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Table 2 Multivariable Cox proportional hazards examining associations with death-censored kidney transplant failure in UK patients transplanted under 30 years of age

From: Associations with kidney transplant survival and eGFR decline in children and young adults in the United Kingdom: a retrospective cohort study

Variable

Hazard

Ratio

95% confidence interval

p-value

Lower

Upper

Female sex

1.13

1.00

1.28

0.049

Live donor (cf. deceased donor)

0.86

0.76

0.97

0.01

Human Leucocyte Antigen mismatchesa

[One DR & two B locus OR two DR locus mismatches]

1.50

1.19

1.89

0.001

Higher first reported eGFR post-transplantb

(per 10 mL/min/1.73 m2)

0.82

0.79

0.86

< 0.0001

Glomerular diseasesc, d

1.30

1.14

1.48

< 0.0001

Age group (cf. 25–29 years)e

 2–4

0.73

0.44

1.23

0.2

 5–9

0.49

0.33

0.73

< 0.0001

 10–14

0.93

0.73

1.17

0.5

 15–19

1.54

1.29

1.83

< 0.0001

 20–24

1.41

1.20

1.67

< 0.0001

 30–34

0.75

0.60

0.94

0.01

 35–39

0.78

0.54

1.11

0.2

 40–44

0.82

0.39

1.70

0.6

Ethnicity (compared to White)

 Asian

1.02

0.83

1.24

0.9

 Black

1.51

1.15

1.97

0.003

 Mixed/Other

1.02

0.71

1.44

0.9

Year of transplant (cf. 1998–2005)

 2006–2010

1.05

0.91

1.21

0.5

 2011–2014

1.17

0.97

1.42

0.1

  1. Stratified by transplant number in the study period. Standard error adjusted for 4392 clusters
  2. Live donation by ethnic group was as follows: White, 49%; Asian, 32%, Black, 37%; Mixed/Other, 48%
  3. aHLA mismatch groups were derived from the UK 2006 National Kidney Allocation scheme [17]
  4. beGFR post-transplant calculated from the first biochemical data recorded by the UK Renal Registry following transplantation. Returns are annual for paediatrics and quarterly for adults
  5. cPrimary kidney disease was using a 2012 European coding system [27]. The pediatric diagnosis was used where discordant between pediatric and adult databases [28]
  6. dThere was non-proportionality over time between those with and without glomerular diseases. Piecewise Cox regression analyses split at 1 year showed similar effects for glomerular diseases [≤1 year HR 2.05 (1.34, 3.14), p = 0.001; > 1 year HR 1.24 (1.08, 1.43), p = 0.002) and no effect on other HRs; this model presents the overall HR for the entire follow-up period
  7. eThe 45–49-year age group is suppressed due to small numbers (n = 8)