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Biomedical subjects

A Helgesen

Publications and source records attributed to A Helgesen.

6 recordsLinked to original sources

The regional distribution of diabetic retinopathy lesions may reflect risk factors for progression of the disease.

BACKGROUND: Diabetic retinopathy is graded by semi-quantitative assessment of the morphological lesions as seen on fundus photographs. This grading method mainly considers the type and number of retinopathy lesions, implying that the diagnostic value of the regional distribution of retinopathy lesions is largely unknown. DESIGN AND METHODS: Case control design. The study group consisted of fifteen diabetic patients successively examined in a screening clinic, with retinopathy lesions predominantly around the larger vascular arcades. The control group consisted of fifteen patients pairwise matched with the patients in the study group regarding sex, age, diabetes type, and diabetes duration. The two groups were compared with respect to the distribution of individual retinal lesions (microaneurysms/dot haemorrhages, blot haemorrhages, cotton wool spots, and hard exudates) around the larger vascular arcades and in the macular area, hypertensive vascular abnormalities (crossing phenomena, arteriolar narrowing, arteriolar light reflex), metabolic regulation, and blood pressure. RESULTS: The patients in the study group had significantly more microaneurysms and haemorrhages around the larger vascular arcades than had the control group, but there was no difference between the vascular changes in the two groups. The study group had significantly higher blood pressure than had the control group, whereas there was no significant difference in metabolic regulation between the two groups. CONCLUSIONS: The findings suggest the existence of a hypertensive-like retinopathy in diabetic patients with lesions mainly around the larger vascular arcades, but with no increase in hypertensive vascular changes. This pattern is not identified with current semi-quantitative grading methods. Further improvement of clinical decisions made from fundus photographs of diabetic retinopathy requires the development of computerised methods for quantitative assessment of retinal lesions.

Adolescent↗

[Villous adenoma of the rectum with electrolyte imbalance. McKittrick-Wheelock syndrome].

We present a case of villous adenoma of the rectum, associated with severe fluid imbalance in a 69 year-old, previously healthy woman. Severe dehydration with hyponatraemia, hypokalaemia, acidosis/alkalosis and watery diarrhoea is typical. Clinical presentation may include fatigue, confusion, convulsions or coma. Intensive rehydration is the primary intervention, and causal treatment is always surgery. Normally full recovery is achieved.

Adenoma↗

HLA antigens in multiple sclerosis.

The frequency of the MLC activating HLA-Dw2 determinant was found significantly increased to 68% among 37 patients with long-standing multiple sclerosis, compared to 30.2% among healthy controls. A similar (or stronger) degree of association was found with an "Ia-like" B cell specificity, SOW, while the association with HLA-B7 was less apparent. No correlation between HLA-Dw2 and signs of local synthesis of oligoclonal IgG or measles or rubella virus antibodies in the CNS was observed.

B-Lymphocytes↗

Identification of five lymphocyte activating determinants in man.

Eleven putative LD-1 locus homozygous cell donors were found by MLC tests in non-consanguineous families. Lymphocytes from each of them were used as stimulating typing cells in MLC tests together with responding cells from the other homozygous cell donors and from 45 random unrelated individuals. Four of the stimulating typing cells were found to identify a determinant in non-random association with HL-A7; LD-7a, three other cells typed for a determinant non-randomly associated with HL-A8; LD-8a, and one cell seems to identify LD-W5 in non-random association with W5. Two possible additional LD-1 determinants, LD-oh and LD-om, were less well defined with two of the cells. The combined gene frequency of the five possible LD-1 determinants is approximately 0.45 among Norwegians.

Alleles↗