遗传性甲状腺转蛋白淀粉样变性患者短期肾功能下降的自然过程和决定因素:一项法国观察性研究。

IF 5.2 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Julien Dang, Lauriane Segaux, Anissa Moktefi, Thomas Stehlé, Mounira Kharoubi, Khalil El Karoui, Philippe Rémy, Philippe Grimbert, Violaine Plante-Bordeneuve, Soulef Guendouz, Arnault Galat, Sophie Mallet, Silvia Oghina, Gagan Deep Singh Chadha, Amira Zaroui, Pascale Fanen, Florence Canoui-Poitrine, Thibaud Damy, Vincent Audard
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引用次数: 1

摘要

关于遗传性甲状腺转蛋白(ATTRv)淀粉样变患者肾脏受累的数据很少,慢性肾脏疾病(CKD)在该人群中的自然病程仍不清楚。这项观察性研究,包括在法国心脏淀粉样变性参考中心诊断为ATTRv淀粉样变性的成年患者,调查了肾功能结局及其决定因素。多变量logistic回归模型确定了与CKD相关的基线因素。通过多变量线性混合效应模型评估24个月随访期间肾小球滤过率(eGFR)变化的决定因素。总共有232例(78例女性[34%],平均年龄:64岁)患有ATTRv淀粉样变的患者根据其TTR变体进行分类:ATTRV122I (37%), ATTRV30M(29%)和其他变体(34%)。中位基线eGFR为78 ml/min/1.73 m2。72例(31%)患者eGFR低于60 ml/min/1.73m2, 27/137例(20%)患者有明显蛋白尿(尿蛋白/肌酐比值≥30 mg/mmol)。在4例肾脏活检中,所有病例均发现典型的刚果红阳性和trr标记淀粉样蛋白沉积。年龄较大(OR 1.07, p = 0.04)与基线时较高的CKD患病率相关,而在随访12个月和24个月后,较高的左心室整体纵向应变(LVGLS) (OR 0.83, p = 2)分别与较高的CKD患病率相关。eGFR下降与老年独立相关((67-74),系数= -14.35 mL/min/1.73 m2, p 74,系数= -22.93 mL/min/1.73 m2, p 2, p p
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Natural course and determinants of short-term kidney function decline in hereditary transthyretin amyloidosis: a French observational study.

Data regarding renal involvement in patients with hereditary transthyretin (ATTRv) amyloidosis are scarce and the natural course of chronic kidney disease (CKD) in this population remains unclear. This observational study, including adult patients diagnosed with ATTRv amyloidosis at the French Reference Centre for Cardiac Amyloidosis, investigated renal function outcome and its determinants. Multivariable logistic regression models identified factors associated with CKD at baseline. Determinants of the change in estimated glomerular filtration rate (eGFR) over 24 months of follow-up were assessed with a multivariable linear mixed-effects model. In total, 232 patients (78 women [34%], mean age: 64 years) with ATTRv amyloidosis were classified on the basis of their TTR variants: ATTRV122I (37%), ATTRV30M (29%), and other variants (34%). Median baseline eGFR was 78 ml/min/1.73 m2. Seventy-two patients (31%) had an eGFR below 60 ml/min/1.73m2 and 27/137 patients (20%) had significant proteinuria (urine protein/creatinine ratio ≥30 mg/mmol). Renal biopsy, performed in four cases, found typical Congo red-positive and TTR-labelled amyloid deposits in all cases. Older age (OR 1.07, p < .001) and a prior history of hypertension (OR 2.09, p = .04) were associated with a higher prevalence of CKD at baseline, whereas higher left ventricular global longitudinal strain (LVGLS) (OR 0.83, p < .001) was associated with a lower prevalence. The estimated change in eGFR was -7.12 [-9.61, -4.63] and -8.21 [-10.81, -5.60] ml/min/1.73 m2 after 12 and 24 months of follow-up, respectively. eGFR decline was independently associated with older age ((67-74], coefficient= -14.35 mL/min/1.73 m2, p < .01, >74, coefficient = -22.93 mL/min/1.73 m2, p < .001, versus <56), ATTRV122I (coefficient = -17.17 mL/min/1.73m2, p < .01, versus ATTRV30M) and LVGLS (coefficient = 1.22, p < .01). These data suggest that CKD is a common finding in patients with ATTRv amyloidosis, and that eGFR decline is rapid during the first year of evaluation. Older age, lower LVGLS and ATTRV122I were associated with a worse renal outcome. Further studies are now needed to evaluate effects of new targeted therapies on long term renal function.

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来源期刊
Amyloid-Journal of Protein Folding Disorders
Amyloid-Journal of Protein Folding Disorders 生物-生化与分子生物学
CiteScore
10.60
自引率
10.90%
发文量
48
审稿时长
6-12 weeks
期刊介绍: Amyloid: the Journal of Protein Folding Disorders is dedicated to the study of all aspects of the protein groups and associated disorders that are classified as the amyloidoses as well as other disorders associated with abnormal protein folding. The journals major focus points are: etiology, pathogenesis, histopathology, chemical structure, nature of fibrillogenesis; whilst also publishing papers on the basic and chemical genetic aspects of many of these disorders. Amyloid is recognised as one of the leading publications on amyloid protein classifications and the associated disorders, as well as clinical studies on all aspects of amyloid related neurodegenerative diseases and major clinical studies on inherited amyloidosis, especially those related to transthyretin. The Journal also publishes book reviews, meeting reports, editorials, thesis abstracts, review articles and symposia in the various areas listed above.
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