Kidney aging.Geriatric view

L. Merkusheva, N. Runikhina, O. Tkacheva
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引用次数: 1

Abstract

Individuals age >65 years old are the fastest expanding population demographic throughout the developed world. Consequently, more aged patients than before are receiving diagnoses of impaired renal function and nephrosclerosis. In this review, we examine these features of the aged kidney and explore the various validated and putative pathways contributing to the changes observed with aging. Senescence or normal physiologic aging portrays the expected age-related changes in the kidney as compared to chronic kidney disease (CKD) in some individuals. The microanatomical structural changes of the kidney with older age include a decreased number of functional glomeruli from an increased prevalence of nephrosclerosis (arteriosclerosis, glomerulosclerosis, and tubular atrophy with interstitialfibrosis), and to some extent, compensatory hypertrophy of remaining nephrons. Among the macroanatomical structural changes, older age associates with smaller cortical volume. There is reason to be concerned that the elderly are being misdiagnosed with CKD. In addition to the structural changes in the kidney associated with aging, physiological changes in renal function are also found in older adults, such as decreased glomerular filtration rate, vascular dysautonomia, altered tubular handling of creatinine, reduction in sodium reabsorption and potassium secretion, and diminished renal reserve. These alterations make aged individuals susceptible to the development of clinical conditions in response to usual stimuli that would otherwise be compensated for in younger individuals, including acute kidney injury, volume depletion and overload, disorders of serum sodium and potassium concentration, and toxic reactions to water -soluble drugs excreted by the kidneys. Additionally, the preservation with aging of a normal urinalysis, normal serum urea and creatinine values, erythropoietin synthesis, and normal phosphorus, calcium and magnesium tubular handling distinguishes decreased GFR due to normal aging from that due to chronic kidney disease.
肾脏衰老。老年视图
在发达国家,65岁以下的人是人口增长最快的群体。因此,越来越多的老年患者被诊断为肾功能受损和肾硬化。在这篇综述中,我们研究了衰老肾脏的这些特征,并探索了各种有效的和假定的途径,有助于观察到衰老的变化。与慢性肾脏疾病(CKD)相比,某些个体的衰老或正常生理性衰老描绘了预期的肾脏年龄相关变化。随着年龄的增长,肾脏的微观解剖结构变化包括:由于肾硬化(动脉硬化、肾小球硬化和肾小管萎缩伴间质纤维化)患病率的增加,功能性肾小球数量减少,以及在一定程度上,剩余肾单位代偿性肥大。在宏观解剖结构变化中,年龄越大,皮质体积越小。有理由担心老年人被误诊为慢性肾病。除了与衰老相关的肾脏结构变化外,在老年人中还发现肾功能的生理变化,如肾小球滤过率下降、血管自主神经异常、小管肌酐处理改变、钠重吸收和钾分泌减少以及肾储备减少。这些变化使老年人容易对通常的刺激产生临床反应,这些刺激在年轻人中本来可以得到补偿,包括急性肾损伤、容量消耗和过载、血清钠和钾浓度紊乱以及对肾脏排泄的水溶性药物的毒性反应。此外,随着年龄的增长,正常的尿液分析、正常的血清尿素和肌酐值、红细胞生成素合成和正常的磷、钙和镁管处理将正常衰老引起的GFR下降与慢性肾脏疾病引起的GFR下降区分开。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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