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Disrupted myelin lipid metabolism differentiates frontotemporal dementia caused by GRN and C9orf72 gene mutations


Heterozygous mutations in the GRN gene and hexanucleotide repeat expansions in C9orf72 are the two most common genetic causes of Frontotemporal Dementia (FTD) with TDP-43 protein inclusions. The triggers for neurodegeneration in FTD with GRN (FTD-GRN) or C9orf72 (FTD-C9orf72) gene abnormalities are unknown, although evidence from mouse and cell culture models suggests that GRN mutations disrupt lysosomal lipid catabolism. To determine how brain lipid metabolism is affected in familial FTD with TDP-43 inclusions, and how this is related to myelin and lysosomal markers, we undertook comprehensive lipidomic analysis, enzyme activity assays, and western blotting on grey and white matter samples from the heavily-affected frontal lobe and less-affected parietal lobe of FTD-GRN cases, FTD-C9orf72 cases, and age-matched neurologically-normal controls. Substantial loss of myelin-enriched sphingolipids (sulfatide, galactosylceramide, sphingomyelin) and myelin proteins was observed in frontal white matter of FTD-GRN cases. A less-pronounced, yet statistically significant, loss of sphingolipids was also observed in FTD-C9orf72. FTD-GRN was distinguished from FTD-C9orf72 and control cases by increased acylcarnitines in frontal grey matter and marked accumulation of cholesterol esters in both frontal and parietal white matter, indicative of myelin break-down. Both FTD-GRN and FTD-C9orf72 cases showed significantly increased lysosomal and phagocytic protein markers, however galactocerebrosidase activity, required for lysosomal catabolism of galactosylceramide and sulfatide, was selectively increased in FTD-GRN. We conclude that both C9orf72 and GRN mutations are associated with disrupted lysosomal homeostasis and white matter lipid loss, but GRN mutations cause a more pronounced disruption to myelin lipid metabolism. Our findings support the hypothesis that hyperactive myelin lipid catabolism is a driver of gliosis and neurodegeneration in FTD-GRN. Since FTD-GRN is associated with white matter hyperintensities by MRI, our data provides important biochemical evidence supporting the use of MRI measures of white matter integrity in the diagnosis and management of FTD.


FTD is the second most common cause of younger-onset dementia, frequently manifesting before 65 years of age [1, 2]. It is characterised by atrophy of the frontal or temporal lobes and classified into three clinical syndromes: behavioural variant FTD (bvFTD), progressive non-fluent aphasia, and semantic dementia. BvFTD, typified by personality changes, socially inappropriate behaviour and cognitive deficits, is the most common [3]. Pathologically, FTD is associated with intraneuronal aggregates of hyperphosphorylated tau protein or hyperphosphorylated and proteolytically-cleaved 43 kDa TAR DNA-binding protein (TDP-43) in both neurons and glia [4].

A strong family history is reported in nearly half of all bvFTD cases [3]. The two most common genetic causes of familial FTD with TDP-43 inclusions are heterozygous mutations in the gene encoding progranulin (GRN), which accounts for 5–20% of inherited FTD [5, 6]; and hexanucleotide repeat (GGGGCC) expansions in a non-coding region of the C9orf72 gene, accounting for approximately 20% of inherited FTD [7]. C9orf72 repeat expansions are also the most common genetic cause of amyotrophic lateral sclerosis (ALS) [8].

Progranulin is a secreted glycoprotein that is highly expressed by activated microglia [6, 9], interacts with the neuronal receptor sortilin, and localises primarily to neuronal and microglial lysosomes [9, 10]. Heterozygous GRN mutations that cause FTD lead to nonsense-mediated decay of GRN mRNA and reduced progranulin protein levels [5, 6]. Loss of function mutations in both GRN alleles cause the severe lysosomal storage disorder neuronal ceroid lipofuscinosis (NCL), characterised by enlarged lysosomes and accumulation of the auto-fluorescent material lipofuscin [11, 12]. These features are also observed in brains of FTD-GRN cases and Grn-/- mice [13,14,15,16]. Mechanistic studies have demonstrated important functions for progranulin in regulating lysosomal acidification [17], the lysosomal import of proteins required for lipid catabolism [10], and activity of the lysosomal lipase glucocerebrosidase (GCase) [18, 19].

C9orf72 repeat expansions are associated with reduced C9orf72 transcript levels, nuclear RNA foci that interfere with the function of RNA binding proteins, and inclusions comprising dipeptide repeat polymers derived from translation of the repeat expansions [8, 20, 21]. Whether one of these mechanisms predominates in causing neurodegeneration remains a subject of research, since both loss of normal C9orf72 and gain of toxic function promote neurodegenerative phenotypes [22, 23]. Physiologically, C9orf72 is required for endosomal trafficking, autophagy and lysosomal biogenesis [23, 24]. Disrupted lysosomal function may therefore be common to both FTD-GRN and FTD-C9orf72.

Magnetic resonance imaging (MRI) studies show white matter hyperintensities, indicative of focal demyelination, in FTD-GRN but not FTD-C9orf72 cases [25,26,27]. On the other hand, diffusion tensor imaging has shown reduced white matter integrity in both FTD-GRN and FTD-C9orf72, and in bvFTD more generally [28, 29]. Myelin is composed 70% (dry weight) of lipids [30]. The physiological turnover and maintenance of myelin is therefore predicted to require constitutive lipid catabolism in microglial and oligodendrocyte lysosomes. In this study we demonstrate that both FTD-GRN and FTD-C9orf72 are characterised by significant lipid loss in frontal white matter. However, myelin lipid and protein loss was substantially greater in FTD-GRN cases and associated with a pronounced increase in cholesterol esters, suggesting that excess cholesterol and fatty acids resulting from myelin break-down are stored as cholesterol esters in white matter. Markers of phagocytic microglia, TREM2 and CD68, were increased in FTD-C9orf72 and FTD-GRN, indicating that both gene defects promote a phagocytic microglial phenotype, however our evidence indicates that hyperactive myelin lipid catabolism differentiates FTD-GRN from FTD-C9orf72 cases.

Materials and methods

Human brain tissue

Fresh frozen grey and white matter tissue samples from the superior frontal and superior parietal lobe of 11 FTD-C9orf72 cases, 6 FTD-GRN cases, and 11 age-matched neurologically-normal controls were obtained from the Sydney Brain Bank and NSW Brain Tissue Resource Centre. Demographic and clinical information (sex, age at death, cause of death and post-mortem interval (PMI)) is provided in Table 1.

Table 1 Demographic information for cases used in this study. PMI: post-mortem interval. *Cases used for histological analysis. #Cases with co-occurring ALS.

Approximately 100 mg of frozen brain tissue was homogenised for 1 min at 4 °C in 700 µL ice-cold HEPES buffer (50 mM, pH 7.4) containing 5 mM NaF, 2 mM Na3VO4, 10 mM KCl and cOmplete Mini EDTA-free Protease Inhibitor Cocktail (Roche #11836153001), using a bead beater with 425–600 mm acid washed glass beads (Sigma Aldrich #G8772). Samples were centrifuged at 4 °C for 1 min at 1000xg and the homogenate was transferred to a new tube, after which the beads were washed with a further 100 µL of ice-cold HEPES buffer, centrifuged, and the supernatant combined with the previous fraction. The homogenate was stored in 100 µL aliquots at -80 °C. Protein concentration of the homogenates was determined by bicinchoninic acid assay (Thermo Scientific #23225).

Lipid extraction

Lipids were extracted from 100 µL brain homogenate samples (~ 100 µg protein) using a two-phase methyl-tert-butyl ether (MTBE)/methanol/water protocol [31]. Homogenate was combined with 850 µL MTBE and 250 µL methanol containing internal standards: 5 nmoles PC(19:0/19:0); 2 nmoles each of SM(d18:1/12:0), GluCer(d18:1/12:0), PS(17:0/17:0), PE(17:0/17:0), PG(17:0/17:0), CL(14:0/14:0/14:0/14:0), TG(17:0/17:0/17:0), and CholE(17:0); 1 nmole PA(17:0/17:0), PI(d7-18:1/15:0), and d7-Chol; 0.5 nmoles LacCer(d18:1/12:0), ST(d18:1/17:0), Cer(d18:1/17:0), DG(d7-18:1/15:0), MG(d7-18:1), LPC(17:0), LPE(17:1), LPS(17:1); and 0.2 nmoles Sph(d17:1), S1P(d17:1), LPA(17:0), and AcCa(d3-16:0). Samples were sonicated in a 4 °C water bath for 30 min. Phase separation was induced with the addition of 212 µL of mass spectrometry grade water, samples were vortexed and centrifuged at 2000xg for 5 min and the upper organic phase was collected in 5 mL glass tubes. The aqueous phase was extracted twice more with 500 µL MTBE and 150 µL methanol followed by sonication for 15 min and phase separation with 125 µL water. Organic phases from the three extractions were combined and dried under vacuum in a Savant SC210 SpeedVac (ThermoFisher Scientific). Lipids were reconstituted in 400 µL of HPLC grade methanol, then diluted 1:5 in 80% (v/v) methanol:20% water containing 1 mM ammonium formate and 0.2% formic acid.

Lipid quantification using liquid chromatography-tandem mass spectrometry (LC-MS/MS)

Lipidomic data was acquired with a ThermoFisher Q-Exactive HF-X mass spectrometer coupled to a Vanquish HPLC [31]. Lipids were resolved on a 2.1 × 100 mm Waters C18 HPLC column (1.7 μm pore size), using a 27 min binary gradient at a 0.28 mL/minute flow rate: 0 min, 80:20 A/B; 3 min, 80:20 A/B; 5.5 min, 55:45 A/B; 8 min, 36:65 A/B; 13 min, 15:85 A/B; 14 min, 0:100 A/B; 20 min, 0:100 A/B; 20.2 min, 70:30 A/B; 27 min, 70:30 A/B. Solvent A was 10 mM ammonium formate, 0.1% formic acid in acetonitrile:water (60:40); Solvent B was 10 mM ammonium formate, 0.1% formic acid in isopropanol:acetonitrile (90:10). Data was acquired in full scan/data-dependent MS2 mode (resolution 60,000 FWHM, scan range 220–1600 m/z). Sample order was randomised, and data was collected in both positive and negative mode for each sample. The ten most abundant ions in each cycle were subjected to MS2, with an isolation window of 1.4 m/z, collision energy 30 eV, resolution 17,500 FWHM, maximum integration time 110 ms and dynamic exclusion window 10 s. An exclusion list of background ions was based on a solvent blank. An inclusion list of the [M + H]+ and [M-H] ions for all internal standards was used. Mass accuracy was < 5 ppm and %CV for peak elution time was < 2% across the entire sample run.

LipidSearch software (version 4.2, Thermo Fisher) was used for lipid annotation, chromatogram alignment, and peak integration. Lipid annotation required both accurate precursor ion mass (5 ppm mass tolerance) and diagnostic product ions (8 ppm mass tolerance). Molar amounts for each lipid were calculated by taking the ratio to the class-specific internal standard, after which lipid levels were normalised to protein content.

Bis(monoacylglycero)phosphate (BMP) quantification

Resolution of BMP from its mass isomer PG was performed as described [19]. Lipid annotation, chromatogram alignment and peak integration were carried out with TraceFinder software (version 5.1, Thermo Fisher). Correct peak identification was confirmed with the use of commercial standards for BMP(18:1/18:1) and PG(18:1/18:1) (Avanti Polar Lipids #857135 and #840475, respectively). Molar amounts for BMP and PG were calculated relative to the PG(17:0/17:0) internal standard.

Western blots

Whole brain homogenates (10 µg protein for grey matter and 5 µg for white matter) were resolved on Bolt™ 4–12% Bis-Tris Plus gels (ThermoFisher Scientific #NW04125BOX) and transferred to polyvinylidene fluoride membranes. Membranes were blocked for 1 h at RT with 5% skim milk in Tris-buffered saline containing 0.1% Tween-20 (TBST), then incubated overnight at 4 °C with primary antibody in TBST with 3% bovine serum albumin (Sigma Aldrich #A7906). Membranes were then washed 3 times in TBST and incubated in horseradish peroxidase-conjugated secondary antibody diluted 1:5000 in TBST containing 5% skim milk for 2 h at RT. Membranes were imaged with ECL Ultra Western HRP Substrate (Millipore #WBULS0500) using a Bio-Rad ChemiDoc Touch. Bands were quantified by densitometry with Bio-Rad Image Lab software (v6.0.1). Membranes were then stripped with mild stripping buffer (1.5% w/v glycine, 0.1% w/v SDS, 0.1% v/v Tween20, pH 2.2), blocked with 5% skim milk in TBST for 1 h and re-probed with anti-β-actin (Abcam #ab8227, RRID #AB_2305186) or anti-GAPDH (Cell Signalling #2118, RRID #AB_561053) at 1:5000 dilution in TBST with 3% BSA overnight at 4 °C. A common sample was included on each gel as a loading control to normalise between membranes containing different samples.

The following primary antibodies were used at 1:1000 dilution unless specified: rabbit anti-MBP (Abcam, #ab40390, RRID #AB_1141521), rabbit anti-PLP (Abcam #ab28486, RRID #AB_776593) (diluted 1:2000), mouse anti-CNP (11-5B) (Abcam #ab6319, RRID #AB_2082593), mouse anti-NEFL (DA2) (Invitrogen #13–0400, RRID #AB_2532995), mouse anti-tubulin βIII (TUBB3) (BioLegend #801,202, RRID #AB_10063408) (diluted 1:5000), #rabbit anti-LAMP1 (D2D11) XP® (Cell Signalling #9091, RRID #AB_2687579), mouse anti-LAMP2 (Developmental Studies Hybridoma Bank #H4B4, RRID #AB_528129) (diluted 1:200), rabbit anti-Trem2 (Cell Signalling #91,068, RRID # AB_1961900), rabbit anti-CD68 (Abcam # ab213363, RRID #AB_2801637).

Enzyme activity assays

β-glucocerebrosidase (GCase) and β-galactocerebrosidase (GALC) activities were assayed with the fluorometric substrates 4-Methylumbelliferyl β-D-glucopyranoside (Sigma-Aldrich #M3633) and 4-Methylumbelliferyl β-D-galactopyranoside (Sigma-Aldrich #M1633), respectively. All reactions were carried out in triplicate in 96-well white Opti-Plates (PerkinElmer #6005290). For GCase activity, 1 µg homogenate protein was resuspended in 15 µL 0.1 M citric acid/0.2 M disodium phosphate (pH 5) and incubated with 30 µL of 10 mM substrate dissolved in 0.1 M citric acid/0.2 M disodium phosphate (pH 5), 0.5% sodium taurocholate, 0.25% Triton X-100 [32]. Plates were covered with sealing film, shaken, and incubated at 37 °C in the dark for 1 h. Reactions were stopped with 180 µL of ice-cold stop solution (0.2 M glycine/NaOH, pH 10.4). For GALC activity, 20 µg homogenate protein was resuspended in 25 µL citrate/phosphate buffer, pH 4.5, and incubated for 30 min with 25 µL of 1 mM substrate dissolved in 50 mM sodium citrate, pH 4.5, 125 mM NaCl, 0.5% Triton X-100. Reactions were stopped with 50 µL of ice-cold stop solution (0.5 M glycine/0.3 M NaOH, pH 10). Fluorescence was measured on a Tecan M200 Pro plate reader with excitation 360 nm and emission 446 nm. Relative activity was determined after subtraction of the substrate blank.


TDP-43 inclusions were detected with anti-phospho TDP-43 (pS409/410) (Cosmo Bio, CAC-TIP-PTD-M01, RRID # AB_1961900). The type and density of TDP-43 inclusions and dystrophic neurites was assessed by an experienced research neuropathologist.

Formalin-fixed and paraffin embedded Sect. (10 μm) from the superior frontal lobe of 4 FTD-C9orf72 cases, 3 FTD-GRN cases and 5 age-matched controls, indicated by an asterisk in Table 1, were used for luxol fast blue (LFB) staining, and immunofluorescence staining for aspartoacylase (ASPA) and myelin basic protein (MBP). These cases were those for which the tissue had not been subjected to extended fixation (> 2 weeks). Sections were heated in an oven at 60 °C for 1 h, deparaffinised in 2 × 15 min changes of xylene, and rehydrated to deionised water following graded changes of ethanol from 100 to 50%. For LFB staining, sections were rehydrated to 95% ethanol, incubated in 0.1% LFB solution (#S3382, Sigma-Aldrich) at 60 °C for 17 h, then rinsed in 70% ethanol for 2.5 min, followed by distilled water until the water ran clear. Sections were then differentiated in 0.05% lithium carbonate solution for 30 s, then in 70% ethanol for 30 s, and rinsed in distilled water. Sections were then counterstained with 0.1% cresyl violet solution for 30 s and rinsed in distilled water, followed by 95% ethanol for 5 min. Sections were dehydrated in two changes of 100% ethanol, cleared in two changes of xylene, and coverslipped using DPX mounting medium. Myelination scores from 0 to 3 were assigned by two blinded observers, where 0 is complete absence of myelin and 3 is dense myelin [33].

For immunofluorescence, sections were incubated in sodium citrate antigen retrieval buffer (10 mM, pH 6.0, 0.05% Tween 20) at 85 °C for 10 min, blocked in PBS with 0.1% Triton X-100 (PBST), 5% normal goat serum and 0.1% bovine serum albumin (BSA) at RT for 2 h, and incubated overnight at 4 °C with primary antibodies rabbit anti-ASPA (Abcam #ab223269 EPR22072) and mouse anti-MBP (R&D #MAB42282), diluted 1:250 in blocking solution. Sections were incubated in secondary antibodies (AlexaFluor 488 Goat anti-mouse, Cell Signalling #4408, RRID: AB_10694704; and AlexaFluor 647 Goat anti-rabbit, Cell Signalling #4414, RRID: AB_10693544) diluted 1:250 in blocking solution for 2 h, and counterstained with 1 µg/mL diamidino-2-phenylindole dihydrochloride (DAPI). Autofluorescence was quenched with TrueBlack Plus autofluorescence eliminator (Biotium #23,014) per manufacturer’s protocol. Sections were cover-slipped with ProLong Glass antifade mountant (Life Technologies #P36980) before imaging. Slides were imaged with a Zeiss Axioscan slide scanner. The density of ASPA-positive cells (co-localised ASPA and DAPI staining) in white matter was quantified using QuPath (version 0.3.2) [34].

Statistical analysis

Partial least squares-discriminant analysis (PLS-DA) of lipidomic data was carried out in MetaboAnalyst (version 5.0). Lipid levels were log10-transformed and filtered based on interquartile range prior to analysis. Missing values (not detected in that sample) were assigned a value of 1/5 of the minimum observed value for that lipid. Lipid class totals, and individual cholesterol ester or acylcarnitine species, were compared between the three sample groups using one-way ANOVA adjusted for age and PMI, followed by Tukey’s post-hoc test. Values were natural log-transformed to improve normality and ANOVA p values were adjusted for false discovery rate using the Benjamini-Hochberg correction, with adjusted p < 0.05 considered significant. These statistical tests were performed using the car, olsrr, ggplot2, multcomp and dplyr packages in R (version 4.0.3). The heatmap was generated in Tableau Desktop (version 2022.1.1).

Western blot, immunofluorescence, BMP levels, and enzyme activity data were analysed by one-way ANOVA with Tukey’s post-hoc test, using GraphPad PRISM (version 9.3.1). Non-normally distributed data were natural log-transformed to achieve a normal distribution. LFB histological scores were subject to non-parametric Kruskall-Wallis test with Dunn’s post-test. Spearman correlations were performed in GraphPad PRISM.


Case demographics and TDP-43 pathology

This study used post-mortem brain tissue from FTD cases with GRN (n = 6) and C9orf72 (n = 11) mutations, and neurologically normal controls (n = 11) (Table 1). Mean age at death was 70.3 ± 10.0 years for controls, 68.6 ± 9.3 years for C9orf72 cases and 63.0 ± 8.8 years for GRN cases (ANOVA, F = 1.17, p = 0.33). Mean post-mortem interval (PMI) was 28.5 ± 15.5 h for controls, 20.2 ± 12.9 h for C9orf72 cases and 25.7 ± 12.4 h for GRN cases (F = 0.99, p = 0.38). All FTD-GRN and 7 out of 11 FTD-C9orf72 cases exhibited type A TDP-43 inclusions [35], with the rest exhibiting type B. The severity of TDP-43 neuronal cytoplasmic inclusions in frontal grey matter (Fig. 1A-D) or glial cytoplasmic inclusions in frontal white matter (Fig. 1E) did not differ significantly between FTD-GRN and FTD-C9orf72 cases (Fig. 1F-G), nor did the severity of TDP-43-positive dystrophic neurites (Fig. 1H-I), indicating that the FTD-GRN and FTD-C9orf72 cases are well-matched neuropathologically.

Fig. 1
figure 1

TDP-43 cytoplasmic inclusions and dystrophic neurites are similar between FTD-GRN and FTD-C9orf72 cases. (A-D) Representative images of phosphorylated TDP-43 staining in grey matter, showing (A) a control case with no TDP-43 inclusions, (B) mild (score = 1), (C) moderate (score = 2), and (D) severe (score = 3) TDP-43 pathology. (E) Abundant TDP-43-positive dystrophic neurites (score = 3) in frontal white matter of an FTD case. Scale bar, 20 µM. (F-I) Severity of (F) neuronal cytoplasmic TDP-43 inclusions in frontal grey matter, (G) glial cytoplasmic inclusions in frontal white matter, (H) TDP-43-positive dystrophic neurites in frontal grey matter, and (I) dystrophic neurites in frontal white matter of FTD-C9orf72 (n = 11) and FTD-GRN (n = 6) cases

Lipidomic profiles distinguishes FTD-GRN from control and FTD-C9orf72 cases

Lipidomic analysis was performed on the superior frontal grey and white matter, which are heavily affected in bvFTD, and the less affected superior parietal grey and white matter [36, 37]. A total of 821 glycerophospholipid, phospholipid, lysophospholipid, sphingolipid, sterol and acylcarnitine species were quantified (Supplementary Data File 1). Applying partial least squares discriminant analysis (PLS-DA), FTD-GRN cases clustered distinctly from both control and FTD-C9orf72 cases based on lipidomic data from frontal grey matter (Fig. 2A). This was driven by myelin-enriched sphingolipids, specifically sulfatides (ST), monohexosylceramides (Hex1Cer), and dihexosylceramides (Hex2Cer) (Fig. 2B). Hex1Cer comprises both glucosylceramide and galactosylceramide, structural isomers that are indistinguishable using LC-MS/MS with reverse-phase chromatography. However, over 99% of Hex1Cer in the brain is galactosylceramide [38], which makes up 20–25% of myelin lipid [30]. ST (galactosylceramide sulfate) makes up a further 4–5% of myelin lipid [30]. PLS-DA did not effectively differentiate the three sample groups based on parietal grey matter lipids.

Fig. 2
figure 2

Lipid profiles distinguish FTD-GRN from FTD-C9orf72 and control cases. (A) PLS-DA scores plots for control (n = 11, orange), FTD-C9orf72 (n = 11, blue), and FTD-GRN (n = 6, yellow) cases for each brain region, based on the untargeted lipidomic data. Component % refers to the percentage of variance explained by each principal component. (B) Variable Importance in the Projection (VIP) scores for the 15 features that contribute most to separation of the groups in PLS-DA. ST: sulfatide, Hex1Cer: monohexosylceramide, Hex2Cer: dihexosylceramide, SM: sphingomyelin, CholE: cholesterol ester, PC: phosphatidylcholine, PE: phosphatidylethanolamine. (C,D) Levels of CholE species in (C) frontal and (D) parietal white matter. Horizontal bars show mean. Missing values indicate that the specific CholE was below the limit of detection in that sample. Sample groups were compared by one-way ANOVA adjusted for PMI and age, and p values were corrected for false discovery rate. Results of Tukey’s post-test are shown: *p < 0.05; **p < 0.01; ***p < 0.001. (E,F) Total cholesterol esters (CholE)/cholesterol (Chol) in (E) frontal and (F) parietal white matter

FTD-GRN cases also clustered distinctly from controls in frontal and parietal white matter (Fig. 2A), and this was driven by cholesterol esters (Fig. 2B). Many cholesterol ester species were increased by 1–2 orders of magnitude in FTD-GRN compared to FTD-C9orf72 and control cases, particularly in parietal white matter (Fig. 2C-D).

Loss of myelin lipids in FTD-GRN and FTD-C9orf72 cases

To complement the unsupervised statistical analysis of individual lipids and identify metabolic nodes affected by GRN or C9orf72 mutations, lipid class totals were compared across the three sample groups using ANOVA adjusted for age and PMI (Fig. 3A and Supplementary Tables 1–4). The most significant changes were observed in frontal white matter, where 9 of the 27 lipid classes were significantly reduced in the FTD-GRN group. Statistically significant reductions in total ST, Hex2Cer, sphingomyelin (SM), Hex1Cer, lysophosphatidylcholine (LPC), and 1-O-alkyl-lysophosphatidylcholine [LPC(O)] were observed in both FTD-GRN and FTD-C9orf72 relative to control cases, although the magnitude of lipid loss was greater in FTD-GRN cases (Fig. 3A-G). Phosphatidylinositol (PI), lysophosphatidylinositol (LPI), and ceramide were significantly reduced in frontal white matter of FTD-GRN but only trended lower in FTD-C9orf72 cases (Fig. 3A). Similar trends with an overall loss of sphingolipids and phospholipids were observed in the parietal white matter, however these were not statistically significant. Instead, total cholesterol esters, lysophosphatidylethanolamine (LPE), and sphingosine, an intermediate metabolite in sphingolipid catabolism, were significantly increased in the FTD-GRN group (Fig. 3A).

Fig. 3
figure 3

Loss of myelin lipids is common to FTD-GRN and FTD-C9orf72. (A) Mean lipid class totals in FTD-C9orf72 (n = 11) and FTD-GRN (n = 6) cases, expressed as a fold-change relative to the mean of the control group (n = 11) within each brain region. GM: grey matter, WM: white matter. Sample groups were compared by one-way ANOVA adjusted for PMI and age, with p values adjusted for false discovery rate. Asterisks indicate a significant difference compared to the control group in Tukey’s post-test: *p < 0.05; **p < 0.01; ***p < 0.001. (B-H) Total lipid levels in each brain region. (I) Individual acylcarnitine (AcCa) species in frontal grey matter. Horizontal bar shows mean. FGM: Frontal Grey Matter; FWM: Frontal White Matter; PGM: Parietal Grey Matter; PWM: Parietal White Matter; ST: sulfatide; SM: sphingomyelin; Hex2Cer: dihexosylceramide; Hex1Cer: monohexosylceramide; Cer: ceramide; Sph: sphingosine; CholE: cholesterol ester; Chol: cholesterol; PC: phosphatidylcholine; PE: phosphatidylethanolamine; PE(O): alkyl-PE; PE(P): alkenyl-PE (PE plasmalogen); PG: phosphatidylglycerol; PI: phosphatidylinositol; PS: phosphatidylserine; CL: cardiolipin; LPA: lysophosphatidic acid; LPC: lysophosphatidylcholine; LPC(O): alkyl-LPC; LPE: lysophosphatidylethanolamine; LPE(O): alkyl-lysophosphatidylethanolamine; LPI: lysophosphatidylinositol; LPS: lysophosphatidylserine; MAG: monoacylglycerol; DAG: diacylglyerol; TAG: triacylglycerol; AcCa: acylcarnitine

In addition to the sphingolipids ST, Hex1Cer, and SM, myelin is highly enriched in unesterified cholesterol [30]. Although unesterified cholesterol levels trended downwards in white matter of FTD relative to the control cases, this was not statistically significant. However, the ratio of esterified to unesterified cholesterol was an order of magnitude higher in both frontal (F = 24.6, p < 0.0001) and parietal (F = 49.2, p < 0.0001) white matter of FTD-GRN cases (Fig. 2E-F).

A marked increase in acylcarnitines was observed in frontal grey matter of FTD-GRN cases (Fig. 3A and H). Examination of individual acylcarnitine species showed a preferential effect on acylcarnitines with 16–20 carbon acyl chains (Fig. 3I). Acylcarnitines also trended higher in FTD-GRN cases in the parietal grey matter, however no lipid classes reached statistical significance in this region.

FTD-GRN is characterised by severe myelin attrition

In agreement with our lipidomic data, western blotting showed significant loss of the myelin markers proteolipid protein (PLP) (ANOVA, F = 12.03, p = 0.0003), 2’,3’-Cyclic nucleotide 3’-phosphodiesterase (CNP) (F = 11.64, p = 0.0003) and myelin basic protein (MBP) (F = 4.84, p = 0.018), in frontal white matter of FTD-GRN cases (Fig. 4A-B). Although PLP levels were reduced relative to controls in FTD-C9orf72 cases, both PLP and CNP were significantly lower in FTD-GRN compared to FTD-C9orf72 cases, indicating more severe myelin loss in FTD-GRN cases. In parietal white matter, PLP (F = 14.64, p < 0.0001) was significantly reduced in FTD-GRN compared to both control and FTD-C9orf72 cases, whereas CNP (F = 0.88, p = 0.43) and MBP (F = 1.02, p = 0.38) were unchanged across the three sample groups (Fig. 4C-D). The neuronal marker βIII-tubulin was significantly decreased in frontal (Fig. 4A-B) but not parietal (Fig. 4C-D) white matter of FTD-GRN cases, and was not significantly affected in FTD-C9orf72 cases (Kruskal-Wallis test, frontal white matter: H = 7.90, p = 0.019; parietal white matter: ANOVA F = 1.76, p = 0.19). Axonal marker neurofilament-L trended down in frontal white matter of FTD-GRN and FTD-C9orf72 cases, however this was not statistically significant (ANOVA F = 2.32, p = 0.12). No difference was observed for neurofilament-L levels in parietal white matter (ANOVA F = 0.73, p = 0.49).

Fig. 4
figure 4

Pronounced myelin loss in FTD-GRN. (A, C) Representative western blots and (B, D) densitometric quantification of PLP, CNP, MBP, βIII-tubulin (βIII-T) and neurofilament light chain (NF-L) in (A, B) superior frontal white matter, and (C, D) superior parietal white matter from control (n = 11), FTD-C9orf72 (n = 11), and FTD-GRN (n = 6) cases. Protein levels were normalised to β-actin or GAPDH as a loading control, and are expressed relative to the mean of the control group. (E) Representative images and (F) myelination scores from LFB staining of superior frontal gyrus white matter from control (n = 5), FTD-C9orf72 (n = 4), and FTD-GRN (n = 3) cases from which tissue fixed for < 2 weeks was available. (G) Representative ASPA (red) and MBP (green) staining in superior frontal gyrus white matter, and (H) ASPA-positive cell density. Groups were compared by one-way ANOVA with Tukey’s post-test (B,D,H) or Kruskall-Wallis test with Dunn’s post-test (F): *p < 0.05; **p < 0.01; ***p < 0.001

Luxol fast blue staining confirmed the pronounced myelin loss in frontal white matter of FTD-GRN cases (Kruskal-Wallis H = 9.47, p = 0.0002) (Fig. 4E-F). Loss of myelin staining in FTD-GRN cases was uniform and without evidence of focal lesions or plaques. Despite the pronounced myelin loss, mature oligodendrocyte (ASPA-positive) cell density [33, 39] was not reduced in frontal white matter of FTD-GRN cases, and was 60% higher in FTD-C9orf72 compared to control cases (F = 6.15, p = 0.021) (Fig. 4G-H).

Cholesterol esters are inversely correlated with myelin proteins and lipids

Myelin loss could explain the pronounced cholesterol ester accumulation in FTD-GRN cases, as cholesterol released from myelin is metabolised by phagocytic cells [40, 41]. Total cholesterol esters were inversely correlated with PLP, but not MBP or CNP, in frontal and parietal white matter (Table 2). Of all the lipids measured, ST and Hex1Cer are most unique to myelin in the CNS [42]. Cholesterol esters were inversely correlated with total Hex1Cer but not ST in frontal white matter, and both Hex1Cer and ST in parietal white matter. Since not all cholesterol esters were increased in FTD-GRN cases, we performed the same correlation analysis with CholE(22:6), an abundant cholesterol ester that was greatly increased in FTD-GRN (Fig. 1C-D). CholE(22:6) was inversely correlated with all five myelin markers (PLP, MBP, CNP, ST, Hex1Cer) in frontal white matter, and PLP, ST, and Hex1Cer in parietal white matter (Table 2). These inverse correlations support the hypothesis that cholesterol esters are indicative of myelin degradation.

Table 2 Correlations between cholesterol esters and myelin markers in white matter. Spearman’s correlation coefficient (r) and p value are shown for associations between myelin markers and total cholesterol ester (CholE) or CholE(22:6) in frontal and parietal white matter. Significant correlations are in bold font

Lysosomal and phagocytic markers are increased in both FTD-GRN and FTD-C9orf72

GRN mutations are proposed to disrupt lysosomal homeostasis, and hypomyelination is common to many lysosomal storage diseases, including neuronal ceroid lipofuscinosis (NCL) caused by homozygous GRN mutations [11, 12]. Reduced GCase activity has been reported in Grn-/- mice [19, 43], IPSC-derived neurons [18] and brain tissue from FTD-GRN cases [44, 45]. We observed no significant difference in GCase activity between FTD cases and controls, in frontal grey or white matter, or parietal white matter (Fig. 5A-C). However, galactocerebrosidase (GALC) activity, which is required for lysosomal degradation of Hex1Cer and ST, was 64% higher in frontal white matter of FTD-GRN (p = 0.004), and 33% higher in FTD-C9orf72 cases (p = 0.21, not significant), relative to the controls (ANOVA F = 6.94, p = 0.004) (Fig. 5B).

Fig. 5
figure 5

Increased GALC activity in frontal white matter of FTD-GRN cases. (A-C) GALC and GCase enzyme activity in frontal white matter (A), parietal white matter (B) and frontal grey matter (C) of control (n = 11), FTD-C9orf72 (n = 11), and FTD-GRN (n = 6) cases. Data is normalised to the mean of the control group. (D-G) Targeted lipidomic analysis of 18:1/18:1 BMP and 18:1/18:1 PG in frontal grey matter (D), frontal white matter (E), parietal grey matter (F), parietal white matter (G). Groups were compared by one-way ANOVA with Tukey’s post-test: **p < 0.01

Recent studies have also demonstrated loss of the endolysosomal lipid Bis(monoacylglycero)phosphate (BMP), particularly BMP(18:1/18:1) and BMP(22:6/22:6), in mouse models of Grn deficiency [19, 45]. We were able to confidently resolve the abundant BMP(18:1/18:1) species from its mass isomer PG(18:1/18:1), and show here that levels of this BMP were not significantly different in FTD cases compared to controls (Fig. 5D-G, all p > 0.05 by one-way ANOVA), in agreement with another recent publication [45].

Further evidence for disrupted lysosomal homeostasis in FTD-GRN cases has come from reports showing increased levels of lysosomal proteins such as LAMP-1 and LAMP-2 [13, 44]. Western blotting showed increased LAMP-2 levels in frontal grey (F = 12.2, p = 0.0003) (Fig. 6A-B) and white matter (F = 9.7, p = 0.0009) (Fig. 6C-D) of both FTD-GRN and FTD-C9orf72 cases, whereas levels were unchanged in parietal white matter (Fig. 6E-F). LAMP-1 was increased in frontal grey matter of FTD-GRN cases (F = 7.0, p = 0.0042), and parietal white matter of both FTD-GRN and FTD-C9orf72 cases (F = 11.3, p = 0.0004), but was reduced in the frontal white matter of FTD-C9orf72 cases compared to controls (F = 3.9, p = 0.035). Levels of the phagocytic microglial marker CD68 were significantly increased in frontal (F = 6.45, p = 0.0049) and parietal white matter of FTD-C9orf72 (F = 3.9, p = 0.034), but not FTD-GRN cases. However, the microglial lipid receptor TREM2 [40, 46] was increased in frontal grey matter (F = 12.5, p = 0.0002) and parietal white matter (F = 33.6, p < 0.0001) of both FTD-GRN and FTD-C9orf72 cases, and frontal white matter of FTD-GRN cases (F = 4.7, p = 0.019). These results indicate that lysosomal and microglial homeostasis is disrupted in both FTD-C9orf72 and FTD-GRN cases, whereas lipid and myelin protein changes are more pronounced in FTD-GRN cases.

Fig. 6
figure 6

Lysosomal and phagocytic markers are increased in both FTD-GRN and FTD-C9orf72. (A, C, E) Representative western blots and (B, D, F) densitometric quantification for LAMP1, LAMP2, TREM2 and CD68 in (A, B) frontal grey matter, (C, D) frontal white matter and (E, F) parietal white matter of control (n = 11), FTD-C9orf72 (n = 11), and FTD-GRN (n = 6) cases. Protein levels were normalised to β-actin or GAPDH as a loading control, and expressed relative to the mean of the control group. Asterisks indicate significant difference in Tukey’s post-test after one-way ANOVA: *p < 0.05; **p < 0.01; ***p < 0.001


This study presents the first comprehensive biochemical evidence that FTD-GRN is characterised by pronounced myelin loss. Significant loss of myelin-enriched sphingolipids was observed in white matter of both FTD-GRN and FTD-C9orf72 cases, however FTD-GRN cases displayed a distinct lipidomic profile characterised by greater white matter lipid loss, increased levels of cholesterol esters in white matter, and increased acylcarnitines in grey matter. Levels of lysosomal markers and the microglial lipid receptor TREM2 were increased in both FTD-C9orf72 and FTD-GRN cases, whereas galactocerebrosidase activity, required for catabolism of the myelin lipids galactosylceramide and ST, was only significantly increased in FTD-GRN cases. These changes point to a specific effect of GRN mutations in promoting myelin lipid catabolism and myelin degeneration, supported by the marked loss of myelin proteins and luxol fast blue staining in FTD-GRN relative to FTD-C9orf72 and control cases. TDP-43 pathology did not differ significantly between the FTD-GRN and FTD-C9orf72 cases, suggesting that heterozygous GRN mutations and C9orf72 repeat expansions may promote TDP-43 deposition and bvFTD through distinct biochemical mechanisms.

Our study establishes that substantial white matter lipid loss is common to both FTD-C9orf72 and FTD-GRN. Relative to age-matched controls, mean levels of the myelin-enriched sphingolipids ST, Hex1Cer, Hex2Cer, and SM were 43–64% lower in frontal white matter of FTD-C9orf72 and 58–71% lower in FTD-GRN cases. Loss of phospholipids (PI) and lysophospholipids (LPC, LPI) in white matter of FTD-GRN cases probably also reflects myelin loss [42]. A previous study showed marked demyelination and gliosis in regions corresponding to white matter hyperintensities in a single FTD-GRN case [47]. Our study expands substantially on this, presenting several lines of biochemical evidence (myelin lipid loss, myelin protein loss, and histological staining) from multiple FTD-GRN cases to demonstrate that pronounced myelin loss is characteristic of FTD-GRN. The observation of severe myelin loss in FTD-GRN but not FTD-C9orf72 cases is in agreement with reported observations of white matter hyperintensities in FTD-GRN but not FTD-C9orf72 cases [25,26,27]. However, our demonstration of significant lipid loss and a reduction in the major myelin protein PLP in frontal white matter of FTD-C9orf72 cases demonstrates some myelin loss, in agreement with a recent study reporting decreased MBP immunoreactivity in frontal cortex of FTD-C9orf72 cases [48]. Mature oligodendrocyte density did not decrease in FTD-GRN cases, implying that demyelination does not stem from oligodendrocyte loss. However, given the significant frontal lobe atrophy in bvFTD [1], equivalent oligodendrocyte density likely indicates an overall loss of oligodendrocytes relative to the age-matched controls. This could explain the increased mature oligodendrocyte density in FTD-C9orf72 cases.

FTD-GRN were differentiated from FTD-C9orf72 cases by pronounced accumulation of cholesterol esters in white matter, relative to both protein content and unesterified cholesterol. Boland et al. very recently reported a modest increase in sterol esters in middle frontal gyrus of FTD cases with GRN mutations but not sporadic cases with TPD-43 inclusions [45], however it was unclear if grey or white matter was used and control cases were limiting. We observed significantly-increased cholesterol esters only in white matter. Cholesterol esters are formed during myelin break-down and accumulate in demyelinating conditions, as microglia and infiltrating macrophages phagocytose cholesterol released from compact myelin [40, 41, 49, 50]. Since cholesterol cannot be broken down by CNS cells, this free cholesterol is stored in esterified form and eventually cleared by excretion [51]. In the CNS, myelin phagocytosis and degradation is carried out by microglia and macrophages [40, 41, 52], which are the cell types that express GRN most abundantly. Although cholesterol ester accumulation in white matter of FTD-GRN cases is probably associated with excessive myelin break-down, it is also possible that this phenotype results from a defect in cholesterol break-down and clearance caused by GRN haploinsufficiency. In this regard, a recent study reported that GRN deficiency impairs clearance of myelin debris by cultured microglia [53]. Cholesterol overload in microglia triggers lysosome rupture and NLRP3 inflammasome activation [41], which could fuel neuroinflammation in FTD-GRN cases. Cholesterol ester formation also appears to be an important driver of amyloid β and neurofibrillary tangle pathology in Alzheimer’s disease models [54, 55].

Diffusion tensor imaging studies have shown loss of white matter integrity in C9orf72, GRN and MAPT mutation carriers up to 30 years prior to estimated symptom onset [28, 29], suggesting that myelin deterioration begins early in FTD pathogenesis. Using post-mortem tissue samples, it is difficult to determine if white matter changes precede axon degeneration, or vice-versa. Loss of myelin markers in frontal white matter of FTD-GRN cases was accompanied by a significant reduction in βIII-tubulin but not neurofilament-L by western blotting. In contrast, we observed significant myelin lipid loss in FTD-C9orf72 cases without evidence for loss of axonal markers by western blotting, although noting that this could be attributed to the more quantitative nature of our lipidomic analysis in comparison to western blotting and densitometry. In the less affected parietal white matter, the pronounced increase in cholesterol esters without significant loss of myelin lipids or axonal markers suggests that cholesterol ester storage is an early phenotype resulting from GRN haploinsufficiency.

Another differentiating feature of FTD-GRN was increased levels of long chain (C16-C20) acylcarnitines in frontal grey matter. Acylcarnitines are formed to import fatty acids into mitochondria for β-oxidation, and their accumulation is commonly associated with impaired β-oxidation of fatty acids [56]. Defective fatty acid β-oxidation can produce a brain energy deficit, which could partly explain the hypometabolic phenotype of FTD [57]. Acylcarnitine accumulation attributed to impaired β-oxidation of very long chain fatty acids in peroxisomes is a defining feature of X-linked adrenoleukodystrophy [58], also characterised by cholesterol ester accumulation [50]. Further research is required to determine if impaired fatty acid oxidation is a feature of FTD-GRN. Alternatively, the increased acylcarnitines could be indicative of a metabolic shift favouring lipid oxidation for energy production at the expense of lipid synthesis, thus causing myelin degeneration [59].

Levels of the microglial lipid receptor TREM2 were significantly higher in grey and white matter of both FTD-GRN and FTD-C9orf72 cases, indicating the presence of phagocytic microglia. Lipid sensing by TREM2 promotes microglial activation and myelin phagocytosis [40, 52]. Our data therefore provides important evidence from human FTD cases confirming the observation that microglia from C9orf72 and Grn knockout mice exhibit a phagocytic microglial phenotype [60, 61]. In addition to phagocytosing myelin, activated microglia promote neurodegeneration through increased secretion of inflammatory cytokines and complement proteins, and synaptic pruning [61, 62]. In fact, complement proteins secreted by GRN-/- microglia are sufficient to induce TDP-43 granules and cell death in excitatory neurons [62]. Our data also establishes that lysosomal protein markers LAMP-1, LAMP-2, and CD68 are deregulated in FTD-C9orf72 cases, and demonstrates that this phenotype is shared with FTD-GRN. C9orf72 colocalises with Rab family proteins and regulates endocytosis, lysosome biogenesis and phagosome maturation [23, 63]. Prior work had shown increased LAMP-1 and CD68 immunoreactivity in ALS cases with C9orf72 repeat expansions [63, 64], however C9orf72-/- motor neurons and those from ALS-C9orf72 cases have fewer lysosomes, despite higher LAMP-2 content in lysosomal membranes [23].

Current evidence suggests that progranulin is required for full activity of lysosomal lipid hydrolases, particularly GCase [19, 43, 44]. Higher levels of the GCase substrate glucosylsphingosine have been reported in plasma of FTD-GRN cases [19], whereas another study showed unchanged levels in the inferior frontal gyrus [44]. Decreased GCase activity has been attributed to a role for progranulin in regulating the delivery of prosaposin to lysosomes and its proteolytic cleavage into saposins [10, 18], which serve as cofactors for lysosomal sphingolipid hydrolases such as GCase. Others have proposed a direct interaction between progranulin and GCase [43], or that progranulin regulates lysosomal enzyme functions through a direct interaction with BMP [19, 45]. Further evidence for lysosomal dysfunction comes from the recent demonstration of gangliosidosis in frontal cortex of FTD-GRN cases [45]. We did not find reduced BMP content in FTD-GRN cases compared to controls, indicating that not all molecular phenotypes of Grn-/- mice accurately reflect changes in FTD cases with heterozygous GRN mutations. GCase activity trended lower (14% reduction) in frontal grey matter of FTD-GRN cases, in line with modest reductions reported in two prior studies [44, 45], however this was not statistically significant. We note that GCase activity reductions are modest even in Grn-/- mice, with one study reporting a decrease of ~ 10% [44], and were not seen in mice bearing the R493X Grn mutation found in FTD [45].

In contrast to the absence of any change in GCase activity, the clear and significant increase in GALC activity in frontal white matter of FTD-GRN cases aligns with our observation of significantly reduced sulfatide and Hex1Cer levels in the same samples. GALC activity in frontal white matter of FTD-C9orf72 cases was lower than FTD-GRN but higher than the control cases (not significant), in agreement with the lipidomic results. Increased GALC (b-galactosidase) activity was also seen in frontal cortex of Grn-/- mice [44], and GALC RNA levels are higher in motor cortex of ALS cases compared to age-matched controls [65]. Overall, decreased sphingolipids in FTD-GRN cases, together with increased levels of the sphingolipid catabolic intermediate sphingosine in parietal white matter, support the concept that GRN mutations disrupt brain sphingolipid metabolism. Future studies with cell culture models will be necessary to resolve whether GRN haploinsufficiency causes a block in lysosomal catabolism that leads to accumulation of cholesterol esters, sphingosine, and acylcarnitines; or whether these features are biomarkers of accelerated myelin break-down, as indicated by the increased GALC activity in frontal white matter.

Our lipidomic results with FTD cases are in broad agreement with a recent paper reporting decreased SM, ceramide, and some phospholipids, and increased cholesterol esters and triglycerides, in motor cortex white matter of ALS cases [65]. Decreased myelin-enriched sphingolipids (GalCer, ST, SM) are also observed in motor cortex of people with multiple system atrophy [66], which is characterised by a-synuclein aggregates in oligodendrocytes. In contrast, the more common synucleinopathy Parkinson’s disease is characterised by increased BMP in the heavily-affected substantia nigra [67], and increased diacylglycerol in frontal cortex [68]. In Alzheimer’s disease (AD), marked depletion of myelin sphingolipids and myelin proteins was seen in superior frontal grey matter, but not frontal white matter [69, 70]. Given that both AD and bvFTD affect the superior frontal lobe, it is interesting that the pattern of myelin loss differs between AD and bvFTD, with a much more pronounced effect on the frontal white matter seen in the familial bvFTD cases examined herein. Accordingly, the burden of white matter hyperintensities is higher in bvFTD than AD and is thought to contribute substantially to cognitive deficits [71, 72].

A limitation of our study was the absence of sporadic FTD cases. It will be important in future studies to determine whether the lipidomic signature and pronounced myelin loss in FTD-GRN cases is shared with a subset of sporadic FTD cases with TDP-43 inclusions. This seems likely, since (i) MRI studies have demonstrated loss of white matter integrity in sporadic bvFTD [72, 73] and (ii) rare variants in genes whose loss of function is associated with the severe inherited leukodystrophies hypomyelinating leukodystrophy (TMEM106B gene), Nasu-Hakola disease (TREM2), metachromatic leukodystrophy (ARSA), and cerebrotendinous xanthomatosis (CYP27A1), are also known to cause FTD with TDP-43 deposition [74].

In conclusion, this study presents the first evidence of severe myelin lipid loss in FTD-GRN and FTD-C9orf72. More severe white matter lipid and myelin protein loss in FTD-GRN, together with marked accumulation of cholesterol esters in white matter and increased GALC activity, imply a pronounced susceptibility for myelin lipid loss, leading to white matter attrition, in GRN mutation carriers. These results are consistent with a requirement for progranulin in restricting myelin lipid catabolism. In fact, our data shows that FTD-GRN displays features of metabolic leukodystrophies, including myelin loss, gliosis, and cholesterol ester storage [50]. MRI studies underscore the importance of myelin attrition in the behavioural deficits that define bvFTD [71, 72], and our data provides biochemical evidence underpinning the use of myelin MRI as a diagnostic and prognostic tool in FTD management. Since myelin is essential for neuronal health and neurological functions, accelerated myelin loss may be a key driver of neurodegeneration caused by progranulin haploinsufficiency.

Data Availability

The complete lipidomic dataset is included as Supplementary Data File 1 and available at Metabolomics Workbench [75], study ST002452, DOI: All other raw data is available from the corresponding author upon reasonable request.





Alzheimer’s disease


Amyotrophic Lateral Sclerosis






Bovine Serum Albumin


Behavioural Variant FTD


Chromosome 9 open reading frame 72






Cholesterol Ester




2’,3’-Cyclic Nucleotide 3’-Phosphodiesterase




Diamidino-2-Phenylindole Dihydrochloride


Frontotemporal Dementia












Luxol Fast Blue


Lysophosphatidic acid
















Myelin Basic Protein


Magnetic Resonance Imaging


Methyl-Tert-Butyl Ether


Neuronal Ceroid Lipofuscinosis








Alkenyl-PE(PE plasmalogen)






Myelin Proteolipid Protein


Partial Least Squares-Discriminant Analysis


Post-Mortem Interval












Tris Buffered Saline, 0.1% Tween 20


TAR DNA-binding protein 43


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Brain tissue was provided by Sydney Brain Bank, which is supported by Neuroscience Research Australia, and the NSW Brain Tissue Resource Centre, University of Sydney, which is supported by award R28AA012725 from the National Institute of Alcohol Abuse and Alcoholism, National Institutes of Health, USA. We would like to thank Heather McCann from the Sydney Brain Bank for TDP-43 scoring, and gratefully acknowledge subsidised access to the Sydney Mass Spectrometry and Sydney Microscopy and Microanalysis core facilities.


This research was supported by Project grant APP1163249 (J.B.K. and A.S.D.) and Ideas grant APP1100626 (A.S.D.) from the National Health and Medical Research Council of Australia. O.C.M., H.S. and J.Y.L. are supported by Australian government Research Training Program scholarships. G.M.H. is supported by an NHMRC Senior Leadership Fellowship (1176607).

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OCM performed experiments, analysed data, and wrote the manuscript.

JDT and HS performed experiments.

JYL analysed data.

JBK obtained funding and performed genotyping.

RLR and GH contributed to study design, case ascertainment, and editing of the manuscript.

ASD conceived and planned the study, obtained funding and ethics approval, and wrote the manuscript.

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Correspondence to Anthony S. Don.

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This research project was carried out under University of Sydney Human Research Ethics Committee approval (#2019/750). Since the research used post-mortem brain bank tissue samples obtained from the Sydney Brain Bank and NSW Brain Tissue Resource Centre, consent to participate is not required.

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Supplementary Data File 1

Supplementary Table 1

. Lipid Class Totals (nmoles/mg protein) in frontal white matter and one-way ANOVA results. BH FDR: Benjamini-Hochberg false discovery rate-corrected p value (q value). P values for Tukey’s post-test are also given. Supplementary Table 2. Lipid Class Totals (nmoles/mg protein) in frontal grey matter and one-way ANOVA results. BH FDR: Benjamini-Hochberg false discovery rate-corrected p value (q value). P values for Tukey’s post-test are also given. Supplementary Table 3. Lipid Class Totals (nmoles/mg protein) in parietal white matter and one-way ANOVA results. BH FDR: Benjamini-Hochberg false discovery rate-corrected p value (q value). P values for Tukey’s post-test are also given. Supplementary Table 4. Lipid Class Totals (nmoles/mg protein) in parietal grey matter and one-way ANOVA results. BH FDR: Benjamini-Hochberg false discovery rate-corrected p value (q value). P values for Tukey’s post-test are also given.

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Marian, O.C., Teo, J.D., Lee, J.Y. et al. Disrupted myelin lipid metabolism differentiates frontotemporal dementia caused by GRN and C9orf72 gene mutations. acta neuropathol commun 11, 52 (2023).

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