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. 2018 Oct 30;19:301. doi: 10.1186/s12882-018-1107-y

Table 4.

Comparison of clinical parameters between UMOD positive and negative patients with non-polycystic genetic kidney diseases

Clinical parameter UMOD positive UMOD negative Significance level (p < 0.0036)
Age at presentation [years] 9–57, median 39, n = 21 0–80, median 35, n = 66 p = 0.882*
Age at RRT [years] 27–66, median 47, n = 27 9–84, median 41, n = 61 p = 0.116*
Gout 15/33 patients (45%) 30/78 (38%) p = 0.493**
Allopurinol use 13/35 patients (37%) 22/78 (28%) p = 0.342**
Hypertension at presentation 31/35 patients (89%) 69/78 (88%) p = 1.0***
Hyperuricaemia (Uric acid > 0.35 umol/l) 24/26 patients (92%) 50/61 patients (82%) p = 0.328***
Uric Acid [umol/l] 0.28–0.79, median 0.45, n = 25 0.12–0.85, median 0.495, n = 60 p = 0.155*
Proteinuria 8/22 patients (36%) 48/62 patients (77%) p = 0.0004**
Protein Creatinine Ratio [mg/g] 0–2761, median 234.5, n = 18 53–20,398, median = 2150, n = 52 p < 0.001*
Anaemia pre RRT (Hb < 100 g/l) 4/27 patients (15%) 25/68 patients (37%) p = 0.036**
Microscopic haematuria 1/27 patients (4%) 24/63 patients (38%) p = 0.001**
Renal cysts 4/21 patients (19%) 6/51 patients (12%) p = 0.463***
Normal renal size at presentation (renal diameter > 9 cm) 11/23 patients (48%) 30/48 patients (63%) p = 0.241**
Electrolyte abnormalities 6/32 patients (19%) 2/67 patients (3%) p = 0.013***

A Bonferroni correction was employed to adjust the significance level for the number of performed tests (i.e. the adjusted significance level is p < 0.05/14)

* = Mann Whitney U, ** = χ2, *** = Fisher’s Exact test