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Epidemiologic data of primary glomerular diseases in western France

机译:法国西部原发性肾小球疾病的流行病学数据

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Epidemiologic data of primary glomerular diseases in western France. Between January 1, 1976, and December 31, 2002, histologic diagnosis of primary glomerular diseases (PGD) was made in 898 patients born and living at the time of diagnosis in a region of France, comprising 412,735 inhabitants, of whom 391,265 were aged from 10 to 85 years. The prevalence of PGD during a 75-year exposure to risk (10 to 85 years of age) was evaluated to 6.9 in 1000 (8.2 in 1000 males and 5.1 in 1000 females) during the 27-year period. The most common PGD was IgA nephropathy (IgAN) with a prevalence of 2.4 in 1000 (3.6 in 1000 males and 1.3 in 1000 females). The annual incidence of PGD was evaluated separately for two consecutive 10-years periods: period A (1976 to 1985), period B (1986 to 1995) and for one 7-year period: period C (1996 to 2002). Within each of these three periods, annual incidence of PGD was 89, 76, and 65 per million inhabitants. During this 27-year period, the annual incidences of membranoproliferative glomerulonephritis (GN) and membranous nephropathy were declining and the incidence of crescentic proliferative GN was strongly progressing, whereas annual incidence of nephrosis remained stable. The incidence of IgAN remained the same throughout the three periods: 28, 28, and 26 per million inhabitants. Whereas the incidence of IgAN was three- to fourfold higher in the adult aged from 20 to 59 years than in the elderly during the periods A (38 vs. 11 per million inhabitants) and B (37 vs. 12 per million inhabitants), the incidence became similar whatever age groups during the last period C (20 to 59 years, 25 per million inhabitants; 60 to 79 years, 27 per million inhabitants; and 80 years and over, 28 per million inhabitants. The stability of annual incidence according to period and age, which is demonstrated for the first time during the last period, provides a new evidence of a role for genetic factors in the pathogenesis of IgAN.
机译:法国西部原发性肾小球疾病的流行病学数据。 1976年1月1日至2002年12月31日期间,法国地区的898例出生和生活中的原发性肾小球疾病(PGD)的组织学诊断为412,735名居民,其中391,265岁来自10至85年。在27年的时间段内,将75年的风险暴露(10至85岁年龄段)中PGD的患病率评估为千分之6.9(男性为8.2,男性为1000,女性为5.1)。最常见的PGD是IgA肾病(IgAN),患病率为2.4 / 1000(1000男性中为3.6,1000女性中为1.3)。对PGD的年发病率分别连续两个10年进行评估:A期(1976年至1985年),B期(1986年至1995年)和7年期:C期(1996年至2002年)。在这三个时期中,PGD的年发生率分别为每百万居民中的89、76和65。在这27年中,膜增生性肾小球肾炎(GN)和膜性肾病的年发病率呈下降趋势,新月型增生性GN的发病率呈强势增长,而肾病的年发病率保持稳定。在三个时期中,IgAN的发生率均保持不变:每百万居民中28、28和26。在A(38人口/百万居民11)和B(37百万人口/ 12居民)期间,年龄20至59岁的成年人的IgAN发病率比老年人高三至四倍,在最后一个时期C中,无论年龄组别,其发病率都变得相似(20至59岁,每百万居民25岁; 60至79岁,每百万居民27岁; 80岁以上,每百万居民28岁。在最后一个时期首次证明了这一时期和年龄,这为遗传因素在IgAN发病机理中的作用提供了新的证据。

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