4.6 Article

Genetic, Environmental, and Disease-Associated Correlates of Vitamin D Status in Children with CKD

Journal

Publisher

AMER SOC NEPHROLOGY
DOI: 10.2215/CJN.10210915

Keywords

-

Funding

  1. Kuratorium fur Heimdialyse Foundation for Preventive Medicine
  2. European Renal Association-European Dialysis and Transplant Association
  3. German Federal Ministry of Education and Research [01EO0802]
  4. Pfizer Deutschland GmbH
  5. Emmy Noether Programme of the German Research Foundation [KO3598/2-1]
  6. National Institutes for Diabetes and Digestive and Kidney Diseases [R01DK082394]
  7. Kidney Research UK [RP39/2013] Funding Source: researchfish

Ask authors/readers for more resources

Background and objectives Vitamin D deficiency is endemic in children with CKD. We sought to investigate the association of genetic disposition, environmental factors, vitamin D supplementation, and renal function on vitamin D status in children with CKD. Design, setting, participants, & measurements Serum 25-hydroxy-vitamin D, 1,25-dihydroxy-vitamin D, and 24,25-dihydroxy-vitamin D concentrations were measured cross-sectionally in 500 children from 12 European countries with CKD stages 3-5. All patients were participants of the Cardiovascular Comorbidity in Children with Chronic Kidney Disease Study, had CKD stage 3-5, and were age 6-18 years old. Patients were genotyped for single-nucleotide polymorphisms in the genes encoding 25-hydroxylase, vitamin D binding protein, 7-dehydrocholesterol reductase, and 24-hydroxylase. Associations of genetic status, season, local solar radiation, oral vitamin D supplementation, and disease-associated factors with vitamin D status were assessed. Results Two thirds of patients were vitamin D deficient (25-hydroxy-vitaminD <16 ng/ml). 25-Hydroxy-vitamin D concentrations varied with season and were twofold higher in vitamin D supplemented patients (21.6 [14.1] versus 10.4 [10.1] ng/ml; P<0.001). Glomerulopathy, albuminuria, and girls were associated with lower 25-hydroxy-vitamin D levels. 24,25-dihydroxy-vitamin D levels were closely correlated with 25-hydroxy-vitamin D and 1,25-dihydroxy-vitamin D (r=0.87 and r=0.55; both P<0.001). 24,25-dihydroxy-vitamin D concentrations were higher with higher c-terminal fibroblast growth factor 23 and inversely correlated with intact parathyroid hormone. Whereas 25-hydroxy-vitamin D levels were independent of renal function, 24,25-dihydroxy-vitamin D levels were lower with lower eGFR. Vitamin D deficiency was more prevalent in Turkey than in other European regions independent of supplementation status and disease-related factors. Single-nucleotide polymorphisms in the vitamin D binding protein gene were independently associated with lower 25-hydroxy-vitamin D and higher 24,25-dihydroxy-vitamin D. Conclusions Disease-related factors and vitamin D supplementation are the main correlates of vitamin D status in children with CKD. Variants in the vitamin D binding protein showed weak associations with the vitamin D status.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

Review Pediatrics

Nutritional management of the infant with chronic kidney disease stages 2-5 and on dialysis

Vanessa Shaw, Caroline Anderson, An Desloovere, Larry A. Greenbaum, Dieter Haffner, Christina L. Nelms, Fabio Paglialonga, Nonnie Polderman, Leila Qizalbash, Jose Renken-Terhaerdt, Stella Stabouli, Jetta Tuokkola, Johan Vande Walle, Bradley A. Warady, Rukshana Shroff

Summary: Proper nutritional management is crucial for children with chronic kidney disease (CKD) to maintain normal growth and development. Infants with CKD have specific nutritional needs, and inadequate nutrition can lead to growth impairment and abnormal neurodevelopment.

PEDIATRIC NEPHROLOGY (2023)

Review Pediatrics

A rare cause of nephrotic syndrome-sphingosine-1-phosphate lyase (SGPL1) deficiency: 6 cases and a review of the literature

Tugba Tastemel Ozturk, Nur Canpolat, Seha Saygili, Umut Selda Bayrakci, Oguz Soylemezoglu, Fatih Ozaltin, Rezan Topaloglu

Summary: Patients with SGPL1 mutations have a poor prognosis, and may exhibit involvement of various organs/systems beyond adrenal insufficiency.

PEDIATRIC NEPHROLOGY (2023)

Article Transplantation

Armed conflicts and kidney patients: a consensus statement from the Renal Disaster Relief Task Force of the ERA

Mehmet S. Sever, Raymond Vanholder, Valerie Luyckx, Kai-Uwe Eckardt, Mykola Kolesnyk, Andrzej Wiecek, Ewa Pawlowicz-Szlarska, Daniel Gallego, Rukshana Shroff, Andrej Skoberne, Ionut Nistor, Mohamed Sekkarie, Dmytro Ivanov, Edita Noruisiene, Serhan Tuglular

Summary: During conflicts, people with kidney disease may face additional threats due to medical and logistical challenges. Acute kidney injury and treatment interruptions can worsen kidney function, and limitations in dialysis and availability of immunosuppressive medications increase the risk of complications. Local preparedness, adjustments in treatment, telemedicine support, and referrals to higher-level hospitals are important measures to address these challenges.

NEPHROLOGY DIALYSIS TRANSPLANTATION (2023)

Article Pediatrics

Changes in bone biomarkers in response to different dosing regimens of cholecalciferol supplementation in children with chronic kidney disease

Nivedita Kamath, Arpana Iyengar, Hamsa Reddy, Jyoti Sharma, Jyoti Singhal, Sudha Ekambaram, Susan Uthup, Sumithra Selvam, Mandy Wan, Anja Rahn, Dagmar Christiane-Fischer, Rukshana Shroff

Summary: This study analyzed the effects of different dosing regimens of cholecalciferol supplementation on bone biomarkers. The results showed that cholecalciferol supplementation significantly increased bone formation, and the three dosing regimens had similar effects on bone biomarkers.

PEDIATRIC NEPHROLOGY (2023)

Review Pediatrics

Management of pediatric dialysis and kidney transplant patients after natural or man-made disasters

Lale Sever, Gulseren Pehlivan, Nur Canpolat, Seha Saygili, Ayse Agbas, Ebru Demirgan, Jun Oh, Elena Levtchenko, Dymtro D. Ivanov, Rukshana Shroff

Summary: Pediatric patients on kidney replacement therapy are highly vulnerable during disasters due to limitations in dialysis treatments and shortage of medical resources. Proper measures and support are crucial to mitigate risks and provide necessary care.

PEDIATRIC NEPHROLOGY (2023)

Article Audiology & Speech-Language Pathology

Hearing Loss Related to Gene Mutations in Distal Renal Tubular Acidosis

Ezgi Ay, Emre Gurses, Filiz Aslan, Bora Gulhan, Asuman Alniacik, Ali Duzova, Munir Demir Bajin, Levent Sennaroglu, Gulsum Aydan Genc, Fatih Ozaltin, Rezan Topaloglu

Summary: This study aimed to determine the characteristics of hearing loss in patients with dRTA caused by different gene mutations. The results showed that LVAS is common in dRTA patients and may influence the type and severity of hearing loss. Therefore, regular audiological follow-up is essential for early detection of possible late-onset or progressive hearing loss in dRTA patients.

AUDIOLOGY AND NEURO-OTOLOGY (2023)

Editorial Material Urology & Nephrology

Genetic Association Analysis of Chronic Kidney Disease Progression in a Small Korean Cohort Study

Sahar Ghasemi, Matthias Wuttke

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2023)

Article Genetics & Heredity

Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine

Pascal Schlosser, Nora Scherer, Franziska Grundner-Culemann, Sara Monteiro-Martins, Stefan Haug, Inga Steinbrenner, Burulca Uluvar, Matthias Wuttke, Yurong Cheng, Arif B. Ekici, Gergely Gyimesi, Edward D. Karoly, Fruzsina Kotsis, Johanna Mielke, Maria F. Gomez, Bing Yu, Morgan E. Grams, Josef Coresh, Eric Boerwinkle, Michael Kottgen, Florian Kronenberg, Heike Meiselbach, Robert P. Mohney, Shreeram Akilesh, Miriam Schmidts, Matthias A. Hediger, Ulla T. Schultheiss, Kai-Uwe Eckardt, Peter J. Oefner, Peggy Sekula, Yong Li, Anna Koettgen

Summary: The kidneys play a critical role in removing waste products and retaining valuable solutes in the body. Genetic studies of plasma and urine metabolites have identified important associations and provided insights into kidney function, such as glycerol transport and protein localization. Shared genetic determinants of metabolite-disease combinations offer potential for understanding metabolic diseases. Expanding genetic studies of the metabolome beyond plasma allows for a better understanding of processes at the interface of body compartments.

NATURE GENETICS (2023)

Article Pediatrics

Diagnosis and management of mineral and bone disorders in infants with CKD: clinical practice points from the ESPN CKD-MBD and Dialysis working groups and the Pediatric Renal Nutrition Taskforce

Justine Bacchetta, Claus Peter Schmitt, Sevcan A. Bakkaloglu, Shelley Cleghorn, Maren Leifheit-Nestler, Agnieszka Prytula, Bruno Ranchin, Anne Schoen, Stella Stabouli, Johan van de Walle, Enrico Vidal, Dieter Haffner, Rukshana Shroff

Summary: Infants with CKD are highly susceptible to mineral and bone disorders, and this position paper provides guidelines for diagnosing and managing CKD-MBD in infants. The paper includes 34 clinical practice points, such as dietary control of calcium and phosphate, and medication recommendations. The strength of the statements in the paper may vary and should be tailored to individual patient needs by the treating physician.

PEDIATRIC NEPHROLOGY (2023)

Article Pediatrics

Nutritional management of children with acute kidney injury-clinical practice recommendations from the Pediatric Renal Nutrition Taskforce

Molly R. Wong Vega, Dana Cerminara, An Desloovere, Fabio Paglialonga, Jose Renken-Terhaerdt, Johan Vande Walle, Vanessa Shaw, Stella Stabouli, Caroline Elizabeth Anderson, Dieter Haffner, Christina L. Nelms, Nonnie Polderman, Leila Qizalbash, Jetta Tuokkola, Bradley A. Warady, Rukshana Shroff, Larry A. Greenbaum

Summary: The nutritional management of children with AKI is complex due to the dynamic nature of the condition. The PRNT has developed CPRs to guide dietitians in providing optimal nutrition support in line with AKI medical treatments. Collaboration between dietitians and physicians is crucial in addressing challenges in nutrition assessment and adapting recommendations to individual patient needs.

PEDIATRIC NEPHROLOGY (2023)

Article Multidisciplinary Sciences

Imputation-powered whole-exome analysis identifies genes associated with kidney function and disease in the UK Biobank

Matthias Wuttke, Eva Koenig, Maria-Alexandra Katsara, Holger Kirsten, Saeed Khomeijani Farahani, Alexander Teumer, Yong Li, Martin Lang, Burulca Goecmen, Cristian Pattaro, Dorothee Guenzel, Anna Koettgen, Christian Fuchsberger

Summary: A genotype imputation approach was applied to whole exome sequencing data from the UK Biobank, resulting in the discovery of 158 rare variants and 105 genes significantly associated with kidney function traits. This approach boosts statistical power and provides a comprehensive resource for directing experimental and clinical studies of kidney disease.

NATURE COMMUNICATIONS (2023)

Article Transplantation

Recommended calcium intake in adults and children with chronic kidney disease-a European consensus statement

Pieter Evenepoel, Hanne Skou Jorgensen, Jordi Bover, Andrew Davenport, Justine Bacchetta, Mathias Haarhaus, Ditte Hansen, Carolina Gracia-Iguacel, Markus Ketteler, Louise McAlister, Emily White, Sandro Mazzaferro, Marc Vervloet, Rukshana Shroff, European Renal Osteodystrophy EUROD, European Renal Assoc ERA, European Soc Pediat Nephrology ESPN

Summary: Mineral and bone disorders are commonly seen in patients with chronic kidney disease, which can lead to adverse health outcomes. The management of calcium intake is crucial for maintaining a neutral calcium balance and preventing bone diseases and fractures. However, current clinical practice guidelines lack specific recommendations on calcium intake. Therefore, experts in the field have provided key practice points to assist healthcare professionals, but these recommendations should be individualized based on patient needs.

NEPHROLOGY DIALYSIS TRANSPLANTATION (2023)

Editorial Material Transplantation

Haemodiafiltration for all: are we CONVINCEd?

Rukshana Shroff, Carlo Basile, Frank van der Sande, Sandip Mitra

NEPHROLOGY DIALYSIS TRANSPLANTATION (2023)

Article Pediatrics

Acute kidney injury in children with moderate-severe COVID-19 and multisystem inflammatory syndrome in children: a referral center experience

Tugba Tastemel Ozturk, Ali Duzova, Pembe Derin Oygar, Demet Baltu, Pelin Ozcilingir Hakverdi, Sibel Lacinel Gurlevik, Eda Didem Kurt-Sukur, Hayrettin Hakan Aykan, Seza Ozen, Ilker Ertugrul, Selman Kesici, Bora Gulhan, Fatih Ozaltin, Yasemin Ozsurekci, Ali Bulent Cengiz, Rezan Topaloglu

Summary: This study investigated the characteristics of acute kidney injury (AKI) in pediatric COVID-19 and MIS-C, and found that the frequency of AKI was 22.7% in COVID-19 and 15.3% in MIS-C. Independent risk factors for AKI in COVID-19 patients were the need for vasoactive/inotropic agents and vomiting/diarrhea, while in MIS-C patients it was the need for vasoactive/inotropic agents and severe inflammation. The study emphasizes the association between AKI and age in MIS-C patients and suggests the need for long-term follow-up for kidney functions.

PEDIATRIC NEPHROLOGY (2023)

Article Medicine, Research & Experimental

SLC26A1 is a major determinant of sulfate homeostasis in humans

Anja Pfau, Karen I. Lopez-Cayuqueo, Nora Scherer, Matthias Wuttke, Annekatrin Wernstedt, Daniela Gonzalez Fassrainer, Desiree E. C. Smith, Jiddeke M. van de Kamp, Katharina Ziegeler, Kai-Uwe Eckardt, Friedrich C. Luft, Peter S. Aronson, Anna Koettgen, Thomas J. Jentsch, Felix Knauf

Summary: Sulfate is important for various physiological processes in the human body. The transporter SLC26A1 plays a crucial role in sulfate reabsorption in the kidney. Through genetic analysis and functional experiments, it is confirmed that SLC26A1 is a sulfate transporter in humans. Rare SLC26A1 variants are associated with lower plasma sulfate levels at the population level.

JOURNAL OF CLINICAL INVESTIGATION (2023)

No Data Available