IgA Glomerulonephritis is a kind of primary glomerular disease, characterized
by recurrent gross (or microscopic) hematuria, hyperplasia of glomerular
Mesangial cells (GMCs), and increasing of matrix, along with wide IGA
deposition. It is also called Berger Disease, as Berger described it in 1968 for
the first time. Besides, IgA Glomerulonephritis can also be referred to as
IgA-IgG Mesangial sedimentary nephritis and IgA Mesangial nephritis, etc.
The incidence, reported from all over the world, quite differs from each
other, while the most frequent area is likely to be the Western Pacific Region.
Of the proved patients with glomerular disease by biopsy, Japan is reported to
take up 50%, the Europe about 10% to 30%, yet America less than 2%. And the
reports from china vary in different areas, approximately accounting for 20% to
30%. The result is obviously impacted by the native renal biopsy indications and
urine census, e.g. it is more or less than 5% in Britain. Nevertheless, this
data in a group of asymptomatic hematuria biopsy from Scotland goes up to 37%.
The disease is more common in men and male to female ratio is about 2:1. There
are also differences between races. For example, the Indians in New Mexico take
up 35%, while it is very rare in the black. Although it is founded out that the
IgA2m(1)in the black is obviously low than that in the white, it has not been
confirmed that it is definitely connected with the low incidence.
Since 1998, it is indicated in some reports that the disease tend to be a
familial one, and at least that there exits genetic predisposition in some
patients with chronic IgA nephropathy. HLA is analyzed to be connected with BW35
and DR4. A recent group of analysis about ESRF caused by IgA point out that B 27
and DR1 are on the increase while DR 2 is on the decline.
[Clinical Manifestation] How to Reverse Chronic Glomerulonephritis Is There a Natural Cure for Glomerulonephritis Do You Recommend Astragalus for Chronic Nephritis Patients Can Homeopathic Treatment Cure Glomerulonephritis
For typical cases, it usually takes the patients several hours to two days to
have gross hematuria after infected in the upper respiratory tract. The symptom
lasts for several hours to several days, some even up to 1 week. The total
number of such patients accounts for about 40% to 50%, slightly higher in
children. Some individuals may suffer from severe backache and stomachache,
which may be related to intestinal IgA vasculitis. The other common
manifestation of this disease is asymptomatic hematuria and/or proteinuria,
accounting for 30 % to 40%. 20% to 25% of the above–mentioned may encounter
gross hematuria one or more times during the process.Home Remedies for Chronic Glomerulonephritis Both Kidneys Are Shrunk with Glomerulonephritis How Long to Cure Glomerulonephritis
Nephrotic syndrome can be found in 5% to 20% of patients, most of whom are
children and youngsters. It is a type of diffuse proliferative disease with or
without glomerulosclerosis. In addition, at times the phenomenon that mainly
refers to Mesangial IgA deposition can also appear in the minimal change
nephropathy, which is characterized by foot process fusion. Some less than 10%
of the patients represent acute renal failure, and all of them can relieve
themselves, 20% to 25% of whom are required to be dialyzed due to the
(crescentic glomerulonephritis) CGN. In the procedure, patients that are
subjected to nitrogenous matter retention take up about 25%, and that with high
blood pressure at the onset about 10%, which significantly increases in patients
over 30 years old; along with prolonged process, patients associated with high
blood pressure exceed 4
[Prognosis]
The disease may have spontaneous remission, which takes up about 4% to 20%.
Each year, about 1% to 2% of the patients get caught into the end stage of renal
failure. Statistic analysis from life table shows that 80% to 90% of the
patients can survive for 10 years, and about 35% of the patients are estimated
to develop into uremia while others suffer persistent hematuresis or
proteinuria. The elements which caused the poor prognosis are as follows: onset
with renal insufficiency, proteinuria exceeding 1.5g/d, high blood pressure and
no gross hematuria; symptoms can be detected with renal biopsy, such as
glomeralosclerosis, interstitial fibrosis, invasion of glomerular capillary,
diffuse hyperplasia and crescent formation, etc.