Mitochondrial Complex I Deficiency among Egyptian Pediatric Patients with Steroid-Resistant Nephrotic Syndrome.

IF 1.7 Q3 UROLOGY & NEPHROLOGY
International Journal of Nephrology Pub Date : 2021-05-18 eCollection Date: 2021-01-01 DOI:10.1155/2021/6645373
Doaa M Abdou, AbdelAal Mohamed, Mohamed Abdulhay, Sara El Khateeb
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引用次数: 0

Abstract

Results: Positive consanguinity was a remarkable finding in 44 patients among the SRNS group (73%), compared with 33 patients among the SSNS group (55%). Complex I activity was significantly lower in the SRNS group (0.2657 ± 0.1831 nmol/ml/min), than in the SSNS group (0.4773 ± 0.1290 nmol/ml/min) (p < 0.001). There was a significant positive correlation between complex I activity and the heaviness of proteinuria among the SRNS group (r 0.344, p < 0.001). There were statistically significant differences in serum C3 and C4 levels between both groups (p < 0.001, 0.053, respectively).

Conclusion: Mitochondrial complex I deficiency in patients who have a nephrotic syndrome complaint may play a role in their responsiveness to steroid therapy and the development of SRNS and even the prognosis of their illness.

Abstract Image

埃及儿童类固醇耐受性肾病综合征患者线粒体复合体 I 缺乏症。
结果在 SRNS 组中,有 44 名患者(73%)的血缘关系呈阳性,而在 SSNS 组中,有 33 名患者(55%)的血缘关系呈阳性。SRNS 组的复合体 I 活性(0.2657 ± 0.1831 nmol/ml/min)明显低于 SSNS 组(0.4773 ± 0.1290 nmol/ml/min)(p < 0.001)。在 SRNS 组中,复合物 I 活性与蛋白尿的严重程度呈明显的正相关(r 0.344,p < 0.001)。两组患者的血清 C3 和 C4 水平差异有统计学意义(P < 0.001,0.053):结论:肾病综合征主诉患者线粒体复合体 I 缺乏可能会影响其对类固醇治疗的反应性、SRNS 的发生甚至预后。
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来源期刊
International Journal of Nephrology
International Journal of Nephrology UROLOGY & NEPHROLOGY-
CiteScore
3.40
自引率
4.80%
发文量
44
审稿时长
17 weeks
期刊介绍: International Journal of Nephrology is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies focusing on the prevention, diagnosis, and management of kidney diseases and associated disorders. The journal welcomes submissions related to cell biology, developmental biology, genetics, immunology, pathology, pathophysiology of renal disease and progression, clinical nephrology, dialysis, and transplantation.
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