Association of hypertension and genetic variants in MYH9 and BMPR1B with increased proteinuria in sickle cell disease

Increased total proteinuria is highly prevalent in this young cohort, indicating early onset of kidney damage. Relative systemic hypertension is a major modifiable risk factor, underscoring the need for rigorous blood pressure control. The instability of the initial genetic signal for MYH9-rs4821469, coupled with its strong linkage disequilibrium with APOL1, suggests that the observed association is likely confounded by ungenotyped APOL1 variants. This highlights the critical importance of including APOL1 analysis in future SCN genetic studies in African-ancestry populations.

Authors

Institutions

Publication Details

Journal
Clinical Biochemistry
Published
2025-11-20
DOI
https://doi.org/10.1016/j.clinbiochem.2025.111058
Primary Topic
Hemoglobinopathies and Related Disorders
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Association of hypertension and genetic variants in MYH9 and BMPR1B with increased proteinuria in sickle cell disease

Rokhaya Dione, Moussa Seck, El Hadj Ousmane Sene, Pape Matar Kandji et al.
Clinical Biochemistry
Hemoglobinopathies and Related Disorders
article

Association of hypertension and genetic variants in MYH9 and BMPR1B with increased proteinuria in sickle cell disease

Rokhaya Dione, Moussa Seck, El Hadj Ousmane Sene, Pape Matar Kandji, Khuthala Mnika, Serigne Saliou Mbacke, Ibrahima Diagne, Nènè Oumou Kesso Barry, Papa Madièye Guéye, Ambroise Wonkam, El Hadji Malick Ndour, Saliou Diop, Rokhaya Ndiaye Diallo, Coumba Kamby, Aynina Cissé, Victoria Nembaware, Jean Pascal Demba Diop, Moustapha Djité, Indou Déme Ly, Philomène Lopez Sall, Fatou Guèye Tall, Mara Sokhna
article en

Abstract

Increased total proteinuria is highly prevalent in this young cohort, indicating early onset of kidney damage. Relative systemic hypertension is a major modifiable risk factor, underscoring the need for rigorous blood pressure control. The instability of the initial genetic signal for MYH9-rs4821469, coupled with its strong linkage disequilibrium with APOL1, suggests that the observed association is likely confounded by ungenotyped APOL1 variants. This highlights the critical importance of including APOL1 analysis in future SCN genetic studies in African-ancestry populations.

Clinical BiochemistryVol. 141
National Health Laboratory Service (ZA), Université Gaston Berger (SN), Johns Hopkins University (US), University of Cape Town (ZA), University of the Witwatersrand (ZA), Johns Hopkins Medicine (US), Centre Hospitalier National Universitaire de Fann (SN)
Openalex Percentile: Top 49%
Hemoglobinopathies and Related Disorders
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.