The spectrum of glomerular and vascular kidney pathology associated with myeloproliferative neoplasms

医学 肾硬化 肾脏疾病 血栓性微血管病 骨髓纤维化 病理 内科学 人口 原发性血小板增多症 肾小球硬化 胃肠病学 真性红细胞增多症 骨髓 疾病 蛋白尿 环境卫生
作者
Thibaut d’Izarny-Gargas,Pierre Isnard,Idris Boudhabhay,David Buob,Anissa Moktefi,Charel Linster,Aurélie Hummel,Emmanuel Estève,Vincent Audard,Hélène Lazareth,N. Maroun,Alexandre Hertig,Clément Gosset,Charlotte Jouzel,S. Permal,Catherine Domenger,Olivier Kosmider,Marion Rabant,Alexandre Karras,Jean‐Paul Duong Van Huyen
出处
期刊:Kidney International [Elsevier BV]
卷期号:104 (6): 1206-1218 被引量:2
标识
DOI:10.1016/j.kint.2023.09.010
摘要

A high prevalence of chronic kidney disease (CKD) occurs in patients with myeloproliferative neoplasms (MPN). However, MPN-related glomerulopathy (MPN-RG) may not account for the entirety of CKD risk in this population. The systemic vasculopathy encountered in these patients raises the hypothesis that vascular nephrosclerosis may be a common pattern of injury in patients with MPN and with CKD. In an exhaustive, retrospective, multicenter study of MPN kidney biopsies in four different pathology departments, we now describe glomerular and vascular lesions and establish clinicopathologic correlations. Our study encompassed 47 patients with MPN who underwent a kidney biopsy that included 16 patients with chronic myeloid leukemia (CML) and 31 patients with non-CML MPN. Fourteen cases met a proposed definition of MPN-RG based on mesangial sclerosis and hypercellularity, as well as glomerular thrombotic microangiopathy. MPN-RG was significantly associated with both myelofibrosis and poorer kidney survival. Thirty-three patients had moderate-to-severe arteriosclerosis while 39 patients had moderate-to-severe arteriolar hyalinosis. Multivariable models that included 188 adult native kidney biopsies as controls revealed an association between MPN and chronic kidney vascular damage, which was independent of established risk factors such as age, diabetes mellitus and hypertension. Therefore, MPN-RG is associated with myelofibrosis and has a poor kidney prognosis. Thus, our findings suggest that the kidney vasculature is a target during MPN-associated vasculopathy and establish a new link between MPN and CKD. Hence, these results may raise new hypotheses regarding the pathophysiology of vascular nephrosclerosis in the general population.
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