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A novel variant in the PDE4D gene is the cause of Acrodysostosis type 2 in a Lithuanian patient: a case report

Abstract

Background

Acrodysostosis is a rare hereditary disorder described as a primary bone dysplasia with or without hormonal resistance. Pathogenic variants in the PRKAR1A and PDE4D genes are known genetic causes of this condition. The latter gene variants are more frequently identified in patients with midfacial and nasal hypoplasia and neurological involvement. The aim of our study was to analyse and confirm a genetic cause of acrodysostosis in a male patient.

Case presentation

We report on a 29-year-old Lithuanian man diagnosed with acrodysostosis type 2. The characteristic phenotype includes specific skeletal abnormalities, facial dysostosis, mild intellectual disability and metabolic syndrome. Using patient’s DNA extracted from peripheral blood sample, the novel, likely pathogenic, heterozygous de novo variant NM_001104631.2:c.581G > C was identified in the gene PDE4D via Sanger sequencing. This variant causes amino acid change (NP_001098101.1:p.(Arg194Pro)) in the functionally relevant upstream conserved region 1 domain of PDE4D.

Conclusions

This report further expands the knowledge of the consequences of missense variants in PDE4D that affect the upstream conserved region 1 regulatory domain and indicates that pathogenic variants of the gene PDE4D play an important role in the pathogenesis mechanism of acrodysostosis type 2 without significant hormonal resistance.

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Background

Acrodysostosis (MIM 101800) refers to a group of rare genetic disorders mainly affecting skeletal growth and resulting in primary skeletal dysplasia. Two types of acrodysostosis are known and has been separated by distinct references on OMIM database. Acrodysostosis type 1 with or without hormone resistance (ACRDYS1, MIM 101800) is caused by pathogenic variants in chromosome 17 (locus 17q24.2) of the PRKAR1A gene. Acrodysostosis type 2 with or without hormone resistance (ACRDYS2, MIM 614613) is associated with the PDE4D gene, which is located in the 5q11.2-q12.1 chromosomal region. According to the new classification proposed by Thiele et al. (2016), ACRDYS1 belongs to the group of inactivating parathyroid hormone (PTH) / PTH-related peptide (PTHrP) signalling disorders 4 (iPPSD4), while ACRDYS2 belongs to iPPSD5 [1]. Acrodysostosis have several overlapping clinical features with another disorder called hypertension and brachydactyly syndrome (HTNB; MIM 112410) classified as iPPSD6. However, this syndrome is caused by heterozygous mutations in PDE3A gene which is functionally similar to PDE4D [1]. Acrodysostosis is inherited in an autosomal dominant manner. In the literature, most of the patients who have been reported on have de novo pathogenic variants. Characteristic clinical features include skeletal abnormalities, resistance to multiple hormones, and neurological involvement. Skeletal dysplasia is specific and includes disproportional short stature with short extremities and brachydactyly, multiple cone-shaped epiphyses, scoliosis or kyphosis with spinal stenosis, and advanced bone maturation. The facial phenotype is also distinctive and characterized by midfacial and nasal hypoplasia, hypertelorism, epicanthal folds, and low set ears. Patients often show some degree of hormone resistance, including resistance to parathyroid and thyroid stimulating hormones, as well as signs of developmental delay and moderate or mild intellectual disability [2, 3]. Although the two types of acrodysostosis are distinguished primarily on a molecular basis, several clinical differences can also be observed. Patients with pathogenic variants in the PRKAR1A gene more frequently have resistance to multiple hormones, while facial dysostosis and neurological involvement are more common in patients with PDE4D pathogenic variants [2, 4].

We report on a patient, who has clinical features of acrodysostosis type 2 and a molecularly confirmed novel pathogenic variant in the PDE4D gene.

Case presentation

The 29-year-old male patient is the first child of healthy unrelated Lithuanian parents. The proband was born at full term. Psychomotor development of the proband was delayed. He attended a regular school until the age of 16 years and was further educated in a professional school. An IQ evaluation at the age of 20 showed a score of 69. At his latest evaluation at the age of 29 years, his height was 164 cm, his weight was 85 kg, his BMI was 31 kg/m2, and the circumference of his head was 60 cm (90 centile). Other anthropometric measurements were thus: total upper limb length of 66 cm, upper arm length of 35 cm, forearm length of 25 cm, hand length of 15 cm, palm length of 8.5 cm, middle finger length of 6.5 cm, total lower limb length of 87 cm on the left and 86 cm on the right, thigh length of 42 cm on both sides, calf length of 45 cm on the left and 44 cm on the right, and feet length of 23 cm. The patient has minor facial anomalies (Fig. 1), including flat face, sloping forehead with prominent supraorbital ridges, sparse and broad brows, depressed nasal ridge, short nose, long philtrum, and malar hypoplasia. Additionally, dental malocclusion, parodontosis, red and sparse scalp hair, male pattern baldness, and short neck are apparent. The patient is overweight and has limited elbow extension, brachydactyly of both hands, short rectangular nails, a single palmar crease, valgus deformation of the knees, brachydactyly of toes II–V of both feet, short rectangular toenails, and relative hyperplasia of the halluces (Fig. 2). The patient complained of premature tiredness, excessive perspiration, and poor fine motor function. He has primary arterial hypertension, and a cardiac ultrasound showed a mitral valve prolapse. An ophthalmological examination revealed hypermetropia. Hormonal screening was remarkable for elevated levels of serum PTH (13.9 pmol/l (n = 1.6–7.3 pmol/l)) and somatotropin (12.2 mIU/l (n < 9.0 mIU/l)). Elevated PTH levels were probably secondary to vit. D deficiency. TSH, T3, T4, FSH, LH, testosterone, cortisole and ACTH were within normal limits. 25-OH vitamin D was 51.4 nmol/l (n = 75–100 nmol/l), serum calcium was 2.58 mmol/l (n = 2.10–2.55 mmol/l), serum phosphorus 0.82 mmol/l (n = 0.74–1.52 mmol/l), serum glucose was 6.09 mmol/l (n = 4.2–6.1 mmol/l). The glucose tolerance test was normal. The ultrasound of the thyroid gland and MRI scan of the hypophyseal gland showed no abnormalities. The X-ray of the hands showed very short and broad tubular bones. Metacarpals II–V are proximally pointed. Coning of phalanges are present in the middle and proximal phalanges of the second to fifth fingers. There is relative sparing of the thumb. The metatarsal bones and phalanges are markedly shortened and there is disproportionate plumpness of the tubular bones of the hallux (Fig. 2). Considering all clinical features and physical examination results, the diagnosis of acrodysostis type 2 was assigned for our proband.

Fig. 1
figure1

The photographs of the patient at 29 years of age. Note the minor facial anomalies (a-b), including flat face, depressed nasal bridge, short nose, and long philtrum

Fig. 2
figure2

The photographs and X-ray pictures of hands and feet of the patient. The photographs of hands (a-b) and feet (d) show brachydactyly of both hands, a single palmar crease, short rectangular nails, brachydactyly of toes II–V of both feet, short rectangular toenails, and relative hyperplasia of the halluces. X-ray pictures (c, e) show the short broad metacarpals and phalanges

To identify DNA sequence variants in the gene PDE4D and analyze segregation, Sanger sequencing was conducted for the proband and his parents. Phenol-chloroform-isoamyl alcohol extraction method was used to isolate genomic DNA from peripheral blood of all three patients. The PDE4D exons 2, 3, 6, 7, 13, 15 were amplified by PCR with specific primers (designed using the Primer Blast software, NCBI, USA) and sequenced in the DNA sample of the proband. PDE4D exon 2 was amplified and sequenced in the parents’ DNA samples to investigate inheritance pattern of the identified variant. Target PCR products from all three individuals were sequenced with BigDye® Terminator v3.1 Cycle Sequencing Kit (Applied Biosystems, USA) and the capillary electrophoresis was carried out with ABI3130xl Genetic Analyser (Applied Biosystems, USA). Sanger sequencing results were analysed with Sequence Analysis v5.1 software (Applied Biosystems, USA). The reference sequence of the PDE4D gene (NCBI: NM_001104631.2) was used for aligning the obtained sequences. Primers and PCR conditions are available from the authors upon request. The pathogenicity of identified DNA sequence variant was evaluated by using several bioinformatics tools: SIFT (https://sift.bii.a-star.edu.sg/), PolyPhen-2 (http://genetics.bwh.harvard.edu/pph2/), MutationTaster2 (http://www.mutationtaster.org/), PROVEAN (http://provean.jcvi.org/about.php). PDE4D nucleotide sequence conservation analysis was performed using multiple sequence alignment tool Clustal Omega (EMBL-EBI, https://www.ebi.ac.uk/Tools/msa/clustalo/).

Heterozygous missense variant NM_001104631.2:c.581G > C (NP_001098101.1:p.(Arg194Pro)) located in exon 2 of the gene PDE4D was detected in the proband’s DNA sample by Sanger sequencing. Family segregation analysis of the identified variant revealed it’s de novo occurrence. Different in silico tools predicted this variant to be likely pathogenic: SIFT damaging (0,00), PolyPhen-2 (0,99), MutationTaster2 disease causing (0,99), PROVEAN deleterious (− 5,60). The pathogenicity of detected variant was classified according to the guidelines proposed by American College of Medical Genetics and Genomics [5].

Discussion and conclusions

Pathogenic variants in the PDE4D gene were first identified as the cause of acrodysostosis in 2012 [2, 3]. Since then there have been investigations about a possible genotype-phenotype correlation between the two types of acrodysostosis. A few studies showed that ACRDYS1 patients had hormone resistance and short stature, but normal intellect and no facial dysostosis, while the ACRDYS2 group exhibited characteristic facial features, intellectual disability, and no hormone resistance [2, 4]. The distinction between the two types of acrodysostosis was not so obvious in other studies, which suggested that mild short stature with brachydactyly, facial dysostosis, spinal stenosis, a variable degree of developmental disability, and variable endocrine abnormalities may be present in both ACRDYS1 and ACRDYS2 patients [3, 6, 7]. The main clinical features of our patient are mild intellectual disability, facial dysostosis, and specific skeletal abnormalities. Additionally, the presence of increased blood pressure, a documented increased fasting glucose level and abdominal obesity indicated metabolic syndrome. Considering the young age of the patient, we cannot exclude that metabolic syndrome and hypertension are part of this syndrome. Identification of the pathogenic variant in the PDE4D gene confirmed the diagnosis of ACRDYS2.

Both PRKAR1A and PDE4D genes encode proteins essential in the cAMP signaling pathway. PRKAR1A is a crucial part of type I protein kinase A (PKA), the main mediator of cAMP signaling in mammals, while PDE4D is a cAMP specific cyclic nucleotide phosphodiesterase (PDE) that maintains the cellular concentrations of cyclic nucleotides. Cyclic nucleotides are essential messengers that regulate cellular responses to extracellular signals such as hormones or neurotransmitters. Phosphodiesterases (PDEs) contribute greatly to the cAMP signaling pathway and play a role in desensitisation, feedback regulation, and signal compartmentalisation of cells [8]. While there are twelve families of PDEs identified [9], isoforms of the PDE4 family are accountable for most cAMP hydrolysing activity.

The structure of PDE4 consists of a highly conserved catalytic domain in between other domains with regulatory functions. Two of the latter, called upstream conserved regions 1 and 2 (UCR1, UCR2), have been suggested to have major regulatory impact on the PDE4 catalytic unit [10]. UCR1 and linker region 2, which is located between UCR2 and catalytic domain, were detected as the major regions undergoing the process of phosphorylation. This post-translational modification plays a role in regulating the enzymatic activity of PDE4D [11]. Depending on the presence of upstream conserved regions, PDE4 isoforms are divided into categories: long, short, and super-short [9]. Long isoforms have both UCR1 and UCR2, while short isoforms lack UCR1, as do super-short isoforms, which also have truncated UCR2 [12]. When these regulatory domains are defective due to a point mutation of the PDE4D gene, the catalytic domain becomes more active and catalysis of cAMP increases abnormally, which leads to the acrodysostosis phenotype. This dominant negative effect of PDE4D coding changes has been confirmed in functional studies [6, 13]. On the other hand, haploinsufficiency renders PDE4D completely dysfunctional and results in a mirror phenotype to that of acrodysostosis characterised by long limbs, fingers and toes, specific facial features, and low BMI [6].

A novel NM_001104631.2:c.581G > C, NP_001098101.1:p.(Arg194Pro) missense variant detected in our patient affects the UCR1 regulatory domain of the PDE4D protein. The UCR1 functional domain of the protein is the most affected site, followed by catalytic and UCR2 domains, in previously reported, affected patients (Fig. 3a) [2,3,4, 6, 7, 13,14,15,16,17,18]. The missense c.581G > C variant was not observed in approximately 6300 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. It leads to nonsynonymous substitution of positively charged arginine to nonpolar proline. This substitution occurs at a position that is conserved across species (Fig. 3b), and in silico analysis predicts this variant is probably damaging to protein function. Healthy parents have been confirmed to not possess the same variant, which further contributes to the notion of its pathogenicity. Four missense variants located more proximally in the UCR1 have been previously reported, supporting the functional importance of this region of the protein [1]. Other PDE4D gene variants that have been described to date are presented in Fig. 3a.

Fig. 3
figure3

Pathogenic variants of the PDE4D gene previously reported in the reviewed literature (a). All DNA variants are depicted according to their position in the PDE4D gene transcript (NM_001104631.2) and in the PDE4D protein (NP_001098101.1) domains. The novel missense variant of the PDE4D gene detected in the present study is also shown. Nucleotide sequence conservation analysis (b) showed that altered G nucleotide position is conserved in several animal species (ClustalOmega tool at EMBLEBI website was used)

In summary, this study adds to the literature a novel pathogenic PDE4D missense variant that results in clinical features specific to acrodysostosis type 2 without significant hormone resistance. By reviewing the literature and combining the clinical and molecular findings of our patient with previously published data, we further expand the knowledge of the consequences of missense variants in the PDE4D gene that affect the UCR1 regulatory domain.

Availability of data and materials

The dataset of the exon 2 of the gene PDE4D chromatograms generated and analysed during the current study is available in Zenodo repository (https://doi.org/10.5281/zenodo.4644688). Any additional information is available from the authors upon request.

Abbreviations

ACRDYS1:

Acrodysostosis type 1

ACRDYS2:

Acrodysostosis type 2

ACTH:

Adrenocorticotropic hormone

BMI:

Body mass index

cAMP:

Cyclic adenosine monophosphate

FSH:

Follicle-stimulating hormone

HTNB:

Hypertension and brachydactyly syndrome

iPPSD4:

Inactivating parathyroid hormone / PTH-related peptide signalling disorders 4

iPPSD5:

Inactivating parathyroid hormone / PTH-related peptide signalling disorders 5

iPPSD6:

Inactivating parathyroid hormone / PTH-related peptide signalling disorders 6

LH:

Luteinizing hormone

MRI:

Magnetic resonance imaging

NHLBI:

National Heart, Lung and Blood Institute

PCR:

Polymerase chain reaction

PDE:

Acronym for proteins phosphodiesterases

PDE4:

A proteins family of phosphodiesterases 4

PDE3A :

Gene symbol for gene that encodes a phosphodiesterase 3A

PDE4D :

Gene symbol for gene that encodes a protein phosphodiesterase 4D

PKA:

Protein kinase A

PRKAR1A :

Gene symbol for gene that encodes protein kinase cAMP-dependent type I regulatory subunit alpha

PTH:

Parathyroid hormone

PTHrP:

PTH-related peptide

T3:

Triiodothyronine

T4:

Thyroxine

TSH:

Thyroid-stimulating hormone

UCR1:

Upstream conserved region 1, a regulatory domain of protein PDE4D

UCR2:

Upstream conserved region 2, a regulatory domain of protein PDE4D

References

  1. 1.

    Thiele S, Mantovani G, Barlier A, Boldrin V, Bordogna P, Sanctis L, et al. From pseudohypoparathyroidism to inactivating PTH/PTHrP signalling disorder (iPPSD), a novel classification proposed by the EuroPHP network. Eur J Endocrinol. 2016;175:P1–P17.

    CAS  Article  Google Scholar 

  2. 2.

    Michot C, Le Goff C, Goldenberg A, Abhyankar A, Klein C, Kinning E, et al. Exome sequencing identifies PDE4D mutations as another cause of acrodysostosis. Am J Hum Genet. 2012;90:740–5.

    CAS  Article  Google Scholar 

  3. 3.

    Lee H, Graham JM, Rimoin DL, Lachman RS, Krejci P, Tompson SW, et al. Exome sequencing identifies PDE4D mutations in acrodysostosis. Am J Hum Genet. 2012;90:746–51.

    CAS  Article  Google Scholar 

  4. 4.

    Michot C, Le Goff C, Blair E, Blanchet P, Capri Y, Gilbert-Dussardier B, et al. Expanding the phenotypic spectrum of variants in PDE4D/PRKAR1A: from acrodysostosis to acroscyphodysplasia. Eur J Hum Genet. 2018;26:1611–22.

    CAS  Article  Google Scholar 

  5. 5.

    Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, et al. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet Med. 2015;17(5):405–24.

    Article  Google Scholar 

  6. 6.

    Lindstrand A, Grigelioniene G, Nilsson D, Pettersson M, Hofmeister W, Anderlid B-M, et al. Different mutations in PDE4D associated with developmental disorders with mirror phenotypes. J Med Genet. 2014;51:45–54.

    CAS  Article  Google Scholar 

  7. 7.

    Hoppmann J, Gesing J, Silve C, Leroy C, Bertsche A, Wolfgang Hirsch F, et al. Phenotypic variability in a family with Acrodysostosis type 2 caused by a novel PDE4D mutation affecting the serine target of protein kinase-a phosphorylation. J Clin Res Pediatr Endocrinol. 2017;14:360–5.

    Article  Google Scholar 

  8. 8.

    Conti M, Richter W, Mehats C, Livera G, Park J-Y, Jin C. Cyclic AMP-specific PDE4 phosphodiesterases as critical components of cyclic AMP signaling. J Biol Chem. 2003;278:5493–6.

    CAS  Article  Google Scholar 

  9. 9.

    Houslay MD. PDE4 cAMP-specific phosphodiesterases. Prog Nucleic Acid Res Mol Biol. 2001;69:249–315.

    CAS  Article  Google Scholar 

  10. 10.

    Beard MB, Olsen AE, Jones RE, Erdogan S, Houslay MD, Bolger GB. UCR1 and UCR2 domains unique to the cAMP-specific phosphodiesterase family form a discrete module via electrostatic interactions. J Biol Chem. 2000;275:10349–58.

    CAS  Article  Google Scholar 

  11. 11.

    Mika D, Conti M. PDE4D phosphorylation: a coincidence detector integrating multiple signaling pathways. Cell Signal. 2016;28:719–24.

    CAS  Article  Google Scholar 

  12. 12.

    Houslay MD, Adams DR. PDE4 cAMP phosphodiesterases: modular enzymes that orchestrate signalling cross-talk, desensitization and compartmentalization. Biochem J. 2003;15:3701–18.

    Google Scholar 

  13. 13.

    Kaname T, Ki C-S, Niikawa N, Baillie GS, Day JP, Yamamura K-I, et al. Heterozygous mutations in cyclic AMP phosphodiesterase-4D (PDE4D) and protein kinase a (PKA) provide new insights into the molecular pathology of acrodysostosis. Cell Signal. 2014;26:2446–59.

    CAS  Article  Google Scholar 

  14. 14.

    Mitsui T, Kim O-H, Hall CM, Offiah A, Johnson D, Jin D-K, et al. Acroscyphodysplasia as a phenotypic variation of pseudohypoparathyroidism and acrodysostosis type 2. Am J Med Genet. 2014;164A:2529–34.

    Article  Google Scholar 

  15. 15.

    Lynch DC, Dyment DA, Huang L, Nikkel SM, Lacombe D, Campeau PM, et al. Identification of novel mutations confirms PDE4D as a major gene causing acrodysostosis. Hum Mutat. 2012;34:97–102.

    Article  Google Scholar 

  16. 16.

    Linglart A, Fryssira H, Hiort O, Holterhus PM, Perez de Nanclares G, Argente J, et al. PRKAR1A and PDE4D mutations cause acrodysostosis but two distinct syndromes with or without GPCR-signaling hormone resistance. J Clin Endocrinol Metab. 2012;97:E2328–38.

    CAS  Article  Google Scholar 

  17. 17.

    Briet C, Pereda A, Le Stunff C, Motte E, de Dios G-DJ, de Nanclares GP, et al. Mutations causing acrodysostosis-2 facilitate activation of phosphodiesterase 4D3. Hum Mol Genet. 2017;26:3883–94.

    CAS  Article  Google Scholar 

  18. 18.

    Elli FM, Bordogna P, de Sanctis L, Giachero F, Verrua E, Segni M, et al. Screening of PRKAR1A and PDE4D in a large Italian series of patients clinically diagnosed with Albright hereditary Osteodystrophy and/or Pseudohypoparathyroidism. J Bone Miner Res. 2016;31:1215–24.

    CAS  Article  Google Scholar 

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Acknowledgements

We are very thankful to the family for taking part in this study.

Funding

This research was funded by a grant (No. S-MIP-17-19/LSS-150000-1179) from the Research Council of Lithuania. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

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Authors

Contributions

All authors contributed to the study conception and design. Patient’s data collection and analysis were performed by LC, DK, EP and AM. Genetic investigations were performed by VM and GP. AU supervised the findings of this work. The first draft of the manuscript was written by KŠ and GP and all authors commented on previous versions of the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Gunda Petraitytė.

Ethics declarations

Ethics approval and consent to participate

This study was performed in line with the principles of the Declaration of Helsinki. The study was approved by the Vilnius Regional Biomedical Research Ethics Committee of Lithuania. Written informed consent for genetic investigations was obtained from the family.

Consent for publication

The patient’s parents provided the written consent for the case report to be published. Informed consent from parents regarding photographs for publication has been obtained. The parents signed on behalf of the patient because of his cognitive deficit. A copy of informed consent is available to the journal.

Competing interests

The authors declare that they have no competing interests.

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Petraitytė, G., Šiaurytė, K., Mikštienė, V. et al. A novel variant in the PDE4D gene is the cause of Acrodysostosis type 2 in a Lithuanian patient: a case report. BMC Endocr Disord 21, 71 (2021). https://doi.org/10.1186/s12902-021-00741-6

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Keywords

  • Acrodysostosis
  • ACRDYS2
  • PDE4D
  • Skeletal abnormalities
  • Intellectual disability
  • Case report