Ze-Xu Chen
Wan-Nan Jia
Yong-Xiang Jiang- 1Eye Institute and Department of Ophthalmology, Eye & ENT Hospital, Fudan University, Shanghai, China
- 2NHC Key Laboratory of Myopia (Fudan University); Key Laboratory of Myopia, Chinese Academy of Medical Sciences, Shanghai, China
- 3Shanghai Key Laboratory of Visual Impairment and Restoration, Shanghai, China
Marfan syndrome (MFS, OMIM: 154700) is a heritable multisystemic disease characterized by a wide range of clinical manifestations. The underlying molecular defect is caused by variants in the FBN1. Meanwhile, FBN1 variants are also detected in a spectrum of connective tissue disorders collectively termed as ‘type I fibrillinopathies’. A multitude of FBN1 variants is reported and most of them are unique in each pedigree. Although MFS is being considered a monogenic disorder, it is speculated that the allelic heterogeneity of FBN1 variants contributes to various manifestations, distinct prognoses, and differential responses to the therapies in affected patients. Significant progress in the genotype–phenotype correlations of MFS have emerged in the last 20 years, though, some of the associations were still in debate. This review aims to update the recent advances in the genotype-phenotype correlations of MFS and related fibrillinopathies. The molecular bases and pathological mechanisms are summarized for better support of the observed correlations. Other factors contributing to the phenotype heterogeneity and future research directions were also discussed. Dissecting the genotype-phenotype correlation of FBN1 variants and related disorders will provide valuable information in risk stratification, prognosis, and choice of therapy.
Introduction
Marfan syndrome (MFS, OMIM: 154700) is an autosomal dominant connective tissue disorder, characterized by ectopia lentis (EL), aortic dilation, and a combination of skeletal features (Judge and Dietz, 2005). In the latest nosology, MFS is exclusively associated with pathogenic variants in the FBN1 gene, although a diagnosis of MFS is possible in the absence of genetic testing. However, variants in FBN1 are also associated with a spectrum of phenotypes (Loeys et al., 2010a). The severe end of this clinical continuum is neonatal MFS characterized by early-onset congestive heart failure secondary to progressive valve problems (Hennekam, 2005; Loeys et al., 2010a). Conditions at the mild end include the MASS syndrome (myopia, mitral valve prolapse, borderline and non-progressive aortic root dilatation, skeletal findings and striae), mitral valve prolapse syndrome, and EL syndrome (Faivre et al., 2012). Some patients with pathogenic FBN1 variants had features that are different from or even opposite to the manifestations of MFS, such as the skin thickening in stiff skin syndrome (SSS, OMIM: 184900), progeroid appearance in marfanoid–progeroid–lipodystrophy syndrome (MFLS, OMIM: 616914), and short extremities in acromelic dysplasia, which include geleophysic dysplasia (GD, OMIM: 231050), acromicric dysplasia (AD, OMIM: 102370), and type II Weill-Marchesani syndrome (WMS2, OMIM: 608328) (Loeys et al., 2010b; Sakai and Keene, 2019; Muthu and Reinhardt, 2020; Yang et al., 2021). Therefore, patients with FBN1 variants are collectively termed ‘type I fibrillinopathy’ (Hayward and Brock, 1997; Faivre et al., 2008).
Molecular testing of FBN1 has become an integral part of clinical management in patients with MFS. FBN1 is positioned at chromosome 15q21.1, which encodes a large glycoprotein consisting of 2871 amino acids, with a predicted molecular mass of 350 kDa (Biggin et al., 2004; Loeys et al., 2004). It comprises 47 epidermal growth factor-like domains (EGF-like), among which 43 are calcium-binding (cb EGF-like), seven transforming growth factor β-binding protein domains (TGFBP), two hybrid domains, a proline-rich domain, a 4-Cys motif LTBP-like domain, an NH2 unique domain, a COOH unique domain, and a fibulin-like domain (Figure 1A) (Du et al., 2021). FBN1 polymerizes into microfibrils which are responsible for the elasticity or force-bearing capacity of connective tissue, such as lens zonule, aortic wall, heart valves, and tubular bones (Shin and Yanagisawa, 2019). To date, more than 3000 FBN1 variants have been recorded including the full spectrum of variant types throughout the 65 coding exons and interspersed introns of the gene (Groth et al., 2017). Approximately 30% of cases are caused by new or spontaneous variants and about 12% of all reported FBN1 variants are recurrent (Collod-Béroud et al., 2003).
FIGURE 1. The demonstration of protein architecture and mutation classification strategy of FBN1 gene. (A) The protein architecture of FBN1. The regions in previous genotype-phenotype studies or mechanism studies were shown in colored blocks, including N terminus (exons 1–21), middle region (exons 22–42), C-terminus (exons 43–65), FUN-EGF region (exons 1–11), neonatal region (exons 24–32), TGFβ-regulating region (exons 43–65), DN-CD region (exons 25–36 and exons 43–49). Exons of strong genotype-phenotype correlations were marked, including exon 25 (poorest prognosis), exon 26 (microspherophakia), exon 37 (stiff skin syndrome), exons 41–42 (geleophysic and acromicric dysplasia), exon 64 (marfanoid–progeroid–lipodystrophy syndrome). (B) The strategy of mutation classification of FBN1. Mutations were first broadly divided into HI and DN groups. DN mutations were further classified according to the affected residue or affected regions. DN mutations were classified as DN (-Cys), DN (+Cys), and DN (Calcium-binding), and DN (Others) based on the affected residues. The classification of affected regions was demonstrated in (A). DN, dominant-negative effect; DN (-Cys), DN mutations eliminating cysteine; DN (+Cys), DN mutations creating cysteine; DN (Calcium-binding), DN mutations affecting conserved calcium-binding motif; DN (Others), DN mutations not belonging to the above groups; Ex, exon; HI, haploinsufficiency.
Despite high penetrance, one of the unexplained features of MFS and related fibrillinopathies is the prominent phenotype variation in the timing of onset, tissue distribution, and severity of manifestations. A number of studies have tried to explain the phenotypic diversity by the allelic heterogeneity of FBN1 variants in the last 20 years. Significant correlations have emerged in characteristics, disease progression, risk stratification, and therapeutic responses, encompassing a full range of phenotypes in multiple systems. In this review, we provide an overview of recent advances in the genotype-phenotype correlations of MFS and related fibrillinopathies, list potential molecular bases or mechanisms, and comment on the future research directions, hoping to present illuminating readings for both clinicians and researchers.
Genotype and phenotype correlation
The first genotype-phenotype correlation came from the clinical observations that variants in patients with neonatal and severe MFS tend to cluster in the exons 24–32 of FBN1 genes, which were referred to as the neonatal region (Putnam et al., 1996). From then on, more and more studies explore the complexity of the genotype-phenotype correlations. The classification of the FBN1 variants is summarized in Figure 1B. The genotype-phenotype studies with a sample size of over 50 were summarized in Supplementary Table S1 and visualized in Figure 2. Although no clear-cut manifestations are predictable for a given type of variant, the relative risk for specific organ involvement shows some statistically significant correlations.
FIGURE 2. The visualization analysis of genotype-phenotype correlations in patients with MFS and related fibrillinopathies. A heatmap was applied to describe the major conclusions of genotype-correlation studies, with the positive correlations in red, negative correlations in blue; insignificant correlations in green; not-studied correlations in yellow. Minor conclusions or special considerations were shown in the note column. The proportions of positive correlations were shown in the last row.
Genotype and clinical manifestations
Cardiac manifestations
As the major causes of early mortality in MFS, cardiovascular manifestations were the most investigated phenotypes in relation to FBN1 genotypes. Major cardiovascular involvement includes aortic dilatation and dissection. The dilated aorta generally develops at the aortic root, but the enlargement or dissection of any part of the aorta is possible (Hiratzka et al., 2010). A solid correlation has the potential to optimize the risk stratification of disease monitoring and decision-making in prophylactic surgeries. Schrijver et al. initially classified FBN1 variants into dominant-negative (DN) variants, encompassing missense variants and inframe deletions or insertions, and haploinsufficiency (HI) groups, including nonsense variants and frameshift variants. It was found that ascending aortic dissections were more common in the HI group than that in the DN group (Schrijver et al., 2002). Salvi et al. found that patients with HI variants exhibited a higher degree of arterial stiffness than that with DN variants, which supports the notion that the aortic involvement is more serious in the HI group (Salvi et al., 2018). Later studies confirmed the above conclusions in independent cohorts; however, this correlation became insignificant in several studies (Figure 2). The potential reasons underlying the inconsistent results may be the different definitions of the aortic events, such as aortic dilation, aortic dissection, or prophylactic surgeries, and the different enrolled patients, such as pediatric patients, classical MFS, or atypical ones.
One big issue is the heterogeneity of the FBN1 variants. The location of nonsense or frameshift variants did not affect the severity of aortic phenotypes (Faivre et al., 2009a; Takeda et al., 2018). However, the variants in the DN group are of considerable heterogeneity. Missense variants affecting the critical structures, such as disulfide-bond forming cysteines and the conserved calcium-binding motif of the tandem cb EGF-like domains were proved to correlate with more severe MFS (Comeglio et al., 2007; Zhang et al., 2021). Thus, further subgrouping of DN variants is an important step to enlighten the real risk loci within the different types of DN variants. Stengl et al. extracted variants eliminating cysteines (-Cys) from the DN variants and combined them with the HI group. It was found that patients with HI or DN (-Cys) variants had a significantly higher aortic involvement rate than DN variants creating cysteines (+Cys) and other DN variants (Others). When it comes to aortic surgery, patients with DN (-Cys) had the highest risks than HI or other DN variants (Stengl et al., 2020). Arnaud et al. and Faivre et al. also found that DN (-Cys) had a higher severity of aortic dissection or surgery than DN (+Cys) and DN (Others) variants in independent cohorts (Faivre et al., 2007; Arnaud et al., 2021a). Aubart et al. divided MFS patients into severe phenotype group and benign phenotype group based on aortic diameter and aortic surgery history and showed more DN (-Cys) and HI variants in the severe phenotype group but more DN (+Cys) variants in the benign phenotype group (Aubart et al., 2018). Comeglio et al. selected DN variants affecting calcium-binding residues in cb EGF-like domains (Calcium-binding) and combined them with DN (-Cys), which were significantly associated with more severe MFS phenotypes (Comeglio et al., 2007).
Another classification strategy is based on the location of the variants (Figures 1A,B). The most well-known example is the neonatal region (exons 24–32), which correlated with globally higher severity and more complete phenotypes of MFS. Faivre et al. revealed that variants in the neonatal region were associated with a higher probability of ascending aortic dilatation, aortic surgery, and shorter survival, even when cases of neonatal MFS were excluded (Faivre et al., 2007). Similar conclusions were also reported by other studies (Faivre et al., 2009b; Arnaud et al., 2021a). Takeda et al. further extended the risk regions to exon 25–36 and 43–49 based on extreme phenotype sampling and verified the conclusions in an independent cohort (Takeda et al., 2018). DN variants affecting cysteine residues and in-frame deletion variants in exons 25–36 and 43–49 (named DN-CD variants) had larger aortic root Z-scores and a 6.3-fold higher risk of aortic events compared with other patients, which was more deleterious than variants within exons 24–32 and comparable to patients in HI group (Takeda et al., 2018). To sum up, DN variants are a heterogeneous group. DN (-Cys) variants and those located in neonatal or DN-CD region have higher risks of developing aortic events.
Besides aortopathy, other cardiac manifestations are also studied in relation to FBN1 variants. The HI variants, DN (-Cys) variants, DN variants in the neonatal region, and FBN1 variants located in TGFBP domains or cb EGF-like domains were associated with higher risks for mitral valve surgery (Faivre et al., 2007; Faivre et al., 2009b; Kühne et al., 2013; Arnaud et al., 2021a). Variants in exons 24–32 were associated with ventricular tachycardia (Aydin et al., 2013). Earlier onset of pulmonary artery dilatation was found in MFS children with DN variants (Stark et al., 2020).
Ocular manifestations
Ectopia lentis (EL), the dislocation of the lens from its physiological position, was first documented as part of MFS by Börger in 1914 (Über zwei, 1914), and has been recognized as a major criterion or cardinal feature when diagnosing MFS. (Loeys et al., 2010a). The prevalence of EL ranges from 33% to 72% (Konradsen and Zetterstrom, 2013; Chandra et al., 2014), thus, a number of studies aim to address why subsets of patients are exempt from developing EL. Contrary to aortic events, EL was more prevalent in patients harboring DN variants (Becerra-Muñoz et al., 2018; Li et al., 2019), especially the DN (-Cys) or DN (+Cys) ones (Faivre et al., 2007; Baudhuin et al., 2015; Meester et al., 2022). Chen et al. and Guo et al. further proved independently that DN variants were associated with a higher degree of EL compared to the HI ones in cohorts of congenital EL (Chen et al., 2021a; Guo et al., 2021). The variants associated with EL also cluster in the N-terminus of the FBN1 gene (Comeglio et al., 2007; Faivre et al., 2007; Baudhuin et al., 2015; Meester et al., 2022). And patients harboring variant in the neonatal region also had a higher incidence of EL (Faivre et al., 2007). As a special form of EL, microspherophakia is characterized by the globular laxity of the zonules and the lens growth of which is arrested by insufficient mechanical stretching (Kumar et al., 2019). Microspherophakia was found in about 10% of patients with MFS and the surgical management of which is different from other types of EL (Chen et al., 2021b; Chen et al., 2022). Chen et al. revealed that variants in exons 22–42, especially exon 26, had higher risks of combined microspherophakia in patients with MFS (Chen et al., 2021c).
In recent years, more and more studies of the correlation between ocular manifestations and FBN1 variants have emerged. The axial length (AL) is the distance from the corneal surface to the retinal pigment. Increased AL was associated with myopia and risks for retinal detachment in patients with MFS (Fan et al., 2014), which has been listed as a minor criterion in Ghent 1 nosology (De Paepe et al., 1996). However, the AL of MFS has considerable individual variations, with short AL in about 30% of MFS patients in a full age range (Drolsum et al., 2015; Chen et al., 2021b). Chen et al. showed that variants in the C-terminus (exons 43–65), especially the TGF-β regulating region (exons 44–49), were associated with longer AL (Chen et al., 2021a). Zhang et al. further showed that DN (-Cys) and DN (Calcium-binding) variants in cb EGF-like domains positively contributed to AL elongation (Zhang et al., 2021). The HI variants and variants in the neonatal region were associated with thinner central corneal thickness (Chen et al., 2021a), which probably explained the conflicting observations of the corneal thickness in MFS (Heur et al., 2008; Konradsen et al., 2012). Posterior staphyloma and ciliary body cysts were more frequently observed in patients with variants in the C-terminus (Chen et al., 2021a). Patients with DN variants tend to show higher corneal astigmatism compared to HI variants (Guo et al., 2021). The correlation between FBN1 variants and ocular features other than EL only received attention in a few studies, which demand further studies for verification.
Skeletal and other manifestations
Skeletal manifestations were the most prominent features for MFS patients, including higher arm span/height ratio, lower upper/lower segment ratio, arachnodactyly, kyphosis or scoliosis, and classic craniofacial features (Sakai et al., 2016). Most of the genotype-phenotype correlations studied a combination of skeletal features or systemic scores. Patients harboring HI variants or variants in the neonatal region often show more prominent skeletal features than those with DN ones (Schrijver et al., 2002; Comeglio et al., 2007; Arnaud et al., 2021a; Meester et al., 2022). DN (-Cys) variants were also associated with more severe skeletal manifestations than DN (+Cys) and DN (Others) (Faivre et al., 2009b; Arnaud et al., 2021a). Scoliosis is a sideways curvature of the spine if a Cobb’s angle exceeds 20° on radiographs (Sponseller et al., 1995), which is found in 45%–54% of MFS patients (Faivre et al., 2007; Arnaud et al., 2021a). Taniguchi et al. dissect the genotype-phenotype correlations in MFS already having scoliosis and found that HI variants and variants in the neonatal region were associated with severe scoliosis and faster progression (Taniguchi et al., 2021). Higher systematic scores were observed in the HI group than that in the DN group (Stark et al., 2020). Striae, the stretch marks of the skin, appeared more frequently in patients with HI variants (Faivre et al., 2007). and similar correlations were found in dura ectasia, the stretching of the dural sac (Franken et al., 2015). Hernia occurred earlier in the DN group than that in the HI group (Stark et al., 2020). All in all, like cardiovascular manifestations, skeletal features were more prominent in patients harboring HI variants and those located in the neonatal region.
Other type I fibrillinopathies
Strong genotype-phenotype correlations exist in some of the subtypes of type I fibrillinopathies. In 2010, Graul-Neumann et al. detected a heterozygotic FBN1 c.8155_8156del variant in the exon 64 from a 27-year-old patient with congenital lipodystrophy, a progeroid facial appearance, and some signs of MFS (Graul-Neumann et al., 2010). This observation was further supported by independent studies that FBN1 variants associated with progeroid phenotypes all clustered within exon 64, which is the extreme C-terminus (Goldblatt et al., 2011; Horn and Robinson, 2011; Takenouchi et al., 2013; Jacquinet et al., 2014; Romere et al., 2016; Lin et al., 2020). The term, MFLS, is proposed to recognize the clinically distinct form of fibrillinopathy (Passarge et al., 2016). GD and AD were known as “the mirror image” of MFS, which are characterized by short stature, short extremities, joint limitation, skin thickening, cardiac valvular thickening, and pseudomuscular build (Marzin et al., 2021). FBN1 variants associated with GD and AD are exclusively distributed in exons 41–42 (Le Goff et al., 2011), indicating that the corresponding region, the fifth TGFBP domain, is associated with short tubular bones and stiff joints. FBN1 variants causing SSS all cluster within exon 37, corresponding to the fourth TGFBP domain, the disease of which is characterized by joint stiffness and flexion contractures secondary to hard and thick skin (Loeys et al., 2010b). Like GD and AD, WMS2 also belongs to acromelic dysplasia but had a higher prevalence of EL. Most of the FBN1 variants associated with WMS2 were located in the exons 41–42 (Newell et al., 2017; Cheng et al., 2018), though inframe deletion of exons 9–11 was also reported in a proband of WMS2 (Sengle et al., 2012). Thus, different presentations of FBN1 variant carriers probably reflect the distinct roles of FBN1 segments.
Genotype and prognostication
Recent studies not only showed the correlation between FBN1 variant types and clinical presentation but also revealed that they have prognostic implications on disease progression and survival in MFS patients. The life expectancy of MFS is largely threatened by aortic dissection or rupture, which is the major cause of premature death (Roman and Devereux, 2020). Franken et al. found more rapid aortic dilation in patients with HI than those with DN variants, especially at the aortic root and at the tubular ascending aorta, leading to a 3.3-fold increased risk of death and dissections (Franken et al., 2017). Franken et al. also observed the long-term survival of patients carrying different types of FBN1 variants. The study demonstrated that individuals with HI variants had a 1.6-fold increased risk for any aortic complication a 2.4-fold increased risk for the combined endpoint comprising death and dissection, and a 2.5-fold increased risk for cardiovascular death compared to patients with a DN variant (Franken et al., 2016). Thus, MFS individuals carrying HI variants should benefit from closer follow-up and more vigorous medical treatment. However, these correlations failed to replicate in an independent cohort of MFS children who had aortic Z-score > 3 (Meester et al., 2022). Thus, the predictive value of FBN1 variants and disease progression requires further investigations in larger cohorts with appropriate age stratification.
Another set of variants well-known for their poor prognosis is those located in the neonatal region. Though FBN1 variants located in the neonatal region were neither a sufficient nor necessary condition for developing neonatal MFS, they were overrepresented in MFS patients with severe involvements and were associated with shorter overall survival (Faivre et al., 2007; Faivre et al., 2009b). Faivre et al. conducted in-depth research on variants located in the neonatal region and found that variants in exon 25 were associated with the shortest survival (Faivre et al., 2009a). This observation was further replicated by Stheneur et al. in MFS patients diagnosed before 1 year old (Stheneur et al., 2011). Thus, parents and clinicians caring for young MFS patients with variants in exon 25 should be made aware of the suboptimal prognosis. It is worth noting that patients with a HI located in exons 24–32 rarely displayed a neonatal or severe MFS presentation. The overall MFS phenotype was less severe in HI variants in the neonatal region than in DN variants in the same area (Faivre et al., 2009a). In summary, individuals with DN variants in exons 24–32 and especially exon 25 generally had a poorer prognosis than other variants.
Genotype and medication
Prophylactic usage of β-blockers is recommended for MFS patients to ameliorate aortic dilation by reducing stress on the aorta (Hiratzka et al., 2010; Erbel et al., 2014). Animal models of Marfan syndrome showed promising outcomes for losartan, an angiotensin II type 1 receptor blocker, as a potential therapy to attenuate aortic dilation (Habashi et al., 2006; Habashi et al., 2011). However, the beneficial effect of losartan was controversial and inconsistent among clinical studies (Groenink et al., 2013; Lacro et al., 2014; Milleron et al., 2015; van Andel et al., 2020). Franken et al. showed that losartan reduced aortic root dilatation rate significantly in adult MFS patients from the HI group instead of the DN group (Franken et al., 2015). Meester et al. conducted a similar clinical trial in MFS children with the Z-score > 3. However, the curative effects of atenolol or losartan did not differ much in patients with DN variants or HI variants (Meester et al., 2022). Thus, it warrants further investigation whether the conflicting results come from the age difference or other potential confounding factors within the two studies. Den Hartog et al. observed that patients with an HI variant showed improvement in biventricular end diastolic volume and stroke volume upon losartan treatment independent of changes in blood pressure, which is not found in DN variant carriers (den Hartog et al., 2016). Despite some inconsistent observations, these studies provide novel insights into the personalized medication for MFS patients based on genetic background.
Molecular relevance
The correlation between the FBN1 variant and diverse presentations is not a coincidence but has its molecular relevance. FBN1 is a large glycoprotein with complex multidomain structures and plays different roles in multiple tissues. Thus, the mutation effects are not only complicated by the variant type but also involve the affected loci, tissue diversity, and associated proteins. It is worth noting that most of the experimental evidence is indirect and should be considered regarding the limitations. The underlying mechanism warrants more studies.
Composition and conformation diversity
The composition of FBN1 microfibril is tissue-dependent. Microfibrils are subgrouped into three categories depending on the association of elastin, including fibers that are elastin-rich microfibril bundles (ERMB), elastin-free microfibril bundles (EFMB), and a continuum intermediate phase (Gawlik, 1965). FBN1 plays a crucial role in elastogenesis, acting as an organized network for the soluble precursor of elastin (tropoelastin). Tropoelastin molecules are deposited extracellularly onto the FBN1 scaffold and are subsequently processed by the lysyl oxidase enzyme for the formation of cross-links (Shin and Yanagisawa, 2019). The organization of elastin-associating microfibrils also differs in organs, which suits the functional integrity of the tissue. The elastic fibers form fenestrated concentric rings that support tissue compliance in the thoracic aorta while organizing as a loose meshwork in the skin, contributing to the pliability of the skin (Ramirez and Sakai, 2010). At the dermal-epidermal junction, the fibers run parallel to the epidermis with turn-offs coursing anchoring the deeper elastic fibers to the basement membrane (Sakai et al., 2016). ERMBs are more elastic in nature and are enriched in the tunica media of the aorta (Shin and Yanagisawa, 2019). The stiffness increases in the aorta of MFS and the pathological findings include elastic lamellae degradation and focal cystic medial necrosis (Nataatmadja et al., 2003; Salvi et al., 2018). There are more EFMBs in tissue where strength and rigidity are needed, including lens zonules and periodontal ligaments. The zonule is a radially oriented apparatus suspending the lens at the optic center and exerting force from the ciliary body in accommodation (Bassnett, 2020). Electron microscopy studies revealed fragmented, wavy, disorientated zonule fibers in eyes of MFS (Farnsworth et al., 1977; Pessier and Potter, 1996). Besides elastin, the presence of some microfibril-associated proteins also differs in organs, including Fibulin-2 (Reinhardt et al., 1996), Perlecan (Tiedemann et al., 2005), and LTBP2 (Hirani et al., 2007). Together, the complex roles of FBN1 and associated proteins in different tissue probably shed light on the organ selectivity of certain FBN1 variants.
There are also ultrastructure differences of microfibrils, which may correlate with the unique function in specific tissues. Though the exact packing models are still in debate, microfibrils display a typical “beads-on-a-string” appearance with uniform diameters (10–12 nm) and lengths (160 nm) (Cain et al., 2006; Jensen et al., 2012). Eckersley et al. compared the microfibrils isolated from the human eye and those in the skin and found that microfibrils differed in bead morphology and regional proteolytic susceptibility (Eckersley et al., 2018). Specifically, microfibrils in the eye had a higher central bead height and more lytic peptides between the cb EGF-like domains 38–43 than that of the skin, while the inter-bead periodicity was similar (Eckersley et al., 2018). However, only minor differences were observed between bovine adult aorta- and ciliary zonule-derived microfibrils (Lu et al., 2006). To sum up, the above evidence provides fundamental insights into the tissue-specific functions of microfibril but more studies were demanded to further clarify their relationship with the observed genotype-phenotype correlations.
Mutation effects
At the molecular level, FBN1 variants are mainly associated with two variant effects: 1) DN effect and 2) HI effect. DN effect generally happens in missense and inframe variants when the incorporation of mutated FBN1 monomers impairs polymerization, thereby creating structurally inferior microfibrils. About 80% of individuals with cysteine substitutions had normal levels of FBN1 synthesis but the secretion was significantly delayed (Schrijver et al., 1999). Experiments showed that both the newly synthesized FBN1 of the normal and mutated allele was retained intracellularly, consistent with the DN effects (Schrijver et al., 1999). The HI effect leads to the degradation of mutant mRNA by the nonsense-mediated decay system, commonly seen in frameshift, nonsense, and splicing variants. In the majority of samples with frameshift or nonsense variants, synthesis of normal FBN1 at protein level measured by pulse-chase analysis of cultured fibroblasts was around 50% of control levels (Schrijver et al., 2002). This decrease leads to the enhanced activation of TGF-β signaling, which results in increased apoptosis, disordered arrangement of smooth muscle cells, and impaired biochemical properties (Granata et al., 2017). Inhibition of TGFβ signaling by neutralizing antibody or losartan, which is an upstream regulator of TGFβ, is effective in preventing aortic aneurysms in Fbn1 mutant mice (Habashi et al., 2011). However, the association between TGFβ signaling and the pathogenesis of MFS is complicated. The knock-out of TGF-β2 or its receptor has been shown to facilitate aneurysm formation (Lindsay et al., 2012; Wei et al., 2017). And the neutralizing antibody of TGF-β was found to increase the aortic dissection death in another mice model of MFS which was delayed but not prevented by losartan (Cook et al., 2015). Meanwhile, the activation of TGF-β signaling seems to have minimal effects on the microfibril in lens zonules, since variants of genes in TGF‐β signaling could lead to Loeys‐Dietz syndrome with Marfanoid phenotypes in the absence of EL (Meester et al., 2017).
Several studies were devoted to revealing the mechanism differences underlying the HI and DN variants. Xu et al. confirmed the cardinal pathological findings in the aorta of MFS but found that elastic fibers and smooth muscle cells were sparser in patients with HI variants than those observed in patients with DN variants (Xu et al., 2020). Verhagen et al. compared the transcriptomic and proteomic profiles of the aorta aneurysm between HI and DN variants and observed impaired mitochondrial respiration only in HI variants, indicating the critical role of mitochondrial dysfunction in the pathogenesis of aortic aneurysm (Verhagen et al., 2021). Burger et al. revealed reduced SMA expression, decreased pSMAD2/SMAD2 ratio, and impaired transdifferentiation potential upon TGFβ stimulation in the skin fibroblast of DN variants rather than HI variants (Burger et al., 2021). However, this discrepancy is of uncertain significance since the obtained vascular smooth muscle cell-like cells from the transdifferentiation exhibited comparable contractility and migration capacity between the two groups (Burger et al., 2021). However, these studies only studied limited cell types from a small number of patients within DN or HI groups. Thus, more evidence is needed to elucidate the discrepancy underlying DN and HI variants.
However, the ultimate effect of an FBN1 variant at the protein level is hard to predict on the basis of sequence information alone. FBN1 variants with premature termination codons might escape nonsense-mediated decay in specific circumstances and produce a truncated protein exerting the DN effect. Alternatively, predicted DN variants can produce a protein that gets trapped in the endoplasmic reticulum and thus leads to diminished FBN1 deposition in the extracellular matrix (Whiteman and Handford, 2003). Moreover, how to classify splicing variants of FBN1 is another big issue. Previous studies classified splicing variants as HI variants, DN variants, or an independent group. Some of them perform in silico prediction or functional experiments, the others excluded splicing variants from analysis (Supplementary Table S2). Though most splicing variants of FBN1 were predicted to be inframe, the stability of the mutated protein is severely impaired, which showed a similar effect as HI (Liu et al., 2001). Some splicing variants also had multiple outcomes, which further complicated the evaluation (Hu et al., 2022). Cryptic splice sites in the coding sequences also demand more attention in case of misclassification of splicing variants into the DN group, especially for genes with multiple exon-intron junctions like FBN1 (Sadusky et al., 2004).
Sequence-specific function
Patients with nonsense or frameshift variants seemed to have phenotypes independent of termination sites (Faivre et al., 2009a; Takeda et al., 2018), probably because of a similar effect on FBN1 degradation (Lykke-Andersen and Jensen, 2015). In contrast, patients with DN variants display a broad spectrum of presentations, indicating that the coding regions affected by DN variants are probably of diverse functions. FBN1 not only serves mechanical roles but is also involved in cell signal pathways which are mediated by specific sequences. Thus, variants in different regions of FBN1 are likely to have diverse functions.
The N-terminus of FBN1 serves as an important platform to interact with a multitude of extracellular components. Thomson et al. summarized that the most FBN1-binding proteins interact with FBN1 through the N-terminus (Thomson et al., 2019), including both the extracellular architectures, such as ADAMTS6 (Cain et al., 2016), ADAMTSL2 (Sengle et al., 2012), and CLSTN1 (Cain et al., 2009), as well as signaling modulators encompassing LTBP1 (Ono et al., 2009) and BMP-2, 4, 5, 7, 10 (Wohl et al., 2016). Some of them were associated with congenital EL, such as LTBP2 (Hirani et al., 2007) and ADAMTS10 (Kutz et al., 2011). The N-terminus is also indispensable in the self-assembly of FBN1. Yadin et al. found that the N-terminal sequence to the first three EGF-like domains (FUN-EGF3) interacted with the heparan sulfate near the cell membrane to promote the oligomerization of the C-terminal cb EGF-like domains 41–43, which thereafter competed with the binding of FUN-EGF3 to heparan sulfate, resulting in the regulated end-to-end assembly of FBN1 (Yadin et al., 2013). They also revealed that the Arg62 is the crucial residue for the self-assembly, the missense variant of which is one of the frequent pathogenic variants for congenital EL in a Chinese cohort (Chen et al., 2021c).
FBN1 has a modular structure with a tandem array of EGF-like domains, 43 of which are capable of calcium-binding, the cb EGF-like domains. These domains contain the calcium-binding consensus motif D/N-XD/N-E/Q-Xm-D/N-Xn-Y/F (where m and n are variable), which provides microfibril a rigid rod-like conformation (Downing et al., 1996). An increased protease susceptibility due to reduced calcium affinity is a mechanism reported for missense variants (Booms et al., 2000; Reinhardt et al., 2000). Disulphide bonds formed among the six cysteine residues in EGF-like and cb EGF-like domains, in a C1-C3, C2-C4, and C5-C6 pattern, further contribute to further stabilizing FBN1 (Werner et al., 2000). Variants affecting the cysteines resulted in protein misfolding, leading to defective secretion and stimulation of endoplasmic reticulum stress (Whiteman and Handford, 2003; Suk et al., 2004). These pathological mechanisms emphasize the importance of calcium-binding and disulphide-forming for the structural integrity of FBN1. Thus, the studies above probably explain more severe phenotypes observed in patients with DN (-Cys) and DN (Calcium-binding) variants (Comeglio et al., 2007; Zhang et al., 2021). The neonatal region includes the central longest stretch of 12 cb EGF-like repeats while the newly defined DN-CD region incorporated more arrays of cb EGF-like repeats into the neonatal region (Takeda et al., 2018). Smallridge et al. showed that the 12-13th cb EGF-like domains possess the highest calcium affinity of any other domains in FBN1, which are located in the center of the neonatal region (Smallridge et al., 1999). Thus, the high calcium affinity is crucial for the rigidity of the neonatal region and could probably explain why variants in this region were at risk of severe phenotypes.
Interspersing the cb EGF-like array are the TGFBP domains, which were characterized by four pairs of disulphide bonds in a C1-C3, C2-C6, C4-C7, C5-C8 arrangement with a hydrophobic core. In contrast to the cb EGF-like domains, the TGFBP domains contribute to the flexibility of FBN1 by interacting with flanking cb EGF-like domains (Kielty et al., 2005). A strong correlation is found in TGFBP domains that all FBN1 variants associated with SSS are all located within the fourth TGFBP domains (exon 37), the unique feature of which is the Arg-Gly-Asn sequence for integrin binding (Bax et al., 2007). Loeys et al. found that FBN1 variants in exon 37 resulted in excessive and tightly packed microfibril and impaired integrin interaction in SSS, which is distinct from that of MFS (Loeys et al., 2010b). Meanwhile, FBN1 variants found in individuals with GD and AD are located in the fifth TGFBP domain (exons 41–42) (Loeys et al., 2010b). Jensen et al. compared the synthesis and deposition profile of FBN1 variants causing SSS, AD, and MFS and concluded that the primary pathology of SSS and AD was the defective cell-surface interactions which were distinct from the defect in FBN1 synthesis or assembly in MFS (Jensen et al., 2015). Therefore, FBN1 variants in TGFBP domains have distinct mechanisms associated with SSS, GD, or AD.
Increased TGFβ bioavailability has been correlated with FBN1 variants and contributed to the pathogenesis of aortic dilation. Beyond sequestering the latent complex of the TGF-β, FBN1 also modulates TGF-β signaling through fragments of exons 44–49, which is named as TGF-β regulating sequence. Chaudhry et al. found the recombinant protein fragments encoded by exons 44–49 strongly bind to the N‐terminus of FBN1, which facilitated the displacement of large latent complex and subsequent release of TGF‐β. It is hypothesized that this fragment degraded from FBN1 protein in pathological situations where there is increased proteolysis or inflammation might contribute to the phenotype in Marfan syndrome (Chaudhry et al., 2007). This evidence potentially correlates with the progressive aortic involvement and elongated axial length of the eyeball associated with the variants in this region (Takeda et al., 2018; Chen et al., 2021a). More studies were warranted to further validate the genotype-phenotype correlations in this region.
The extreme C-terminus of FBN1 has a unique role as a circulating hormone, which was discovered by studying the genotype-phenotype correlation. In 2016, Romere et al. identified a novel glucogenic adipokine, asprosin, based on the fact that FBN1 variants in the exon 64 were associated with atypical ‘MFS’ patients with progeria and lipodystrophia. Asprosin is the C-terminal of pro-FBN1 which is cleaved by the protease furin (Romere et al., 2016). It was secreted by white adipose, triggering the liver glycogenolysis and the release of insulin (Romere et al., 2016). It was further proved to be a centrally-acting orexigenic hormone, which promoted appetite and body weight (Duerrschmid et al., 2017). The discovery of asprosin based on genotype-phenotype correlation studies provides a novel therapeutic target to treat diabetes and obesity.
Other factors contributing to phenotype
At present, it is not possible to predict the phenotype solely based on FBN1 variant. Recurrent variants may lead to distinct phenotypes in different probands, let alone the intrafamilial variability, re-enforcing the notion that factors other than the causative variant also contribute to the phenotypic heterogeneity of MFS.
The mutational effects of the FBN1 gene are modulated at multiple levels from the mRNA transcription and translation to protein multimerization, and from the incorporation into the extracellular matrix to the degradation hereafter. Therefore, the resulting clinical phenotype cannot easily be predicted based on variants at the genomic level alone. One hypothesis is that the phenotype of MFS is modulated by the residual mRNA expression of the unaffected allele. Aubart et al. cultured the skin fibroblasts from a cohort of MFS with HI variants and quantified the expression level of mRNA synthesized from the wild-type allele (Aubart et al., 2015). It was found that a lower residual expression of FBN1 protein accounts for higher risk of EL, pectus abnormality, and aortic dilatation (Aubart et al., 2015). However, it demanded further studies on whether the mRNA expression of FBN1 could explain the intrafamily variability. (De Backer et al., 2007). Quantitation of FBN1 protein synthesis and matrix deposition seems to be the ultimate method to correlate the MFS phenotype. Aoyama et al. developed ‘Fibrillin phenotyping’ which divided patients with FBN1 variants into five groups based on the synthesis and deposition of FBN1 protein from the skin fibroblasts (Aoyama et al., 1994). It was found that most missense variants did not affect the synthesis of FBN1 protein while both the missense and frameshift variants can lead to decreased deposition of FBN1. More severe cardiac complications at an earlier age were seen in groups with FBN1 deposition < 35% (Aoyama et al., 1995).
The incorporated microfibrils also interacted with other extracellular proteins. Thus, an alternative explanation for the individual variation is the involvement of modifier genes. Aubart et al. identified co-occurrence of rare variants in SMAD3 and COL4A1 and modifier loci containing ECE1, PKG1, and SLN in MFS patients with severe aortic phenotype (Aubart et al., 2018). Common variants of the COL1A1 had been shown to exert a protective effect on scoliosis while rare variants of MYH11 were associated with ectopia lentis (Gentilini et al., 2019). Epigenetic factors were found to influence the aortic manifestations and progression in patients with MFS too. Van Andel et al. identified 28 differentially methylated regions (DMPs) associated with aortic diameters, 7 DMPs with aortic diameter growth, and 5 DMPs with aortic events by genome-wide DNA-methylation profiling of peripheral whole-blood samples (van Andel et al., 2021). Meanwhile, around 0.64% of MFS patients carried more than one FBN1 gene variant which could be overlooked in routine examinations (Arnaud et al., 2017). Somatic mosaicism for a mutant FBN1 allele was associated with milder manifestations, compared to those of germ-line transmission (Montgomery et al., 1998; Arnaud et al., 2021b).
Discussion
In monogenic disorders, an established correlation between genotype and phenotype is a premise for predicting prognosis, enabling prophylaxis, and promoting clinical follow-up in affected patients. In the last 20 years, a number of studies tried to dissect the complexity of the genotype-phenotype correlation of MFS and related fibrillinopathies. Though some observations were inconsistent, statistically significant correlations emerged which provided illuminating readings to understand the pathophysiology of MFS. However, most of the reviews focus on the correlations regarding aortic events and lack a summary of potential molecular relevance. (Loeys, 2016; Stengl et al., 2021). In this review, we update the latest genotype-phenotype correlation studies on the full range of the phenotypes of MFS and related fibrillinopathies and provide potential explanations for the observed correlations at the molecular level.
Early studies on genotype-phenotype correlation began with the susceptibility to EL and aortic dilatation (Schrijver et al., 2002; Loeys et al., 2004). Later studies expanded the studied phenotypes to almost all aspects of the MFS manifestations, including the axial length of the eyeball (Chen et al., 2021a), astigmatism of the cornea (Guo et al., 2021), severity of scoliosis (Taniguchi et al., 2021), and incidence of ventricular tachycardia (Aydin et al., 2013). Meanwhile, detailed parameters were applied instead of a broad description of aortic events, such as the aortic root diameters and the aortic stiffness (Franken et al., 2017; Salvi et al., 2018). The long-term survival, disease progression, and response to medication were also explored in relation to the FBN1 variants (Franken et al., 2015; Franken et al., 2017; den Hartog et al., 2016). The subjects investigated also include various populations, from the Ghent-positive to atypical ones (Faivre et al., 2009c; Baudhuin et al., 2015), and from the adult (Franken et al., 2015; den Hartog et al., 2016) to pediatric patients (Faivre et al., 2009b; Meester et al., 2022). Some correlations even help to establish a new nosology of fibrillinopathies (Loeys et al., 2010b; Passarge et al., 2016; Marzin et al., 2021) and assisted in identifying a novel hormone, i.e., asprosin (Romere et al., 2016; Duerrschmid et al., 2017). In summary, the DN variants are associated with a higher prevalence of EL while severe cardiac and skeletal phenotypes are more common in the HI variant carriers. The DN variants in the neonatal region and DN (-Cys) variants were correlated with globally more severe MFS phenotypes. Thus, molecular testing of FBN1 variants will play an increasingly important role in the precise medicine of MFS in the near future. However, the correlations regarding ocular and skeletal manifestations received less attention, and qualified research has just emerged in recent years. The disease progression and long-term prognosis of these phenotypes demands more studies. Most studies were cross-sectional and adapted Kaplan-Meier analyses to control the phenotype variation caused by age difference. Nevertheless, the studies of disease progression in long-term follow-up cohorts will provide more valuable insights.
The classifications of FBN1 variants also evolve as the research goes on (Figures 1A,B). Dividing the FBN1 variants into DN and HI is commonly seen. It is widely accepted that patients with DN variants have higher risks of EL while those with HI variants are more likely to develop aortic events. However, the associations between HI variants and aortic involvements seem to be less reproductive, even in some large cohorts (Figure 2) (Comeglio et al., 2007; Faivre et al., 2007; Meester et al., 2022) Later researchers came to realize the heterogeneity of DN variants and proposed two subgrouping schemes. The first one was based on the affected amino acid, which divided the DN variants into DN (-Cys), DN (+Cys), or DN (Calcium-binding) variants. The second one classified DN variants based on the affected region, including the N-terminus, C-terminus, and neonatal region. Recent studies suggested that DN (-Cys) variants and variants in the neonatal region were closer to HI variants in nature than other DN variants, (Faivre et al., 2009b; Stengl et al., 2020), while DN (+Cys) variants were associated with fewer aortic events but similarly high incidence of EL when compared to DN (-Cys) (Faivre et al., 2007; Stengl et al., 2020; Arnaud et al., 2021a). A new region was also identified by taking both the protein structure and the variant clusters of extreme phenotypes (Takeda et al., 2018). Thus, it would be interesting to apply these newly developed classification methods to more phenotypes and independent cohorts.
In 2016, Verstraeten et al. proposed that completion of the mechanistic puzzle of MFS might be feasible within the next 10–15 years (Verstraeten et al., 2016). The sparse and disorganized elastin fibers, the overactivation of TGFβ signaling and subsequent tissue remodeling, and the apoptosis of smooth muscle cells were cardinal mechanisms in aortopathy of MFS (Schrenk et al., 2018). Recently, inflammation, endoplasmic reticulum stress, and mitochondrial dysfunction were also reported to contribute to the molecular mechanism (Siegert et al., 2019; Verhagen et al., 2021; Lim et al., 2022). However, it seems that the mechanism underlying the phenotypic diversity of FBN1 variant carriers demanded more time to elucidate. We summarized the molecular relevance of the observed genotype-phenotype correlations, beyond the widely accepted DN and HI theories. The tissue-specific monomer conformation and polymer composition provided the fundamental insights for the organ selectivity of the same variant while the unique function among certain regions of FBN1 partially explains the variant effects among different variants. However, most of these evidences were indirect and the functional studies of genotype-phenotype correlations of FBN1 variants are limited. Most of them tested the tissue or fibroblasts derived from the patients or expressed recombinant segments of FBN1 in cultured fibroblasts (Schrijver et al., 1999; Whiteman and Handford, 2003; Burger et al., 2021). Meanwhile, the molecular genotype-phenotype studies were complicated by the large molecular weight and multiple involved cell types. Patient-derived induced pluripotent stem cells (iPSC) have certain potential in tackling the above troubles and are powerful to tools to study genotype-phenotype correlations in certain diseases (Nevin et al., 2017; Kathuria et al., 2020). iPSCs derived from MFS patients were shown to mimic the skeletal and aortic pathology of MFS (Quarto et al., 2012; Granata et al., 2017; Park et al., 2017). Establishing iPSC models of desired types of FBN1 variants and differentiating them into target cells will be helpful in understanding the molecular mechanism underlying genotype-phenotype correlations.
There is a lack of clear-cut genotype-phenotype correlations of MFS so far. Though FBN1 variants related to some fibrillinopathies, such as GD, AD, SSS, and MFLS exclusively clustered in certain regions, the variants in the same region also led to classical MFS, which is hard to predict without the comprehensive phenotype analysis of the patient. Variants in neonatal region can also occur in patients with mild and atypical MFS (Faivre et al., 2009a; Zhang et al., 2021). Thus, patients with variants of high risks of aortic events should receive more frequent examinations while those carrying less deleterious variants should not be exempted from follow-up, considering the life-long risks of aortic dissection (Gaudry et al., 2021). Researchers have explored other factors contributing to the phenotypes, including FBN1 expression at mRNA and protein level (Aoyama et al., 1994; Aubart et al., 2015), modifying genes (Aubart et al., 2018), and epigenetic factors (van Andel et al., 2021). Thus, a prediction model of phenotype and prognosis is warranted in the future which should incorporate both genotypes and modifying factors.
Though genetic testing is not mandatory to establish the diagnosis of MFS, with the growing knowledge of genotype-phenotype correlation, FBN1 sequencing plays an increasingly important role in the clinical management of MFS and related fibrillinopathies in terms of risk stratification, disease monitoring, and personalized medication. Clinical studies of large sample size and long-term follow-up were warranted to settle the inconsistent correlations. More molecular studies would be beneficial which provide more solid evidence for the established correlations.
Author contributions
Z-XC reviewed the literature and wrote the paper. W-NJ critically reviewed the manuscript. Y-XJ proposed the topic and supervised the project.
Funding
This study was supported by the Shanghai Science and Technology Commission (Scientific Innovation Action Plan, grant no. 20Y11911000). The sponsors played no role in the study design, data collection, data analysis, manuscript preparation, nor the decision to submit the manuscript for publication.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fgene.2022.943083/full#supplementary-material
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Keywords: FBN1, type I fibrillinopathy, genotype-phenotype correlation, dominant negative effect, haploinsufficiency
Citation: Chen Z-X, Jia W-N and Jiang Y-X (2022) Genotype-phenotype correlations of marfan syndrome and related fibrillinopathies: Phenomenon and molecular relevance. Front. Genet. 13:943083. doi: 10.3389/fgene.2022.943083
Received: 13 May 2022; Accepted: 01 July 2022;
Published: 16 August 2022.
Edited by:
Owen Murray Rennert, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NIH), United StatesReviewed by:
Pauline Arnaud, Inserm U1148 LVTS, FranceKálmán Dr. Benke, Semmelweis University, Hungary
Mingyao Luo, Chinese Academy of Medical Sciences, China
Kim M. Summers, University of Queensland, Australia
Copyright © 2022 Chen, Jia and Jiang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Yong-Xiang Jiang, yongxiang_jiang@163.com
†ORCID: Ze-Xu Chen, orcid.org/0000-0002-7371-1765; Yong-Xiang Jiang, orcid.org/0000-0001-9770-5733