Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where James B. McCormick is active.

Publication


Featured researches published by James B. McCormick.


JAMA | 2000

Circadian relationship of serum uric acid and nitric oxide.

Eugene L. Kanabrocki; Jane L.H.C. Third; May Ryan; Bernard A. Nemchausky; Parvez Shirazi; Lawrence E. Scheving; James B. McCormick; Ramon C. Hermida; W. Fraser Bremner; Debbie A. Hoppensteadt; Jawed Fareed; J. H. Olwin

To the Editor: Nitric oxide–mediated damage has been implicated in a number of neurological diseases including stroke1, 2 and multiple sclerosis (MS).3 For instance, monocytes expressing high levels of nitric oxide synthetase have been found in plaques from the brains of patients with MS.4 The proximal agent of neuronal cell damage may be peroxynitrite, which is formed in vivo from the synthesis of nitric oxide and superoxide.


American Heart Journal | 2000

Relation between circadian patterns in levels of circulating lipoprotein(a), fibrinogen, platelets, and related lipid variables in men.

W. Fraser Bremner; Robert B. Sothern; Eugene L. Kanabrocki; May Ryan; James B. McCormick; Susan Dawson; Eileen S. Connors; Renee Rothschild; Jane L.H.C. Third; Sabera Vahed; Bernard M. Nemchausky; Parvez Shirazi; John H. Olwin

BACKGROUND A correlation has been reported between lipoprotein(a) [Lp(a)] concentration and risk for coronary artery disease. High concentrations of Lp(a) might be markers for vascular or tissue injury or might be associated with other genetic or environmental factors that can cause acute myocardial infarction. METHODS We measured the circadian characteristics of circulating Lp(a), fibrinogen, platelets, cholesterol, triglycerides, high-density lipoprotein cholesterol, and low-density lipoprotein cholesterol for a group of adult male volunteers who had no clinical symptoms. We obtained samples every 3 hours around the clock to assess the normal degree of variation within a 24-hour period and to test for similarities in circadian patterns and correlations with level of Lp(a). RESULTS Each variable displayed a highly significant circadian rhythm. Lp(a), fibrinogen, high-density lipoprotein cholesterol, and low-density lipoprotein cholesterol peaked in the morning. Cholesterol and platelets peaked in the late afternoon, and triglycerides peaked in the evening. CONCLUSIONS Although peak levels of Lp(a) and fibrinogen coincide with reported morning peak frequencies of myocardial infarction and stroke, the platelet peak appears to coincide with late afternoon peak frequencies of sudden cardiac death and fatal stroke. The data suggest that proper timing of single samples may improve the usefulness and accuracy of diagnosis, risk assessment, and therapy.


Chronobiology International | 1990

REFERENCE VALUES FOR CIRCADIAN RHYTHMS OF 98 VARIABLES IN CLINICALLY HEALTHY MEN IN THE FIFTH DECADE OF LIFE

Eugene L. Kanabrocki; Robert B. Sothern; Lawrence E. Scheving; David L. Vesely; T. H. Tsai; J. Shelstad; C. Cournoyer; J. Greco; H. Mermall; H. Ferlin; B. M. Nemchausky; D. L. Bushnell; Ervin Kaplan; S. Kahn; G. Augustine; E. Holmes; J. Rumbyrt; R. P. Sturtevant; F. Sturtevant; F. Bremner; J. L.H.C. Third; James B. McCormick; S. Dawson; L. Sackett-Lundeen; E. Haus; Franz Halberg; J. E. Pauly; J. H. Olwin

Nine clinically healthy men, 41-47 yr of age, served as subjects in a 24-hr study conducted at the Edward Hines Jr Veterans Administration Hospital in the Chicago area in May 1988. Physiologic measurements, and blood and urine samples were collected at 3-hr intervals over a single 24-hr period beginning at 1900. The number of variables measured or calculated (total = 98) included: 6 vital signs (oral temperature, pulse, blood- and intraocular pressures); 16 in whole blood (counts and differentials); 50 in serum (SMAC-24, lipids, hormones, electrophoresis of LDH and proteins); and 26 in urine (solids, proteins, creatinine, catecholamines, melatonin, cortisol, electrolytes and metals). Data were analyzed for time effect by analysis of variance (ANOVA) and for circadian rhythm by single cosinor. Individual rhythm characteristics for each variable were summarized for the group by population mean cosinor. The vast majority of variables revealed statistically significant within-day changes in values as validated by one-way ANOVA. All vital signs (except for intraocular pressures) and all serum hormones displayed a prominent circadian rhythm for the group, as did most variables in whole blood, while only about half of the variables in urine demonstrated a significant group rhythm. The results obtained are meant to: (a) document the circadian time structure; and (b) serve as reference values for circadian rhythm characteristics (range of change, mesor, amplitude and acrophase) for a defined group of individuals: clinically-healthy adult men in the prime of life.


Clinical and Applied Thrombosis-Hemostasis | 1999

Circadian interrelationships among levels of plasma fibrinogen, blood platelets, and serum interleukin-6.

Eugene L. Kanabrocki; Robert B. Sothern; Harry L. Messmore; Beatrice Roitman-Johnson; James B. McCormick; Susan Dawson; Fraser W. Bremner; Jane L.H.C. Third; Bernard A. Nemchausky; Parvez Shirazi; Lawrence E. Scheving

Circadian (24 h) rhythms of fibrinogen, interleu kin-6 (IL-6), and platelet levels were studied in 11 males ages 46 to 72 years. Since there is a known circadian rhythm for fibrinogen and IL-6, we postulated that the peak level (acro phase) of fibrinogen would follow the acrophase of IL-6, based on the fact that IL-6 is the stimulus for fibrinogen production in the liver. Platelet levels were measured to show whether there was any correlation with the IL-6 acrophase because it has been reported that IL-6 affects megakaryocytes and platelets in dogs. We found that the acrophase for IL-6 occurred at 02:03 h and the acrophase for fibrinogen occurred at 09:16 h. Platelet counts peaked at 16:56 h. Thus, there was a positive correlation between IL-6 and fibrinogen acrophases and a negative corre lation of each with the acrophase for platelets. The positive linkage of IL-6 with fibrinogen in this study suggests that sup pression of IL-6 production would lower those peak fibrinogen levels that occur in the morning in association with arterial ischemic events. This could result in fewer arterial ischemic events, especially in the morning. Key Words: Circadian— Fibrinogen—Interleukin—6 (IL-6)—Platelets—Arterial ischemia.


Chronobiology International | 1988

Ten-year-replicated circadian profiles for 36 physiological, serological and urinary variables in healthy men

Eugene L. Kanabrocki; Robert B. Sothern; Lawrence E. Scheving; Franz Halberg; John E. Pauly; J. Greco; Bernard A. Nemchausky; M. Debartolo; Ervin Kaplan; James B. McCormick; J. H. Olwin; Gayle E. Marks; T. Bird; Redmond Dp; R. C. Graeber; A. Ferrara; William J. M. Hrushesky

At 3-hr intervals over a 24-hr span, 36 systemic, serologic and urinary variables were examined in 7 men in their mid 20s in the Spring of 1969, and again in the same 7 men in the Spring of 1979 under a similar chronobiologic protocol, using the same chemical and numerical analytical procedures. The variables examined for rhythms by cosinor were: vital signs--blood pressure (systolic, diastolic, pulse pressure and mean arterial pressure), heart rate, intraocular pressure (left and right), oral temperature; serum components--albumin, albumin/globulin ratio, total bilirubin, calcium, carbon dioxide, chlorides, bilirubin, cholesterol, globulin, glucose, potassium, sodium, sodium/potassium ratio, transaminase, triglycerides, total protein, urea nitrogen; and urine components--calcium, calcium/magnesium ratio, creatinine, magnesium, pH, potassium, sodium, sodium/potassium ratio, urea clearance, urea nitrogen, volume and zinc. Although all subjects appeared clinically healthy in 1969 and in 1979, certain inter-study differences were observed in a number of rhythm parameters of different variables. Statistically significant increases in mesor for the group as a whole were observed for serum Ca, cholesterol, Cl, CO2, K, Na, and while statistically significant mesor decreases for a group as a whole were noted in serum glucose and transaminase. Statistically significant increases in amplitude for the group as a whole were observed in serum chloride and urinary Na/K ratio, while statistically significant decreases were observed in amplitude for blood pressure, heart rate, serum albumin, A/G ratio, globulin, glucose, protein, sodium and transaminase.(ABSTRACT TRUNCATED AT 250 WORDS)


American Journal of Nephrology | 1996

Circadian Relationships between Circulating Atrial Natriuretic Peptides and Serum Sodium and Chloride in Healthy Humans

Robert B. Sothern; David L. Vesely; Eugene L. Kanabrocki; Fraser W. Bremner; Jane L.H.C. Third; James B. McCormick; Susan Dawson; May Ryan; Joseph Greco; Jeff T. Bean; Bernard M. Nemchausky; Parvez Shirazi; Lawrence E. Scheving

Long-acting natriuretic peptide (LANP), vessel dilator (VSDL), and atrial natriuretic factor (ANF) consisting of amino acids 1-30, 31-67, and 99-126 of the 126 amino acid ANF prohormone, respectively, circulate in humans and have potent natriuretic properties. To determine whether these peptides have a direct relationship to serum Na and/or Cl, we examined 21 24-hour profiles of these peptides and Na and Cl in 14 healthy humans. LANP, VSDL, ANF, and Cl had significant (p < 0.001) circadian rhythms with peak concentrations at 04.00 h. The circadian rhythm of serum Na was exactly opposite. Sodium correlated negatively with LANP (p = 0.021) and ANF (p = 0.007), while Cl correlated positively with LANP (p = 0.003) and VSDL (p = 0.001). These data suggest that the atrial peptides may be important for the maintenance of serum Na and Cl within their normal ranges and in the modulation of their daily circadian rhythms.


American Journal of Anatomy | 1983

Circadian variation in the urinary excretion of electrolytes and trace elements in men

Eugene L. Kanabrocki; Lawrence E. Scheving; J. H. Olwin; Gayle E. Marks; James B. McCormick; Franz Halberg; John E. Pauly; J. Greco; M. De Bartolo; Bernard A. Nemchausky; Ervin Kaplan; Robert B. Sothern


JAMA | 1976

Classification Criteria for Systemic Lupus Erythematosus: Frequency in Normal Patients

Leon Wolf; Michael Sheahan; James B. McCormick; Beno Michel; Roland W. Moskowitz


American Journal of Clinical Pathology | 1967

Semi-micro prothrombin time test chamber.

James B. McCormick; Kopp Jb


American Journal of Clinical Pathology | 1959

Improved tissue-embedding method for paraffin and carbowax, using Tissue-Tek system.

James B. McCormick

Collaboration


Dive into the James B. McCormick's collaboration.

Top Co-Authors

Avatar

Eugene L. Kanabrocki

United States Department of Veterans Affairs

View shared research outputs
Top Co-Authors

Avatar

Lawrence E. Scheving

University of Arkansas for Medical Sciences

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Bernard A. Nemchausky

United States Department of Veterans Affairs

View shared research outputs
Top Co-Authors

Avatar

J. H. Olwin

Rush University Medical Center

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Ervin Kaplan

United States Department of Veterans Affairs

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar

J. Greco

United States Department of Veterans Affairs

View shared research outputs
Top Co-Authors

Avatar

Susan Dawson

Swedish Covenant Hospital

View shared research outputs
Researchain Logo
Decentralizing Knowledge