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Biomedical subjects

T Sahi

Publications and source records attributed to T Sahi.

34 records · Page 2Linked to original sources
PubMed1983

Etiology of mild acute infectious myocarditis. Relation to clinical features.

The etiology of mild myocarditis, diagnosed on the basis of serial ECG changes during an acute infection, was studied in 126 consecutive conscripts. A fourfold rise in the antibody titers in the paired serum samples was required for a positive etiologic diagnosis. An etiologic diagnosis was made probable in 47% of the patients. Adenovirus was incriminated in 19 patients, vaccinia in 12, influenza A in eight, beta-hemolytic Streptococcus in six, mononucleosis in five and Mycoplasma in three. Chlamydia, influenza B and Coxsackie B4 were each found in two patients; parainfluenza, mumps and adult Still's disease were each found in one patient. The incidence of vaccinia myocarditis was 1/10000 smallpox vaccinations. Clear-cut myopericarditis was usually noted during vaccinia, mononucleosis, Mycoplasma, Chlamydia and Coxsackie B4 infections. Adenovirus and influenza A myocarditis was most often subclinical, being mostly detected only because of ECG screening of patients without cardiac symptoms. Frequent recent ventricular extrasystoles were most often triggered by a beta-hemolytic Streptococcus infection. The etiology of infectious myocarditis seems to reflect the overall profile of viruses and other infective agents in the study population at that particular time. Cardiotrophic viruses such as Coxsackie B only rarely cause myocarditis outside epidemics.

Acute Disease↗
PubMed1983

Hypolactasia in a fixed cohort of young Finnish adults. A follow-up study.

Selective late-onset hypolactasia (lactose malabsorption) was examined in a fixed cohort of Finnish adolescents, now aged 17 to 25 years. This was the third examination of the same subjects. In the first examination 10 years ago the prevalence of hypolactasia was 6.2%. In the second examination 5 years ago three more cases of hypolactasia were diagnosed, and the prevalence was 9.3%. In this examination the prevalence was 10.3% (10/97); 2 newly manifested hypolactasia cases were diagnosed. If those subjects were included who were not examined this time but whose hypolactasia was diagnosed previously or who were at least 20 years old at the second examination, the prevalence of hypolactasia was 12.7% (13/102). In the 17- to 20-year-olds the prevalence was 15.4%, and in the 21- to 25-year-olds it was 11.1%. The results were in agreement with our previous conclusions that hypolactasia manifests itself in the Finnish population mostly between 10 and 20 years of age and that the prevalence in adults is 17%. Eight of the 13 subjects with hypolactasia had weekly abdominal symptoms; all except one of them had symptoms after the lactose tolerance test. Nine subjects had realized milk intolerance; six of them had symptoms from one glass of milk or less. Symptoms varied considerably from person to person, the commonest symptom being meteorism. The reason was probably the variation in the remaining small-intestinal lactase activity and in the functional stability of the colon.

Adolescent↗
PubMed1983

Resting- and postexercise-ECG findings in an adult Lapp population.

Resting electrocardiograms were recorded in 412 and postexercise-ECGs in 186 Lapp men and women over the age of 40. Abnormalities in the resting-ECG suggestive of old myocardial infarction by the Minnesota code were found in 7% of the men and in 1% of the women. ST-depression compatible with myocardial ischaemia in the resting-ECG were found in 3% of men aged 40-49 years and in 5% of women of the same age; and increased with age up to 11% and 24% in men and women, respectively, over the age of 60. Postexercise ST-depressions of "ischemic type" were found in 18% of the men and in 13% of the women, but there was no clear age dependence. The frequency of high amplitude R-waves of the left type was high compared with most normal populations, especially in men (29%). These prevalences were very similar to those previously reported in a Finnish population.

Adult↗
PubMed1978

Manifestation and occurrence of selective adult-type lactose malabsorption in Finnish teenagers. A follow-up study.

In 1969--1970, a simple random sample of 129 Finnish school-aged children was examined to study selective adult-type lactose malabsorption (SLM) in this age category. SLM was found in 8 children. All subjects were reexamined 5 years later. SLM was reconfirmed in these 8 persons and found in 3 additional subjects who had normal lactose absorption in the first examination. The prevalence of SLM was 9.3%, being 8.5% in the age category 12--15 years and 9.9% in that 16--20 years. Low rise of blood glucose in the lactose tolerance test of the first examination, very low milk consumption, milk intolerance, and history of gastrointestinal symptoms were found to be of low predictive value as indicators of SLM. It was also concluded that information about dietetic sources of lactose is important to persons with SLM, but categorical exclusion of lactose from the diet is not necessary, at least in the Finnish population.

Adolescent↗
PubMed1977

Serum lipids and proteins in lactose malabsorption.

It has been suggested that dietary lactose may reduce the intestinal absorption of fat and protein in individuals with lactase deficiency. On the other hand, it is known that a high carbohydrate diet increases serum lipids. The purpose of this study was to examine whether there are differences in the fasting serum lipid and protein concentrations between people with lactose malabsorption and people with normal lactose absorption. Therefore in the connection of a family study serum lipids and proteins were measured in 409 subjects belonging to 11 families. Of these 288 were relatives of the 11 index persons and 121 were spouses or relatives of the spouses. The weight, height, and milk consumption of each person were recorded. When the age, sex, relative weight and milk consumption effects were taken into account there was a statistical difference between the lactose malabsorption and lactose absorption groups for the concentration of serum triglycerides, but not for the other variables. Besides, serum triglyceride values of over 200 mg/100 ml were significantly fewer in people with lactose malabsorption. It was hypothesized that increased intestinal motility may disturb the absorption of fats and cause the observed difference at least in the Finnish population.

Adolescent↗
PubMed1977

More evidence for the recessive inheritance of selective adult type lactose malabsorption.

Selective adult type lactose malabsorption appears in childhood or adolescence because of the great decline in jejunal lactase activity. There is strong evidence that this is a genetically determined disorder. Specifically, selective adult type lactose malabsorptions seem to be inherited by a single autosomal recessive gene. In the present prospective study the transition from the state of lactose absorption to that of lactose malabsorption was documented for the first time in two Finnish boys who were at risk for selective adult type lactose malabsorption because the parents of both boys had the disorder. At the age of 14 and 9 years, respectively, the boys had normal lactose absorption. Three years and 7 months and 4 years and 5 months later, respectively, the boys were shown to have lactose malabsorption. The period of documented transition averaged less than 4 years. These manifestations clearly strengthen the genetic model proposed.

Adolescent↗