Printer Friendly

Follow-up Findings in a Turkish Girl with Pseudohypoparathyroidism Type Ia Caused by a Novel Heterozygous Mutation in the GNAS Gene.

What is already known on this topic?

Pseudohypoparathyroidism type Ia (PHP-Ia) is characterized by multihormone resistance and Albright hereditary osteodystrophy. Heterozygous mutations in GNAS gene may result with decreased Gsa activity.

What this study adds?

Longitudinal follow-up of a PHP-Ia patient seems to be lacking in the literature. In our case, heterotopic ossification, subclinical hypothyroidism, and cerebral calcification developed late during the 8-year follow-up period. To our knowledge, this is the first report about bioinactive growth hormone associated with PHP-Ia. GNAS gene analysis revealed a novel mutation.

Introduction

Pseudohypoparathyroidism (PHP) is defined as an endorgan resistance to parathormone (PTH) and is characterized by hypocalcemia, hyperphosphatemia, and increased PTH levels (1).

PHP-Ia is a subtype of PHP, caused by heterozygous inactivating mutations in GNAS which encodes Gsa. This gene is located on chromosome 20q13.11 and contains 13 exons and 12 introns. Gsa is essential for the actions of PTH and of many other hormones (2,3). PHP-Ia patients express resistance to hormones that act via Gs-coupled receptors, such as PTH, thyroid-stimulating hormone (TSH), gonadotropins, growth hormone-releasing hormone (GHRH). These patients, also known as cases of Albright hereditary osteodystrophy (AHO), show a constellation of features including short stature, short neck, round face, centripedal obesity, brachydactyly, ectopic ossifications, and mild mental retardation.

Low serum calcium, elevated serum phosphorus and high PTH are frequent findings in laboratory analyses. In some cases, calcium and phosphorus are within the normal range and only PTH is elevated (2,4).

The differential diagnosis among subtypes of PHP is very difficult. Table 1 shows subtypes of PHP with the classification based on the level of serum calcium, phosphorus, PTH, urinary cyclic AMP (cAMP), phosphaturia response to PTH, Gsa activity, and presence of AHO phenotype. PHP-I can be differentiated by the presence (PHP-Ia and PHP-Ic) or absence (PHP-Ib) of AHO. The only way to distinguish PHP-Ia from the much rarer PHP-Ic is to measure Gsa activity because of the identical clinical and biochemical features.

In this case report, we present the follow-up results of a longitudinal observation of clinical and biochemical profiles of a girl with typical phenotype of AHO and a novel mutation in GNAS gene.

Case Report

This 6.5-year-old girl patient was referred to our outpatient clinic for short stature and brachydactyly. She was born at term to non-consanguineous parents. Neither brachydactyly, short stature, nor any specific feature of AHO phenotype were present in either parent. The patient's birth weight was 2300 g (<10 p) and her birth height was 45 cm (<10 p). Developmental dysplasia of the hip was noted on neonatal examination. Her motor development was also delayed. She was reported to first smile to her mother at 3 months, to have acquired head control at 9 months, sitting at 24 months, walking at age 3 years. Physical examination revealed short stature [height: 109 cm, -1.75 standard deviation (SD)], a low body mass index (BMI=13.5 kg/m (2), -1.59 SD), round face, full cheeks, depressed nasal bridge, short neck, brachydactyly of all digits of the hand (hand length: 9.5 cm, <3th centile) and feet (Figure 1 A-1C and Table 2). Subcutaneous heterotopic ossification at the level of the right iliac crest (diameter 3x2 cm) was also noted.

The first laboratory examination revealed normal serum calcium (9.7 mg/dL) and phosphorus (5.3 mg/dL) levels, with an elevated serum PTH (138.1 pg/mL) level. The subsequent measurements of PTH concentrations were 98.5 pg/mL and 111.2 mg/mL, respectively. The serum levels of free triiodothyronine (f[T.sub.3]), free thyroxine (f[T.sub.4]), TSH, alkaline phosphatase (ALP), creatinine, and 25-hydroxyvitamin D (25-OHD) were normal. X-rays revealed marked shortness and thickness of metacarpal and metatarsal bones with cone-shaped epiphyses in all tubular bones of the hand (Figure 1E, 1F) and coxa valga with acetabular dysplasia. The patient's bone age was compatible with her chronological age. Cranial magnetic resonance imaging findings were normal. Chromosomal analysis revealed 46,XX karyotype. Audiological and ophthalmological examination showed bilateral minimal conductive hearing loss and retinitis pigmentosa, respectively.

Gsa function was found as 48.1% of normal, suggesting impaired activity. Based on these clinical and biochemical findings, the most likely diagnosis was thought to be PHP-Ia. A heterozygous novel missense mutation (c.128T>C) was detected in exon 1 in the GNAS gene.

The patient was followed up until 14.5 years of age. At age 9 years, her height was 122 cm (-1.86 SD) and her BMI was 14.8 kg/m (2) (-0.86 SD) (Table 2). Borderline intellectual disability (IQ: 83) was detected in Stanford-Binet test at age 9 years. Pubertal development was Tanner stage II and appropriate to her age. Hormonal profile showed subclinical hypothyroidism (f[T.sub.3]: 3.51 pg/mL, f[T.sub.4]: 1.27 ng/dL, TSH: 5.97 mIU/L). [The diagnosis of subclinical hypothyroidism was based on a serum TSH value of >4.2 [micro]U/mL (reference interval=0.27-4.2 [micro]U/mL), while serum f[T.sub.3] (reference interval=2-4.4 pg/mL) and f[T.sub.4] (reference interval=0.93-1.7 ng/dL) levels were within the reference ranges].

Antithyroid antibodies were within normal limits and thyroid ultrasound was normal. Thus, increased TSH (6.02 mIU/L) with normal f[T.sub.3] and f[T.sub.4] levels in subsequent measurements suggested TSH resistance. Elevated PTH levels (138.1 pg/mL) were still evident, while serum calcium, phosphorous, and ALP concentrations were normal. Nephrocalcinosis was not detected in ultrasonography. Cranial computerized tomography (CT) scan did not reveal any basal ganglion calcification. L-T4 supplementation was initiated at a dose of 1.25 [micro]g/kg/day.

The most remarkable findings of the physical examination at age 14.5 years were the increase in number of mobile subcutaneous heterotopic ossifications and bilateral calcification of the globus pallidus in cranial CT scan (Figure 1D). In addition to the initial lesion at the right iliac crest level, there were three new subcutaneous ossifications in the both hands and in the left foot. Her height was 143 cm (-2.80 SD) and her weight was 35 kg (-2.54 SD) (Table 2). While pubertal development was at Tanner stage IV, menarche had not occurred yet. During the 8 years of longitudinal follow-up, her pubertal development had been normal, indicating that there was no gonadotropin resistance. The patient's bone age was 13 years. Her height standard deviation score (SDS) regressed to -2.80 with a growth velocity of 5 cm/year. Growth hormone (GH) stimulation tests were performed. They revealed sufficient GH secretion (after clonidine stimulation GH peak: 14 ng/mL). Insulin-like growth factor 1 (IGF-1) stimulation test was performed to see if there was a response of IGF-1 increment to exogenous GH. This test revealed an increased response [baseline IGF-1 level: 262.1 ng/mL (-2.086 SD), peak IGF1 level: 393.5 ng/mL, [DELTA]IGF1: 131.4 ng/mL, 50.1% increase] suggesting GH bioinactivity. [The IGF-1 generation test was performed as follows: Exogenous GH injections (100 [micro]g/kg s.c. daily) were administered at 21:00 h for four days. Blood samples for IGF-1 were taken on day 0 before the first injection and 12 hours later after the last injection (a serum IGF-1 level increment greater than 20% was defined as GH bioinactivity). Baseline serum IGF-1 standard deviation calculation was performed (5)].

Molecular Methodology

The activity of Gsa protein from erythrocyte membranes of patients was investigated in heparinized blood samples.

After solubilization, the Gsa protein from patient-derived erythrocyte membranes was incubated with GTP?S. Adenylyl cyclase from turkey red cell membranes were added, and the generated cAMP in the presence of ATP by RIA (Immuno Biological Laboratories, Hamburg, Germany) was measured. Results obtained in triplicate were expressed as percent of the mean of healthy controls (normal range: 85-115%).

For molecular genetic analysis, genomic DNA derived from peripheral leukocytes was isolated by standard procedures (Qiaquick DNA kit, Qiagen, Hilden, Germany). GNAS exon 1-13, (RefSeq NM_000516.4) including all intron/exon boundaries were amplified in 11 fragments by polymerase chain reaction (PCR) (primer sequences available upon request). PCR-amplified DNA was sequenced by direct cycle sequencing using the BigDye Terminator v1.1 Cycle Sequencing Kit (Applied Biosystems, Foster City, CA) and an ABI 3130 capillary sequencer (Applied Biosystems, Foster City, CA).

Discussion

The hand and feet X-rays of this patient (clinical findings: short stature, short neck, round face, brachydactyly, and borderline intellectual disability) revealed marked shortness of metacarpals and metatarsals. The patient was also found to have high PTH levels, subclinical hypothyroidism, and heterotopic ossifications. While patients with AHO are usually obese, the BMI level of our patient was in the underweight group according to the World Health Organization guidelines. With these findings, the patient was diagnosed as a case of Albright PHP. Heterotopic ossifications and brachydactyly are the most unique features of AHO phenotype that distinguishes true AHO from a variety of clinical phenocopies (6,7). While brachydactyly was evident in the first evaluation of our patient, heterotopic ossification became apparent at the right iliac crest at 9 years of age. Moreover, the subcutaneous ossifications were observed to have increased in number at different parts of the body in the last follow-up examination.

Almost all features of PHP-Ia including hormone resistance, are also common in acrodysostosis syndrome. PHP-Ia can be differentiated from this syndrome only by the presence of GNAS mutation and of heterotopic ossifications (8). The differential diagnosis among subtypes of PHP is very difficult. In our patient, PHP-Ib and PHP-Ic were excluded by decreased Gsa activity and PHP-II by both decreased Gsa activity and mutation. Gsa activity of our case was reduced to 48.1%, a finding that was consistent with PHP-Ia rather than PHP-Ib, -Ic, and -II.

The GNAS gene analysis revealed a novel heterozygous mutation (c.128T>C). This mutation results in the change of the aminoacid leucine at codon 43 with the aminoacid proline (p. Leu43Pro). There is a moderate physicochemical difference between Leu and Pro [Grantham dist.: 98 (0-215)] and the amino acid leucine at codon 43 is conserved between species up to C. elegans. It is possible that the mutation is pathogenic and causal for AHO in this patient. This mutation, as far as we know, has never been described before and was not detected in the GNAS gene. Thus, we have concluded that the mutation is meaningful.

Formerly, the term pseudopseudohypoparathyroidism (PPHP), was used for patients who display AHO features and carry heterozygous inactivating Gsa mutations without evidence of hormone resistance. Previous studies were reporting maternal inheritance of GNAS mutations results in AHO together with hormone resistance and named as PHP-Ia, while paternal inheritance of the same mutation was reported to lead only to AHO phenotype and was termed as PPHP (2,3). However, in a recent publication, mild PTH resistance besides AHO phenotype was reported in a PPHP patient, and ascertainment of the parental origin of the mutation was declared as the most effective diagnostic procedure in differentiating PPHP from PHP-Ia (9).

While Gsa is biallelically expressed in most tissues, it is predominantly maternally expressed in certain tissues such as renal proximal tubules, the thyroid, the gonads, and the pituitary. Paternal allele is suppressed in these tissues. Tissue-specific imprinting nature of GNAS gene is responsible for this difference (1,10). This might explain why the multihormone resistance in PHP-Ia patients primarily involves four hormones: PTH, TSH, gonadotropins, and GHRH (1,11).

While PTH resistance associated later with TSH resistance was apparent in our patient, resistance to gonadotropins or GHRH was not detected. The most important hormone resistance in PHP-Ia that results in clinically evident signs is renal resistance to PTH. Most patients present with hypocalcemia, hyperphosphatemia, and elevated levels of PTH. Despite presence of PTH resistance, some cases may have normal serum calcium and phosphorus levels. PHP-Ia patients have a reduced phosphatidic response to PTH, which leads to hyperphosphatemia. Besides hyperphosphatemia, proximal tubule resistance to PTH leads to decreased 1,25-dihydroxyvitamin D production, thus causing hypocalcemia. Unlike patients with primary hypoparathyroidism, PHP cases do not develop hypercalciuria, which shows that the anti-calciuric effect of PTH in the thick ascending limb remains intact (3). Some patients may show osteopenia and signs of rickets. Skeletal deformities like short ulna, genu varum-valgum, cubitus valgus may be seen (12).

TSH resistance becomes clinically apparent during the adolescence period (1). This resistance is mostly not severe, with TSH levels only slightly elevated or thyroid hormone levels slightly less than normal (11). Our patient developed subclinical hypothyroidism at 9 years of age.

Although short stature became apparent in the follow-up of our patient, she showed a normal GH response to clonidine stimulation test. Clonidine is a selective a-receptor agonist and causes GH release via GHRH. This normal response suggests that our patient did not have GHRH resistance. GH bioinactivity was diagnosed by detecting a 50.1% increment to IGF1 stimulation test. This diagnosis predicates that endogenously produced GH is inactive, probably due to disorders of GH gene. To our knowledge, this is the first report about the bioinactive GH associated with PHP-Ia. However, without GH gene analysis, this diagnosis is not precise. Reports on GH deficiency in patients with PHP-Ia are variable. While some authors reported GH deficiency in PHP-Ia (11,13,14,15), there are a few studies reporting patients without GH deficiency (16,17) as noted in the case of our patient.

However, our inability to perform a PTH infusion test and a GNAS gene analysis in the parents represent the main limitations of this case report, limitations which made the differential diagnosis more complicated in terms of PHP-Ia and PPHP. Also, we had no possibility to analyze neither the DNA samples of the parents nor the ribonucleic acid sample of the patient to be able to show the origin of the mutation, in other words, whether it was paternally or maternally expressed. Accordingly, the patient could also be classified as PPHP in the light of current literature and case reports.

In conclusion, clinicians should take into consideration PHP-Ia and PPHP in patients referred with short stature, and the subjects with AHO phenotype must be further evaluated for hormone resistance, GNAS gene mutation, Gsa activity. Repeated physical and laboratory examinations should be performed in order to detect changes which may occur in hormone resistance.

Ethics

Informed Consent: It was taken.

Peer-review: Externally peer-reviewed.

Authorship Contributions

Concept: Beyhan Tuysuz, Design: Beyhan Tuysuz, Data Collection or Processing: Beyhan Tuysuz, Analysis or Interpretation: Beyhan Tuysuz, Olcay Evliyaoglu, Sezgin Sahin, Olaf Hiort, Susanne Thiele, Literature Search: Beyhan Tuysuz, Olcay Evliyaoglu, Sezgin Sahin, Writing: Beyhan Tuysuz, Olcay Evliyaoglu, Sezgin Sahin.

Financial Disclosure: The authors declared that this study received no financial support.

References

(1). Weinstein LS, Yu S, Warner DR, Liu J. Endocrine manifestations of stimulatory G protein a-subunit mutations and the role of genomic imprinting. Endocr Rev 2001;22:675-705.

(2). Bastepe M, Juppner H. GNAS locus and pseudohypoparathyroidism. Horm Res 2005;63:65-74. Epub 2005 Feb 9

(3). Mantovani G, Spada A. Mutations in the Gs a gene causing hormone resistance. Best Pract Res Clin Endocrinol Metab 2006;20:501-513.

(4). Levine MA. An update on the clinical and molecular characteristics of pseudohypoparathyroidism. Curr Opin Endocrinol Diabetes Obes 2012;19:443-451.

(5). Carrillo AA, Bao Y. Hormonal dynamic tests and genetic tests used in pediatric endocrinology. In: Lifshitz F (ed). Pediatric endocrinology 5th ed. Marcel Dekker Inc, New York, 2007:737-767.

(6). de Sanctis L, Vai S, Andreo MR, Romagnolo D, Silvestro L, de Sanctis C. Brachydactyly in 14 genetically characterized pseudohypoparathyroidism type Ia patients. J Clin Endocrinol Metab 2004;89:1650-1655.

(7). Mantovani G.Clinical review: Pseudohypoparathyroidism: diagnosis and treatment. J Clin Endocrinol Metab 2011;96:3020-3030. Epub 2011 Aug 3

(8). Silve C, Le-Stunff C, Motte E, Gunes Y, Linglart A, Clauser E. Acrodysostosis syndromes. Bonekey Rep 2012;1:225.

(9). Turan S, Thiele S, Tafaj O, Brix B, Atay Z, Abali S, Haliloglu B, Bereket A, Bastepe M. Evidence of hormone resistance in a pseudo-pseudohypoparathyroidism patient with a novel paternal mutation in GNAS. Bone 2015;71:53-57. Epub 2014 Oct 18

(10). Liu J, Chen M, Deng C, Bourc'his D, Nealon JG, Erlichman B, Bestor TH, Weinstein LS. Identification of the control region for tissue-specific imprinting of the stimulatory G protein a-subunit. Proc Natl Acad Sci USA 2005;102:5513-5518. Epub 2005 Apr 5

11. Mantovani G, Spada A. Resistance to growth hormone releasing hormone and gonadotropins in Albright's hereditary osteodystrophy. J Pediatr Endocrinol Metab 2006;19(Suppl 2):663-670.

(12). Kidd GS, Schaaf M, Adler RA, Lassman MN, Wray HL. Skeletal responsiveness in pseudohypoparathyroidism: A spectrum of clinical disease. Am J Med 1980;68:772-781.

(13). Mantovani G, Maghnie M, Weber G, de Menis E, Brunelli V, Cappa M, Loli P, Beck-Peccoz P, Spada A. Growth hormone releasing hormone resistance in pseudohypoparathyroidism type ia: new evidence for imprinting of the Gs a gene. J Clin Endocrinol Metab 2003;88:4070-4074.

(14). Germain-Lee EL, Groman J, Crane JL, Jan de Beur SM, Levine MA. Growth hormone deficiency in pseudohypoparathyroidism type 1a: another manifestation of multihormone resistance. J Clin Endocrinol Metab 2003;88:4059-4069.

(15). de Sanctis L, Bellone J, Salerno M, Faleschini E, Caruso-Nicoletti M, Cicchetti M, Concolino D, Balsamo A, Buzi F, Ghizzoni L, de Sanctis C. GH secretion in a cohort of children with pseudohypoparathyroidism type Ia. J Endocrinol Invest 2007;30:97-103.

(16). Faull CM, Welbury RR, Paul B, Kendall-Taylor P. Pseudohypoparathyroidism: its phenotypic variability and associated disorders in a large family. Q J Med 1991;78:251-264.

(17). Erdeve SS, Berberoglu M, Siklar Z, Evliyaoglu O, Hiort O, Ocal G. Long-Term Follow-up of a Pseudohypoparathyroidism Type 1A Patient with Missense Mutation (Pro115Ser) in exon 5. J Clin Res Pediatr Endocrinol 2010;2:85-88.

Sezgin Sahin (1), Olaf Hiort (2), Susanne Thiele (2), Olcay Evliyaoglu (3), Beyhan Tuysuz (4)

(1) Istanbul University Cerrahpasa Faculty of Medicine, Department of Pediatric Rheumatology, Istanbul, Turkey

(2) University of Lubeck, Department of Pediatrics, Lubeck, Germany

(3) Istanbul University Cerrahpasa Faculty of Medicine, Department of Pediatric Endocrinology, Istanbul, Turkey

(4) Istanbul University Cerrahpasa Faculty of Medicine, Department of Pediatric Genetics, Istanbul, Turkey

Address for Correspondence: Beyhan Tuysuz MD, Istanbul University Cerrahpasa Faculty of Medicine, Department of Pediatric Genetics, Istanbul, Turkey

Phone: +90 212 4143192 E-mail: beyhan@istanbul.edu.tr

Conflict of interest: None declared

Received: 30.03.2016

Accepted: 16.07.2016

DOI: 10.4274/jcrpe.3191
Table 1. Clinical fndings of our patient and differential diagnosis in
cases of pseudohypoparathyroidism

                    PHP-Ia        PHP-Ib         PHP-Ic
AHO (**)            Yes           No             Yes

Hormone resistance  PTH, TSH,     PTH,           PTH, TSH, Gn, GHRH
                    Gn (***),     sometimes TSH
                    GHRH (****)
Ca P[down arrow]    Mostly yes    Mostly yes     Mostly yes
Serum PTH           Elevated      Elevated       Elevated
PTH infusion        Urine cAMP    Urine cAMP     Urine cAMP
                    Phosphaturia  Phosphaturia   Phosphaturia
GNAS gene defect    Inactivating  Imprinting     No
                    mutations     Dysregulation
Gsa activity        Reduced       Normal         Normal

                    PHP-II        PPHP (*)      Present patient
AHO (**)            No            Yes           Yes

Hormone resistance  PTH           None
Ca P[down arrow]    Mostly yes    No            No
Serum PTH           Elevated      Normal        Elevated
PTH infusion        Urine cAMP    Urine cAMP    Not performed
                    Phosphaturia  Phosphaturia
GNAS gene defect    No            Inactivating  Yes
                                  mutations
Gsa activity        Normal        Reduced       Reduced

(*) PPHP: pseudopseudohypoparathyroidism,
(**) AHO: Albright hereditary osteodystrophy,
(***) Gn: gonadotropins,
(****) GHRH: growth hormone-releasing hormone.
PHP: Pseudohypoparathyroidism, PTH: parathormone, TSH:
thyroid-stimulating hormone, Ca: calcium, P: phosphor

Table 2. Results of anthropometry and hormone measurements during the
follow-up of the patient

                                Birth  Age 6.5 years  Age 9 years

Weight, kg
SDS                              2.3    16 (-2.29)     22 (-1.75)
Height, cm
SDS                             45     109 (-1.75)    122 (-1.86)
BMI, kg/[m.sup.2]
(z-score)                       NA      13.5 (-1.59)   14.8 (-0.86)
PTH, pg/mL                      NA     138.1          138
TSH, mIU/L                      NA       2.53           6.02
GH bioinactivity                NA     NA             NA
Subcutaneous ossifcation level  ND     CI             CI
LH, LF
Intracranial calcifcation       NA     ND             ND

                                Age 14.5 years

Weight, kg
SDS                              35 (-2.54)
Height, cm
SDS                             143 (-2.80)
BMI, kg/[m.sup.2]
(z-score)                        17.1 (-1.03)
PTH, pg/mL                      101.3
TSH, mIU/L                        5.72
GH bioinactivity                Present
Subcutaneous ossifcation level  CI, RH,
LH, LF
Intracranial calcifcation       Globus pallidus

NA: not available, ND: not detected, CI: Crista iliaca, RH: Right hand,
LH: left hand, LF: Left foot, SDS: standard deviation score, BMI: body
mass index, PTH: parathormone, TSH: thyroid-stimulating hormone, GH:
growth hormone
COPYRIGHT 2017 Galenos Yayinevi Tic. Ltd.
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2017 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Title Annotation:CASE REPORT
Author:Sahin, Sezgin; Hiort, Olaf; Thiele, Susanne; Evliyaoglu, Olcay; Tuysuz, Beyhan
Publication:Journal of Clinical Research in Pediatric Endocrinology
Article Type:Case study
Date:Mar 1, 2017
Words:3396
Previous Article:Uniparental Isodisomy of Chromosome 1 Unmasking an Autosomal Recessive 3-Beta Hydroxysteroid Dehydrogenase Type II-Related Congenital Adrenal...
Next Article:Clinical and Molecular Genetic Analysis in Three Children with Wolfram Syndrome: A Novel WFS1 Mutation (c.2534T>A).
Topics:

Terms of use | Privacy policy | Copyright © 2021 Farlex, Inc. | Feedback | For webmasters |