IGF-I levels reflect hypopituitarism severity in adults with pituitary dysfunction

被引:6
|
作者
Tirosh, Amit [1 ,2 ]
Toledano, Yoel [2 ,3 ]
Masri-Iraqi, Hiba [1 ,2 ]
Eizenberg, Yoav [2 ,4 ]
Tzvetov, Gloria [1 ,2 ]
Hirsch, Dania [1 ,2 ]
Benbassat, Carlos [1 ,2 ]
Robenshtok, Eyal [1 ,2 ]
Shimon, Ilan [1 ,2 ]
机构
[1] Beilinson Med Ctr, Rabin Med Ctr, Endocrine Inst, Petah Tiqwa, Israel
[2] Tel Aviv Univ, Sackler Fac Med, Tel Aviv, Israel
[3] Helen Schneider Hosp Women, Rabin Med Ctr, Div Maternal Fetal Med, Endocrinol Clin, Petah Tiqwa, Israel
[4] Tel Aviv Jaffa Dist Clalit Hlth Serv, Tel Aviv, Israel
关键词
Adult; Hypopituitarism; IGF-I; Pituitary; GROWTH-HORMONE DEFICIENCY; GH DEFICIENCY; ENDOCRINE-SOCIETY; SOMATOMEDIN-C; DIAGNOSIS; SECRETION; REPRODUCIBILITY; ASSOCIATION;
D O I
10.1007/s11102-016-0718-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To evaluate the utility of Insulin-like growth factor I (IGF-I) standard deviation score (SDS) as a surrogate marker of severity of hypopituitarism in adults with pituitary pathology. We performed a retrospective data analysis, including 269 consecutive patients with pituitary disease attending a tertiary endocrine clinic in 1990-2015. The medical files were reviewed for the complete pituitary hormone profile, including IGF-I, and clinical data. Age-adjusted assay reference ranges of IGF-I were used to calculate IGF-I SDS for each patient. The main outcome measures were positive and negative predictive values of low and high IGF-I SDS, respectively, for the various pituitary hormone deficiencies. IGF-I SDS correlated negatively with the number of altered pituitary axes (p < 0.001). Gonadotropin was affected in 76.6 % of cases, followed by thyrotropin (58.4 %), corticotropin (49.1 %), and prolactin (22.7 %). Positive and negative predictive values yielded a clear trend for the probability of low/high IGF-I SDS for all affected pituitary axes. Rates of diabetes insipidus correlated with IGF-I SDS values both for the full study population, and specifically for patients with non-functioning pituitary adenomas. IGF-I SDS can be used to evaluate the somatotroph function, as a valid substitute to absolute IGF-I levels. Moreover, IGF-I SDS predicted the extent of hypopituitarism in adults with pituitary disease, and thus can serve as a marker of hypopituitarism severity.
引用
收藏
页码:399 / 406
页数:8
相关论文
共 50 条
  • [21] Leptin after IGF-I Generation Test in a Patient with Hypopituitarism and Myotonic Dystrophy Disease
    Gómez J.M.
    Martínez-Matos J.A.
    Pituitary, 1999, 1 (2) : 121 - 123
  • [22] Skeletal effects of growth hormone and IGF-I in adults
    Marcus, R
    HORMONE RESEARCH, 1997, 48 : 60 - 64
  • [23] Skeletal effects of growth hormone and IGF-I in adults
    Marcus, R
    ENDOCRINE, 1997, 7 (01) : 53 - 55
  • [24] SERUM IGF-I LEVELS DURING CHILDHOOD AND ADOLESCENCE
    RULAND, A
    HEINRICH, U
    HARTMANN, K
    SCHONBERG, D
    ACTA PAEDIATRICA SCANDINAVICA, 1988, : 238 - 239
  • [25] IGF-I INCREASES INTEGRIN LEVELS AND OSTEOBLAST ADHESION
    GRONOWICZ, G
    MCCARTHY, M
    LIEGEOT, A
    JOURNAL OF BONE AND MINERAL RESEARCH, 1993, 8 : S308 - S308
  • [26] TNF α and IGF-I levels in Down Syndrome (DS)
    Mehta, Pankaj D.
    Patrick, Bruce A.
    Dalton, Arthur J.
    FASEB JOURNAL, 2008, 22
  • [27] Raloxifene lowers IGF-I levels in acromegalic women
    Attanasio, R
    Barausse, M
    Cozzi, R
    EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2003, 148 (04) : 443 - 448
  • [28] IGF-I levels in the cerebrospinal fluid in patients with acromegaly
    Catrina, S. B.
    Botusan, Ileana
    Cucu, C.
    Radian, S.
    Caragheorgheopol, Andra
    Coculescu, M.
    ACTA ENDOCRINOLOGICA-BUCHAREST, 2008, 4 (02) : 143 - 149
  • [29] Effects of tamoxifen an GH and IGF-I levels in acromegaly
    Cozzi, R
    Attanasio, R
    Oppizzi, G
    Orlandi, P
    Giustina, A
    Lodrini, S
    DaRe, N
    Dallabonzana, D
    JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 1997, 20 (08) : 445 - 451
  • [30] Serum leptin and IGF-I levels in cystic fibrosis
    Arumugam, R
    LeBlanc, A
    Seilheimer, DK
    Hardin, DS
    ENDOCRINE RESEARCH, 1998, 24 (02) : 247 - 257