Skip to main content
. 2022 Jan 11;7(3):580–590. doi: 10.1016/j.ekir.2021.12.028

Table 5.

Clinical characteristics and prognosis of patients with m.3243 A>G by pathologic diagnosis

Characteristics of cases with mtDNA point mutation (N = 44) Pathologic diagnosis
FSGS (n = 21) Nephrosclerosis (n = 5) Diabetic nephropathy (n = 7)
Data at kidney biopsy, median (IQR)
 Age (yr) 25.0 (18.0–30.0) 30.0 (25.0–31.0) 43.0 (33.0–61.0)
 eGFR (ml/min per 1.73 m2) 82.3 (56.8–108.9) 44.6 (31.6–47.5) 43.9 (33.7–85.8)
 Proteinuria (g/g Cre) 1.99 (1.330–4.41) 0.24 (0.04–0.97) 1.28 (0.60–2.35)
Observation time for initiation of RRT, median (IQR) (yr)a 14.0 (8.0–16.0) 6.0 (5.0–8.0) 13.0 (5.0–18.0)
Initiation RRT, n (%) 15 (71.4) 1 (20.0) 2 (42.9)
Observation time for all-cause mortality, median (IQR) (yr)a 16.0 (9.0–24.0) 8.0 (6.0–12.0) 13.0 (6.0–23.0)
All-cause mortality, n (%) 4 (19.1) 1 (20.0) 6 (85.7)
eGFR declining slope (ml/min per 1.73 m2/yr), median (IQR) 8.3 (4.7–13.6) 2.9 (1.7–4.5) 3.3 (0.02–16.4)

Cre, creatinine; eGFR, estimated glomerular filtration rate; FSGS, focal segmental glomerular sclerosis; IQR, interquartile range; mtDNA, mitochondrial DNA; RRT, renal replacement therapy.

a

Time from onset of renal manifestations.