic effects of lithium in depression treatment, whereas the binding of aluminium by melatonin could provide insight into the role of this element in the aetiology of Alzheimer's disease.


Subject(s)
Melatonin/metabolism , Metals/metabolism , Serotonin/metabolism , Aluminum/metabolism , Alzheimer Disease/etiology , Alzheimer Disease/metabolism , Animals , Brain/metabolism , Calcium/metabolism , Electrochemistry , Humans , In Vitro Techniques , Lithium/metabolism , Lithium/pharmacology , Melatonin/chemistry , Metals/chemistry , Potassium/metabolism , Psychopharmacology , Serotonin/chemistry , Sodium/metabolism
3.
J Neurol Neurosurg Psychiatry ; 67(4): 457-62, 1999 Oct.
Article in English | MEDLINE | ID: mdl-10486391

ABSTRACT

OBJECTIVES AND METHODS: Transcranial real time sonography (TCS) was applied to 49 patients with Huntington's disease and 39 control subjects to visualise alterations in the echotexture of the basal ganglia. For comparison T1 weighted, T2 weighted, and fast spin echo MRI was performed in 12 patients with Huntington's disease with and in nine patients without alterations of the basal ganglia echotexture as detected by TCS and T1 weighted, T2 weighted, and fast spin echo MRI. Furthermore, the widths of the frontal horns, third ventricle, and the lateral ventricles were depicted in TCS examinations and correlations examined with corresponding CT slices. RESULTS: Eighteen out of 45 (40%) of the patients with Huntington's disease with adequate insonation conditions showed hyperechogenic lesions of at least one basal ganglia region. In 12 patients TCS depicted hyperechogenic lesions of the substantia nigra; in six patients the head of the caudate nucleus was affected. The lentiform nucleus (n=3) and the thalamus (n=0) were less often affected or spared. Hyperechogenic lesions were significantly more frequent in patients with Huntington's disease than in 39 control subjects, who had alterations of the echotexture in 12.8% (4/39) of the examinations. The number of CAG repeats and the clinical status correlated with the identification of hyperechogenic lesions of the substantia nigra (p<0.01). Hyperechogenic lesions of the caudate nucleus were associated with an increased signal intensity in T2 weighted MR images (p<0.05). All TCS parameters indicating brain atrophy correlated with CT findings (p<0.0001). CONCLUSIONS: TCS detects primarily abnormalities of the caudate nucleus and substantia nigra in Huntington's disease. These changes in the echotexture may represent degenerative changes in the basal ganglia matrix and are partially associated with CAG repeat expansion and the severity of clinical findings.


Subject(s)
Basal Ganglia/diagnostic imaging , Brain Diseases/diagnostic imaging , Huntington Disease/diagnostic imaging , Adult , Aged , Atrophy/diagnostic imaging , Atrophy/pathology , Basal Ganglia/pathology , Brain Diseases/pathology , Female , Humans , Huntington Disease/pathology , Male , Middle Aged , Ultrasonography, Doppler, Transcranial
4.
J Neurol ; 246(6): 459-61, 1999 Jun.
Article in English | MEDLINE | ID: mdl-10431771

ABSTRACT

Serum neuron-specific enolase (s-NSE) and s-100 protein (s-100) are sensitive markers of various brain diseases. We investigated both of these markers in nine patients within 5 min, 6 h, 12 h, and 48 h after a single tonic-clonic seizure. The mean peak s-NSE level was significantly higher after 5 min (11.97 +/- 8.56 microg/l) and 48 h (10.31 +/- 8.92 microg/l, P < 0.05) than the levels of seizure-free, age-matched controls. Five patients had increased s-NSE levels regarding the upper limit of normal as mean + 3 SD. s-100 was not detected either in controls or epileptic patients. These data indicate that s-NSE in contrast to s-100 may be an in vivo marker after generalized seizures in some patients.


Subject(s)
Epilepsy, Tonic-Clonic/blood , Phosphopyruvate Hydratase/blood , S100 Proteins/blood , Adult , Biomarkers/blood , Case-Control Studies , Epilepsy, Tonic-Clonic/diagnosis , Epilepsy, Tonic-Clonic/enzymology , Female , Humans , Male , Middle Aged
5.
Surg Clin North Am ; 67(1): 1-14, 1987 Feb.
Article in English | MEDLINE | ID: mdl-3544261

ABSTRACT

Injury and death from burns have reached epidemic levels in the United States during the past quarter-century. Yet preventive action on both local and national administrative levels has been dismally inadequate and underfunded. Identifying and recognizing both the etiologies of burn injuries and the statistical magnitude of the problem will, it is hoped, stimulate dedication of more resources and personnel to reducing the hazards of fire and the resulting loss of life, productivity, and property in the next two decades. Public education and national awareness are first steps to creation of a consumer and popular demand worthy of national action.


Subject(s)
Fires/prevention & control , Adolescent , Adult , Aged , Burns/prevention & control , Child , Child, Preschool , Female , Humans , Infant , Infant, Newborn , Male , Middle Aged , United States
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