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1.
Ugeskr Laeger ; 153(40): 2836-7, 1991 Sep 30.
Article in Danish | MEDLINE | ID: mdl-1926623

ABSTRACT

We report a typical case of histiocytic necrotizing lymphadenitis (Kikuchi's disease). To our knowledge this is the first reported case in Denmark. Histiocytic necrotizing lymphadenitis is a benign self-limiting disorder, which mainly involves the cervical lymph nodes. The disease commonly affects young women of Asian origin, but it is seen more and more often in other populations. Clinically and histologically it can be misdiagnosed as malignant lymphoma. The etiology is unknown.


Subject(s)
Histiocytosis/pathology , Lymphadenitis/pathology , Adult , Denmark , Female , Humans , Necrosis , Syndrome , Vietnam/ethnology
3.
Acta Endocrinol (Copenh) ; 125(2): 127-31, 1991 Aug.
Article in English | MEDLINE | ID: mdl-1897329

ABSTRACT

Circulating levels of calciotropic hormones were measured during one year of treatment with either 200 IU of salmon calcitonin daily or placebo as a nasal spray in 20 postmenopausal women with a former Colles' fracture. A supplement of 0.5 gram elemental calcium was given to all participants. Serum levels of parathyroid hormone and human calcitonin were determined with radioimmunoassays, and serum levels of vitamin D metabolites were determined with protein binding assays. We did not find any significant differences between the two groups with respect to serum levels of calciotropic hormones. In the salmon calcitonin treated group there was a tendency towards a small decrease in serum levels of human calcitonin and an increase in serum levels of calcitriol. Our results suggest that treatment with 200 IU of salmon calcitonin daily as a nasal spray does not markedly affect fasting serum levels of parathyroid hormone, human calcitonin, and vitamin D metabolites.


Subject(s)
Calcitonin/pharmacology , Calcitriol/blood , Parathyroid Hormone/blood , Administration, Intranasal , Aged , Animals , Calcitonin/blood , Female , Humans , Middle Aged , Time Factors
4.
Ugeskr Laeger ; 153(27): 1914-20, 1991 Jul 01.
Article in Danish | MEDLINE | ID: mdl-1858170

ABSTRACT

Cross-section regression analyses of some of the world's populations suggest a direct linear relationship between mean blood pressure and mean salt-intake. Since such investigations have hitherto been partly based on information about dietary salt intake, which is a questionable measure, we performed an analysis including 28 male populations and an analysis including 21 female populations solely based on 24 hour sodium urinary excretion. The regression analysis confirmed that a direct linear relationship between blood pressure and 24 hour sodium urinary excretion existed, since the blood pressure in a population was about 7 mmHg/6 mmHg higher than in a population which consumed 100 mmol less salt. We were, however, not able to correct for confounders. This was done in the recently published "Intersalt" study in which the linear relationship between median blood pressure and median salt intake disappeared after correction for weight and alcohol intake. From the regression coefficients from "Intersalt" it can be deduced that a reduction in salt intake from 150 mmol to 75 mmol may reduce blood pressure by 1.6/0.05 mmHg. Most epidemiological studies have not been able to demonstrate a correlation between salt intake and blood pressure within population. Still, on the basis of uncontrolled clinical studies it has been claimed that salt-restriction may reduce blood pressure. Consequently we also performed a meta-analysis of 15 controlled clinical trials dealing with the effect of salt-restriction on blood pressure within a population. This meta-analysis including 704 patients showed that a reduction in average salt intake from 150 mmol to 75 mmol may reduce blood pressure by 2.4/1.4 mmHg.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Diet, Sodium-Restricted , Hypertension/prevention & control , Meta-Analysis as Topic , Blood Pressure Determination , Female , Humans , Male , Regression Analysis , Sodium/urine
5.
Calcif Tissue Int ; 48(5): 302-7, 1991 May.
Article in English | MEDLINE | ID: mdl-2054714

ABSTRACT

Forty postmenopausal women with a former Colles' fracture were enrolled in a 1-year study to determine the dose-effect relationship of nasal salmon calcitonin (SCT) on bone mass. They were randomized to receive either placebo, 50, 100, or 200 IU per day of SCT given as a nasal spray. The rate of change in the bone mineral content of the lumbar spine was 0.7, 0.2, 1.1, and 2.0 gHA per year, respectively, and the rate of change in the bone mineral content in the forearm was -0.4, -0.1, 0.0, and -0.1 AU per year, respectively. The rate of change in the bone mineral content of the lumbar spine in patients receiving 200 IU of SCT per day differed significantly from zero (P less than 0.01). Except for one patient, who experienced intolerable nausea, no systemic side effects were observed. Seven patients withdrew, two patients from nasal intolerance to the spray. These preliminary data suggest that SCT given by the nasal route has a positive and dose-dependent effect on spinal bone mass, but affects forearm bone mass only minimally.


Subject(s)
Bone Density/drug effects , Calcitonin/administration & dosage , Osteoporosis, Postmenopausal/drug therapy , Administration, Intranasal , Aged , Bone Density/physiology , Calcitonin/adverse effects , Dose-Response Relationship, Drug , Double-Blind Method , Female , Humans , Middle Aged , Osteoporosis, Postmenopausal/metabolism
6.
Calcif Tissue Int ; 46(1): 5-8, 1990 Jan.
Article in English | MEDLINE | ID: mdl-2153040

ABSTRACT

To investigate the effect of low doses of intranasal salmon calcitonin on plasma cyclic AMP (cAMP) and serum ionized calcium, 40 healthy postmenopausal women were randomized to receive a single dose of either placebo or 50, 100, or 200 IU of salmon calcitonin as a nasal spray. Blood samples were collected throughout an 8-hour period. None of the doses could provoke detectable hypocalcemia, whereas 100 and 200 IU of salmon calcitonin were associated with an increase in plasma cAMP after 15 minutes. Measurable plasma levels of salmon calcitonin were demonstrated in all active treatment groups, and the calculated areas under the curves showed a dose-dependent increase.


Subject(s)
Calcitonin/pharmacology , Calcium/blood , Cyclic AMP/blood , Administration, Inhalation , Aged , Calcitonin/administration & dosage , Calcitonin/blood , Calcitonin/metabolism , Cyclic AMP/metabolism , Dose-Response Relationship, Drug , Female , Humans , Middle Aged , Random Allocation
7.
Eur J Obstet Gynecol Reprod Biol ; 27(3): 197-201, 1988 Mar.
Article in English | MEDLINE | ID: mdl-2965038

ABSTRACT

Atrial natriuretic peptide (ANP) is a recently discovered cardiac hormone involved in blood-volume homeostasis. Known stimulating factors for ANP release are rise in atrial pressures or atrial distension, suggesting that blood volume regulates ANP release. This study was undertaken to test the hypothesis that plasma levels of ANP are high and increase during normal pregnancy secondary to the expanding plasma volume. In a cross-sectional study plasma concentrations of ANP were measured in 99 normal pregnant women at different gestational ages and compared with the values found in an age-matched non-pregnant control group. Mean plasma ANP was already significantly increased in the first trimester as opposed to the non-pregnant women, but despite a continuously expanded plasma volume there was no further increase during pregnancy. Our findings suggest that other factors must interact with plasma volume in regulating plasma ANP during pregnancy.


Subject(s)
Atrial Natriuretic Factor/blood , Pregnancy/blood , Adult , Blood Pressure , Body Weight , Female , Heart Rate , Humans , Pregnancy Trimester, First , Pregnancy Trimester, Second , Pregnancy Trimester, Third
8.
Calcif Tissue Int ; 42(3): 157-61, 1988 Mar.
Article in English | MEDLINE | ID: mdl-3130164

ABSTRACT

A new method for measuring the bone mineral content (BMC) of the mandible by dual-photon absorptiometry (DPA) has recently been introduced. The purpose of the present investigation therefore was to examine the long-term precision for 32 months in vitro and in vivo for assessment of BMC in the mandible and to examine the relationship in vivo among BMC of the mandible, the forearms, and the lumbar spine as measured by DPA and/or single-photon absorptiometry (SPA). For comparison, the relationship between forearm BMC as measured by DPA and SPA was studied. The long-term precision of the mandibular BMC was 0.8% in vitro, independent of age and change of radioactive source, and 2.1% by assessment in vivo. A significant relationship (P less than 0.01) was found between BMC of the lumbar spine and the forearms and between the two sets of forearm BMC measured by DPA and SPA. Thus, relative BMC changes of the forearms can be compared without respect to type of forearm bone scanner used. The BMC changes of the mandible can only be evaluated by scanning of the mandible itself. The present DPA bone scanner is suitable for follow-up analyses of the BMC changes of the mandible and the forearms.


Subject(s)
Mandible/diagnostic imaging , Minerals/analysis , Radius/diagnostic imaging , Spine/diagnostic imaging , Ulna/diagnostic imaging , Adult , Bone and Bones/analysis , Female , Forearm/diagnostic imaging , Humans , In Vitro Techniques , Male , Radionuclide Imaging
9.
Scand J Clin Lab Invest ; 47(7): 745-8, 1987 Nov.
Article in English | MEDLINE | ID: mdl-2961046

ABSTRACT

A highly sensitive and accurate radio-immunoassay for measurement of atrial natriuretic peptide in human plasma has been established. All reagents are commercially available. The sensitivity of the method is 1 pmol/l. The 50% intercept of the standard curve was at 22 fmol/tube and inter- and intra-assay precision were 10.9 and 5.3%, respectively. Plasma immunoreactive atrial natriuretic peptide levels measured in healthy subjects, during pregnancy, and in congestive cardiac failure were within the limits reported in the literature.


Subject(s)
Atrial Natriuretic Factor/blood , Heart Failure/blood , Pregnancy/blood , Adult , Female , Humans , Male , Middle Aged , Radioimmunoassay/methods , Reference Values
11.
Br Med J (Clin Res Ed) ; 294(6586): 1508-10, 1987 Jun 13.
Article in English | MEDLINE | ID: mdl-2955845

ABSTRACT

The concentration of plasma immunoreactive atrial natriuretic peptide is positively associated with right atrial and pulmonary capillary wedge pressure, suggesting that blood volume and hence atrial pressure govern its release. Expansion of plasma volume is a central physiological adjustment in normal pregnancy. Conversely, pregnancies complicated by pre-eclampsia are associated with a reduction in plasma volume and central venous pressure. A study was therefore undertaken to test the hypothesis that plasma atrial natriuretic peptide concentrations are low in pre-eclampsia owing to deficient secretion. Concentrations of the peptide were measured by a specific radioimmunoassay. The mean plasma immunoreactive atrial natriuretic peptide concentration in healthy pregnant women (n = 22; third trimester) was higher (56 (1 SD 29) ng/l) than in 25 young, non-pregnant controls (37 (19) ng/l). Concentrations in patients suffering from mild pre-eclampsia (n = 9) were higher (127 (60) ng/l) than in normal pregnant women, and in patients with severe pre-eclampsia (n = 6) concentrations were higher still (392 (225) ng/l). Despite failure of plasma volume expansion and low central venous and pulmonary capillary wedge pressures in pre-eclampsia this condition is associated with greatly increased plasma concentrations of plasma immunoreactive atrial natriuretic peptide, which increase still further with the severity of the disease. These findings are clear evidence that atrial pressure may not be the principal determinant of the release of the natriuretic peptide in pre-eclampsia.


Subject(s)
Atrial Natriuretic Factor/blood , Pre-Eclampsia/blood , Adult , Female , Humans , Pregnancy , Radioimmunoassay
12.
Am J Cardiol ; 59(14): 73G-77G, 1987 May 29.
Article in English | MEDLINE | ID: mdl-2884856

ABSTRACT

In a double-blind multicenter study, the new alpha 1-adrenoceptor inhibitor doxazosin was compared with atenolol for efficacy, safety and effect on serum lipids. One hundred and twenty-six patients with mild to moderate hypertension were randomly assigned to receive either doxazosin (n = 63) or atenolol (n = 63). The mean final dosages, administered once daily, to obtain 24-hour blood pressure (BP) control were doxazosin 12 mg (range 1 to 16) and atenolol 91.8 mg (range 50 to 100). Of 12 doxazosin and 7 atenolol patient withdrawals from the study, 7 doxazosin and 4 atenolol patients withdrew for treatment-related reasons. No statistically significant differences between treatment groups were found after 20 weeks in changes from baseline in standing and sitting BPs measured 24 hours after administration. Sitting BP (systolic/diastolic) was reduced by 10.5/9.8 mm Hg after doxazosin treatment and by 10.9/10.7 mm Hg after atenolol therapy. Standing BP was reduced by 8.8/7.7 mm Hg after doxazosin administration and 9.7/9.3 mm Hg after treatment with atenolol. Supine BP was measured in a small cohort of the study population, and doxazosin had a smaller effect than atenolol. After 20 weeks of treatment, both drugs reduced heart rate with atenolol producing a statistically significantly greater decrease than doxazosin (standing, doxazosin 5 beats/min, atenolol 16.2 beats/min, p less than 0.001; sitting, doxazosin 5 beats/min, atenolol 13.1 beats/min, p less than 0.001). Side effects were reported by 37 patients receiving doxazosin therapy and 34 patients receiving atenolol therapy.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Adrenergic alpha-Antagonists/therapeutic use , Antihypertensive Agents/therapeutic use , Atenolol/therapeutic use , Hypertension/drug therapy , Prazosin/analogs & derivatives , Adrenergic alpha-Antagonists/adverse effects , Adult , Aged , Antihypertensive Agents/adverse effects , Atenolol/adverse effects , Clinical Trials as Topic , Double-Blind Method , Doxazosin , Female , Heart Rate/drug effects , Humans , Hypertension/blood , Lipoproteins/blood , Male , Middle Aged , Prazosin/adverse effects , Prazosin/therapeutic use
13.
J Clin Pharmacol ; 27(1): 18-21, 1987 Jan.
Article in English | MEDLINE | ID: mdl-3316301

ABSTRACT

Tiapamil is an investigational calcium-channel antagonist that is chemically related to verapamil. The antihypertensive efficacies of tiapamil and hydrochlorothiazide (HCTZ) were compared in a randomized double-blind trial. Thirty patients, age 44 to 80 years, with mild to moderate hypertension (World Health Organization stage I-II) entered and completed the study. Previous therapy, if any, was stopped for at least one week prior to study initiation, and patients received placebo tablets for two weeks. The participants were then given active medication, which was titrated for the next three weeks; HCTZ 25 to 50 mg bid or tiapamil 300 to 600 mg bid was given until supine diastolic blood pressure (BP) was no higher than 90 mm Hg or the ceiling dose was reached. Both drugs caused a significant reduction in systolic as well as in diastolic blood pressure (P less than .01). The reduction was seen in both the supine and erect position. The median decrease in supine systolic blood pressure from baseline to the end of treatment was 20 mm Hg in the tiapamil group and 27 mm Hg in the hydrochlorothiazide group, whereas the median decrease in supine diastolic blood pressure was 14 mm Hg and 18 mm Hg, respectively. The median difference in supine diastolic BP reduction after HCTZ and tiapamil administration was 3.8 mm Hg (not significant). There were no significant changes in heart rate. Dizziness occurred in one patient taking tiapamil and in three receiving HCTZ. One patient receiving HCTZ developed acute arthritis urica.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Calcium Channel Blockers/therapeutic use , Hydrochlorothiazide/therapeutic use , Hypertension/drug therapy , Propylamines/therapeutic use , Adult , Aged , Aged, 80 and over , Calcium Channel Blockers/adverse effects , Clinical Trials as Topic , Double-Blind Method , Female , Humans , Hydrochlorothiazide/adverse effects , Male , Middle Aged , Propylamines/adverse effects , Random Allocation , Tiapamil Hydrochloride
15.
Acta Med Scand ; 219(2): 215-9, 1986.
Article in English | MEDLINE | ID: mdl-3485891

ABSTRACT

Sunshine exposure increased the serum concentration of 25-hydroxyvitamin D (25-OHD) in 9 hemodialyzed patients. Mean 1,25-dihydroxyvitamin D (1,25-(OH)2D) was unchanged, but in two patients with low initial 25-OHD values this increase was accompanied by a rise in circulating 1,25-(OH)2D, although not to normal levels. One hemodialyzed patient developed liver insufficiency with a resultant reduction of serum 25-OHD concentration accompanied by a decrease in serum 1,25-(OH)2D concentration. The results indicate that the circulating levels of 1,25-(OH)2D in patients with end-stage renal failure are to some extent regulated by the serum 25-OHD concentrations. Injection of parathyroid hormone (PTH) induced minor increases in serum concentrations of 1,25-(OH)2D in patients with end-stage renal failure and even in anephric patients, suggesting the existence of an extrarenal PTH-sensitive 1-alpha-hydroxylase. However, the enzyme was stimulated by supraphysiological concentrations of PTH, and therefore not necessarily of importance in the normal regulation of calcium metabolism.


Subject(s)
Dihydroxycholecalciferols/metabolism , Kidney Diseases/metabolism , Nephrectomy , Parathyroid Hormone/administration & dosage , Renal Dialysis , Sunlight , 24,25-Dihydroxyvitamin D 3 , Adult , Female , Humans , Hydroxycholecalciferols/metabolism , Injections, Intravenous , Male , Middle Aged , Mixed Function Oxygenases/metabolism
17.
Clin Rheumatol ; 4(2): 143-9, 1985 Jun.
Article in English | MEDLINE | ID: mdl-4006384

ABSTRACT

Long-term glucocorticoid treatment might interfere with the vitamin D metabolism. The serum concentrations of 25-OHD were significantly reduced whereas the circulating levels of 1,25-(OH)2D were normal in 50 patients with rheumatoid arthritis on long-term treatment with small doses of prednisone. The bone mineral content of the forearm was significantly reduced, but the degree of bone loss did not correlate with duration of treatment or dose of prednisone given. Quantitative bone histomorphometry was performed in 18 patients. Apart from a significant correlation between serum 25-OHD and the fractional trabecular bone volume, no relationships were observed between bone histomorphometry and vitamin D metabolites or serum iPTH. The results indicate that the bone loss was due to a decreased osteoblastic activity rather than to an impaired vitamin D metabolism.


Subject(s)
Arthritis, Rheumatoid/metabolism , Bone and Bones/metabolism , Glucocorticoids/adverse effects , Minerals/deficiency , Vitamin D/metabolism , Adult , Aged , Arthritis, Rheumatoid/drug therapy , Bone and Bones/pathology , Calcium/blood , Dihydroxycholecalciferols/blood , Female , Humans , Hydroxycholecalciferols/blood , Kidney/drug effects , Kidney/metabolism , Magnesium/blood , Male , Middle Aged , Parathyroid Hormone/blood , Phosphorus/blood , Time Factors
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