Evidence map›Paper›PMID 36986200›Full record

ArticleNutrients2023

Serum and Urinary Soluble α-Klotho as Markers of Kidney and Vascular Impairment.

Julia Martín-Vírgala, Sara Fernández-Villabrille, Beatriz Martín-Carro, Isaac Tamargo-Gómez, Juan F Navarro-González, Carmen Mora-Fernández, Laura Calleros, Elena Astudillo-Cortés, Noelia Avello-Llano, Guillermo Mariño and 6 more

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.8field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
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  4. [Potential of early diagnosis and targeted therapy for Klotho protein in chronic kidney disease].Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 5 institutions in 2 countries.

Julia Martín-VírgalaBone and Mineral Research Unit, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Hospital Universitario Central de Asturias (HUCA), Universidad de Oviedo, 33011 Oviedo, Spain.
Sara Fernández-VillabrilleBone and Mineral Research Unit, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Hospital Universitario Central de Asturias (HUCA), Universidad de Oviedo, 33011 Oviedo, Spain.
Beatriz Martín-CarroBone and Mineral Research Unit, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Hospital Universitario Central de Asturias (HUCA), Universidad de Oviedo, 33011 Oviedo, Spain.ORCID 0000-0002-1683-6617
Isaac Tamargo-GómezDepartamento de Biología Funcional, Facultad de Medicina, Universidad de Oviedo, 33006 Oviedo, Spain.ORCID 0000-0002-9907-2543
Juan F Navarro-GonzálezRedes de Investigación Cooperativa Orientadas a Resultados en Salud (RICORS), RICORS2040 (Kidney Disease), 28040 Madrid, Spain.
Carmen Mora-FernándezRedes de Investigación Cooperativa Orientadas a Resultados en Salud (RICORS), RICORS2040 (Kidney Disease), 28040 Madrid, Spain.
Laura CallerosRedes de Investigación Cooperativa Orientadas a Resultados en Salud (RICORS), RICORS2040 (Kidney Disease), 28040 Madrid, Spain.
Elena Astudillo-CortésDivision of Nephrology, Hospital Universitario Central de Asturias (HUCA), 33011 Oviedo, Spain.
Noelia Avello-LlanoLaboratorio de Medicina, Hospital Universitario Central de Asturias (HUCA), 33011 Oviedo, Spain.
Guillermo MariñoDepartamento de Biología Funcional, Facultad de Medicina, Universidad de Oviedo, 33006 Oviedo, Spain.ORCID 0000-0003-1960-1677
Adriana S DussoBone and Mineral Research Unit, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Hospital Universitario Central de Asturias (HUCA), Universidad de Oviedo, 33011 Oviedo, Spain.
Cristina Alonso-MontesBone and Mineral Research Unit, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Hospital Universitario Central de Asturias (HUCA), Universidad de Oviedo, 33011 Oviedo, Spain.
Sara PanizoBone and Mineral Research Unit, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Hospital Universitario Central de Asturias (HUCA), Universidad de Oviedo, 33011 Oviedo, Spain.
Jorge B Cannata-AndíaBone and Mineral Research Unit, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Hospital Universitario Central de Asturias (HUCA), Universidad de Oviedo, 33011 Oviedo, Spain.
Manuel Naves-DíazBone and Mineral Research Unit, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Hospital Universitario Central de Asturias (HUCA), Universidad de Oviedo, 33011 Oviedo, Spain.
Natalia Carrillo-LópezBone and Mineral Research Unit, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Hospital Universitario Central de Asturias (HUCA), Universidad de Oviedo, 33011 Oviedo, Spain.ORCID 0000-0002-4227-4144
Universidad de Oviedo · ESHospital Universitario Central de Asturias · ESHospital Universitario Nuestra Señora de Candelaria · ESUniversidad de Alcalá · ESUniversidad de La Laguna · ES

Funding

Fundación Renal Luis HernandoInstituto de Salud Carlos III PI16/00637Instituto de Salud Carlos III PI19/00532Instituto de Salud Carlos III PI20/00573Instituto de Salud Carlos III PI20/00633Instituto de Salud Carlos III Retic REDinREN (RD16/0009/0017)Instituto de Salud Carlos III RICORS2040 (Kidney Disease)Plan de Ciencia, Tecnología e Innovación 2013-2017 y 2018-2022 del Principado de Asturias GRUPIN14-028, IDI-2018-000152, IDI-2021-000080
6 · The paper itself

Abstract

This study was designed to investigate the controversy on the potential role of sKlotho as an early biomarker in Chronic Kidney Disease-Mineral Bone Disorder (CKD-MBD), to assess whether sKlotho is a reliable marker of kidney α-Klotho, to deepen the effects of sKlotho on vascular smooth muscle cells (VSMCs) osteogenic differentiation and to evaluate the role of autophagy in this process. Experimental studies were conducted in CKD mice fed a normal phosphorus (CKD+NP) or high phosphorus (CKD+HP) diet for 14 weeks. The patients' study was performed in CKD stages 2-5 and in vitro studies which used VSMCs exposed to non-calcifying medium or calcifying medium with or without sKlotho. The CKD experimental model showed that the CKD+HP group reached the highest serum PTH, P and FGF23 levels, but the lowest serum and urinary sKlotho levels. In addition, a positive correlation between serum sKlotho and kidney α-Klotho was found. CKD mice showed aortic osteogenic differentiation, together with increased autophagy. The human CKD study showed that the decline in serum sKlotho is previous to the rise in FGF23. In addition, both serum sKlotho and FGF23 levels correlated with kidney function. Finally, in VSMCs, the addition of sKlotho prevented osteogenic differentiation and induced autophagy. It can be concluded that serum sKlotho was the earliest CKD-MBD biomarker, a reliable indicator of kidney α-Klotho and that might protect against osteogenic differentiation by increasing autophagy. Nevertheless, further studies are needed to investigate the mechanisms of this possible protective effect.

Indexed as

Chronic Kidney Disease-Mineral and Bone DisorderRenal Insufficiency, ChronicAnimalsBiomarkersFibroblast Growth FactorsGlucuronidaseHumansKidneyKlotho ProteinsMiceMineralsOsteogenesisPhosphorusBiomarkersFibroblast Growth FactorsGlucuronidaseKlotho ProteinsMineralsPhosphoruschronic kidney diseaseosteogenic differentiationserum CKD-MBD biomarkerssKlothovascular calcification

Identifiers

PMID36986200
PMCPMC10057552
OpenAlexW4327975688

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.