Decline in haemoglobin A1c values in diabetic patients receiving interferon-alpha and ribavirin for chronic hepatitis C

被引:18
作者
Greenberg, P. D.
Rosman, A. S.
Eldeiry, L. S.
Naqvi, Z.
Brau, N.
机构
[1] Bronx Veterans Affairs Med Ctr, Infect Dis Sect 111F, Bronx, NY 10468 USA
[2] CUNY Mt Sinai Sch Med, Div Endocrinol, New York, NY 10029 USA
[3] CUNY Mt Sinai Sch Med, Div Gastroenterol, New York, NY 10029 USA
[4] CUNY Mt Sinai Sch Med, Div Infect Dis, New York, NY 10029 USA
[5] CUNY Mt Sinai Sch Med, Div Liver Dis, New York, NY 10029 USA
关键词
diabetes mellitus; haemoglobin A1c; hepatitis C; interferon-alpha; ribavirin; therapy;
D O I
10.1111/j.1365-2893.2006.00729.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Haemoglobin A1c (A1c) levels are lower during haemolysis because of the shorter exposure of haemoglobin (Hb) to plasma glucose. Ribavirin (RBV) used in combination with interferon-alpha (IFN) for chronic hepatitis C causes reversible haemolytic anaemia. This study examined the extent to which RBV treatment influences A1c levels in diabetic patients. A retrospective analysis identified 32 diabetic patients who underwent hepatitis C treatment with IFN and RBV. Each subject had at least three measures of A1c, Hb and glucose: before, during and after therapy. A1c values decreased from a mean pretreatment level of 7.2% to an on-treatment A1c level of 5.2% [mean paired difference -2.01%; 95% confidence interval (CI) -1.59% to -2.43%; P < 0.001]. During therapy, mean Hb levels decreased from 15.1 g/dL at baseline to a nadir of 11.7 g/dL (P < 0.001) with a rise in lactose dehydrogenase levels and reticulocyte counts, and unchanged mean corpuscular volume values confirming haemolysis. At the same time, glucose levels declined by a mean of 38.4 mg/dL (95% CI 13.4-63.5 mg/dL; P = 0.002) as did body weights by a mean of 3.15 kg (P < 0.001). According to published glucose-A1c correlation tables, this decline of glucose concentration by 38.4 mg/dL correlates to a decline in A1c level of 1.08%. In conclusion, reductions of A1c levels by a mean of 2.01% during hepatitis C therapy with IFN + RBV are due to a combination of decreased glucose levels (1.08%) and RBV-induced haemolysis (0.93%). A1c levels should not be measured during hepatitis C treatment with IFN + RBV because they do not adequately reflect glycaemic control.
引用
收藏
页码:613 / 617
页数:5
相关论文
共 18 条
  • [1] American Diabetes Association, 2004, Diabetes Care, V27 Suppl 1, pS5, DOI 10.2337/diacare.27.2007.S5
  • [2] ATABANI GS, 1989, ACTA HAEMATOL-BASEL, V81, P140
  • [3] BIOSYNTHESIS OF HUMAN HEMOGLOBIN A1C - SLOW GLYCOSYLATION OF HEMOGLOBIN INVIVO
    BUNN, HF
    HANEY, DN
    KAMIN, S
    GABBAY, KH
    GALLOP, PM
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1976, 57 (06) : 1652 - 1659
  • [4] Hemolytic anemia induced by ribavirin therapy in patients with chronic hepatitis C virus infection: Role of membrane oxidative damage
    De Franceschi, L
    Fattovich, G
    Turrini, F
    Ayi, K
    Brugnara, C
    Manzato, F
    Noventa, F
    Stanzial, AM
    Solero, P
    Corrocher, R
    [J]. HEPATOLOGY, 2000, 31 (04) : 997 - 1004
  • [5] Ribavirin treatment for patients with chronic hepatitis C: Results of a placebo-controlled study
    Dusheiko, G
    Main, J
    Thomas, H
    Reichard, O
    Lee, C
    Dhillon, A
    Rassam, S
    Fryden, A
    Reesink, H
    Bassendine, M
    Norkrans, G
    Cuypers, T
    Lelie, N
    Telfer, P
    Watson, J
    Weegink, C
    Sillikens, P
    Weiland, O
    [J]. JOURNAL OF HEPATOLOGY, 1996, 25 (05) : 591 - 598
  • [6] EBERENTZLHOMME C, 1984, DIABETES METAB, V10, P304
  • [7] HO CH, 1990, EUR J HAEMATOL, V45, P139
  • [8] HISTOLOGICAL GRADING AND STAGING OF CHRONIC HEPATITIS
    ISHAK, K
    BAPTISTA, A
    BIANCHI, L
    CALLEA, F
    DEGROOTE, J
    GUDAT, F
    DENK, H
    DESMET, V
    KORB, G
    MACSWEEN, RNM
    PHILLIPS, MJ
    PORTMANN, BG
    POULSEN, H
    SCHEUER, PJ
    SCHMID, M
    THALER, H
    [J]. JOURNAL OF HEPATOLOGY, 1995, 22 (06): : 696 - 699
  • [9] Interferon-α improves glucose tolerance in diabetic and non-diabetic patients with HCV-induced liver disease
    Konrad, T
    Vicini, P
    Zeuzem, S
    Toffolo, G
    Briem, D
    Lormann, J
    Herrmann, G
    Wittmann, D
    Lenz, T
    Kusterer, K
    Teuber, G
    Cobelli, C
    Usadel, KH
    [J]. EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES, 1999, 107 (06) : 343 - 349
  • [10] Lindsey Cameron C, 2004, Diabetes Technol Ther, V6, P370, DOI 10.1089/152091504774198070