G220 Changing patterns of growth in prader-willi syndrome

Autor: Neophytou, GI, Frixou, M, Shaikh, MG, Kyriakou, A
Zdroj: Archives of Disease in Childhood; 2018, Vol. 103 Issue: Supplement 1 pA91-A91, 1p
Abstrakt: Introduction/aimChildren with Prader-Willi syndrome (PWS) show alterations in infantile, childhood and pubertal growth. Growth Hormone (GH) therapy is recommended due to reported improvements in height velocity (HV) and body composition. The aim was to describe the patterns of growth in PWS and the influence of both changes in clinical practice and GH therapy.MethodsHeight SDS(HSDS), BMISDS and HVSDS of children attending a dedicated PWS clinic, 2000–2017, were analysed. To identify changes in growth we compared growth parameters between 2000–2012 and 2013–2017. In 21 children who received GH(median age at GH start 4.92 years (2.27,8.1)), consecutive measurements were available at −1, 0,+1 and+2 years from GH start.ResultsOverall, 60 children(31 F/29 M) were included. Three phases of growth after the age of 1 year were identified: 1–5 years, with acceleration in both HSDS(r, 0.310, p,<0.0001) and BMISDS(r, 0.602, p,<0.0001); 6–12 years, with stabilisation in both HSDS(r, 0.063, p, 0.417) and BMISDS(r, −0.154, p, 0.087); and 13–18 years, with deceleration in HSDS(r, −0.383, p,<0.0001) and unchanged BMISDS(r, 0.015, p, 0.896).Abstract G220 Table 1Age1 year 5 years 12 years 16, 17 years Number 32 30 16 31 HSDS −1.82 (-3.99,–0.08) −0.76 (-4.16,2.25)* −0.59 (-4.27,1.59) −2.66 (-4.27,–0.64)** BMISDS −0.83 (-3.27,1.85) 2.51 (-2.36,5.63)* 1.94 (-0.13,4.3) 2.52 (-1.5,4.18) * p,<0.0001 vs age 1 ** p,<0.0001 vs age 5 and age 12At age 5, children in 2013–2017 (n,12) had higher HSDS [median,−0.08 (-1.74,1.54) vs −1.04(−4.16,0.5)] than those in 2000–2012 (n,18) (p,0.03). At age 12, children in 2013–2017 (n,5) had higher HSDS [median, 1.13 (-0.62,1.59) vs −1.35 (-4.27,0.23)] (p,0.027) and lower BMISDS [median, 1.05 (-0.13,2.14) vs 2.44 (0.13,4.3)] (p,0.032) than those in 2000–2012 (n,11). After 2 years on GH, median HSDS improved from −1.43 (-4.59,0.95) to −0.11(−3.53,1.57) (p,<0.0001) and median HVSDS from 0.62 (-5.9,4.17) to 2.8(−2.2,5.2) (p,0.027). BMISDS was unchanged (Table 1).ConclusionWe were able to delineate 3 distinct phases of growth in PWS. Changes in our clinical practice have led to improvements in both height and BMI. GH therapy was associated with an increase in height and stabilisation of BMI.
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