Urinary glycosaminoglycan excretion in NIDDM subjects: Its relationship to albuminura

被引:0
|
作者
McAuliffe, AV
Fisher, EJ
McLennan, SV
Yue, DK
Turtle, JR
机构
[1] Department of Life Sciences, University of Sydney, Sydney, NSW
[2] Department of Medicine, University of Sydney
关键词
diabetic nephropathy; NIDDM; urinary glycosaminoglycans;
D O I
10.1002/(SICI)1096-9136(199608)13:8<758::AID-DIA160>3.0.CO;2-T
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Nephropathy is a serious microvascular complication of diabetes mellitus which is preceded by a period of microalbuminura. Increased loss of proteoglycan (PG) from glomerular basement (GEM) has been postulated to alter glomerular charge selectivity which contributes to urinary loss of albumin. In this study we measured the excretion of urinary glycosaminoglycans (GAG), the degradation products of PG, in 82 non-insulin-dependent (NIDDM) (Type 2) diabetic and 34 non-diabetic subjects. We found that diabetic subjects had a significantly higher GAG urinary excretion rate compared to non-diabetic subjects (12.54 +/- 5.67 vs 8.80 +/- 3.99 mu g glucuronic acid min(-1), p = 0.0001). Categorizing for albuminuric status shows that the diabetic normo-, micro- and macroalbuminuric groups have a higher GAG excretion rate than non-diabetic subjects. Heparan sulphate (HS) GAG urinary excretion was measured in 25 samples from diabetic subjects and 18 non-diabetic subjects. Diabetic subjects excreted more HS GAG than controls both as a rate or as a percentage of total GAG (3.70 +/- 1.94 vs 2.38 +/- 1.48 mu g glucosamine min(-1), p = 0.02; 31.6 % +/- 12.5 vs 23.1 % +/- 10.4, p = 0.02). Categorizing for albuminuric status shows that micro- and macro-albuminuric groups have a significantly higher HS GAG excretion rate than non-diabetic subjects. We conclude that, as in IDDM, excretion of GAG and HS GAG is higher in NIDDM and may precede the development of microalbuminuria.
引用
收藏
页码:758 / 763
页数:6
相关论文
共 50 条
  • [21] Urinary glycosaminoglycan excretion in patients with primary nocturnal enuresis
    Budak, Yasemin U.
    Huysal, Kagan
    Guray, Atilla
    ITALIAN JOURNAL OF PEDIATRICS, 2010, 36 : 13
  • [22] Relationship between circadian changes in renal hemodynamics and circadian changes in urinary glycosaminoglycan excretion in normal rats
    Pons, M
    Forpomes, O
    Espagnet, S
    Cambar, J
    CHRONOBIOLOGY INTERNATIONAL, 1996, 13 (05) : 349 - 358
  • [23] STUDY OF URINARY-EXCRETION OF CHLORPROMAZINE AND OF ITS METABOLITES IN SCHIZOPHRENIC SUBJECTS
    KANABUS, P
    MATSUMOTO, H
    STENCKA, K
    PIETRUSZEWSKA, I
    THERAPIE, 1975, 30 (04): : 625 - 627
  • [24] RELATIONSHIP BETWEEN PRA AND DAILY RATE OF URINARY SODIUM EXCRETION IN NORMAL SUBJECTS
    SALVETTI, A
    SASSANO, P
    ARZILLI, F
    GAZZETTI, P
    JOURNAL OF NUCLEAR BIOLOGY AND MEDICINE, 1974, 18 (03): : 119 - 122
  • [25] URINARY-EXCRETION OF ACID GLYCOSAMINOGLYCANS AND ITS RELATIONSHIP TO PROTEINURIA
    KIRCHER, S
    LUBEC, G
    NEPHRON, 1986, 42 (03): : 275 - 276
  • [26] Prepubertal urinary estrogen excretion and its relationship with pubertal timing
    Shi, Lijie
    Remer, Thomas
    Buyken, Anette E.
    Hartmann, Michaela F.
    Hoffmann, Philipp
    Wudy, Stefan A.
    AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2010, 299 (06): : E990 - E997
  • [27] URINARY GLYCOSAMINOGLYCAN (GAG) EXCRETION IN PROSTATIC-CANCER PATIENTS
    DEKLERK, DP
    WERELY, C
    JOURNAL OF UROLOGY, 1986, 135 (04): : A340 - A340
  • [28] Circadian changes in urinary glycosaminoglycan excretion in normal rat.
    Pons, M
    Forpomes, O
    Espagnet, S
    Mellado, M
    Cambar, J
    PATHOLOGIE BIOLOGIE, 1996, 44 (03): : 189 - 195
  • [29] Urinary glycosaminoglycan excretion in healthy and stone-forming children
    Harangi, F
    Gyorke, Z
    Melegh, B
    PEDIATRIC NEPHROLOGY, 1996, 10 (05) : 555 - 558
  • [30] SIMPLE SPECTROPHOTOMETRIC QUANTIFICATION OF URINARY-EXCRETION OF GLYCOSAMINOGLYCAN SULFATES
    PANIN, G
    NAIA, S
    DALLAMICO, R
    CHIANDETTI, L
    ZACHELLO, F
    CATASSI, C
    FELICI, L
    COPPA, GV
    CLINICAL CHEMISTRY, 1986, 32 (11) : 2073 - 2076