Kowarski syndrome

Kowarski syndrome
Other namesShort stature due to growth hormone qualitative anomaly
This condition is inherited in an autosomal recessive manner.

Kowarski syndrome[1] describes cases of growth failure (height and bone age two standard deviations below the mean for age), despite the presence of normal or slightly high blood growth hormone by radioimmunoassay (RIA-GH) and low serum IGF1 (formerly called somatomedin), and who exhibit a significant increase in growth rate following recombinant GH therapy.[2]

Cause

Allen Avinoam Kowarski et al.[3] described the first two cases of the Kowarski syndrome in 1978. The group speculated that their patients' growth impairment was caused by a mutation in the growth hormone gene, which altered the structure of their secreted growth hormone, reducing its biological activity while retaining its ability to bind the antibodies used in the RIA-GH. Their RIA-GH measured growth hormone of reduced bioactivity. The children retained the ability to respond to treatment with active growth hormone.

The speculation of Kowarski et al. was confirmed by Valenta et al in 1985, Takahshi et al in 1996 and 1997 and Besson et al in 2005. Valenta et al[4] studied a case of Kowarski syndrome where they confirmed a structural abnormality of the growth hormone molecule. 60 to 90% of circulating growth hormone of the patient was in the form of tetramers and dimers (normal, 14% to 39% in plasma) and the patients' growth hormone polymers were abnormally resistant to conversion into monomers by urea.

Takahashi et al.[5] reported a case of a boy with short stature who was heterozygous for a mutation in the GH1 gene. In this child, growth hormone not only could not activate the GH receptor (GHR) but also inhibited the action of wild type GH because of its greater affinity for GHR and GH-binding protein (GHBP) that is derived from the extracellular domain of the GHR. Thus, a dominant-negative effect was observed.

Takahashi et al.[6] demonstrated in a girl with short stature, a biologically inactive growth hormone resulting from a heterozygous mutation in the GH1 gene. At age 3 years, the girl's height was 3.6 standard deviations below the mean for age and sex. Bone age was delayed by 1.5 years. She had a prominent forehead and a hypoplastic nasal bridge with normal body proportions. She showed lack of growth hormone action despite high immunoassayable GH levels in serum and marked catch-up growth to exogenous GH administration. Results of other studies were compatible with the production of a bioinactive GH, which prevented dimerization of the growth hormone receptor, a crucial step in GH signal transduction.

Besson et al[7] described in 1955 a Serbian patient with Kowarski syndrome who was homozygous for a mutation in the GH1 gene that disrupted the first disulfide bridge in growth hormone. The parents were each heterozygous for the mutation and were of normal stature.

Diagnosis

Diagnostic criteria

The discovery of the Kowarski syndrome created a dilemma. The first diagnostic test for the syndrome was subjecting the suspected children to six month of growth hormone therapy. Kowarski syndrome was assumed to be a very rare disorder (officially recognized as an “orphan disease”). Researchers could not justify subjecting children to a trial period of growth hormone therapy to confirm the diagnosis of a rare syndrome. There is a need for a reliable and practical diagnostic procedure for the syndrome.

Reliability of testing

The standard test for growth hormone deficiency is the growth hormone stimulation test. Peak levels of growth hormone below normal are considered confirmation of a growth hormone deficiency. Growth-impaired children with a normal stimulation test were considered suspect for having the Kowarski syndrome that may benefit from treatment with growth hormone.

Zadik et al.[8] reported in 1990 that the growth hormone stimulation test is not reliable, suggesting the use of the more reliable 24-hour integrated concentration of growth hormone (IC-GH) as a better test. In 1995, it was also suggested[9] that some cases of the neurosecretory growth failure syndrome might have the Kowarski syndrome.

Albertsson-Wikland Kerstin confirmed in 1992[10] that the IC-GH test is a reproducible test for growth hormone deficiency and Carel et al. confirmed in 1997[11] that the reliability of the growth hormone stimulation tests was poor.

A 1987 study by Bistrizer et al [12] suggested a diagnostic procedure that may be used to diagnose the Kowarski syndrome. Their study was based on the requirement for the growth hormone molecule to bind a specific binding molecule on the wall of the responsive cells to elicit its activity. Their study demonstrated a decrease ability of the growth hormone from children with the Kowarski syndrome to bind with living IM-9 cells. The test involved measuring the ratio between the levels of growth hormone by a radioreceptor assay (RRA-GH) to the level of growth hormone determined by the established radioimmunoassay (RIA-GH). The study found that the RRA-GH/RIA-GH ratio in NS subjects was normal but significantly below normal (P<0.005) in the Kowarski syndrome patients. The authors proposed the use of their test for the diagnosis of the Kowarski syndrome.

Bistrizer, Chalew and Kowarski demonstrated in 1995 [9] that a modified RRA-GH/RIA-GH ratio test was a predictor for the responsiveness of growth-impaired children to growth hormone therapy.

The RRA-GH/RIA-GH ratio assay proposed by Bistrizer et al.[9] can be used for screening of patients who may have the Kowarski syndrome thus more likely to respond to Growth Hormone therapy. Advances in the methodology for identifying spot mutations in the DNA of individuals demonstrated that the "Kowarski Syndrome is caused by various mutations in the GH1 gene (17q22-q24) that result in structural GH anomalies and a biologically inactive molecule." Testing individual patient for such mutation is offered on the Internet.[13]

References

  1. ↑ OMIM Database entry for Kowarski syndrome
  2. ↑ Mullis, 6th ESPE Advanced Seminar in Developmental Endocrinology, Bern, May 10–11, 2012; volume editor, Primus-E. Developmental biology of GH secretion, growth, and treatment. Basel: Karger. p. 75. ISBN 9783318022445. {{cite book}}: |first= has generic name (help)
  3. ↑ Kowarski AA, Schneider J, Ben-Galim E, Weldon VV, Daughaday WH (August 1978). "Growth failure with normal serum RIA-GH and low somatomedin activity: somatomedin restoration and growth acceleration after exogenous GH". J. Clin. Endocrinol. Metab. 47 (2): 461–4. doi:10.1210/jcem-47-2-461. PMID 263308.
  4. ↑ Valenta LJ, Sigel MB, Lesniak MA, Elias AN, Lewis UJ, Friesen HG, Kershnar AK (January 1985). "Pituitary dwarfism in a patient with circulating abnormal growth hormone polymers". N. Engl. J. Med. 312 (4): 214–7. doi:10.1056/NEJM198501243120405. PMID 3965948.
  5. ↑ Takahashi, Yutaka; Kaji, Hidesuke; Okimura, Yasuhiko; Goji, Katsumi; Abe, Hiromi; Chihara, Kazuo (1996). "Short Stature Caused by a Mutant Growth Hormone". New England Journal of Medicine. 334 (7): 432–436. doi:10.1056/NEJM199602153340704. ISSN 0028-4793. PMID 8552145.
  6. ↑ Takahashi Y, Shirono H, Arisaka O, Takahashi K, Yagi T, Koga J, Kaji H, Okimura Y, Abe H, Tanaka T, Chihara K (September 1997). "Biologically inactive growth hormone caused by an amino acid substitution". J. Clin. Invest. 100 (5): 1159–65. doi:10.1172/JCI119627. PMC 508291. PMID 9276733.
  7. ↑ Besson A, Salemi S, Deladoëy J, Vuissoz JM, Eblé A, Bidlingmaier M, Bürgi S, Honegger U, Flück C, Mullis PE (May 2005). "Short stature caused by a biologically inactive mutant growth hormone (GH-C53S)". J. Clin. Endocrinol. Metab. 90 (5): 2493–9. doi:10.1210/jc.2004-1838. PMID 15713716.
  8. ↑ Zadik Z, Chalew SA, Gilula Z, Kowarski AA (November 1990). "Reproducibility of growth hormone testing procedures: a comparison between 24-hour integrated concentration and pharmacological stimulation". J. Clin. Endocrinol. Metab. 71 (5): 1127–30. doi:10.1210/jcem-71-5-1127. PMID 2229276.
  9. 1 2 3 Bistritzer T, Chalew SA, Kowarski AA (1995). "Growth failure with plasma GH that is normal by RIA but low by radioreceptor assay: responsiveness to exogenous GH". Horm. Res. 43 (6): 261–5. doi:10.1159/000184306. PMID 7607611.
  10. ↑ Albertsson-Wikland K, Rosberg S (February 1992). "Reproducibility of 24-h growth hormone profiles in children". Acta Endocrinol. 126 (2): 109–12. doi:10.1530/acta.0.1260109. PMID 1543014.
  11. ↑ Carel JC, Tresca JP, Letrait M, Chaussain JL, Lebouc Y, Job JC, Coste J (July 1997). "Growth hormone testing for the diagnosis of growth hormone deficiency in childhood: a population register-based study". J. Clin. Endocrinol. Metab. 82 (7): 2117–21. doi:10.1210/jcem.82.7.4106. PMID 9215281.
  12. ↑ Bistritzer, Tzvy; Chalew, Stuart A; Lovohik, Judith C; Kowarski, A Avlnoam (1987). "Decreased Growth Hormone (Gh) Binding to Im-9 Cells in Children with Biologically Inactive Gh Syndrome (Bi)". Pediatric Research. 21 (4): 244A. doi:10.1203/00006450-198704010-00461. ISSN 0031-3998.
  13. ↑ "Short stature due to growth hormone qualitative anomaly". orphanet.
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