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. 2023 Mar 30;34(6):1105–1119. doi: 10.1681/ASN.0000000000000132

Table 1.

Study cohort characteristics

Characteristics UPJO (n=321) UVJO (n=178) COU-NOS (n=234) Overall COU Cohort (n=733)
Sex
 Female 117 (36.4) 51 (28.7) 63 (26.9) 231 (31.5)
 Male 204 (63.6) 127 (71.3) 171 (73.1) 502 (68.5)
Laterality
 Bilateral 31 (9.7) 35 (19.7) 64 (27.4) 130 (17.7)
 Left 164 (51.1) 95 (53.4) 95 (40.6) 354 (48.3)
 Right 94 (29.3) 33 (18.5) 62 (26.5) 189 (25.8)
 Unknown 32 (10) 15 (8.4) 13 (5.6) 60 (8.2)
Genetically determined ancestry
 European participants 264 (82.2) 148 (83.1) 187 (79.9) 599 (81.7)
 Admixed participants 40 (12.5) 22 (12.4) 27 (11.5) 89 (12.1)
 Hispanic participants 6 (1.9) 5 (2.8) 12 (5.1) 23 (3.1)
 South Asian participants 5 (1.6) 2 (1.1) 2 (0.9) 9 (1.2)
 African participants 3 (0.9) 1 (0.6) 4 (1.7) 8 (1.1)
 East Asian participants 3 (0.9) 0 2 (0.9) 5 (0.7)
Additional renal phenotype
 Bladder defect 2 (0.6) 3 (1.7) 5 (2.1) 10 (1.4)
 DCS 8 (2.5) 5 (2.8) 2 (0.9) 15 (2)
 Ectopia 5 (1.6) 4 (2.2) 4 (1.7) 13 (1.8)
 Glomerular 3 (0.9) 0 2 (0.9) 5 (0.7)
 KHD 19 (5.9) 5 (2.8) 7 (3) 31 (4.2)
 Nephronopthisis 1 (0.3) 0 0 1 (0.1)
 Reflux nephropathy 14 (4.4) 23 (12.9) 10 (4.3) 47 (6.4)
 Tubular defect 0 0 1 (0.4) 1 (0.1)
Nonurinary defect
 Neural 8 (2.5) 5 (2.8) 1 (0.4) 14 (1.9)
 Craniofacial 8 (2.5) 7 (3.9) 4 (1.7) 19 (2.6)
 Cardiac 5 (1.6) 5 (2.8) 9 (3.8) 19 (2.6)
 Musculoskeletal 6 (1.9) 8 (4.5) 4 (1.7) 18 (2.5)
 Gastrointestinal 6 (1.9) 5 (2.8) 1 (0.4) 12 (1.6)
 Genital 12 (3.7) 5 (2.8) 10 (4.3) 27 (3.7)
 General developmental delay 6 (1.9) 8 (4.5) 4 (1.7) 18 (2.5)
 Other syndromesa 0,00 0,00 2 (0.9) 2 (0.3)
Family history of kidney disease 47 (14.6) 35 (19.7) 82 (35) 164 (22.4)

Presented as n (%). UPJO, ureteropelvic junction obstruction; UVJO, ureterovesical junction obstruction; COU-NOS, congenital obstructive uropathy—not otherwise specified; COU, congenital obstructive uropathy; DCS, duplex collecting system; KHD, kidney hypodysplasia.

a

Other syndromes include Currarino syndrome and Beckwith–Wiedemann.