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Featured researches published by Bernard E. Statland.


Clinical Biochemistry | 1976

Variation of serum iron concentration in young healthy men: Within-day and day-to-day changes.

Bernard E. Statland; Per Winkel; Henning Bokelund

1. Serum iron concentration values were determined on a group of 11 healthy young men on blood specimens which were drawn at various hours of the day: 800 h, 1100 h, and 1400 h; on each of four separate days. 2. using a three-way ANOVA (analysis of variance) model, we determined the diurnal variation both for the group as a whole (main hour effect) and for the individual subjects (subject-hour and subject-day-hour interactions). 3. the total combined within-day variation as expressed in coefficients of variation was 12.9% with the peak value seen at 1400 h. 4. on a separate study, blood specimens were obtained at 1100 h on five separate days during a two week period on the same volunteers. 5. using a two-way ANOVA model (subject and day) the day-to-day coefficient of variation was found to be 26.6% for the group. In both cases (within-day and day-to-day) the biological variation was considerably greater than the analytic variation.


Clinica Chimica Acta | 1976

The effect of a short burst of exercise on activity values of enzymes in sera of healthy young men

Steven W. King; Bernard E. Statland; John Savory

We report the effect of exercise on the activity values of five enzymes in sera as studied in four healthy male volunteers. The underlying purpose of this present study was to produce an increase in the activity values in the sera of selected enzymes found in muscle. Then by observing the decay rate of these enzymes, we computed the inter-individual differences in clearance rates serum half-life) of these enzymes. Blood specimens were collected just prior to exercise, 1 h after excerise, and on eight additional times up to 93 h after exercise. All specimens were assayed on one occasion for activity values of creatine kinase, asparate aminotransferase, alanine aminotransferase, alkaline phosphatase, and lactate dehydrogenase. We found increases in the three muscle enzymes with average increases being: creatine kinase, +116%; asparate aminotransferase, +41%; and lactate dehydrogenase, +32%; all of which remained above baseline values for 53 h or longer. In the case of creatine kinase, a monoexponential decay curve depicted the data (from the 19-h specimen to the 67-h specimen). The calculated apparent serum half-life for creatine kinase varied from 38 h to 118 h in the subjects tested.


Clinical Obstetrics and Gynecology | 1985

Abruptio placentae with coagulopathy: a rational basis for management.

Geoffrey Sher; Bernard E. Statland

Abruptio placentae rarely produces severe maternal complications while the fetus is alive in utero. The advent of fetal death (grade III) indicates a severe form of abruptio placentae and a real risk that an overt coagulopathy might develop (grade IIIB). Overt coagulopathy associated with a live fetus is, however, uncommon. The advent of an overt coagulopathy should be viewed as ominous. Treatment of abruptio placentae with overt coagulopathy should be directed toward obtaining a rapid and atraumatic vaginal delivery. Once delivery has occurred, spontaneous reversal of the coagulopathy can be anticipated. In the opinion of one of the authors (G.S.), the advent of severe consumption coagulopathy and/or uterine inertia is an indication for intravenous therapy with aprotinin. It has been shown that such therapy will limit DIC, reverse fibrinolysis, reawaken uterine activity, and lead to rapid vaginal delivery within 6-8 hours. Aprotinin is not commercially available for clinical use in the United States. Prolongation of the abruption-delivery interval will worsen maternal prognosis. Accordingly, the advent of uterine inertia prior to complete cervical dilatation is an indication for immediate cesarean section in circumstances where aprotinin is not available. Following delivery, the physician should be on the lookout for postpartum hemorrhage, which may necessitate immediate transfusion, the administration of oxytocics, and/or uterine manipulation. Surgical intervention is rarely indicated in such cases. The patient should also be carefully observed over the ensuing days and weeks for the evolution and resolution of complications, such as renal failure, pulmonary insufficiency, and panhypopituitarism.


Clinica Chimica Acta | 1976

Daily variation of lipids and hormones in sera of healthy subjects

John E. Hammond; Peter Wentz; Bernard E. Statland; J.C. Phillips; Per Winkel

The physiological day-to-day variation of selected hormone and lipid concentration values in sera of healthy subjects was studied. We drew blood specimens from 14 healthy volunteers, aged 22 to 40 years, (8 male and 6 female) at 0800 h on six separate days over a ten day interval. On one occasion all the twelve specimens from each subject (6 days X 2 replicates) were assayed for the hormones: thyroxine and cortisol; and the lipips: cholesterol and triglyceride which were analyzed by enzymatic methods. The assays were performed on one occasion in order to eliminate the batch-to-batch analytical variation which would tend to blur the physiological day-to-day variation. Using an analysis of variance technique, the total variation was separated into the physiological intraindividual day-to-day variation, the biological inter-individual variation, and the within-batch analytical variation. The mean physiological day-to-day variations in terms of percent coefficient of variation were 7.5% for thyroxine, 26.6% for cortisol, 4.8% for cholesterol, , and 25.0% for triglycerides.


Metabolism-clinical and Experimental | 1983

Alterations in human serum alkaline phosphatase and its isoenzymes by hypolipidemic agents: Colestipol and clofibrate

Jeffrey L. Probstfield; Bernard E. Statland; Linda Gorman; Donald B. Hunninghake

Total serum alkaline phosphatase (TSAP) determinations were done as part of the biochemical screening in comparative studies of lipid lowering agents in type lla hyperlipoproteinemic patients. TSAP determinations were made by using a modification of the Bessey-Lowry method and the Statland method. Increases in TSAP following colestipol treatment of 20% (P less than 0.05) and 32% (P less than 0.005) were seen by using the respective methods. Isoenzymatic determinations were done by employing the Statland method and all fractions were increased from baseline levels during colestipol therapy. Clofibrate was associated with 34% (P less than 0.005) and 28% (P less than 0.005) reductions in TSAP activity by using the respective methods; significant reductions in both bone and other isoenzymatic components occurred. Gamma-glutamyltransferase (gamma GT) results did not consistently reflect TSAP or liver isoenzyme results.


Clinical Chemistry | 1974

Factors Contributing to Intra-Individual Variation of Serum Constituents: 4. Effects of Posture and Tourniquet Application on Variation of Serum Constituents in Healthy Subjects

Bernard E. Statland; Henning Bokelund; Per Winkel


Clinical Chemistry | 1973

Factors Contributing to Intra-Individual Variation of Serum Constituents: 2. Effects of Exercise and Diet on Variation of Serum Constituents in Healthy Subjects

Bernard E. Statland; Per Winkel; Henning Bokelund


Clinical Chemistry | 1973

Factors Contributing to Intra-Individual Variation of Serum Constituents: 1. Within-Day Variation of Serum Constituents in Healthy Subjects

Bernard E. Statland; Per Winkel; Henning Bokelund


Clinical Chemistry | 2000

The Role of Total Laboratory Automation in a Consolidated Laboratory Network

Richard S. Seaberg; Robert O. Stallone; Bernard E. Statland


American Journal of Clinical Pathology | 1977

Relationship of Day-to-day Variation of Serum Iron Concentrations to Iron-binding Capacity in Healthy Young Women

Bernard E. Statland; Per Winkel

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R H Ng

Boston Medical Center

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Per Winkel

University of North Carolina at Chapel Hill

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Dennis E. Freer

University of North Carolina at Chapel Hill

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Henning Bokelund

University of North Carolina at Chapel Hill

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Geoffrey Sher

University of North Carolina at Chapel Hill

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B. Douglas Morton

University of North Carolina at Chapel Hill

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Ernest N. Kraybill

University of North Carolina at Chapel Hill

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