Prolonged untreated hypopituitarism results in a considerable deficit in final height. Untreated children achieve final height standard deviation scores of -4 to -6.[22]Wit JM, Kamp GA, Rikken B. Spontaneous growth and response to growth hormone treatment in children with growth hormone deficiency and idiopathic short stature. Pediatr Res. 1996 Feb;39(2):295-302.
http://www.ncbi.nlm.nih.gov/pubmed/8825803?tool=bestpractice.com
[23]Ranke MB, Price DA, Albertsson-Wikland K, et al. Factors determining pubertal growth and final height in growth hormone treatment of idiopathic growth hormone deficiency: analysis of 195 patients of the Kabi Pharmacia International Growth Study. Horm Res. 1997;48(2):62-71.
http://www.ncbi.nlm.nih.gov/pubmed/9251922?tool=bestpractice.com
The long-term effects of GHD on cardiovascular morbidity and mortality are unclear. However, adults with GHD have an increased fat mass and decreased lean body and bone mass, are often overweight, and have elevated lipids. They are often low in mood with an impaired quality of life. GH treatment can reverse and reduce many of these abnormalities.[80]Amato G, Carella C, Fazio S, et al. Body composition, bone metabolism, and heart structure and function in growth hormone (GH)-deficient adults before and after GH replacement therapy at low doses. J Clin Endocrinol Metab. 1993 Dec;77(6):1671-6.
http://www.ncbi.nlm.nih.gov/pubmed/8263158?tool=bestpractice.com
[81]Carroll PV, Christ ER, Bengtsson BA, et al. Growth hormone deficiency in adulthood and the effects of growth hormone replacement: a review. Growth Hormone Research Society Scientific Committee. J Clin Endocrinol Metab. 1998 Feb;83(2):382-95.
https://academic.oup.com/jcem/article/83/2/382/2865179
http://www.ncbi.nlm.nih.gov/pubmed/9467546?tool=bestpractice.com
Adult bone mineral density is improved with continuous as opposed to discontinuous treatment. Therefore, in the future, treatment may be routinely recommended for adults with severe GHD.
The finding of an undescended posterior pituitary in patients with "idiopathic" isolated GHD has also been shown to be a specific marker of permanent GHD (although other studies have shown that this is not always so), and is associated with a 2-fold risk of developing combined pituitary hormone deficiencies (CPHD) as compared with isolated GHD.[82]Maghnie M, Ghirardello S, Genovese E. Magnetic resonance imaging of the hypothalamus-pituitary unit in children suspected of hypopituitarism: who, how and when to investigate. J Endocrinol Invest. 2004 May;27(5):496-509.
http://www.ncbi.nlm.nih.gov/pubmed/15279086?tool=bestpractice.com
[83]Léger J, Danner S, Simon D, et al. Do all patients with childhood-onset growth hormone deficiency (GHD) and ectopic neurohypophysis have persistent GHD in adulthood? J Clin Endocrinol Metab. 2005 Feb;90(2):650-6.
https://academic.oup.com/jcem/article/90/2/650/2836543
http://www.ncbi.nlm.nih.gov/pubmed/15546901?tool=bestpractice.com
[84]Pellini C, di Natale B, De Angelis R, et al. Growth hormone deficiency in children: role of magnetic resonance imaging in assessing aetiopathogenesis and prognosis in idiopathic hypopituitarism. Eur J Pediatr. 1990 May;149(8):536-41.
http://www.ncbi.nlm.nih.gov/pubmed/2112091?tool=bestpractice.com
[85]Bozzola M, Mengarda F, Sartirana P, et al. Long-term follow-up evaluation of magnetic resonance imaging in the prognosis of permanent GH deficiency. Eur J Endocrinol. 2000 Oct;143(4):493-6.
http://www.eje-online.org/content/143/4/493.long
http://www.ncbi.nlm.nih.gov/pubmed/11022195?tool=bestpractice.com
[86]Chen S, Léger J, Garel C, et al. Growth hormone deficiency with ectopic neurohypophysis: anatomical variations and relationship between the visibility of the pituitary stalk asserted by magnetic resonance imaging and anterior pituitary function. J Clin Endocrinol Metab. 1999 Jul;84(7):2408-13.
https://academic.oup.com/jcem/article/84/7/2408/2864272
http://www.ncbi.nlm.nih.gov/pubmed/10404812?tool=bestpractice.com
Additionally, the absence of the pituitary stalk has been associated with CPHD as opposed to isolated GHD.[2]Mehta A, Hindmarsh PC, Mehta H, et al. Congenital hypopituitarism: clinical, molecular and neuroradiological correlates. Clin Endocrinol (Oxf). 2009 Sep;71(3):376-82.
http://www.ncbi.nlm.nih.gov/pubmed/19320653?tool=bestpractice.com
[85]Bozzola M, Mengarda F, Sartirana P, et al. Long-term follow-up evaluation of magnetic resonance imaging in the prognosis of permanent GH deficiency. Eur J Endocrinol. 2000 Oct;143(4):493-6.
http://www.eje-online.org/content/143/4/493.long
http://www.ncbi.nlm.nih.gov/pubmed/11022195?tool=bestpractice.com
These data imply that magnetic resonance imaging may be of prognostic use in patients with isolated GHD. Patients who have GHD in association with CPHD (especially if there are ≥3 other hormone deficits) are likely to be GH deficient as adults.