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. 2020 Nov 3;20:504. doi: 10.1186/s12887-020-02393-2

Where the congenital heart disease meets the pulmonary arterial hypertension, FLNA matters: a case report and literature review

Xiaoxian Deng 1, Shanshan Li 1, Qiu Qiu 1, Bowen Jin 1, Menghuan Yan 1, Yuanpin Hu 2, Yang Wu 3, Hongmei Zhou 1, Gangcheng Zhang 1, Xuan Zheng 1,2,✉
PMCID: PMC7607646  PMID: 33143682

Abstract

Background

Pediatric patients with genetic disorders have a higher incidence of pulmonary arterial hypertension (PAH) regardless of their heart defects. Filamin A (FLNA) mutation is recently recognized to be associated with pediatric pulmonary disorders, however, the clinical courses of PAH related to the mutation were reported in limited cases. Here, we presented a case and pooled data for better understanding of the correlation between FLNA mutation and pediatric PAH.

Case presentation

The patient was a 8-month-old female with repeated episodes of pneumonia. Physical examination revealed cleft lip, cleft palate and developmental retardation. Imaging examination showed a small atrial septal defect (ASD), central pulmonary artery enlargement, left upper lobe of lung atelectasis, and pulmonary infiltration. Genetic test showed she carried a de novo pathogenic variant of FLNA gene (c.5417-1G > A, p.-). Oral medications didn’t slow the progression of PAH in the patient, and she died two years later.

Conclusions

FLNA mutation causes rare but progressive PAH in addition to a wide spectrum of congenital heart disease and other comorbidities in pediatric patients. We highly recommend genetic testing for pediatric patients when suspected with PAH. Given the high mortality in this group, lung transplantation may offer a better outcome.

Keywords: Pulmonary arterial hypertension, Congenital heart disease, Filamin A

Background

Pediatric pulmonary arterial hypertension (PAH) is a rare disease with high mortality. Left-to-right shunting, lung diseases and genetic disorders are most common causes leading to PAH in children[1]. Filamin A (FLNA) is a 280-kD protein widely expressed in the body and regulating cell shape and migration. Among the broad range of diseases associated with FLNA mutation, lung diseases have been seen in most patients, such as pneumonia, and respiratory failure. In addition, PAH in pediatric patients with FLNA mutation was fatal despite of their congenital heart disease (CHD), and required early lung transplantation[2]. Here we report a female patient with FLNA mutation, who presented with recurrent pneumonia, arterial septal defect (ASD), mild developmental delay and rapidly progressive PAH.

Case presentation

An 8-month-old female patient was referred to our center due to severe cough, short of breath, fatigue and fever. The patient had nine episodes of pneumonia and cardiomegaly since she was two-month-old. Physical examination revealed cleft lip, which was surgical repaired when she was 6 months old, and cleft palate. Her finger oxygen saturation was 94%. Transthoracic echocardiography showed there was a 0.5 × 0.6 cm ASD with a 2.4 cm right atrium. Laboratory test showed NT-proBNP was 963 pg/ml. Some of autoimmune antibodies, including dsDNA-antibody, SSA/Ro 60kD antibody, anti-cardiolipid antibody, and anti-β2GPI antibody, were positive. Erythrocyte sedimentation rate (ESR) and C-reaction protein (CRP) were normal. IgG was slightly elevated at 18.40 g/L, and C3 was 0.83 g/L. Significantly increased pulmonary vascular resistance (PVR, 17 WU) was seen in her first right heart catheterization despite of the slightly increased pulmonary artery pressure (PAP, 38/17/24 mmHg). Oral furosemide and antisterone were given since then. She was also suggested to inhale oxygen at home even though she maintained her daily activities without additional requirement of oxygen. The patient was re-hospitalized several times because of recurrent pneumonia and heart failure thereafter. Her finger oxygen saturation dropped to 75% at lowest, and stayed at 95% or higher when given nasal catheter oxygen inhalation. Hemodynamic parameters turned worse in the second measurements, where PAP increased along with PVR (PAP, 100/50/67 mmHg; PVR, 42 WU). Further examination included chest computed tomography (CT) scan. CT showed infiltration in upper lobes at both sides (Fig. 1a, b), and lung atelectasis in left upper lobe (Fig. 1b). Pulmonary artery and right atrium were significantly dilated (Fig. 1b, star; d). No thrombosis was seen in pulmonary artery. The patient and her parents received whole exome sequencing test. A new splicing variant (exon34: c.5417-1G > A, p.-) in the FLNA gene was found only in the patient. Diuretics, dopamine, and oral Bosentan (12.5 mg twice daily) were used to relieve her symptoms. No intubation or other advanced life supports were required during hospitalizations. Patient’s family refused any further intervention during her last hospitalization at age of 2 years. She became significantly cyanosis after last discharge. Unfortunately, the patient didn’t response well to medication therapy, and she died from a severe pneumonia 5 months later.

Fig. 1.

Fig. 1

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Chest CT. a Infiltration in both upper lobes of lung; b Main pulmonary artery was dilated (*). There was atelectasis in left upper lobe of lung; c Slightly infiltration in lower lobes; d Dilated right atrium. 

Discussion and conclusions

PAH is a clinical symptom characterized by increased pulmonary artery pressure more than 25 mmHg. Pediatric PAH shares similarities with adult PAH in some etiology. However, specialists have addressed that pediatric patients have higher prevalence of idiopathic PAH, PAH associated with congenital heart disease (CHD), and pulmonary disorders [3]. With the attempt to explore mechanism underlying, next generation sequencing reveals the genetic defects associated with pediatric PAH.

FLNA gene was firstly related to neurologic disorder defect periventricular heterotopia (PVNH) in 1998 [4]. A broad range of diseases were observed with FLNA mutation thereafter, such as otopalatodigital syndrome (OPD) [5], frontometaphyseal dysplasia (FMD) [6], and Melnick-Needles syndrome (MNS) [5], FG syndrome (FGS), chronic idiopathic intestinal pseudoobstruction (CIIP) [7], cardiac valvular disease (CVD) [8], and others. However, lung disease was noticed in patients with FLNA mutation first by de Wit MC, et al. in 2010 [9]. Patients with lung disease related to FLNA mutation had higher incidence of pneumonia, lung developmental defects and respiratory failure, however, PAH were uncommon [10–12]. Among the reported cases, there were 19 of them having early onset PAH (including this case). Their clinical characteristics are summarized in Table 1. Developmental delay was observed in 6 patients, while CHD were seen in all. Fourteen patients had surgical correction of CHD, 6 of which had lung transplantation at the same time. Only one patient died after lung transplantation, nonetheless, mortality among pediatric PAH patients with FLNA mutation is as high as 35%.

Table 1.

Summary of pediatric PAH associated with FLNA mutation

Mutation Sex Age at diagnose CHD Chest CT Lung transplantation Medicine Outcome
Masurel-Paulet 2011[13] mosaic nonsense mutation c.994delG(p.K331X) male 3 months PDA Bilateral atelectasis; lung cysts; tracheobronchomalacia; pulmonary emphysema; congenital lobar emphysema; N None ND
Reinstein 2013 [14] De novo c.2193C > A (p.Tyr731X) female 6 months PDA Areas of focal hyperinflation associated with minimal patchy atelectasis N Sildenifil ND
De novo deletion of exons 2,5 and 13 female 18 months VSD N/A N Bosentan ND

De novo

c.5498_5504delCACCCACinsAC

 male 2 months

ASD;VSD;

PDA

 N/A N None Died
Lord 2014 [12] Truncating filamin A mutation(c.5683G-T, p.G1895*) female 4 months ASD

Bilateral pulmonary atelectasis and cysts,

tracheobronchomalacia, Areas of hyperinflation alternating with heterogeneous areas of

atelectasis; alveolar simplification

 N Inhaled nitric oxide; sidenafil; bosentan ND
Eltahir 2016 [13] c.3153dupC in exon 21 female 2 months PDA Bilateral lung emphysema with basal atelectasis; bronchospasm N None Died
Burrage 2017 [15]

Heterozygous

c.4596dupG

(p.Ser1533Glufs*12) (de novo)

 female 4 months PFO, PDA Multifocal atelectasis; perinflation and hyperlucency; atelectasis; central pulmonary artery enlargement; tracheobronchomalacia Y Sildenafil Alive

Heterozygous

c.5290G > A

(p.Ala1764Thr)

(de novo)

 female 2 months PFO, PDA, VSD Perinflation hyperlucency; atelectasis; central pulmonary artery enlargement; tracheobronchomalacia Y Sildenafil Died

Heterozygous

c.4446_4447dupAT(p.Leu1483Tyrfs* 19) (de novo)

 female 1month PFO,PDA Perinflation hyperlucency; atelectasis; central pulmonary artery enlargement; tracheobronchomalacia Y Sildenafil Alive

Heterozygous

c.4617_4618delGC(p.Leu1540Alafs*)

 female 2 months PFO, PDA Perinflation hyperlucency; atelectasis; central pulmonary artery enlargement; tracheobronchomalacia Y Sildenafil Alive

Heterozygous

c.6585dupT

(p.Pro2196Serfs*3) (de novo)

 female 7 montsh PFO;PDA Perinflation hyperlucency; atelectasis; central pulmonary artery enlargement; tracheobronchomalacia Y Sildenafil Alive

Heterozygous

c.2807A > G

(p.Lys936Arg) (VUS)

 female 5 months PFO, PDA Perinflation hyperlucency; atelectasis; central pulmonary artery enlargement; tracheobronchomalacia Y Sildenafil Alive
Shelmerdine 2017 [10]

Heterozygous for

c.88delG, p.(Ala30fs)

 female ND PDA;PFO Left lung hyperinflation; interstitial thickening in left; mediastinal shift to the right; right lobe consolidation N None Died

Heterozygous for c.6496dupA, p.

(lle2166fs)

 female ND PDA Progressive right lung hyperinflation; mediastinal shift to the left; right upper and middle lobe over inflation; coarse septal thickening; lower lobe atelectasis; patchy ground glass changes in lower lobes N Sildenafil Alive

Heterozygous for

c.2190_2193delTTAC,

p(tyr731fs)

 female ND ASD;PDA Right upper lobe hyperinflation; right middle lobe and left lower lobe atelectasis; right upper and middle, left upper lobe over-inflation; coarse septal thickening; lower lobe atelectasis N None Alive
Kinane 2017 [16] c.6577delC; p.Arg2193AlafsX14[R219AfsX14 female 7w PFO; VSD; PDA Wilson–Mikity syndrome (pulmonary dysmaturity syndrome) N None ND
Sasaki 2018 [17] Deletion c.6670-1delG male neonate PDA Bilateral dependent and subsegmental atelectasis, scattered opacity N None Died
Cannaerts 2018 [18] cis-located c.7921C > G,p.Pro2641Ala,c.7923delC,p.Tyr2642Thrfs*63 female ND ASD ND N None Died
This case splicing c.5417-1G > A (exon 34) female 22 months ASD Central pulmonary artery enlargement; left upper lobe atelectasis N Bosentan Died
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FLNA Filamin A; CT computed tomography; PDA patent ductus arteriosus; VSD ventricle septal defect; ASD atrial septal defect; N no; Y yes; ND Not provided

Interstitial lung disease (ILD) may cause PAH in pediatric patients, and FLNA mutation has been called for attention in ILD [17], but pediatric PAH patients with FLNA mutation don’t always present with characteristically pulmonary pathologic changes of ILD. Moreover, high prevalence of CHD in patients with FLNA mutation may confuse the real cause of the rapidly progressive PAH [19]. In our experience, genetic testing is more helpful to offer early-stage and accurate diagnose. Moreover, lung transplantation would bring higher survival in these patients based on previous reports.

Acknowledgements

We would like to thank the patient’s family for their consent to publish this report. We also appreciated our medical team and their efforts to treat the patient.

Abbreviations

FLNA

Filamin A

CHD

Congenital heart disease

ASD

Atrial septal defect

VSD

Ventricle septal defect

PDA

Patent ductus arteriosus

PFO

Patent foramen ovale

RHC

Right heart catheterization

PAH

Pulmonary arterial hypertension

NT-proBNP

N-terminal prohormone of brain natriuretic peptide

ESR

Erythrocyte sedimentation rate

CRP

C-reaction protein

PVR

Pulmonary vascular resistance

WU

Wood unites

PAP

Pulmonary artery pressure

CT

Computed tomography

PVNH

Periventricular heterotopia

OPD

Otopalatodigital syndrome

FMD

Frontometaphyseal dysplasia

MNS

Melnick-Needles syndrome

FGS

FG syndrome

CIIP

Chronic idiopathic intestinal pseudoobstruction

CVD

Cardiac valvular disease

Authors’ contributions

XD, SL, XZ management of the patient, drafting the article, critical revision of the article; QQ, BJ, MY literature review, critical revision of the article; H data collection; YW imaging evaluation; HZ, GZ critical revision of the article. All authors read and approved the final manuscript.

Funding

The authors declare that they did not receive any source of funding for the preparation of the manuscript.

Availability of data and materials

The datasets used in current study are available from the corresponding author on reasonable request.

Ethics approval and consent to participate

The study was performed according to the Declaration of Helsinki. Written informed consent was obtained from the patient’s parents for publication of this case report and accompanying images.

Consent for publication

Written informed consent was obtained from the patient’s parents for publication of this case report and accompanying images.

Competing interests

The authors declare that they have no competing interests.

Footnotes

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The datasets used in current study are available from the corresponding author on reasonable request.

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