15 results match your criteria: "Center for Kidney Health Research[Affiliation]"

Older age is linked with poorer self-care in the chronic kidney disease (CKD) setting. Informal health supporters (family members and friends) are critical sources of self-care support, but much remains unclear about the characteristics and implications of received support among this patient population. We examined how received self-care support (amount and type) related to positive (CKD management self-efficacy) and negative (depressive symptoms) psychosocial health correlates of self-care in 536 adults aged 65 years and older with non-dialysis-dependent CKD.

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Key Points: Using transcriptome-wide association studies, we identified an association between splicing out of exon 27 of COL4A4 and hematuria. We confirmed the presence of COL4A4 exon 27 splicing in an independent cohort. Functional assays revealed that the COL4A4 transcript with exon 27 spliced out affects collagen IV trimer assembly and secretion.

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Background: Self-measurement of blood pressure (SMBP) is endorsed by current guidelines for diagnosing and managing hypertension (HTN). We surveyed individuals in a rural healthcare system on practices and attitudes related to SMBP that could guide future practice.

Methods: Survey questions were sent via an online patient portal to a random sample of 56,275 patients with either BP > 140/90 mm Hg or cardiovascular care in the system.

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Our GWAS of hematuria in the UK Biobank identified 6 loci, some of which overlap with loci for albuminuria suggesting pleiotropy. Since clinical syndromes are often defined by combinations of traits, generating a combined phenotype can improve power to detect loci influencing multiple characteristics. Thus the composite trait of hematuria and albuminuria was chosen to enrich for glomerular pathologies.

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Article Synopsis
  • This study examines autosomal dominant Alport Syndrome (ADAS), a genetic disorder affecting 1 in 106 people, and its varied symptoms and severity.
  • Researchers analyzed data from over 174,000 individuals to identify 403 who had likely harmful gene variants, finding that those with these variants had higher risks of kidney-related issues but not hearing loss.
  • The findings stress the importance of genotype in predicting disease severity and highlight a need for better screening and treatment options for affected individuals.
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Estimated Glomerular Filtration Rate, Albuminuria, and Adverse Outcomes: An Individual-Participant Data Meta-Analysis.

JAMA

October 2023

Department of Nephrology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.

Article Synopsis
  • * This study analyzes data from over 27 million individuals to assess the impact of low eGFR and severe albuminuria on health outcomes like kidney failure, mortality, and cardiovascular events.
  • * Results indicate differing health risks associated with the methods of estimating kidney function, revealing significant correlations between lower eGFR and adverse health outcomes over time.
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Blockbuster Medications for Obesity: A Primer for Nephrologists.

Am J Kidney Dis

December 2023

Center for Kidney Health Research, Departments of Population Health Sciences and Nephrology, Geisinger, Danville, Pennsylvania. Electronic address:

The prevalence of obesity in the United States and across the world continues to climb, imparting increased risk of chronic disease. This impact is doubly felt in nephrology because obesity not only increases the risk of chronic kidney disease (CKD) but also exacerbates existing cardiovascular morbidity and mortality. The role of medical weight loss therapy in CKD has been debated, but increasing evidence suggests that intentional weight loss is protective against adverse kidney and cardiovascular outcomes.

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Article Synopsis
  • A study analyzed data from 174,418 participants to investigate the phenotypic spectrum of autosomal dominant Alport Syndrome (AS), focusing on 403 individuals identified as heterozygous for likely pathogenic variants.
  • The analysis revealed that heterozygous individuals were significantly more likely to experience kidney-related issues such as hematuria, decreased kidney function, and end-stage kidney disease, but not hearing loss.
  • Patients with specific genetic mutations (glycine missense variants) had higher risks for these conditions, yet many patients lacked appropriate screening and treatment, indicating a need for more research on early diagnosis and management of AS.
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Are Digital Health Technologies and Models of Nutrition Care the Future of Chronic Kidney Disease Management?

J Ren Nutr

November 2023

Centre for Health Services Research, Faculty of Medicine, The University of Queensland, Brisbane, Queensland, Australia; Healthcare Excellence and Innovation, Metro North Hospital and Health Service, Brisbane, Australia.

Article Synopsis
  • * While these technological approaches have shown benefits in improving diet quality and patient outcomes, there are significant barriers to their widespread adoption in nephrology and nutrition care, including issues related to patients, clinicians, and healthcare systems.
  • * The paper reviews current digital health programs for CKD nutrition, highlights their potential effectiveness, and discusses future trends and opportunities for kidney dietitians to enhance patient-centered care through technology.
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Individuals heterozygous for ALG8 protein-truncating variants are at increased risk of a mild cystic kidney disease.

Kidney Int

March 2023

Department of Nephrology, Geisinger, Danville, Pennsylvania, USA; Center for Kidney Health Research, Department of Population Health Sciences, Geisinger, Danville, Pennsylvania, USA. Electronic address:

ALG8 protein-truncating variants (PTVs) have previously been described in patients with polycystic liver disease and in some cases cystic kidney disease. Given a lack of well-controlled studies, we determined whether individuals heterozygous for ALG8 PTVs are at increased risk of cystic kidney disease in a large, unselected health system-based observational cohort linked to electronic health records in Pennsylvania (Geisinger-Regeneron DiscovEHR MyCode study). Out of 174,172 patients, 236 were identified with ALG8 PTVs.

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Importance: Most studies of autosomal dominant polycystic kidney disease (ADPKD) genetics have used kidney specialty cohorts, focusing on PKD1 and PKD2. These can lead to biased estimates of population prevalence of ADPKD-associated gene variants and their phenotypic expression.

Objective: To determine the prevalence of ADPKD and contributions of PKD1, PKD2, and other genes related to cystic kidney disease in a large, unselected cohort.

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Background Limited data exist on the benefits of lifestyle behavior change delivered using telehealth and web-based applications with varied support on blood pressure (BP). Methods and Results We conducted a 2-site randomized controlled trial at Geisinger (January 2019-March 2021) to compare the efficacy of 2 remotely delivered strategies using web-based applications in participants with 24-hour systolic BP 120-160 mm Hg and body mass index ≥25 kg/m. Both arms received access to web-based applications and the same lifestyle guidance per American Heart Association guidelines.

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