Evidence map›Paper›PMID 42503547›Full record

ArticlePediatric nephrology (Berlin, Germany)2026

PROGRESS Study: Longitudinal analysis of antioxidant status and its relationship with heat shock proteins in children with chronic kidney disease.

Zeynep Nagehan Yuruk Yildirim, Sebahat Usta Akgul, Harika Alpay, Bagdagul Aksu, Fatma Savran Oguz, Aysel Kiyak, Nurver Akinci, Sevgi Yavuz, Gul Ozcelik, Asuman Gedikbasi and 15 more

Abstract read
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In one paragraph

Article in Pediatric nephrology (Berlin, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

25 authors.

Zeynep Nagehan Yuruk YildirimIstanbul Faculty of Medicine, Division of Pediatric Nephrology, Istanbul University, 34390, Capa, Istanbul, Turkey. znyuruk@gmail.com.ORCID http://orcid.org/0000-0003-2891-2231
Sebahat Usta AkgulIstanbul Faculty of Medicine, Department of Medical Biology, Istanbul University, Istanbul, Turkey.
Harika AlpayDivision of Pediatric Nephrology, Marmara University Medical Faculty, Istanbul, Turkey.
Bagdagul AksuIstanbul Faculty of Medicine, Institute of Child Health, Istanbul University, Division of Pediatric Nephrology and Istanbul University, Istanbul, Turkey.
Fatma Savran OguzIstanbul Faculty of Medicine, Department of Medical Biology, Istanbul University, Istanbul, Turkey.
Aysel KiyakDivision of Pediatric Nephrology, Kanuni Sultan Suleyman Education and Research Hospital, Istanbul, Turkey.
Nurver AkinciDivision of Pediatric Nephrology, Sisli Etfal Education and Research Hospital, Istanbul, Turkey.
Sevgi YavuzDivision of Pediatric Nephrology, Basaksehir Cam and Sakura City Hospital, Istanbul, Turkey.
Gul OzcelikDivision of Pediatric Nephrology, Sisli Etfal Education and Research Hospital, Istanbul, Turkey.
Asuman GedikbasiIstanbul Faculty of Medicine, Institute of Child Health, Istanbul University, Division of Pediatric Nutrition and Metabolism and Istanbul University, Istanbul, Turkey.
Ibrahim GokceDivision of Pediatric Nephrology, Marmara University Medical Faculty, Istanbul, Turkey.
Nese OzkayinDivision of Pediatric Nephrology, Trakya University School of Medicine, Istanbul, Turkey.
Nurdan YildizDivision of Pediatric Nephrology, Marmara University Medical Faculty, Istanbul, Turkey.
Cemile PehlivanogluDivision of Pediatric Nephrology, Koc University School of Medicine, Istanbul, Turkey.
Nilufer GoknarFaculty of Medicine, Division of Pediatric Nephrology, Medeniyet University, Istanbul, Turkey.
Seha SaygiliDivision of Pediatric Nephrology, Istanbul University-Cerrahpasa, Cerrahpasa School of Medicine, Istanbul, Turkey.
Sebahat TulparDivision of Pediatric Nephrology, Bakirkoy Sadi Konuk Education and Research Hospital, Istanbul, Turkey.
Nuran KucukDivision of Pediatric Nephrology, Kartal Education and Research Hospital, Istanbul, Turkey.
Ilmay BilgeDivision of Pediatric Nephrology, Koc University School of Medicine, Istanbul, Turkey.
Mehmet TasdemirDivision of Pediatric Nephrology, Istınye University, Bahcesehir Liv Hospital, Istanbul, Turkey.
Ayse AgbaşDivision of Pediatric Nephrology, Istanbul University-Cerrahpasa, Cerrahpasa School of Medicine, Istanbul, Turkey.
Ahmet DiricanIstanbul Faculty of Medicine, Department of Biostatistics, Istanbul University, Istanbul, Turkey.
Sevinc EmreIstanbul Faculty of Medicine, Division of Pediatric Nephrology, Istanbul University, 34390, Capa, Istanbul, Turkey.
Ahmet NayirIstanbul Faculty of Medicine, Division of Pediatric Nephrology, Istanbul University, 34390, Capa, Istanbul, Turkey.
Alev YilmazIstanbul Faculty of Medicine, Division of Pediatric Nephrology, Istanbul University, 34390, Capa, Istanbul, Turkey.ORCID http://orcid.org/0000-0003-1743-1491

Funding

Türkiye Bilimsel ve Teknolojik Araştırma Kurumu 115S365
6 · The paper itself

Abstract

backgroundChronic kidney disease (CKD) progresses via complex mechanisms, including oxidative stress and impaired antioxidant defenses. We aimed to investigate longitudinal changes in serum and urinary levels of superoxide dismutase (SOD), catalase, and glutathione in children with CKD, and to assess their relationship with heat shock proteins (HSPs), which we have previously reported to be altered in this population.

methodsA total of 117 children with CKD and 56 healthy children were enrolled in the study. The CKD group was followed prospectively for 24 months. Serum and urinary levels of SOD, catalase, and glutathione were measured using ELISA at baseline, 12 months, and 24 months. Longitudinal changes and associations with kidney outcomes and CKD progression were analyzed using mixed-effects and logistic regression models.

resultsSerum SOD and catalase levels, as well as urinary SOD, catalase, and glutathione levels were higher in the CKD group than in the control group. Serum and urinary SOD and catalase levels steadily decreased over time, similarly to urinary HSP levels. Most antioxidant biomarkers were not significantly associated with longitudinal kidney outcomes. However, higher longitudinal urinary catalase levels were modestly associated with better kidney function over time, and higher baseline urinary catalase was independently associated with a lower risk of CKD progression. In contrast, higher baseline serum SOD levels were associated with an increased risk of progression. Antioxidant biomarkers showed strong correlations with serum and urinary HSP levels.

conclusionAlthough urinary catalase consistently associates with kidney function and CKD progression, most antioxidant biomarkers alone have limited predictive value. Children with CKD show altered antioxidant defenses that decline over time, and their correlations with HSPs suggest that they may act together in response to oxidative stress.

Indexed as

Antioxidant defenseCatalaseChronic kidney diseaseGlutathioneHeat shock proteins (HSPs)Oxidative stressSuperoxide dismutase (SOD)

Identifiers

PMID42503547

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