TY - JOUR
T1 - Clinical efulness of Measurement of Serum Fructosamine in Diabetics
T2 - Influence of Renal Failure, Liver Cirrhosis, and Thyroid Dysfunction
AU - Sako, Yasuhiro
AU - Umeda, Fumio
AU - Hashimoto, Toshihiko
AU - Inoguchi, Toyoshi
AU - Mimura, Kazuo
AU - Kunisaki, Makoto
AU - Tajiri, Yuji
AU - Ishii, Hidehiro
AU - Yamashita, Tsukasa
AU - Yamauchi, Teruaki
AU - Nawata, Hajime
N1 - Copyright:
Copyright 2016 Elsevier B.V., All rights reserved.
PY - 1988
Y1 - 1988
N2 - Measurement of serum fructosamine (FRA) by means of a Roche kit is a simple and reliable method for estimating glycosylated serum proteins. The level of FRA can be affected by hyperglycemia in diabetics and an abnormal metabolic state of serum proteins such as albumin in patients with renal failure, liver cirrhosis, and thyroid dysfunction. We measured FRA in diabetics and these patients. The average FRA level was 2.58 ± 0.08 (mean ± SE) mmol/l in the normal controls (n=18), 4.60±0.67 in patients with IDDM (n=8), and 3.61±0.10 in patients with NIDDM (n=63). In the patients with non-diabetic renal failure, while the FRA level was significantly (p<0.05) low, FRA corrected by total protein concentration was not different from that of the normal controls. The FRA level in liver cirrhosis without hyperbilirubinemia was not significantly different from that of normal controls. In the patients with thyroid disease, the FRA level was 2.08±0.03 in hyperthyroidism and 3. 11 ±0.07 in hypothyroidism. Moreover, the FRA level was negatively correlated with the thyroid hormones T3 and T4 (p<0.001). It is concluded that measurement of FRA is clinically useful for evaluating short-term glycemic control in diabetics even when there is complicating nephropathy or liver cirrhosis. However, its level in diabetic patients with hyperbilirubinemia or thyroid dysfunction must be cautiously interpreted.
AB - Measurement of serum fructosamine (FRA) by means of a Roche kit is a simple and reliable method for estimating glycosylated serum proteins. The level of FRA can be affected by hyperglycemia in diabetics and an abnormal metabolic state of serum proteins such as albumin in patients with renal failure, liver cirrhosis, and thyroid dysfunction. We measured FRA in diabetics and these patients. The average FRA level was 2.58 ± 0.08 (mean ± SE) mmol/l in the normal controls (n=18), 4.60±0.67 in patients with IDDM (n=8), and 3.61±0.10 in patients with NIDDM (n=63). In the patients with non-diabetic renal failure, while the FRA level was significantly (p<0.05) low, FRA corrected by total protein concentration was not different from that of the normal controls. The FRA level in liver cirrhosis without hyperbilirubinemia was not significantly different from that of normal controls. In the patients with thyroid disease, the FRA level was 2.08±0.03 in hyperthyroidism and 3. 11 ±0.07 in hypothyroidism. Moreover, the FRA level was negatively correlated with the thyroid hormones T3 and T4 (p<0.001). It is concluded that measurement of FRA is clinically useful for evaluating short-term glycemic control in diabetics even when there is complicating nephropathy or liver cirrhosis. However, its level in diabetic patients with hyperbilirubinemia or thyroid dysfunction must be cautiously interpreted.
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U2 - 10.11213/tonyobyo1958.31.929
DO - 10.11213/tonyobyo1958.31.929
M3 - Article
AN - SCOPUS:85007978583
SN - 0021-437X
VL - 31
SP - 929
EP - 935
JO - Journal of the Japan Diabetes Society
JF - Journal of the Japan Diabetes Society
IS - 12
ER -