Focal segmental glomerulosclerosis epidemiology and demographics
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor-In-Chief:’’’ Olufunmilola Olubukola M.D.[2]
Overview
Epidemiology & Demographics
Focal segmental glomerulosclerosis (FSGS) is considered the most common cause of nephrotic syndrome worldwide.[1]FSGS remains the most common primary glomerulonephropathy across ethnic and racial distribution in the United States. [2]Data from the United States Renal Data System (USRDS) collected over 21 years shows that FSGS is the most common renal pathology identified in end-stage renal disease (ESRD) patients in the United States.[1]
Incidence and Prevalence
The prevalence of FSGS as a lesion associated with ESRD has risen. In 1980, FSGS was the cause of ESRD in only 0.2 percent of patients; by 2000, it was responsible for 2.3 percent of cases of ESRD. [3] Around the world, there are contrary evidences as to FSGS being the most common cause of Nephrotic Syndrome. Though, FSGS accounts for 15 to 45% of all primary glomerular diseases worldwide, higher incidence and prevalence of FSGS are seen only in America, India, Brazil and Saudi Arabia.[4]
In Asia, Europe and Australia however, IgA nephropathy remains the most common cause of Idiopathic Nephrotic Syndrome accounting for about 40 to 45% cause of primary glomerulopathy [4] while in Africa, MCD is the most common cause of Idiopathic Nephrotic Syndrome accounting for 16.5% of all causes of primary NS. [5]
Age
The disease is considered a disease of the adult population (vs. minimal change disease which is much more common among children). In a 21-year follow-up study that excludes HIV-associated nephropathy, the median age of FSGS ESRD is 40-49 years in black adults and 70-79 in white and Asian adults.[1]
Gender
The male to female ratio is 1.5-2 to 1.[1]
Race
FSGS is the most common primary renal cause of end-stage renal disease (ESRD) in whites and blacks, contributing to approximately 2% of ESRD.[1]
FSGS is more common in blacks. It accounts for approximately 35% of nephrotic syndromes in all cases and approximately 50% of nephrotic syndrome in blacks.[6] FSGS seems to have a higher incidence in Blacks with a familial pattern of inheritance especially in Blacks with family history of ESKD.
References
- ↑ 1.0 1.1 1.2 1.3 1.4 Kitiyakara C, Eggers P, Kopp JB (2004). "Twenty-one-year trend in ESRD due to focal segmental glomerulosclerosis in the United States". Am J Kidney Dis. 44 (5): 815–25. PMID 15492947.
- ↑ Sim JJ, Batech M, Hever A, Harrison TN, Avelar T, Kanter MH; et al. (2016). "Distribution of Biopsy-Proven Presumed Primary Glomerulonephropathies in 2000-2011 Among a Racially and Ethnically Diverse US Population". Am J Kidney Dis. 68 (4): 533–44. doi:10.1053/j.ajkd.2016.03.416. PMID 27138468.
- ↑ Reiser J, Nast CC, Alachkar N (2014). "Permeability factors in focal and segmental glomerulosclerosis". Adv Chronic Kidney Dis. 21 (5): 417–21. doi:10.1053/j.ackd.2014.05.010. PMC 4149759. PMID 25168830.
- ↑ 4.0 4.1 Kitiyakara C, Eggers P, Kopp JB (2004). "Twenty-one-year trend in ESRD due to focal segmental glomerulosclerosis in the United States". Am J Kidney Dis. 44 (5): 815–25. PMID 15492947 : 15492947 Check
|pmid=
value (help). - ↑ Okpechi IG, Ameh OI, Bello AK, Ronco P, Swanepoel CR, Kengne AP (2016). "Epidemiology of Histologically Proven Glomerulonephritis in Africa: A Systematic Review and Meta-Analysis". PLoS One. 11 (3): e0152203. doi:10.1371/journal.pone.0152203. PMC 4806979. PMID 27011216.
- ↑ Hogg R, Middleton J, Vehaskari VM (2007). "Focal segmental glomerulosclerosis--epidemiology aspects in children and adults". Pediatr Nephrol. 22 (2): 183–6. doi:10.1007/s00467-006-0370-5. PMC 1764601. PMID 17151873.