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An MRI-based strategy for differentiation of frontotemporal dementia and Alzheimer’s disease



The differential diagnosis of frontotemporal dementia (FTD) and Alzheimer’s disease (AD) is difficult due to the overlaps of clinical symptoms. Structural magnetic resonance imaging (sMRI) presents distinct brain atrophy and potentially helps in their differentiation. In this study, we aim at deriving a novel integrated index by leveraging the volumetric measures in brain regions with significant difference between AD and FTD and developing an MRI-based strategy for the differentiation of FTD and AD.


In this study, the data were acquired from three different databases, including 47 subjects with FTD, 47 subjects with AD, and 47 normal controls in the NACC database; 50 subjects with AD in the ADNI database; and 50 subjects with FTD in the FTLDNI database. The MR images of all subjects were automatically segmented, and the brain atrophy, including the AD resemblance atrophy index (AD-RAI), was quantified using AccuBrain®. A novel MRI index, named the frontotemporal dementia index (FTDI), was derived as the ratio between the weighted sum of the volumetric indexes in “FTD dominant” structures over that obtained from “AD dominant” structures. The weights and the identification of “FTD/AD dominant” structures were acquired from the statistical analysis of NACC data. The differentiation performance of FTDI was validated using independent data from ADNI and FTLDNI databases.


AD-RAI is a proven imaging biomarker to identify AD and FTD from NC with significantly higher values (p < 0.001 and AUC = 0.88) as we reported before, while no significant difference was found between AD and FTD (p = 0.647). FTDI showed excellent accuracy in identifying FTD from AD (AUC = 0.90; SEN = 89%, SPE = 75% with threshold value = 1.08). The validation using independent data from ADNI and FTLDNI datasets also confirmed the efficacy of FTDI (AUC = 0.93; SEN = 96%, SPE = 70% with threshold value = 1.08).


Brain atrophy in AD, FTD, and normal elderly shows distinct patterns. In addition to AD-RAI that is designed to detect abnormal brain atrophy in dementia, a novel index specific to FTD is proposed and validated. By combining AD-RAI and FTDI, an MRI-based decision strategy was further proposed as a promising solution for the differential diagnosis of AD and FTD in clinical practice.


Frontotemporal dementia (FTD) is one of the main causes of dementia in people under 65, which accounts for nearly 20% of neurodegenerative dementia [1]. Clinical symptoms of FTD overlap with other types of dementia, psychiatric disorders, or Parkinson’s disease. Alzheimer’s disease (AD) is the most common type of dementia and is often difficult to differentiate with FTD, especially in the early stage [2, 3]. Currently, there are no disease-modifying treatments for FTD. Acetylcholinesterase inhibitors widely used in patients with AD could lead to worsening of symptoms in those with FTD [4]. Therefore, accurate diagnosis of FTD and AD may avoid severe consequence in treatment outcome. In addition to clinical practice, the reduction of misdiagnosis is of utility in the differentiation for clinical trials, as well [5].

Structural magnetic resonance imaging (sMRI) is a common non-invasive examination in the diagnosis of dementia. Compared with computed tomography, positron emission tomography, and advanced MRI sequences, sMRI is advantageous in being widely accessible, free of ionizing or nuclear radiation, objective for visualizing brain atrophy, and with good tissue contrast [6]. In clinical practice, neurologists and radiologists use various visual rating scales to evaluate the degree of brain atrophy in MR images [7, 8]. In spite of being convenient to perform, visual rating is highly subjective and dependent on experience which is prone to lead to misdiagnosis and missed diagnosis in practice [9]. Recently, automatic brain segmentation, quantitative analysis, and machine learning have been studied a lot in neurodegenerative diseases [10,11,12,13,14,15,16,17,18]. However, plenty of machine learning-based classification highly rely on limited training data and lack of underlying clinical rationale [19,20,21,22]. Because it is hard for clinicians to understand how and why these artificial intelligence methods made a certain decision, the lack of interpretability limits their applicability in clinical practice [23]. Secondly, most studies were based on samples from a single center and may not be translated to other centers because of the heterogeneity in diagnostic criteria, imaging parameters, and sociodemographic characteristics of patients. Finally, many studies only focus on distinguishing AD from behavioral variant frontotemporal dementia (bvFTD) [24, 25]. But, in fact, due to the presence of either mild or overlapping linguistic deficits, AD with speech impairment can also be confused with the subtypes of FTD, such as primary progressive aphasia (PPA) including semantic variant PPA (svPPA) and non-fluent variant PPA (nfvPPA) [26]. Therefore, it is theoretically desirable and practically meaningful if AD can be differentiated with FTD spectrum disorders.

The primary objective of this study is to investigate the MRI volumetric and atrophic patterns among FTD, AD, and normal controls (NC) collected from multicenter data. Based on these findings, the secondary objective is to derive an atrophy index that is specific to reflect FTD brain atrophy, named FTD index (FTDI). FTDI was an individualized index derived from brain regions with significant volume difference between FTD and AD, which were identified by group-level comparisons, and the differentiation performance of the proposed index was validated using multicenter data from another two databases.

Materials and methods


In this retrospective study, all the subjects were included from the National Alzheimer’s Coordinating Center (NACC), the Alzheimer’s Disease Neuroimaging Initiative (ADNI), and the Frontotemporal Lobar Degeneration Neuroimaging Initiative (FTLDNI) databases (see Additional Material 1). The data are the result of collaborative efforts at three sites in North America.

We first included 47 subjects with FTD (19 bvFTD, 12 svPPA, 2 nfvPPA, and 14 not otherwise specified) from NACC. Then, 47 subjects with probable AD and 47 NC perfectly matching those with FTD (Table 1) in age, educational level, gender, race, and global CDR score (except for NC) using the CDR® Dementia Staging Instrument plus NACC FTLD Behavior & Language Domains [27,28,29] were selected from NACC as well. Subjects were included if their diagnoses were stable (> 1 year) and 3D T1-weighted MRI scans were available ± 6 months of a visit. Scans containing large artifacts were excluded by visual inspection (Fig. 1). After that, as a validation dataset, 50 subjects with AD in the ADNI database and 50 subjects with FTD (20 bvFTD, 10 svPPA, 10 nfvPPA, and 10 not otherwise specified) in the FTLDNI database were included in this study.

Table 1 Demographic characteristics of subjects included
Fig. 1
figure 1

Subject screening from the NACC database

The National Institute of Neurological and Communicative Disorders and Stroke and the AD and Related Disorders Association (NINCDS/ADRDA) criteria [30] and the National Institute on Aging-Alzheimer’s Association (NIA-AA) criteria [31] were applied for the diagnosis of probable AD. The Mckhann et al. and Rascovsky et al. criteria [32, 33] were used for bvFTD, and the Mckhann et al. and Gorno-Tempini et al. criteria [32, 34] for PPA. The inclusion criteria for the NC were normal in general physical status and CDR of 0, suggesting no cognitive impairment.

MRI acquisition and volumetric analysis

MR images from NACC were collected following varying acquisition protocols by different centers, which reflects the real-world scenario. In the ADNI database, the subjects were scanned using 3-T scanners including GE, Philips, or Siemens scanners. For T1-weighted MRI, the inversion recovery-fast spoiled gradient recalled (IR-FSPGR) sequences were used by GE scanners, and magnetization-prepared rapid gradient echo (MP-RAGE) sequences were used by Philips and Siemens scanners. More details concerning the sMRI images are available on the ADNI homepage ( In the FTLDNI database, the subjects were scanned using Siemens TrioTim 3-T scanners at three centers. MP-RAGE sequence was used to acquire T1-weighted MR images [35]. All MRI scans were analyzed using AccuBrain® (BrainNow Medical Technology Limited), a fully automatic neuroanatomical volumetry tool that quantifies brain volumes of various subcortical structures, ventricles, and cortical lobar atrophy within clinically acceptable time. AccuBrain® performs brain structure segmentation based on a multi-atlas image registration scheme. The accuracy of hippocampus segmentation of AccuBrain® was validated using data from the ADNI database [36], and more technical description of AccuBrain® and its comparison with other automatic brain image segmentation schemes were described in our previous work [37,38,39]. Since the main objective of this study is to identify FTD from NC and AD, we focus on the brain regions known to be associated with cognition and behavior, including the brain parenchyma, typical subcortical structures (bilateral hippocampus, amygdala and caudate, etc.), ventricular regions (ventricular system, lateral ventricle, and inferior lateral ventricle), and atrophy of lobar regions (frontal, occipital, temporal, parietal, cingulate, and insular lobe). To correct for the head size difference, we took the relative volume and atrophy as our volumetric brain measures. The relative volume of each region was defined as the absolute volume divided by the total intracranial volume (ICV). The atrophy of a particular lobe was defined as the ratio between the volume of cerebrospinal fluid and brain parenchyma within that lobe. The AD resemblance atrophy index (AD-RAI), representing the similarity of the brain atrophy pattern with AD, was also calculated for each subject in this study. Calculating AD-RAI is a unique function of AccuBrain® and was previously proven to be able to identify AD and estimate the risk of cognitive decline [40, 41].

In addition to AD-RAI, in this study, a novel MRI-based biomarker named FTDI was derived based on the volumetric results of brain regions with significant volume difference between AD and FTD using the NACC data.

To increase the comparability of the numerical metrics, the relative volumes of the involved brain regions and lobe atrophy Ri(j) were normalized to Ri(j), i.e.,

$$ {R}_i^{\prime }(j)=\frac{R_i(j)-\min \left({R}_i\right)}{\max \left({R}_i\right)-\min \left({R}_i\right)} $$

where Ri(j) is the relative volume of the ith volumetric brain measure of the jth subject among all the subjects from NACC included in this study. For the ease of formulation, assume values in the array Ri are arranged so that the first m values are the subjects with FTD and the total number of subjects with FTD and AD is n. The “FTD dominant” structures are the structures with statistically larger Ri values in the FTD group, and the “AD dominant” structures are those with statistically larger Ri values in the AD group. It should be noted that the “FTD/AD dominant” structures did not refer to the abnormal brain regions of FTD/AD patients. They were derived from the group-level comparisons and were the volumetric metrics with the statistically larger values. min(Ri) and max(Ri) represent the minimal and maximal values in the ith volumetric brain measure of all subjects from NACC included in this study, respectively.

As each lobe atrophy contributed uniquely in the differentiation of AD and FTD, a weight wi was calculated for each “FTD dominant” and “AD dominant” structures as the normalized absolute difference of Ri between FTD and AD patients:

$$ {w}_{\boldsymbol{i}}=\frac{\left|\sum \limits_{j=1}^m{R}_i(j)-\sum \limits_{j=m+1}^n{R}_i(j)\right|}{\sum \limits_{j=1}^m{R}_i(j)+\sum \limits_{j=m+1}^n{R}_i(j)} $$

In order to increase the differentiation ability, the FTDI of an individual brain is defined as the ratio between its weighted sum of Ri in the “FTD dominant” structures over that of the “AD dominant” structures.

$$ \mathrm{FTDI}(j)=\frac{\sum \limits_{i=1}^p{w}_i{R}_i^{\prime }(j)}{\sum \limits_{i=p+1}^q{w}_i{R}_i^{\prime }(j)} $$

where i ={1, …, p} are the “FTD dominant” structures and i ={p+1, …, q} are the “AD dominant” structures.

When FTDI was validated using the ADNI and FTLDNI data, the maximum and minimum values from NACC were used in the normalization and any value of Ri ′ (j) below zero would be set to zero.

Visual assessment

All the MRI scans were viewed in the coronal plane and the severity of medial temporal lobe atrophy (MTA) was assessed visually by two experienced neurologists (YRM and YTR) according to a 5-point scale [42]. The single MTA score of each subject was the average score of left and right hemispheres with substantial agreement and high reliability between the two raters (κ =0.75, ICC > 0.9).

Statistical analysis

We compared the demographic characteristics of the three groups (NC, AD, FTD) using ANOVA analysis and chi-square test. Data of volumetric brain measures were not normally distributed and therefore were analyzed statistically with the Friedman M test, and a p value below 0.05 was considered to indicate a significant difference. If significant differences were found, a post hoc analysis would be performed with the Wilcoxon signed-rank test with Bonferroni correction, and a corrected p value below 0.05 was considered to indicate a significant difference. Receiver operating characteristic (ROC) curves were drawn, and the area under the curve (AUC), sensitivity (SEN), and specificity (SPE) were used to verify the diagnostic efficiency of AD-RAI and FTDI. Nonnormally distributed values were described as medians with inter-quartile range. All the statistical analyses were performed with software (SPSS version 25.0, IBM, Armonk, NY).


Demographic and clinical parameters

The characteristics (age, educational level, gender, race, and global CDR score) of subjects from NACC were matched in pairs and the changes among each group showed no significant difference (Table 1). The characteristics of subjects from ADNI and FTLDNI were also displayed (Table 1).

AD-RAI can identify AD and FTD from NC

Compared with the NC group, we found that the AD group showed significant (p < 0.05) atrophy in the brain parenchyma, bilateral hippocampi, temporal lobes, parietal lobes, amygdalae, and left cingulate lobe, and the ventricular system was significantly enlarged (see Additional Table 1). The FTD group showed significant (p < 0.05) atrophy in the brain parenchyma, bilateral frontal lobes, temporal lobes, insular lobes, amygdalae, and left cingulate lobe (see Additional Table 1). These findings are largely consistent with previous studies [43,44,45]. The AD-RAI was significantly different between NC when compared with AD and FTD, respectively (Table 2, Fig. 2a). As we expected, AD-RAI performed well (AUC = 0.88) with 97.9% sensitivity and 73.4% specificity (Fig. 3a). However, when comparing FTD with AD, AD-RAI showed no significant (p = 0.647) difference (Table 2, Fig. 2a).

Table 2 Comparison of AD-RAI and volumetric brain measures among NC, AD, and FTD groups from NACC
Fig. 2
figure 2

Box plots of AD-RAI and volumetric brain measures among NC, AD, and FTD groups from the NACC database. a AD-RAI among NC, AD, and FTD groups. bf Volumetric brain measures which were significantly lower in the FTD group than in AD. gl Volumetric brain measures which were significantly higher in the FTD group than in AD. m, n Relative volumes of bilateral temporal lobes and o QMTA among NC, AD, and FTD groups (*p < 0.05, **p < 0.01, ***p < 0.001)

Fig. 3
figure 3

Diagnostic performance of different indexes. a ROC of AD-RAI using data from the NACC database, AUC = 0.88. b ROC of FTDI using data from the NACC database, AUC = 0.90. c ROC of FTDI using data from ADNI and FTDNI databases, AUC = 0.93. d, e ROC of the single volumetric brain measure which was significantly different between AD and FTD groups

Diagnostic performance of single volumetric brain measure and FTDI

We found that the relative volume of the total hippocampus, left caudate, left frontal lobe, right occipital lobe, bilateral parietal lobes, bilateral insular lobes, and atrophy of bilateral frontal lobes and right occipital lobe were significantly (p < 0.05) different (Table 2, Fig. 2b–l) between AD and FTD groups. However, the temporal lobe, MTA score, and quantitative MTA (QMTA, defined as the ratio between the volumes of the inferior lateral ventricle and hippocampus using AccuBrain and Spearmen correlation of QMTA and MTA score was 0.805 [40]) of AD and FTD all showed significant difference with normal people but no significant difference existed between the two in this study (Table 2, Fig. 2m–o). As previously mentioned, among these structures, those with statistically larger volumetric brain measure in the FTD group were defined as the “FTD dominant” structures and those with statistically larger volumetric brain measure in the AD group were defined as the “AD dominant” structures, and the ratio between the two derived FTDI. When a single volumetric brain measure was used to distinguish FTD from AD in the NACC database, the AUC could only reach 0.63~0.83 (Fig. 3d, e). The parietal lobe, consistent with the previous study [43], provided the highest diagnostic accuracy. When FTDI was used for differential diagnosis of FTD and AD in the NACC database, the AUC could reach 0.90 (Fig. 3b). We chose FTDI > 1.08 as the threshold value according to the optimal Youden Index, which ensures high sensitivity (89.4%) and relatively good specificity (74.5%). When validated in the data from ADNI and FTDNI databases, FTDI performed robustly with 96.0% sensitivity and 70.0% specificity (AUC=0.93, Fig. 3c).


In this study, we developed a novel MRI biomarker for differentiating AD and FTD using their dominant brain volumetric measures derived from statistical analysis of the automated and objective volumetry. The CDR scores of subjects with FTD/AD included from NACC in our study ranged mostly from 0 to 1 (> 93%) and MTA scores using visual rating scale showed no significant difference between the two groups, which means most of them experienced an early stage of AD/FTD and the atrophy patterns of the two may overlap or be too subtle (Fig. 4). Group-level comparisons were firstly applied to find the distinct brain atrophy patterns between FTD and AD (Fig. 5), and FTDI was exactly an individual index derived from those differential volumetric brain measures. By combining with the previously developed AD-RAI, an MRI-based diagnostic strategy was designed (Fig. 6) for the differentiation of FTD and AD. The FTDI model and the threshold value was determined using data from NACC and was validated in a separate cohort of data combined from ADNI and FTDNI databases. The accuracy of AD-RAI in identifying the AD and FTD from NC measured by AUC is 0.88. In this strategy, we set the threshold value of 0.75 with high sensitivity (97.9%) to reduce the rate of missed diagnosis, while maintaining a relatively high specificity (73.4%). When distinguishing FTD from AD, the AUC of FTDI was 0.90, which is comparable and even higher than previous studies [19,20,21,22, 46, 47]. The advantage of FTDI is that it is intuitively interpretable with a clear clinical meaning. Unlike complicated machine learning method or advanced imaging examinations, our work based on sMRI provided a simple logical algorithm and decision strategy to help clinicians understand and use. As the therapeutic strategy needs to be tailored for FTD and AD, the high accuracy in differentiating FTD and AD is more favored. For example, cholinesterase inhibitors effective against AD may aggravate the condition of FTD patients [4]. With this consideration, we chose a threshold value of FTDI of 1.08 with high sensitivity (89.4%) to reduce potential missed diagnosis of FTD. When validated on the independent testing data from ADNI and FTDNI databases, FTDI was proven to be satisfactorily accurate (AUC = 0.93, SEN = 96%). Our research was based on real-world data analysis and hence has high interpretability.

Fig. 4
figure 4

3D T1-weighted MRI scans (classical coronal section) of a FTD with CDR = 0.5, ID NACC204983; b AD with CDR = 0.5, ID NACC162576; c FTD with CDR = 1.0, ID NACC067187; and d AD with CDR = 1.0, ID NACC878860

Fig. 5
figure 5

The distinct brain atrophy patterns between FTD and AD. The red color labeled the brain structures with higher atrophy in FTD including the bilateral frontal lobes, bilateral insular lobes, and left caudate. Likewise, the blue color labeled the brain structures with higher atrophy in AD including the bilateral parietal lobes, right occipital lobe, and total hippocampi

Fig. 6
figure 6

Quantitative evidence-based decision strategy to differentially diagnose AD and FTD from NC

The ideal imaging-assisted diagnosis for clinical use should be objective, economic, simple, and efficient. Therefore, many studies adopted the automatic brain segmentation tool to identify FTD and AD through machine learning. These models need to be trained on a large number of high-quality and uniformly acquired images. Obtaining these images from a population with a low incidence of FTD will be a challenge. In addition, these methods are considered to be the “black box” and difficult for clinicians to understand, so most of them are hard to be adopted in clinical practice. In this study, we acquired enough subjects from three different well-recognized multicenter databases to ensure the robustness of the results that can be translated to the real-world application. Secondly, AccuBrain® is a National Medical Products Administration (NMPA) and CE-marked commercially automated brain segmentation tool that can be readily deployed in the clinic. Thirdly, clinicians without computer expertise can easily apply FTDI to daily clinical practice. Thus, compared with most existing MRI-based FTD classification methods, FTDI has a higher clinical application prospect.

A few studies have attempted to classify the subtypes of FTD based on MRI [20, 46, 47]. The proposed methodology in this study could be further extended into the classification of FTD subtypes. But it is beyond the scope of this study. This study, instead, is focused on a more important clinical problem, which is the differentiation of FTD as a whole with AD. However, different proportion of subtypes of the FTD spectrum disorders may result in a potential patient selection bias. FTDI is a composite index derived from several different volumetric brain measures after weighted. Preliminary validation in this work has proven its good robustness.


This study has several limitations. First of all, pathological diagnosis is not mandatory during subject inclusion, although it may reduce the likelihood of misdiagnosis. However, essentially, there is no recognized in vivo pathological biomarker of FTD [48, 49] and the pathological diagnosis of FTD usually comes from autopsy, which increases the difficulty of acquisition. To ensure adequate sample size, we relied more on the clinical diagnosis as indicated in the database to include the subjects. Another limitation of this study is that it was only tested and validated on three databases. Although inclusion and exclusion criteria of these databases were fairly standard and comparable to those in clinical trials, the CDR status is not reflective of the distribution of analogous patients seen in clinical practice and could bias results. However, the results of this work preliminarily showed the benefits of FTDI and our decision strategy in differentiation of FTD and AD. In addition, this study included 241 subjects in total, which is a relatively modest sample size. Before application to clinical settings, a larger dataset for further test and validation is needed. It can be difficult to collect data and maintain a relatively consistent standard, which may have a significant effect on MRI analysis. Meanwhile, due to the current limited data, the diagnostic efficacy of FTDI is unproven for patients beyond the age range specified in this study.

Although this study has these limitations, it provides a novel algorithm that takes full advantage of the different patterns of brain atrophy in AD and FTD, and it can incorporate more data to make the diagnosis more accurate. Most importantly, through this study, we came up with a method to derive individualized FTDI and provided its threshold value using the data from the NACC database and developed an MRI-based decision strategy, which is obviously more beneficial for clinicians to understand and use than complex machine learning programs.


In this study, the volumetric metrics of structural MRI were investigated in a multicenter cohort of FTD, AD, and NC. These volumetric features and group-level difference were then explored to an FTD atrophy-specific index, named FTDI. Combined with the AD resemblance atrophy index, AD-RAI, we developed a strategy for identifying and differentiating FTD and AD based on MRI-induced volumetric information. Compared with visual rating and machine learning, the proposed strategy is more accurate, objective, and easier to implement.

Availability of data and materials

The datasets used and analyzed during the current study are available from the corresponding author on reasonable request.



Alzheimer’s disease


Frontotemporal dementia


Structural magnetic resonance imaging


Behavioral variant frontotemporal dementia


Primary progressive aphasia


Semantic variant PPA


Non-fluent variant PPA


Normal controls


National Alzheimer’s Coordinating Center


Alzheimer’s Disease Neuroimaging Initiative


Frontotemporal Lobar Degeneration Neuroimaging Initiative


AD resemblance atrophy index


Frontotemporal dementia index


Mild cognitive impairment


Clinical dementia rating


Intracranial volume


Medial temporal atrophy


Interclass correlation coefficient

ROC curve:

Receiver operating characteristic curve


Area under the curve






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We are grateful for the research volunteers, their families, and the investigators at the NACC, ADNI, and FTLDNI databases. The NACC database is funded by National Institutes on Aging/National Institutes of Health (NIA/NIH) Grant U01 AG016976. NACC data are contributed by the NIA-funded ADCs: P30 AG019610 (PI Eric Reiman, MD), P30 AG013846 (PI Neil Kowall, MD), P30 AG062428-01 (PI James Leverenz, MD), P50 AG008702 (PI Scott Small, MD), P50 AG025688 (PI Allan Levey, MD, PhD), P50 AG047266 (PI Todd Golde, MD, PhD), P30 AG010133 (PI Andrew Saykin, PsyD), P50 AG005146 (PI Marilyn Albert, PhD), P30 AG062421-01 (PI Bradley Hyman, MD, PhD), P30 AG062422-01 (PI Ronald Petersen, MD, PhD), P50 AG005138 (PI Mary Sano, PhD), P30 AG008051 (PI Thomas Wisniewski, MD), P30 AG013854 (PI Robert Vassar, PhD), P30 AG008017 (PI Jeffrey Kaye, MD), P30 AG010161 (PI David Bennett, MD), P50 AG047366 (PI Victor Henderson, MD, MS), P30 AG010129 (PI Charles DeCarli, MD), P50 AG016573 (PI Frank LaFerla, PhD), P30 AG062429-01 (PI James Brewer, MD, PhD), P50 AG023501 (PI Bruce Miller, MD), P30 AG035982 (PI Russell Swerdlow, MD), P30 AG028383 (PI Linda Van Eldik, PhD), P30 AG053760 (PI Henry Paulson, MD, PhD), P30 AG010124 (PI John Trojanowski, MD, PhD), P50 AG005133 (PI Oscar Lopez, MD), P50 AG005142 (PI Helena Chui, MD), P30 AG012300 (PI Roger Rosenberg, MD), P30 AG049638 (PI Suzanne Craft, PhD), P50 AG005136 (PI Thomas Grabowski, MD), P30 AG062715-01 (PI Sanjay Asthana, MD, FRCP), P50 AG005681 (PI John Morris, MD), and P50 AG047270 (PI Stephen Strittmatter, MD, PhD).

ADNI data collection and sharing for this project was funded by the NIH Grant U01 AG024904 and DOD ADNI (Department of Defense award number W81XWH-12-2-0012). ADNI is funded by the National Institute on Aging, the National Institute of Biomedical Imaging and Bioengineering, and through generous contributions from the following: AbbVie, Alzheimer’s Association; Alzheimer’s Drug Discovery Foundation; Araclon Biotech; BioClinica, Inc.; Biogen; Bristol-Myers Squibb Company; CereSpir, Inc.; Cogstate; Eisai Inc.; Elan Pharmaceuticals, Inc.; Eli Lilly and Company; EuroImmun; F. Hoffmann-La Roche Ltd. and its affiliated company Genentech, Inc.; Fujirebio; GE Healthcare; IXICO Ltd.; Janssen Alzheimer Immunotherapy Research & Development, LLC.; Johnson & Johnson Pharmaceutical Research & Development LLC.; Lumosity; Lundbeck; Merck & Co., Inc.; Meso Scale Diagnostics, LLC.; NeuroRx Research; Neurotrack Technologies; Novartis Pharmaceuticals Corporation; Pfizer Inc.; Piramal Imaging; Servier; Takeda Pharmaceutical Company; and Transition Therapeutics. The Canadian Institutes of Health Research is providing funds to support ADNI clinical sites in Canada. Private sector contributions are facilitated by the Foundation for the National Institutes of Health ( The grantee organization is the Northern California Institute for Research and Education, and the study is coordinated by the Alzheimer’s Therapeutic Research Institute at the University of Southern California. ADNI data are disseminated by the Laboratory for Neuro Imaging at the University of Southern California.

FTLDNI data collection and sharing for this project was funded by the NIH Grant R01 AG032306. The study is coordinated through the University of California, San Francisco, Memory and Aging Center. FTLDNI data are disseminated by the Laboratory for Neuro Imaging at the University of Southern California.

Partial data used in the preparation of this article were obtained from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) database ( As such, the investigators within the ADNI contributed to the design and implementation of ADNI and/or provided data but did not participate in the analysis or writing of this report. A complete listing of ADNI investigators can be found at

Partial data used in the preparation of this article were obtained from the Frontotemporal Lobar Degeneration Neuroimaging Initiative (FTLDNI) database. The investigators at NIFD/FTLDNI contributed to the design and implementation of FTLDNI and/or provided data, but did not participate in the analysis or writing of this report (unless otherwise listed). The FTLDNI investigators included the following individuals:

Howard Rosen; University of California, San Francisco (PI)

Bradford C. Dickerson; Harvard Medical School and Massachusetts General Hospital

Kimoko Domoto-Reilly; University of Washington School of Medicine

David Knopman; Mayo Clinic, Rochester

Bradley F. Boeve; Mayo Clinic Rochester

Adam L. Boxer; University of California, San Francisco

John Kornak; University of California, San Francisco

Bruce L. Miller; University of California, San Francisco

William W. Seeley; University of California, San Francisco

Maria-Luisa Gorno-Tempini; University of California, San Francisco

Scott McGinnis; University of California, San Francisco

Maria Luisa Mandelli; University of California, San Francisco


This study was funded by the National Natural Science Foundation of China (grant numbers 81870836, 81872261) and the Natural Science Foundation of Guangdong Province (grant number 2020A1515010210). The funding body had no role in the design of the study and collection, analysis, interpretation of data, and writing of the manuscript.

Author information

Authors and Affiliations




QY designed the study, sorted the data, did the statistical analysis, and drafted and revised the manuscript. YRM and YTR scored MTA, interpreted the data, prepared all the figures and tables, and drafted and revised the manuscript. YSL, LZ, WLF, ZYC, YL, and WL sorted and inspected the data and revised the manuscript. SHX, VCM, LS, and JL interpreted the data and revised the manuscript. All authors contributed to the writing and revisions of the paper and approved the final version. Data used in this study were obtained from the NACC, ADNI, and FTLDNI. The investigators within the three provided data but were uninvolved in the data analysis or drafting of this manuscript.

Corresponding authors

Correspondence to Lin Shi or Jun Liu.

Ethics declarations

Ethics approval and consent to participate

This study was approved by the institutional review boards of all participating institutions, and written informed consent was obtained from all participants or their guardians according to the Declaration of Helsinki. A complete listing of ADNI investigators and institutions can be found online (

Consent for publication

Not applicable.

Competing interests

LS is the director of BrainNow Medical Technology Limited. VCM is the chief medical consultant of BrainNow Medical Technology Limited. YSL and LZ are now employed by BrainNow Medical Technology Limited. All other authors report no financial relationships with commercial interests.

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Supplementary Information

Additional file 1: Additional Material 1.

Brief introduction of the databases where data were collected.

Additional file 2: Additional Table 1.

Comparison of all the volumetric brain measures among NC, AD and FTD group from NACC. The comparison was performed with Friedman M test and a post hoc analysis with Wilcoxon signed-rank test with Bonferroni correction. P value would be highlighted in bold when it was below 0.05 and would not be shown if difference was not significant among the three groups. The median with inter-quartile range of AD-RAI and the volumetric brain measures in all three groups were provided. L, left; R, right.

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Yu, Q., Mai, Y., Ruan, Y. et al. An MRI-based strategy for differentiation of frontotemporal dementia and Alzheimer’s disease. Alz Res Therapy 13, 23 (2021).

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  • Frontotemporal dementia
  • Alzheimer’s disease
  • Structural magnetic resonance imaging
  • AD resemblance atrophy index
  • Frontotemporal dementia index