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Biomedical subjects

H Enomoto

Publications and source records attributed to H Enomoto.

At least 199 records · Page 11Linked to original sources

A comparative study of serum alpha 1-microglobulin and beta 2-microglobulin levels in cancerous and other diseases.

The levels of serum alpha 1-microglobulin in 60 normal persons and in 191 patients suffering from a variety of benign and malignant disorders were determined by an enzyme immunoassay, and these values were compared with the levels of beta 2-microglobulin. A discrepancy between the serum levels of these proteins was found in hepatobiliary disorders; that is, an increased serum level of beta 2-microglobulin was observed in 73.9%, while in only 4.3% was there an elevation of alpha 1-microglobulin. In particular, alpha 1-microglobulin levels in patients with liver cirrhosis were well below the normal range, while beta 2-microglobulin levels were elevated. Elevated levels of both proteins were noted in patients with some impairments of renal function, particularly in chronic renal failure, and in immunological diseases. In 81 patients with neoplastic diseases, a high alpha 1-microglobulin value was found in only 15 patients (16.4%), while a high beta 2-microglobulin value in 62 patients (76.5%). The serum levels of both alpha 1-microglobulin and beta 2-microglobulin were especially high in plasma cell dyscrasia with Bence Jones protein, but other neoplastic diseases were mostly associated with beta 2-microglobulin elevation alone.

Adult↗

[The method of T4 radioimmunoassay using filter paper blood samples and its application for the early detection of neonatal hypothyroidism (author's transl)].

We examined the method of radioimmunoassay of the Disc T4 (dried blood spot T4) for the purpose of mass screening of neonatal hypothyroidism and tried the parallel assay of T4 and TSH in dried blood spotted on filter paper at the fifth day of life, and we compared the results. By changing the volumes of T4 antibody and T4 antigen solutions, it is possible to measure thyroxine using two discs 3mm in diameter. Disc T4 values obtained in 45 unknown samples by this method were in good correlation with serum T4 values of the same subjects (Y = 0.97X + 0.06). The coefficients of variation were 5.6 to 18.9% in the range of 5.3 to 10.7 micrograms/100ml of Disc T4 (within assay), and 7.9 to 20.8% in the range of 2.4 to 10.3 micrograms/100ml of Disc T4 (between assay). We measured both Disc T4 and Disc TSH of 26,067 newborn infants born between June 1978 and May 1979. Out of 26,067 measurements, four cases of primary hypothyroidism, fourteen cases of TBG deficiency and two cases of transient hypothyroidism were discovered. Out of the four cases of primary hypothyroidism, three showed low Disc T4 (1.3 to 4.0 micrograms/100ml) and high Disc TSH (200 to 240 micromicrons/ml), one showed normal Disc T4 (7.1 micrograms/100ml) and high Disc TSH (30 micromicrons/ml). It was thought the last case might be mild hypothyroidism. In 14 cases of TBG deficiency, Disc T4 was not detectable to 3.4 micrograms/100ml while Disc TSH was within the normal range. In two cases of transient hypothyroidism, Disc T4 measurements showed normal range (6.5, 10.6 micrograms/100ml), and Disc TSH showed high values (41, 120 micromicrons/ml). Therefore, Disc TSH was more sensitive and showed less false positive cases than did Disc T4 for screening hypothyroidism. Although no secondary hypothyroidism existed in the 26,067 measurements, it continues to be important to measure Disc T4 for the discovery of secondary or tertiary hypothyroidism.

Congenital Hypothyroidism↗

Human alpha 1-microglobulin levels in various body fluids.

alpha 1-Microglobulin levels in serum and urine were estimated by using single radial immunodiffusion, resulting in the following mean values: umbilical cord blood serum, 40.6 mg/l; normal adult serum, 44.2 mg/l; and normal urine, 5.7 mg/24 h urine volume. Slightly higher levels of serum alpha 1-microglobulin were found in infants and the aged. Serum and urine alpha 1-microglobulin levels in patients with renal failure, however, were greatly increased, mean levels being 231.5 mg/l and 100.7 mg/24 h urine volume, respectively. Serum alpha 1-microglobulin levels in these patients correlated well with both serum creatinine and beta 2-microglobulin levels. Serum alpha 1-microglobulin level did not correlate positively with serum levels of other plasma proteins, such as alpha 1-antitrypsin, haptoglobin, complement, etc. Ouchterlony immunodiffusion also revealed the presence of alpha 1-microglobulin in synovial fluid, ascites, pleural effusion, amniotic fluid, cyst fluid, and cerebrospinal fluid. The levels of alpha 1-microglobulin in these fluids were measured by single radial immunodiffusion, except that its level in cerebrospinal fluid was measured by radioimmunoassay. Mean alpha 1-microglobulin concentration was 20.8 mg/l in synovial fluid, 28.7 mg/l in ascites, 21.5 mg/l in pleural effusion, 2.7 mg/l in amniotic fluid, 8.2 mg/l in cyst fluid, and 42.3 ng/ml in cerebrospinal fluid.

Alpha-Globulins↗

[Early detection of congenital hypothyroidism by TSH radioimmunoassay using filter paper blood samples (author's transl)].

It has been reported that mental retardation due to congenital hypothyroidism can be prevented by early detection and early adequate replacement therapy. We have developed a radioimmunoassay for TSH using the dried blood spot and have started screening for newborn congenital hypothyroidism using a part of sample of the inborn metabolic error screening. (1) The dried blood spot TSH of 61,000 newborn infants was assayed in the first half of our screening and that of 74,505 newborn infants was assayed in the latter half of our screening. As a result, although we were not able to detect any cases in the first screening, we were able to detect 9 cases of congenital hypothyroidism in the latter screening. From the results obtained through our investigation of the thyroid function of these 9 infants, we confirmed that mild hypothyroidism can be better detected by the screening of TSH. (2) As to the program of the screening, we chose from the latter half of our screening all the samples in which TSH concentrations contained above 3 percent of each assay and were remeasured on the next assay. (3) As we confirmed that the sensitivity of measurement was increased at very low concentrations, when the volume of antibodies, radioisotopes and eluates used for each assay were decreased, we measured TSH successfully using two 3 mm discs. (4) As we can perform very simple screening by the 3 mm disc method, we are changing the screening method from that with 10 mm disc to one with two 3 mm discs. We intend to extend our screening, and will make every effort to prevent mental retardation due to congenital hypothyroidism.

Blood Preservation↗