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Factors for persistent growth hormone deficiency in young adults with childhood onset growth hormone deficiency

소아청소년기 성장호르몬결핍증의 성인기 지속에 영향을 미치는 요인

  • Lee, Young Ah (Department of Pediatrics, College of Medicine, Seoul National University) ;
  • Chung, Hye Rim (Department of Pediatrics, College of Medicine, Seoul National University) ;
  • Lee, Se Min (Department of Pediatrics, College of Medicine, Hanyang University) ;
  • Kim, Jae Hyun (Department of Pediatrics, College of Medicine, Seoul National University) ;
  • Kim, Ji Hyun (Department of Pediatrics, College of Medicine, Seoul National University) ;
  • Lee, Sun Hee (Department of Pediatrics, College of Medicine, Seoul National University) ;
  • Shin, Choong Ho (Department of Pediatrics, College of Medicine, Seoul National University) ;
  • Yang, Sei Won (Department of Pediatrics, College of Medicine, Seoul National University)
  • 이영아 (서울대학교 의과대학 소아과학교실) ;
  • 정혜림 (서울대학교 의과대학 소아과학교실) ;
  • 이세민 (한양대학교 의과대학 소아과학교실) ;
  • 김재현 (서울대학교 의과대학 소아과학교실) ;
  • 김지현 (서울대학교 의과대학 소아과학교실) ;
  • 이선희 (서울대학교 의과대학 소아과학교실) ;
  • 신충호 (서울대학교 의과대학 소아과학교실) ;
  • 양세원 (서울대학교 의과대학 소아과학교실)
  • Received : 2008.01.13
  • Accepted : 2008.01.27
  • Published : 2009.02.15

Abstract

Purpose : Growth hormone (GH) replacement after retesting is necessary because impairment of body composition and cardiovascular health has been more severe in adult patients with persistent GH deficiency (GHD) from childhood to adulthood. This study aimed to investigate the factors for persistent GHD and define a highly probable group of persistent GHD in young adults with childhood-onset GHD. Methods : GHD was reassessed by insulin tolerance test (ITT) in 55 adult patients (39 males, 16 females) with childhood-onset GHD. Twelve patients presented with idiopathic GHD and 43 patients presented with organic GHD caused by tumors involving the hypothalamus-pituitary (H-P) region (n=33), other brain tumors (n=3), meningitis (n=3), leukemia (n=2) and others (n=2). Results : Forty-nine (89.1%) of 55 patients had persistent GHD. IGF-I was positively correlated with log of peak GH (r=0.57, P<0.001). There was no difference in the proportion of persistent GHD between idiopathic and organic GHD. The percentage of patients with persistent GHD was 40%, 80%, and 95.6% for patients with zero, one, two or more additional pituitary hormone deficiencies (PHDs), respectively (P=0.002). The probability of persistent GHD was higher in patients with diseases involving the H-P region (P=0.003). GHD persisted in 15 of 18 patients treated with cranial irradiation. Conclusion : We suggest that the probability of persistent GHD in adulthood was high in patients with 2 or more additional PHDs, and diseases involving the H-P region.

목 적 : 소아청소년기 GHD 환자들은 성인기에 진단된 환자보다 체성분과 심혈관계의 변화가 심한 것으로 알려져 있어 성인기에도 GHD가 지속되면 성장호르몬 치료를 꼭 받아야 한다. 본 연구에서는 소아청소년기에 GHD로 진단 받은 성인 환자들을 대상으로 ITT를 시행하여 성인기에도 GHD가 지속되는 요인을 살펴보고, 성인기에도 GHD가 지속될 가능성이 높은 대상을 알아보고자 한다. 방 법 : 성인키에 도달한 55명(남 39명, 여 16명)을 대상으로 ITT의 최대 성장호르몬 값이 $3{\mu}g/L$ 미만이면 성인기 GHD로 진단하였다. 특발성 GHD 환자(n=12)는 뇌하수체 구조적인 이상이 있는 2명과 둔위 분만 또는 가사의 병력이 있는 10명이었으며, 기질성 GHD 환자(n=43)는 시상하부-뇌하수체를 침범하는 뇌종양(n=33), 그 외의 뇌종양(n=3), 뇌수막염(n=3), 백혈병(n= 2), 지주막낭종(n=1), 뇌하수체염(n=1)에 해당하였다. 결 과 : 성인기에도 GHD가 지속된 환자는 49명(89.1%)이었다. 최대 성장호르몬 값의 log값은 기저 IGF-I 농도와 양의 상관관계를 보였다(r=0.57, P<0.001). 특발성 GHD 환자의 91.7%가 성인기에도 GHD가 지속되어, 성인기 GHD 여부는 소아청소년기 특발성, 기질성 GHD 여부에 따른 차이가 없었다. 동반된 뇌하수체호르몬 결핍 개수가 많을수록(단독 GHD 40%, 1개의 결핍 동반 80%, 2개 이상 동반 95.6%, P=0.002), 기질성 GHD 환자 중에서 병변이 시상하부-뇌하수체를 일차적으로 침범하는 경우(P=0.003)에 성인기에도 GHD가 지속될 가능성이 높았다. 두개 내 방사선 치료를 받은 18명 중에서 15명이 성인기에도 GHD가 지속되었는데, 시상하부-뇌하수체를 침범하는 종양으로 방사선 치료를 받은 환자들 14명은 모두 방사선조사량에 관계없이 성인기에도 GHD가 지속되었다. 동반된 뇌하수체호르몬 결핍이 있는 경우(P=0.005), 소아청소년기 완전 GHD인 경우(P=0.005)에 성인기에도 GHD가 지속되는 비율이 높았다. 결 론 : 소아청소년기에 GHD로 진단 받은 환자들 중에서 동반 뇌하수체호르몬 결핍이 2개 이상이거나, 기저 질환의 병변이 시상하부-뇌하수체를 포함하면 성인기에도 GHD가 지속될 가능성이 높다.

Keywords

References

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