Compound Heterozygous Mutations with a Novel Variant in Integrin Beta4 Cause Epidermolysis Bullosa with Pyloric Atresia and Urologic Abnormalities.

To the Editor,

Epidermolysis bullosa (EB) with pyloric atresia (PA) is an autosomal recessive form of EB subtype that affects the skin, as well as digestive and frequently urogenital tracts. EB-PA is classified as the simplex form caused by the plectin gene (PLEC) mutations and the junctional form caused by integrin α6β4 genes (ITGA6, ITGB4) mutations.12345 However, the intracellular domain of integrin β4 interacts with other hemidesmosomal components of basal keratinocytes, including plectin.6 A recent review on the transmission electron microscopy (TEM) findings of EB-PA patients who showed absent expression of integrin β4 reported a consistent level of cleavage planes through concurrent low intra-basal epidermal and lamina lucida,7 suggesting that the loss of integrin β4 can lead to this unique ultrastructural finding.

We previously reported a Korean male newborn who presented with PA with mucocutaneous blisters at birth.8 Widespread blisters were found on the entire body and oral mucosa, and they eventually healed without significant scarring. Nail dystrophy was observed on the right thumb. Multiple urologic abnormalities including bilateral hydronephrosis, hydroureter, and a distended trabeculated bladder were noted at 12 months of age. Immunofluorescence mapping and TEM performed at infancy revealed the localization of type IV and VII collagen to the blister base and intra-basal epidermal cleavages with tonofilaments clumping, respectively, leading to a diagnosis of EB simplex, generalized severe, formerly called Dowling-Meara type with PA and urologic abnormalities.8 The patient's father, paternal brother, and sister had reported bullae without any anomalies, which had spontaneously improved. In this report, we describe compound heterozygous mutations in integrin β4 in this patient, which were not previously identified. Next-generation sequencing performed after obtaining informed consent revealed compound heterozygous missense mutations, c.113G>T (p.C38F) in exon 3 and c1274A>C (p.Q425P) in exon 11 of ITGB4 gene, which were confirmed by additional Sanger sequencing (Fig. 1A). Mutations in PLEC or keratin genes have not been detected. Missense mutation of p.Q425P has been reported in EB-PA.91011 p.C38F in ITGB4 was reported as a codon variant, but has not been reported to be associated with EB.12 Two in silico tools, including SIFT and PolyPhen-2, predicted that this amino acid substitution in ITGB4 is likely pathogenic. Cutaneous symptoms improved with age, showing only blistering limited to the extremities and inguinal area at age 22 (Fig. 1B).

Fig. 1

Clinical features and genetic information of the patient. (A) Direct sequencing (Sanger method) of DNA identified compound heterozygous missense mutations in c.113G>T (p.C38F) in exon 3 and c1274A>C (p.Q425P) in exon 11 of ITGB4 in the patient's DNA. (B) Clinical features of the patient at age 22. (C) Representative immunofluorescence staining images of integrin β4, plectin, and integrin β6 in the skin of the patient and healthy individual (scale bars=50 µm).

Integrin β4 consists of an intracytoplasmic domain connected to keratin intermediate filaments via binding to plectin and type XVII collagen and an extracellular domain connected to laminin. ITGB4 mutations are the most frequent cause of EB-PA, and EB-PA caused by ITGB4 mutations has been classified as a form of junctional EB,4 but a previous paper reported that the deletion of a cytoplasmic domain of integrin β4 causes EB simplex without PA.13 This indicated that mutations in the intracytoplasmic domain of integrin β4 may result in intrabasal splits, suggesting EB simplex rather than junctional EB.13 In this case, despite the compound heterozygous missense mutations in the extracellular domain of integrin β4, TEM showed cleavages above the hemidesmosome and keratin clumping in the basal keratinocytes, resembling the finding in EB simplex, generalized severe. Besides, the expression of plectin was reduced in the patient's skin, despite the absence of mutations in PLEC (Fig. 1C). These findings might be possibly due to the impaired stabilization of plectin by integrin β4, which in turn, may affect the interaction with keratin intermediate filaments. However, to exclude the possibility of artificial cleavages within the basal cells or dermo-epidermal junction and to confirm the type of EB-PA, thorough inspection of numerous sections of TEM samples will be further required. Based on the position of ITGB4 mutations, our case is thought to be junctional EB-PA.

The prognosis of junctional EB-PA is generally poor, but spontaneous amelioration of symptoms with aging has been reported in rare cases.1415 Our case is also considered to belong to this rare subgroup.

Among the ITGB4 missense mutations in our case, we found p.C38F in ITGB4. Another mutation at the same codon 38 (p.C38R) has been reported in EB-PA patients,16 but p.C38F has not been reported to be associated with EB-PA. Another interesting finding in our case was that the patient presented with mild skin lesions possibly due to compound heterozygous missense mutations in ITGB4, but relatively severe and multiple congenital urologic abnormalities, suggesting that genotype-phenotype correlations are not always evident in EB-PA with ITGB4 mutations. Collectively, our case expands the genotypic and phenotypic spectrum and ultrastructural findings of EB-PA caused by ITGB4 mutations.