ESPE Abstracts (2014) 82 P-D-1-3-169

ESPE2014 Poster Presentations Growth (2) (13 abstracts)

Recombinant Human GH Therapy Allows to Reach a Normal Final Adult Height in Coeliac Children with GH Deficiency due to Hypophysistis

Lorenzo Iughetti a , Laura Lucaccioni a , Patrizia Bruzzi a , Anna Rita Di Biase a , Anna Maira De Bellis b & Barbara Predieri a


aDepartment of Medical and Surgical Sciences of the Mother, Children and Adults, University of Modena and Reggio Emilia, Modena, Italy; bDepartment of Clinical and Experimental Medicine and Surgery 2, Chair of Endocrinology, Second University of Naples, Naples, Italy


Background: Coeliac disease (CD) can be associated with impaired growth in children after a prolonged period of Gluten-free diet (GFD). A small percentage of CD patients does not show catch-up growth during GFD because of GH secretion deficiency (GHD) that could be associated with antipituitary autoantibodies (APA).

Objective and hypotheses: This study aims to evaluate the efficacy of recombinant human GH (rhGH) therapy on final adult height in children with CD and GHD associated with APA.

Method: We evaluated six CD patients with persistent growth impairment after at least 1 year from the GFD initiation due to GHD. APA and/or antihypothalamus autoantibodies resulted positive at high titers in four out of six CD-GHD patients. They all started rhGH therapy at the recommended weekly dose of 0.233±0.007 mg/kg s.c. for a mean period of 3.21±1.88 years.

Results: Patients showed a significant gain of height SDS from the onset of rhGH therapy to the stop time (−2.09±0.35 vs −1.00±0.43, respectively; P=0.0277) and the final adult height SDS, evaluated after 1 year from the rhGH interruption, was within the target height (−0.81±0.69 vs −0.57±0.61, respectively; P=0.248). Results did not changed analysing data according to APA and/or AHA status (positive vs negative): final adult height was consistent with the target height.

Conclusion: In patients with CD and GHD the association of GFD and rhGH treatment seems to allow an adequate catch-up growth and the achievement of height within target height and presence of LYH seems not to influence the efficacy of the treatment.

Volume 82

53rd Annual ESPE (ESPE 2014)

Dublin, Ireland
18 Sep 2014 - 20 Sep 2014

European Society for Paediatric Endocrinology 

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