Background Fabry disease (FD) is a rare X-linked lysosomal storage disease caused by mutations in the α-galactosidase A gene (GLA) leading to deficiency of α-galactosidase A and ultimately in progressive glycosphingolipid accumulation, especially globotriaosylceramide (Gb3) and its deacylated derivative globotriaosylsphingosine (Lyso-Gb3). The aim of the study was to assess plasma Lyso-Gb3 levels as a possible factor associated with adverse outcomes in FD.
Methods In a cohort of 66 patients with genetically confirmed FD (26 males and 40 females), we analysed serum Lyso-Gb3 as a factor associated with adverse clinical outcomes in a long-term study. The main outcome was a composite endpoint of incident kidney replacement therapy, atrial fibrillation, pacemaker and/or implantable cardioverter defibrillator, cerebrovascular events or death, whichever occurred first.
Results During the median follow-up time of 68 (40–80) months, events occurred in 19 (29%) of the patients. In a Cox multivariate regression analysis, Lyso-Gb3 levels (HR 4.62 (1.55 to 13.81); p=0.006) and the pretreatment exposure to Lyso-Gb3 (HR 3.41 (1.11 to 10.49); p=0.03) (both per SD increase) were significantly associated with adverse outcomes. If pretreatment Lyso-Gb3 exposure was added to multivariable logistic regression models containing age, sex, phenotype and enzyme replacement therapy as other covariates with the composite outcome as dependent variable, the area under the curve for the composite outcome significantly improved from 0.72 to 0.86 (p comparison=0.04).
Conclusion Lyso-Gb3 is a significant risk factor associated with important clinical events. Whether treatment-related amelioration of Lyso-Gb3 levels will be associated with improved long-term outcome needs to be established in prospective intervention trials.
- human genetics
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Fabry disease (FD) is a rare X-linked glycosphingolipid storage disease and a result of mutations in the α-galactosidase A gene (GLA), which leads to reduced activity of the encoded lysosomal exoglycohydrolase, α-galactosidase A (α-Gal A) (EC 220.127.116.11; α-Gal A).1 2 The α-Gal A defect causes the progressive accumulation of globotriaosylceramide (Gb3) and other related glycosphingolipids in lysosomes of patients affected with FD.1
The clinical phenotypes include earlier-onset classic, and the attenuated, so-called later-onset variants.1 3–5 In the classic phenotype, males with little or no residual α-Gal A activity develop marked intracellular Gb3-accumulation, with disease signs and symptoms, such as acroparesthesias, angiokeratoma, corneal opacities, hypohidrosis and gastrointestinal symptoms, occurring in childhood or early adolescence. With advancing age, the progressive deposition of glycosphingolipids, particularly in vascular endothelial lysosomes, cardiomyocytes and kidney podocytes is associated with left ventricular hypertrophy, hypertrophic cardiomyopathy, arrhythmias, kidney failure and cerebrovascular disease. This results in early demise, typically in the fourth or fifth decades of life.6 7 In contrast, males with the later-onset phenotype have residual α-Gal A activity, no microvascular endothelial glycosphingolipid accumulation, and lack the early manifestations seen in classic male Fabry patients. They present in adulthood with cardiac or, less frequently, with kidney disease.3 8–10 Notably, a mild biopsy-proven Fabry nephropathy has also been reported in the cardiac subtype of the attenuated phenotype.11 Female heterozygotes have variable expression of FD, ranging from asymptomatic to severe, primarily associated with skewed X-chromosomal inactivation.12
Recently, the deacylated derivative of Gb3, globotriaosylsphingosine (Lyso-Gb3), has been identified as a hallmark of FD.13 Nonetheless, it remained highly debated, whether Lyso-Gb3 is an independent risk factor for unfavourable clinical events. Arends and colleagues assessed the event-free survival time from birth until the first clinical event using plasma Lyso-Gb3 at the first clinic assessment.5 Thereby, the authors conducted a retrospective analysis rather than a prospective mortality study because measurements of Lyso-Gb3 concentrations had only recently been developed and established.13 Based on these data for a combined cohort of patients with FD, higher Lyso-Gb3 concentrations at first clinical visit were found to be associated with clinical event rate occurring between birth and the time of the Lyso-Gb3 measurement. In contrast, analysing Lyso-Gb3 concentrations only for classic males and females, its levels were not significantly associated with previous clinical event rates, although classic patients more frequently develop clinical events in prospective survival analyses5 and suffer from a more severe phenotype. This lack of clarity reduces the usefulness of Lyso-Gb3 as a biomarker for severity and progression of FD.
Early and accurate risk stratification of patients with FD remains an unmet clinical need. Herein, we have assessed serum Lyso-Gb3 levels as a possible factor associated with adverse outcomes in a prospective long-term study of a large and well-defined population of genetically confirmed Fabry patients. Importantly, all Lyso-Gb3 measurements were performed by the same laboratory and using the same analytical standards,4 14 and their levels as well as clinical covariates were stratified by gender and phenotype.
Study population and treatment
This is a retrospective analysis of a prospective cohort; samples for the Lyso-Gb3 concentrations were prospectively drawn during the routine annual examinations. The entire study period was between September 2013 and April 2020. The study was conducted in accordance with the principles of the Helsinki Declaration. Informed consent for collecting clinical data and blood samples was obtained from all patients. All authors have read and approved the manuscript.
All patients had a confirmed GLA mutation diagnosis and presented for routine annual examinations at our FD centre. The cohort was established in 2001 when enzyme replacement therapy (ERT) was approved and offered to patients with FD. ERT was prescribed at the licensed dose of either 0.2 mg/kg body weight of recombinant agalsidase-α (Replagal) or 1 mg/kg body weight agalsidase-β (Fabrazyme) and given intravenously biweekly. ERT was initiated according to the written local guidelines and prescribed as reported previously.15
We measured Lyso-Gb3 in 66 adult patients (males: n=26 (39%)) at the University Hospital Zurich, Switzerland, between September 2013 and December 2016. If patients had more than one Lyso-Gb3 measurement, the first result was used for the present longitudinal survival analysis. All clinical data were extracted from medical records, and the adverse events were evaluated during annual examinations as reported previously.15
All mutations have been classified as coding for the classic or later-onset phenotype based on genotype and residual α‐Gal A activity in males and are published in the International Fabry Disease Genotype/Phenotype Database (www.dbFGP.org) and in previous studies.4 14 Nonsense, frameshift, consensus splice site (mutations that can affect the splice-donor and splice-acceptor sequences and alter the mature messenger RNA, leading to the production of abnormal proteins16) and some missense mutations encode for 0% to 2% residual α‐Gal A activity and lead to the classic phenotype in males. Alternative splicing mutations and certain other missense mutations encode for >2% of mean normal α‐Gal A activity and cause attenuated, the so-called later‐onset phenotype in males. The phenotypic assignments of the mutations are supported by the clinical manifestations in males, the age of symptom onset and by in vitro expression assays as reported previously.17 18
For serum Lyso-Gb3 levels, blood samples were centrifuged, and serum was immediately frozen at −80°C for a later batch analysis. The samples were measured by high-sensitive electrospray ionisation liquid chromatography tandem mass spectrometry using an adapted method from Gold. A 7-point serum calibrator and an internal standard for Lyso-Gb3 quantification (covering the analytic range from 0 to 120 ng/mL; lower limit of quantification: 0.3 ng/mL) and three-level controls (3, 30 and 100 ng/mL) for quality control were used (ARCHIMED Life Science GmbH, Vienna, Austria; www.archimedlife.com) as previously reported.14
Endpoint definition and evaluation
As a primary endpoint, we defined the composite of requiring kidney replacement therapy (RRT) (kidney transplantation or chronic dialysis), newly diagnosed atrial fibrillation (AF) of any type (paroxysmal/persistent), pacemaker and/or implantable cardioverter defibrillator (ICD) implantation, cerebrovascular events (stroke or transient ischaemic attack (TIA)) diagnosed by a neurologist and death, whichever occurred first after the baseline serum Lyso-Gb3 measurement. These endpoints, with the exception of death, were prospectively defined according to Arends et al.5 In contrast to this study, death was added to the primary endpoint because of the prospective observational period of our study, while this study retrospectively assessed the clinical event rates from birth to first visit. It is important to note that this previous study did not conduct a mortality study, because their patients were included at first visit and retrospectively analysed.5 In our study, the follow-up was censored at the date of the first event after the baseline Lyso-Gb3 measurement to calculate HRs. The follow-up time for patients without events was censored at the 1 April 2020. If the patients died outside of the Fabry Centre, the date of death was evaluated by asking the responsible general practitioner, the family or the nurse administering ERT in the home care setting.
Serum level Lyso-Gb3 at the first measurement (1) and the exposure to Lyso-Gb3 before disease-specific treatment (2) were employed as primary exposure variables. To calculate the cumulative pretreatment exposure to Lyso-Gb3, its serum levels measured at baseline of the observational period, all measured after September 2013, were multiplied by the age in years of the patients at ERT initiation, which was between 2001 and 2019. Additionally, the exposure to Lyso-Gb3 before diagnosis of FD, calculated as product of Lyso-Gb3 levels at baseline and age at diagnosis, was employed as exploratory variable. We did so under a simplified assumption that the levels of Lyso-Gb3 are linear as function of years of age.
Definition of binary covariates
The Lyso-Gb3 measures were classified by their median values, stratified by gender and Fabry phenotype (ie, classic vs later-onset) to generate a binary covariate with ‘0’ corresponding to female gender, later-onset phenotype and Lyso-Gb3 level below the median value for each gender and phenotype strata. The other binary covariates included median age stratified by gender and phenotype at the baseline evaluation, gender, treatment with ERT at the time of baseline evaluation and Fabry phenotype.
We used descriptive statistics for the baseline characteristics at the time of the first Lyso-Gb3 measurement. Categorical variables were expressed as proportions, continuous variables as means with SD or medians with IQRs. Normal distribution was assessed by Shapiro-Wilk test. The primary exposure variables showed a non-parametric distribution and, therefore, were log-transformed for modelling. Comparison of Lyso-Gb3 groups according to sex and phenotype was made using one-way analysis of variance test.
Kaplan-Meier analysis was performed and log-rank test of survival distributions equality for patients with baseline serum level Lyso-Gb3 at the first measurement (1) and the exposure to Lyso-Gb3 before disease-specific treatment (2) above versus below median were calculated.
Cox regression analysis was used to examine the mortality risk associated with Lyso-Gb3 at the first measurement (1) and the exposure to Lyso-Gb3 before disease-specific treatment (2). Multivariable models were applied to adjust for potential confounders using prior knowledge of variables that have been associated with risk in patients with FD in previous studies.5 We defined model 1 as a hierarchical adjustment for age; model 2 for male sex; model 3 for the classic phenotype. These models were used for all multivariable Cox regression analyses.
Receiver-operating characteristic (ROC) curves were generated with multifactor logistic regression models, and the effect of adding a specific covariate was evaluated by testing for significant change in the area under the ROC curve (AUC). The individual contributions of two different measures of Lyso-Gb3 concentrations (baseline Lyso-Gb3 and cumulative Lyso-Gb3 exposure) as well as a comparison of the contribution of each Lyso-Gb3 measure was assessed.
The ROC curves were generated and compared using Stata V.16.1 and the roccomp routine. The other statistical analyses were performed using the SPSS/PC (V.26.0; SPSS). All statistical tests were two-sided, and p values <0.05 were considered significant.
The clinical characteristics at the time of the first Lyso-Gb3 measurement in all patients according to sex and phenotype are shown in online supplemental table 1, the detailed baseline demographical and biochemical characteristics in online supplemental table 2.
In total, 66 patients (26 males and 40 females) with the median age of 44 years were included in the analysis. The highest Lyso-Gb3 levels were measured in the classic males, followed by the classic heterozygous females. All patients on RRT were male. Of 50 patients on ERT, 6 were treated with agalsidase-β, 44 with agalsidase-α, all at the licensed full dose of each preparation.
No patients were lost to follow-up. During the median follow-up time of 68 (40–80) months, the first event occurred in 19 (29%) of the patient population. The clinical outcomes are summarised in table 1 and are shown in detail in online supplemental table 3. Five classic patients (males n=4, females n=1) and none later-onset patients died during the observational period. Clinical events occurred in 18 classic patients (males n=9, females n=9) and in one later-onset male (table 1).
Seven patients underwent pacemaker and/or ICD implantation: three because of a high-degree atrioventricular block, four as primary prophylaxis due to high-degree myocardial hypertrophy and fibrosis; in three patients, a new-onset of AF occurred; one patient received a kidney transplantation, one went on chronic dialysis; in one, a stroke occurred; one suffered myocardial infarction, five patients died. Overall, 21 events occurred in the whole population: one female with pacemaker implantation as first event subsequently suffered from two strokes. The distribution of the incident composite outcome and, separately, death during the observational period, according to sex and phenotype, is shown in table 2. This table also summarises the late disease complications at baseline, when plasma Lyso-Gb3 levels were measured.
In males and females, serum levels of Lyso-Gb3 were significantly higher in patients who developed events versus patients without events (figure 1).
In the Kaplan-Meier analysis, the median of plasma Lyso-Gb3 levels and of the cumulative pretreatment Lyso-Gb3 exposure (figure 2), better than age, sex and phenotype (online supplemental figure 1), separated patients with versus without clinical events.
In the Cox regression analysis, Lyso-Gb3 levels and the pretreatment Lyso-Gb3 exposure were significantly associated with the adverse outcomes in the crude model and after the adjustment for age in model 1, male sex in model 2 and classic phenotype in model 3. This association remained unchanged after the exclusion of the six patients with agalsidase-β: for Lyso-Gb3 levels HR 2.26 (1.38 to 3.71), p=0.001 in crude model; HR 2.50 (1.48 to 4.27), p=0.001 in model 1; HR 4.36 (1.61 to 11.80), p=0.004 in model 2; HR 5.53 (1.80 to 17.00), p=0.003 in model 3; for the pretreatment exposure to Lyso-Gb3 HR 2.93 (1.68 to 5.12), p<0.001 in crude model; HR 2.76 (1.54 to 4.96), p=0.001 in model 1; HR 3.82 (1.66 to 8.79), p=0.002 in model 2; HR 3.59 (1.19 to 10.84), p=0.02 in model 3 (all per SD increase). In addition, the cumulative exposure to Lyso-Gb3 before Fabry diagnosis was significantly associated with the adverse outcomes: HR 2.07 (1.52 to 2.82), p<0.001 in crude model; HR 2.01 (1.47 to 2.77), p<0.001 in model 1; HR 2.21 (1.39 to 3.50), p=0.001 in model 2; HR 2.15 (1.31 to 3.53), p=0.003 in model 3 (all per SD increase).
The ROC curve indicated a moderate to high association of baseline Lyso-Gb3 and the pretreatment Lyso-Gb3 exposure with the composite outcome (figure 3).
If pretreatment Lyso-Gb3 exposure was added to the multivariable logistic regression model containing age, sex, phenotype and ERT as other covariates and the composite outcome as dependent variable, the AUC for the composite outcome significantly improved from 0.72 to 0.86 (p comparison=0.04).
If baseline Lyso-Gb3 levels were added to the multivariable logistic regression model containing the same covariates as above, the AUC for the composite outcome improved not significantly from 0.72 to 0.77 (p comparison=0.16).
In this relatively large well-characterised cohort of genetically proven patients with FD, higher baseline levels of Lyso-Gb3 were associated with a higher risk of complications such as death, stroke/TIA, new manifestation of AF, requirement for RRT, pacemaker or ICD implantation. More importantly, the cumulative exposure to Lyso-Gb3 during the untreated period seems to predispose patients with FD to worse clinical outcomes.
These findings correspond to the fact that Lyso-Gb3 reflects severity of FD, shown by us4 14 and other groups,19 20 and to the fact that Lyso-Gb3 levels in serum correspond to the Gb3 burden in the vital organs.13 In FD, the correct risk stratification based on an understanding of the genotype and phenotype relationship is an urgent but still unmet clinical need. An increased awareness of FD among primary care physicians and specialists as well as systematic screening among high-risk populations21 and newborns22 has been becoming increasingly frequent, leading to an increased detection of mutations with unknown clinical progression.23 24 A specific biomarker could not only fill the diagnostic gap but also improve disease staging and risk stratification as well as support the decision whether a patient should be started on ERT and or if he should be more closely monitored. Of note, patients with FD with low or undetectable Lyso-Gb3 levels can still suffer adverse events because of possibly having genetic and epigenetic modifiers of their phenotype, additional diseases, environmental conditions such as toxins or lifestyle modalities. Thus, no biomarker can replace a thorough clinical multidisciplinary characterisation, genetic testing and the phenotypic descriptions of the family members.
Lyso-Gb3 has been described as a helpful tool for newborn22 and high-risk group screening,21 25 for diagnosis,26–29 as a biomarker for phenotypic assignment,14 a tool reflecting disease severity4 and therapeutic monitoring.30–32 As a result of enzymatic deficiency, Gb3 accumulation occurs in classic phenotype males, already before symptom manifestation.33 34 Lyso-Gb3 may originate from deacylation of the stored Gb3 or be synthesised by sequential glycosylation of accumulating sphingolipid precursors.13 As suggested by our results, the toxic effects of Lyso-Gb3 seem to cumulate during the pretreatment period. A possible explanation could be that Lyso-Gb3 might not only act as a marker of disease severity but also have direct toxic effects as a metabolite. Supporting this, Lyso-Gb3 has been demonstrated to promote Notch1-mediated inflammatory and fibrogenic response in podocytes, potentially contributing to Fabry nephropathy.35 In studies by Sanchez-Niño and colleagues, Lyso-Gb3 has been further shown to disrupt the gut microbiota homeostasis modulating the biofilm formation of healthy enteric bacteria, potentially enhancing the gastrointestinal symptoms of patients with FD.36 37 Furthermore, plantar administration of Lyso-Gb3 stimulated allodynia in healthy mice; in vitro application of Lyso-Gb3 activated Ca2+ uptake of voltage-dependent nociceptive neurons, suggesting that this toxic metabolite may induce pain through direct actions on sensory afferents.38 Moreover, Aerts and colleagues observed that concentrations of Lyso-Gb3, similar to those observed in plasma of symptomatic Fabry patients promoted proliferation of smooth muscle cells in culture.13
Arends and colleagues observed that ERT initiation at a younger age resulted in a more pronounced sustainable decrease of Lyso-Gb3, in classic males.31 Noteworthy, plasma Lyso-Gb3 adequately reflects the cumulative lifetime treatment effect. If adding cumulative pretreatment Lyso-Gb3 exposure to the logistic regression model containing other important risk factors such as age, sex, phenotype and ERT requirement, the AUC for the composite outcome significantly improved. Our studies are the first to analyse the cumulative pretreatment toxic potential of this metabolite. The consequence of this knowledge could be that disease-specific treatment aiming at decrease of Lyso-Gb3 could lower the incidence of the composite endpoint, which could be shown by future studies. A possible design of a Lyso-Gb3-guided study could be to administer two different doses of ERT, which, in the absence of antibodies, would lead to a greater decrease of Lyso-Gb330 32 levels and, presumably, to a lower incidence of clinical events, in patients with the higher dose.
The strength of these studies includes a long observational period for relevant clinical outcomes in a genetically confirmed one-country cohort, where patients are treated similarly and exposed to similar environmental conditions and complete follow-up data. The latter is due to Swiss regulation that the ERT prescription and patient’s follow-up remain reserved for the Fabry Centre. Furthermore, an under-reporting of clinical events is unlikely in a setting like this, where a cohort is personally followed and treated at the same specialised centre and by the same treating physician. Disadvantages like under-reporting of clinical events and lost to follow-up can sometimes limit large registry-based studies.39 In addition, the Lyso-Gb3 measurements were conducted at one laboratory with the same standards of the technical methods.
These studies are also limited since we analysed the cumulative long-term effects of Lyso-Gb3 under the assumption that its levels increase with age in a horizontal linear manner. However, Lyso-Gb3, already increased in classic Fabry male newborns,13 40 continues rising during the presymptomatic phase, representing a metabolic progression to the clinical phenotype, and reaches its plateau at the advent of the early symptoms.33 Then, it rapidly decreases by approximately 70% after 2–3 months of ERT initiation, remaining stable but elevated, in patients without antibodies against ERT.30 In contrast, in patients with antibodies, Lyso-Gb3 gradually increases again after a decrease, following ERT initiation.32 In migalastat-treated patients, Lyso-Gb3 increases, decreases or remains stable dependent of the degree of mutation amenability.41 In our studies, we had to simplify the course of Lyso-Gb3 as linear for the calculation of cumulative Lyso-Gb3 exposure because Lyso-Gb3 had been discovered as a hallmark of FD in 200713 and reliable laboratory measurements were available even later and were applied in this cohort of adult patients starting from 2013.14 Although, Lyso-Gb3 decreases after ERT initiation,30 a simplified assumption of linearity seems to be useful to estimate the pretreatment cumulative effects to Lyso-Gb3 because (1) ERT was initiated relatively late—in the adult age—in this old Fabry cohort, and because (2), following ERT, Lyso-Gb3 decreases but remains greatly elevated above the normal range.30 Of note, we classified the phenotype as published in the International Fabry Disease Genotype/Phenotype Database (www.dbFGP.org) for all mutations reported in this study. However, it needs to be mentioned that patients with the same genotype, sex and similar age can have phenotypic variations as previously shown in our4 and other cohorts,42 possibly caused by concomitant mutations, epigenetic phenomena and environmental conditions. Further limitation is that our results are not entirely in line with previous reports that found Lyso-Gb3 not to be associated with clinical events. Arends and colleagues analysed Lyso-Gb3 concentrations only for classic males and females, its levels were not significantly associated with previous clinical event rates.5 Further limitation is that the number of patients is relatively low due to the nature of a rare disease. Due to this, a predefined composite outcome rather than mortality alone was used to assess risk factors. Therefore, further studies are needed to confirm our findings. Finally, for the use as a clinical biomarker, standardisation of the technical methods and interlaboratory testing is needed in order to compare Lyso-Gb3 measurements among laboratories.
In conclusion, the major metabolite of FD Lyso-Gb3 appears as a potential marker of disease progression and is associated with increased risk of mortality and other significant clinical events. The cumulative pretreatment exposure to Lyso-Gb3 seems to worsen the long-term clinical outcomes, while the disease-specific treatment should ameliorate cumulative toxic Lyso-Gb3 effects.
Contributors AN contributed to conception and design of the work, acquisition, analysis and interpretation of data and drafting the manuscript. FB contributed to interpretation of data and final approval of the last version. VS and DK contributed to acquisition of data, interpretation of data and final approval of the last version. DGW contributed to design of the work, acquisition, analysis and interpretation of data and final approval of the last version.
Funding The Lyso-Gb3 measurements were determined by ARCHIMED Life Science, Vienna, Austria. The ARCHIMED Life Science laboratory member DCK participated in writing and approving the manuscript. The laboratory members were blinded to patients' names and all clinical and biochemical information and had no role in the collection of samples, interpretation of data and the decision to submit the article for publication.
Competing interests AN received lecturing honoraria and research support from Sanofi Genzyme, Takeda and Amicus and received financial publication support for this article from Sanofi Genzyme. DGW serves as a consultant for Amicus, Protalix, and Chiesi Pharma.
Patient consent for publication Not required.
Ethics approval The study was approved by the Zurich Ethics Committee.
Data availability statement Data are available upon reasonable request. All data relevant to the study are included in the article or uploaded as supplementary information. Deidentified participant data is available from the first author upon reasonable request as a data file under the email address email@example.com.
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