Study on the relationship between blood stasis syndrome and clinical pathology in patients with IgA nephropathy.
- Author:
Cheng-Yun WEI
1
;
Xiang-Mei CHEN
;
Dan-Yang ZHAO
;
Yongze ZHUANG
Author Information
- Publication Type:Journal Article
- MeSH: Adolescent; Adult; Aged; Blood Circulation; Blood Viscosity; Diagnosis, Differential; Female; Glomerulonephritis, IGA; classification; diagnosis; pathology; Hematuria; pathology; Humans; Male; Medicine, Chinese Traditional; Proteinuria; pathology
- From: Chinese Journal of Integrated Traditional and Western Medicine 2005;25(8):687-690
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo explore the relationship between blood stasis Syndrome and clinical pathological parameters in patients with IgA nephropathy (IgAN).
METHODSThe clinicopathological data were analyzed of 94 IgAN patients of traditional Chinese medicine blood stasis syndrome.
RESULTSOf the 94 IgAN patients, 61.70% had blood stasis syndrome (BS) and 38.30% had non- blood stasis syndrome (non-BS). In patients with BS, dark purple tongue proper was the symptom most commonly seen; the clinical manifestations were mostly proteinuria with hematuria, often accompanied with hypertension and renal dysfunction. Compared with those in patients without BS, plasma levels of serum creatinine (SCr), triglyceride (TG) and plasma fibrinogen (FIB) were obviously higher, activated partial thromboplastin time (APTT), and urokinase-type plasminogen activators (u-PA) significantly lower; and scores of glomerular sclerosis, tubular interstitial lesions, interstitial inflammatory cell infiltration, interstitial fibrosis, tubular atrophy and vascular sclerosis significantly higher. Besides, the Lee's grades in them of III - V were mostly seen.
CONCLUSIONBlood stasis syndrome of IgAN are correlated with certain clinical parameters and severity of renal pathological changes. The combination of TCM holistic syndrome differentiation and modern medicinal micro-differentiation is more favorable for making clear the nature of blood stasis Syndrome of IgAN.