Prevalence and predictors of Sickle Cell Nephropathy A single-center experience

被引:0
|
作者
Elzorkany, Khaled [1 ,2 ]
Alsalman, Mortadah [1 ]
Alsahlawi, Muthana [1 ]
Alhedhod, Azam [3 ]
Almulhim, Nasser Abdullah [3 ]
Alsultan, Nora Jalal [3 ]
Al-Ali, Eman Mohammed [3 ]
Ali, Eman [1 ]
Omer, Nawal Eltayeb [4 ]
机构
[1] King Faisal Univ, Coll Med, Internal Med Dept, Al Hasa, Saudi Arabia
[2] Menoufia Univ, Fac Med, Internal Med Dept, Nephrol Unit, Menoufia, Egypt
[3] King Faisal Univ, Coll Med, Al Hasa, Saudi Arabia
[4] Hereditary blood Dis Ctr, Al Hasa, Saudi Arabia
来源
SCIENTIFIC REPORTS | 2024年 / 14卷 / 01期
关键词
Sickle cell disease; Hydroxyurea; CKD; sickle cell nephropathy; ERECTILE FUNCTION IIEF; QUALITY-OF-LIFE; INTERNATIONAL INDEX; TESTICULAR CANCER; SURVIVORS;
D O I
10.1038/s41598-024-79345-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Sickle cell disease (SCD) is the most common monogenic disorder in Saudi Arabia, which associates with an increased risk of organs damage, including the kidney. The aim of this study is to investigate the prevalence and predictors of sickle cell nephropathy (SCN) in the Saudi population. A retrospective study was conducted from April to October 2023, and included 343 adult patients with SCD who were recruited from the hereditary blood diseases center (HBDC), Al-Ahsa, Saudi Arabia. Spot protein-to-creatinine ratio was measured and glomerular filtration rate (GFR) was estimated from serum creatinine using the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation. As per KIDGO guidelines, CKD was diagnosed in 93 (27.1%) patients. Based on the CKD-EPI equation, 2% of patients had low GFR (eGFR < 60mL/min), 28.3% had high GFR (eGFR > 140 mL/min), and 69.7% had normal GFR. Among SCD patients, proteinuria was observed in 26.5% of the patients. SCD patients with CKD were significantly older than non-CKD patients (p < 0.001) and had higher prevalence of diabetes mellitus (DM) and hypertension (HTN) (p = 0.045 and 0.001 respectively). The multivariate analysis showed that age (P = 0.001; OR 1.035; 95% CI 1.014-1.056) and low hemoglobin level (p = 0.034; OR -0.851; 95% CI 0.721-0.980) were independent risk factors for the development of SCN. Nephropathy is a common complication among patients with SCD as early as the third decade of life, although they remain asymptomatic. Advances in age and low hemoglobin levels are the main predictors of nephropathy. In addition, SCD patients with coexistent comorbidities, particularly DM and HTN, were at increased risk of developing kidney disease.
引用
收藏
页数:7
相关论文
共 50 条
  • [1] Prevalence of neuropathic pain in adolescents with sickle cell disease: A single-center experience
    Cregan, Melissa
    Puri, Latika
    Kang, Guolian
    Anghelescu, Doralina
    PEDIATRIC BLOOD & CANCER, 2022, 69 (04)
  • [2] Laparoscopic cholecystectomy in 427 adults with sickle cell disease: a single-center experience
    Abdulrahman S. Al-Mulhim
    Abdulmohsen A. Al-Mulhim
    Surgical Endoscopy, 2009, 23 : 1599 - 1602
  • [3] Laparoscopic cholecystectomy in 427 adults with sickle cell disease: a single-center experience
    Al-Mulhim, Abdulrahman S.
    Al-Mulhim, Abdulmohsen A.
    SURGICAL ENDOSCOPY AND OTHER INTERVENTIONAL TECHNIQUES, 2009, 23 (07): : 1599 - 1602
  • [4] Red blood cell utilization in patients with sickle cell disease: A Canadian single-center experience
    Uminski, Kelsey
    Perelman, Iris
    Mack, Johnathan
    Tinmouth, Alan
    TRANSFUSION, 2025, : 476 - 484
  • [5] Moyamoya Syndrome in Children With Sickle Cell Disease in Saudi Arabia: A Single-Center Experience
    Zayed, Abdalla M.
    Al-Muhaimeed, Sulaiman
    Al-Otaibi, Turki
    Ali, Elsayed Mohammed
    Saleh, Rashid
    Ancheta, Shangrila Joy
    Al-Harbi, Fahad
    Waheed, Khawaja Bilal
    Albahli, Yasir
    Alghamdi, Hamid
    CUREUS JOURNAL OF MEDICAL SCIENCE, 2023, 15 (11)
  • [6] Single-center experience of LVAD implantation in patients with sickle-cell trait: A retrospective analysis
    Al Khamees, Khalid
    Grasso, Elena
    Ibrahim, Ahmed
    Abdallah, Hassane
    Adbelhamed, Mohamad I.
    Sayin, Omer
    Lorusso, Roberto
    JOURNAL OF CARDIAC SURGERY, 2022, 37 (12) : 4816 - 4824
  • [7] Clinical and hematological effects of hydroxyurea therapy in sickle cell patients: a single-center experience in Brazil
    Silva-Pinto, Ana Cristina
    Angulo, Ivan Lucena
    Brunetta, Denise Menezes
    Rodrigues Neves, Fabia Idalina
    Bassi, Sarah Cristina
    De Santis, Gil Cunha
    Covas, Dimas Tadeu
    SAO PAULO MEDICAL JOURNAL, 2013, 131 (04): : 238 - 243
  • [8] Characteristics and outcomes of osteomyelitis in children with sickle cell disease: A 10-year single-center experience
    Weisman, Julie K.
    Nickel, Robert Sheppard
    Darbari, Deepika S.
    Hanisch, Benjamin R.
    Diab, Yaser A.
    PEDIATRIC BLOOD & CANCER, 2020, 67 (05)
  • [9] The prevalence of Sickle Nephropathy among children with Sickle Cell Disease
    Eltagui, Mona Hassan
    Abd Elhady, Marwa
    El-Sayed, Dalia
    Momen, Nouran
    Selim, Yasmeen M. M.
    Salam, Mai Abd E. L.
    JOURNAL OF POPULATION THERAPEUTICS AND CLINICAL PHARMACOLOGY, 2023, 30 (07): : E141 - E147
  • [10] Implementation of near-universal hydroxyurea uptake among children with sickle cell anemia: A single-center experience
    Karkoska, Kristine
    Todd, Kevin
    Niss, Omar
    Clapp, Kelly
    Fenchel, Lynette
    Kalfa, Theodosia A.
    Malik, Punam
    Quinn, Charles T.
    Ware, Russell E.
    McGann, Patrick T.
    PEDIATRIC BLOOD & CANCER, 2021, 68 (06)