A novel compound heterozygous variant in SMARCAL1 leading to mild Schimke immune-osseous dysplasia identified using whole-exome sequencing

Abstract

Schimke immuno-osseous dysplasia (SIOD) is a rare autosomal recessive inherited disorder that is caused by the SMARCAL1 mutation. The phenotype can vary from mild to severe on the basis of the patient’s age at onset. Herein, we report the case of a 14-year-old Chinese boy who presented with short stature, focal segmental glomerulosclerosis (FSGS), and facial dysmorphism. Genetic analysis revealed two compound heterozygous missense mutations, including a well-known mutation (c.1933C>T, p.R645C) and a novel mutation (c.2479G>A, p.V827M) in the SMARCAL1 gene, which were inherited from his parents. In silico analyses showed that the c.2479G>A (p.V827M) variant affects a highly conserved residue within the ATPase catalytic domain. Finally, we established the diagnosis of mild SIOD and treated the patient with diuretics and angiotensin receptor blockers. This report expands the mutational spectrum of SMARCAL1 and reinforces the importance of a detailed clinical evaluation, molecular detection, and appropriate genetic counseling.

Keywords

Short stature focal segmental glomerulosclerosis Schimke immuno-osseous dysplasia SMARCAL1 whole exome sequencing novel mutation

Introduction

Schimke immuno-osseous dysplasia (SIOD, OMIM: 242900) is a rare autosomal recessive inherited disorder that was first reported by Schimke in 1971, and its main clinical findings are spondyloepiphyseal dysplasia, focal segmental glomerulosclerosis (FSGS), T-cell immunodeficiency, and facial dysmorphism.^1–3 Clinically, the severity of SIOD is determined primarily by the patient’s age at onset, ultimate lifespan, and accompanying symptoms.⁴ SIOD is divided into the following two forms: 1) severe or infantile; and 2) mild or juvenile on the basis of the age at onset. The severe or infantile form usually manifests early or even in utero with growth retardation and death early in life, whereas the mild or juvenile form usually displays growth failure and survival to adulthood if renal disease is appropriately treated.^3,5 Mortality with SIOD can be significant, particularly if the condition is not recognized. Fortunately, identification of biallelic pathogenic mutations in SMARCAL1 on molecular genetic testing confirms the diagnosis if clinical features are inconclusive.

Boerkoel et al.⁵ first determined that SMARCAL1 (OMIM: 606622; hg19/GRCh37, NM_014140.4) gene mutations were responsible for SIOD. The SMARCAL1 gene, which was mapped to 2q35, is composed of 18 exons, and the first two exons are non-coding. It also encodes the SMARCAL1 protein, which is also known as HepA-related protein (HARP) and has 954 amino acids; this protein plays an important role in transcriptional regulation, replication, repair, recombination, and covalent modification.⁶ A deficiency in the SMARCAL1 protein could lead to impairment of cellular functions due to progressive DNA damage.⁷ In this study, we present the case of a 14-year-old Chinese boy with short stature, FSGS, and some characteristic dysmorphic features. He was diagnosed with mild SIOD on the basis of clinical features and genetic analysis. We also present a review of other cases of mild SIOD in the literature.

Case presentation

A 14-year-old Chinese boy, who was the second child of nonconsanguineous parents, was admitted to our hospital because of foamy urine and lower extremity edema for 1 year. His parents and older brother were healthy, and no family history of short stature or renal disease was reported. He was born at 38⁺³ weeks gestation (birth weight, 2.6 kg) by cesarean section because of oligohydramnios and decreased fetal movement. Protracted diarrhea occurred frequently before 3 years of age, and his weight was 8.3 kg, which is in the <3rd percentile for that age.

On physical examination, he had developmental delay (37.0 kg, weight at 3rd percentile), short stature (137 cm, height <3rd percentile), and he had some characteristic facial features including a triangular shape and a broad nasal bridge with a rounded tip of the nose. He had swollen eyelids, short neck, barrel-shaped chest, protruding abdomen, and two areas of jock itch, one on each of his inner thighs. His teeth appeared small and widely spaced (Figure 1). When walking, his legs made an X shape. Lymphopenia (1.04 × 10⁹/L, 16.7%, Ref: 1.1–3.2 × 10⁹/L, 20%–50%) was observed at different times, and it was further confirmed by flow cytometry analysis, which revealed significantly decreased levels of CD4⁺ T-cells (208/μL, 14.57%, Ref: 550–1440/μL, 27%–51%) and CD4⁺/CD8⁺ T-cells (0.55/μL, Ref: 0.71–2.78/μL). Massive proteinuria (9.31 g) was detected using 24-hour proteinuria quantification, and proteinuria did not improve after treatment. Blood biochemistry evaluation revealed hypoproteinemia due to low total protein (47.3 g/L, Ref: 60–85 g/L) and albumin (24.9 g/L, Ref: 35–55 g/L), as well as dyslipidemia with high total cholesterol (TC; 7.87 mmol/L, Ref: <5.2 mmol/L) and low-density lipoprotein (LDL; 4.27 mmol/L, Ref: <3.61 mmol/L). However, urea nitrogen, creatinine, and glucose levels were all within their respective reference ranges. Endocrine hormone results revealed subclinical hypothyroidism (thyroid stimulating hormone [TSH] 8.75 μIU/mL, Ref: 0.27–4.2 μIU/mL), hypocalcemia (serum calcium 1.91 mmol/L, Ref: 2.0–2.7 mmol/L), and secondary hyperparathyroidism (parathyroid hormone [PTH] 178.1 μIU/mL, Ref: 15–68.3 μIU/mL) because 1,25-dihydroxyvitamin D₃ [1,25(OH)₂D₃] was insufficient (11 ng/μL, Ref: 30–100 ng/μL), whereas cortisol, adrenocorticotropic hormone (ACTH), and sex hormones (including follicle stimulating hormone [FSH], luteinizing hormone [LH], estradiol, prolactin, and progesterone) were all normal. Growth hormone provocation test results indicated that the peak secretion of growth hormone was up to 40,308 pg/mL at 30 minutes after medication (Table 1), with a normal insulin-like growth factor [IGF-1] level (298 ng/mL; Ref: 220–972 ng/mL). High levels were detected for C-reactive protein (CRP; 15.2 mg/L, Ref: 0–10 mg/L), procalcitonin (PCT; 0.061 ng/mL, Ref: 0–0.046 ng/mL), and erythrocyte sedimentation rate (ESR; 39 mm/hour, Ref: 0–15 mm/hour). No hepatitis infection was detected, and the markers of autoimmunity (antinuclear antibodies [ANA], antineutrophil cytoplasmic antibody [ANCA], anti-double-stranded DNA antibody [dsDNA]) were negative. Radiological examination of his hand demonstrated that the patient’s bone age was 14.3 years, which was consistent with his calendar age. Osteoporosis was observed in both feet and ankles using an X-ray bone densitometer, but the features of his vertebrae, pelvis, and femoral heads were not available.

Table 1.

The patient’s growth hormone provocative test results.

	Growth hormone (pg/mL)
When medication was administered	685.9
15 minutes after medication	29297
30 minutes after medication	40308
1 hour after medication	29881
1.5 hours after medication	26718
2 hours after medication	13115

With his parents’ consent, a renal biopsy was performed, and the results showed FSGS and mild mesangial proliferative glomerulonephritis. Whole exome sequencing (WES) revealed two compound heterozygous missense mutations in the SMARCAL1 gene using the Illumina NovaSeq 6000 platform (Illumina, San Diego, CA, USA). Sanger sequencing confirmed that the two missense variants, c.1933C>T (p.R645C) and c.2479G>A (p.V827M), in the SMARCAL1 gene were inherited from his parents (Figure 2). Results of bioinformatic analysis showed all of the five online prediction tools, including Mutation Taster (http://mutationtaster.org/),⁹ Polymorphism Phenotyping v2 (Polyphen_2, http://genetics.bwh.harvard.edu/pph2),¹⁰ Rare Exome Variant Ensemble Learner (REVEL, https://sites.google.com/site/revelgenomics/),¹¹ Sorting Intolerant from Tolerant (SIFT, https://sift.bii.a-star.edu.sg/),¹² and Protein Variation Effect Analyzer (PROVEAN) (http://provean.jcvi.org/index.php),¹³ predicted the two missense mutations as disease-causing/damaging mutations. The prediction results were also supported by the extremely low allele frequencies of the two mutations (Table 2). Additionally, comparative amino acid sequence alignment of other SMARCAL1 proteins across different species revealed that the c.2479G>A (p.V827M) mutation occurred in highly conserved regions within the ATPase catlytic domain using homologene (http://www.ncbi.nlm.nih.gov/homologene) with UGene software (Figure 3).^14,15 In accordance with the ACMG guidelines for interpretation of genetic variants,¹⁶ the c.1933C>T (p.R645C) and c.2479G>A (p.V827M) variants were classified as a “likely pathogenic variant” (PM2+PP4+PM3+PM5+PP3) and a “likely pathogenic variant” (PM2+PP4+PM3+PP3), respectively. Therefore, on the basis of the clinical and genetic features, the patient was diagnosed with mild SIOD. After receiving consent from his parents, the patient was treated with irbesartan, alfacalcidol capsule, levothyroxin sodium tablets, calcium carbonate, vitamin D₃ tablets, and thymopdypeptide enteric-coated tablets to reduce proteinuria, protect kidney function, prevent infection, maintain thyroid function, and regulate immune function. After treatment, his edema and infection improved. We followed-up with the patient until December 2020, and he had normal renal function.

Table 2.

The SMARCAL1 variant pathogenicity was supported by multiple in silico analyses

Variant	Amino acid change	Mutation Taster^a	Polyphen-2^b	REVEL^c	SIFT^d	PROVEAN^e	ExAC (total)^f	1000 Genome (total)^g	gnomAD_exome (total)^h	gnomAD_genome (total)ⁱ
c.1933C>T	p.R645C	Disease-causing (1)	Probably damaging (1.000)	Damaging (0.974)	Damaging (0)	Damaging (−7.28)	–	–	1.219e-05	3.23e-05
c.2479G>A	p.V827M	Disease-causing (1)	Probably damaging (0.997)	Damaging (0.844)	Damaging (0)	Damaging (−2.81)	4.456e-05	0.000199681	1.38e-05	3.229e-05

a: For Mutation Taster, the probability value is the probability of the prediction (i.e., a value close to 1 indicates a high likelihood of prediction).

b: For Polyphen-2, the prediction scores ranged from 0 to 1, with high scores indicating probably or possibly damaging.

c: For REVEL, prediction scores ranged from 0 to 1, with high scores indicating probably or possibly damaging.

d: For SIFT, scores varied between 0 and 1. Variants with scores close or equal to 0 are predicted to be damaging.

e: For PROVEAN, variants with scores lower than −2.5 (cutoff) are predicted to be deleterious.

f: Allele frequency of variation in the total ExAC database.

g: Allele frequency of variation in the 1000 Genomes database.

h: Allele frequency of variation in the total gnomAD (a large database containing 123,136 exome sequences).

I: Allele frequency of variation in the total gnomAD (a large database containing 15,496 whole-genome sequences).

Polyphen-2, polymorphism phenotyping v2; REVEL, Rare Exome Variant Ensemble Learner; SIFT, Sorting Intolerant from Tolerant; PROVEAN, Protein Variation Effect Analyzer; ExAC, Exome Aggregation Consortium; gnomAD, Genome Aggregation database.

Discussion

In the present study, we report the case of a male teenager who exhibited some clinical characteristics and was diagnosed with mild SIOD; these clinical characteristics included short stature, FSGS, and characteristic dysmorphic features. Moreover, there were two areas of jock itch, one on each of his inner thighs, which might have been caused by a fungal infection, and it was confirmed by the laboratory test results. This infection might have been associated with low immunity. The effect of 1,25(OH)₂D₃ on secondary hyperparathyroidism with chronic renal failure was reported previously, and it showed that 1,25(OH)₂D₃ could markedly suppress PTH levels while increasing serum calcium.^17,18 For our patient, hyperparathyroidism was considered to be the result of a 1,25(OH)₂D₃ deficiency. Mild clinical features were compatible with the juvenile form of SIOD at 14 years of age.

As an ATP-dependent annealing helicase, the SMARCAL1 protein, contains two DNA/RNA HARP2 helicases at the C-terminal and has a SNF2 N terminal domain, and the SMARCAL1 protein can catalyze the rewinding of stably unwound DNA (Figure 2).^19,20 The professional HGMD database contains 100 mutations of the SMARCAL1 gene, with 66 missense/nonsense mutations, 9 splicing substitutions, 14 small deletions, 8 small insertions/duplications, 1 small indel, and 2 gross deletions. Usually, the SMARCAL1 missense mutations are typically associated with later onset disease, whereas nonsense, frameshift, and splicing mutations are more frequently detected in severe SIOD. In our patient, a mild phenotypic expression of SIOD was found to be associated with a new genotype consisting of compound heterozygosity for a well-known missense variant (c.1933C>T, p.R645C) and a novel missense variant (c.2479G>A, p.V827M). The missense variant (c.1933C>T, p.R645C) has been previously reported to be pathogenic, and it was detected in a patient who was clinically diagnosed with mild SIOD and survived into adulthood with medical therapy and renal transplantation.²¹ This suggests that the missense variant c.1933C>T (p.R645C) is common in mild SIOD, which was previously reported in other SIOD patients with different ethnic origins.⁵ This missense mutation c.2479G>A (p.V827M) occurred at a highly conserved site of the multi-sequence alignment within the ATPase catalytic domain (Figure 3). This indicates that there may be some residual function of the SMARCAL1 protein with the compound heterozygous missense mutations c.1933C>T (p.R645C) and c.2479G>A (p.V827M).

For a better understanding the phenotype and genotype, we summarized the reported cases of mild SIOD that were reported in the literature (Table 3).^{4–6,20,22–26} Sixteen cases (including four pairs of siblings) with mild SIOD have been summarized. The male-to-female ratio was 7:9, and 81.25% (13/16) of the patients were over 10 years of age. Most mild SIOD cases occurred in people of German descent (4/16), Italian descent (3/16), and Turkish descent (3/16), and only one case was reported in a Chinese population. Skeletal abnormality (16/16) was the most frequent feature, and short stature was the most common reason for admission to the hospital. Nephrotic syndrome (13/16) and facial features (9/16) were also common features. Nine patients underwent renal biopsies, and FSGS was observed in seven patients. Thirteen patients underwent genetic analysis, and all (including four pairs of siblings) had five homozygous mutations (including two pairs of siblings) or eight compound heterozygous mutations in the SMARCAL1 gene. Among these mutations, a nonsense mutation of E848X was identified in five out of 13 patients with a heterozygous mutation, indicating that it should be prevalent in the patients with mild SIOD. Both homozygous missense mutations of R586W and R561C were detected in two pairs of siblings who were born to consanguineous parents. The homozygous R561C mutation was detected in a young boy aged 18 months who presented with significantly diminished CD4⁺ T cells, which is a typical immune defect, and this required long-term follow-up. Another homozygous K647T mutation was detected in a young Algerian woman who was 20 years old. Nine patients underwent kidney transplantation and remained stable because their urea nitrogen and creatinine levels were normal, but the long-term efficacy remains to be further evaluated.

Table 3.

Phenotype and genotype in mild SIOD patients.

Reference	Fam–Ind	Ethnicity	Sex	Age^# (y)	Sk	Fac	Pig	NS	Rec	Lym	TSH	Dys	CNS	Ren	Treatment	Exon	Gene mutation
Hashimoto et al. (1994)²²	1–1	Japanese	F	16	+	+	+	+	−	+	ND	+	−	FSGS	Peritoneal dialysis	−	ND
Boerkoel et al. (2002)⁵	16–1	Scottish/French	M	25.9	+	+	+	+	−	+	ND	ND	−	ND	Kidney transplant	9/12	p.I548N/p.R645C
	18–1*	Italian	M	36.3	+	−	−	+	−	+	ND	ND	−	ND	Kidney transplant	11/11	p.R586W/p.R586W
	18–2*	Italian	F	23.9	+	−	−	+	−	+	ND	ND	−	ND	Kidney transplant	11/11	p.R586W/p.R586W
	27–1	Algerian	F	19.8	+	+	+	+	−	+	ND	ND	−	ND	Kidney transplant	12/12	p.K647T/p.K647T
Lücke et al. (2005)⁴	1–1*	German	M	22	+	−	+	+	−	−	−	ND	−	GS	Kidney transplant	4/17	p.F279S/p.E848X
	1–2*	German	M	19.9	+	+	+	+	+	+, mild	−	ND	+	FSGS	Kidney transplant	4/17	p.F279S/p.E848X
Bökenkamp et al. (2005)²³	1–1*	Turkish	M	10	+	+	−	+	−	+	−	ND	−	FSGS	Enalapril and losartan	10/10	p.R561C/p.R561C
	1–2*	Turkish	M	1.5	−	−	−	−	−	diminished CD4+ cells	ND	ND	ND	ND	−	10/10	p.R561C/p.R561C
Zivicnjak et al. (2009)²⁴	1–1*	German	F	19	+	−	−	+	+(after kidney transplant)	ND	ND	ND	−	MGA	Kidney transplant	12/17	p.R645H/p.E848X
	1–2*	German	F	14	+	−	−	+	+(after kidney transplant)	+	ND	ND	−	ND	Kidney transplant	12/17	p.R645H/p.E848X
Santangelo et al. (2014)⁶	1–1	Italian	F	7	+	−	−	+	−	+	+	ND	−	FSGS	Ramipril and irbesartan	3/17	p.R247P/p.E848X
Yavuz et al. (2015)²⁵	1–1	Brazilian	F	9	+	+	+	+	+	+	+	ND	+	FSGS	Kidney transplant	−	ND
Pedrosa et al. (2016)²⁶	1–1	Turkish	F	10	+	+	+	+	−	+	ND	ND	+	FSGS	Enalapril and losartan	−	ND
Liu et al. (2017)²⁰	1–1	Chinese	F	10.8	+	+	+	−	−	+	ND	+	−	ND	ND	3/12	p.Q149X/p.R645C
Current report	1–1	Chinese	M	14	+	+	−	+	Protracted diarrhea until 3 years old	+	+	+	−	FSGS	Irbesartan	12/16	p.R645C/p.V827M

*1 and 2 are siblings.

^#Age at publication or reported in the paper.

Fam, family; Ind, individual; y, years; Sk, skeleton; Fac, facial features; Pig, pigmentation; NS, nephrotic syndrome; Rec, recurrent infection; Lym, lymphopenia; Dys, dyslipidemia; Ren, renal biopsy; F, female; M, male; TSH, thyroid-stimulating hormone; CNS, central nervous system; ND, no data or not done; GS, global glomerulosclerosis; FSGS, focal segmental glomerulosclerosis; MGA, minor glomerular abnormalities.

Conclusion

We identified a novel missense mutation, c.2479G>A (p.V827M), in the SMARCAL1 gene from a male teenager who was diagnosed with mild SIOD. This report highlights the significance of complete clinical data and molecular detection. Our findings provide some targeted guidance for the treatment and prognosis in patients with mild SIOD, and they also contribute to the information that is available in gene mutation databases.

Footnotes

Acknowledgements

The authors thank the patient and his family members for participation in this study and all of the patient advisers for their assistance with clinical examination and blood specimen collection.

Authors’ contributions

WL designed the study, performed genetic testing, and drafted the initial manuscript. LJJ collected the patient data and current literature. WG made the diagnosis and completed the diagnostic work-up. KXD designed the study and critically reviewed the manuscript. All authors read and approved the final manuscript.

Declaration of conflicting interest

The authors declare that there is no conflict of interest.

Ethics statement

Informed consent was obtained from the patient and his family before participating in our study. The study was approved by the Research Ethics Committee of Zhengzhou University (approval number KS-2018-KY-36), and it complies with the CARE case report guidelines.⁸ All identifying details of the patient’s information have been deleted from the case report, and the identity of the patient cannot be ascertained in any way. The patient and his parents provided written consent for the treatment and publication of this paper.

Funding

This work was supported by the National Key Research and Development Project of China [grant number 2018YFC1002203].

ORCID iD

Xiangdong Kong

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