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Efficacy and neural mechanism of acupuncture treatment in older adults with subjective cognitive decline: study protocol for a randomised controlled clinical trial
  1. Chao-Qun Yan1,2,
  2. Ping Zhou1,
  3. Xu Wang3,
  4. Jian Feng Tu1,
  5. Shang-Qing Hu1,
  6. Jian-Wei Huo4,
  7. Zhong-Yan Wang4,
  8. Guang-Xia Shi1,
  9. Ya-Nan Zhang4,
  10. Jun-Qiu Li4,
  11. Jun Wang2,
  12. Cun-Zhi Liu1
  1. 1School of Acupuncture-Moxibustion and Tuina, Beijing University of Chinese Medicine, Beijing, China
  2. 2Department of Acupuncture and moxibustion, Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine, Beijing, China
  3. 3School of Life Sciences, Beijing University of Chinese Medicine, Beijing, China
  4. 4Beijing Hospital of Traditional Chinese Medicine, Capital Medical University, Beijing, China
  1. Correspondence to Professor Cun-Zhi Liu; lcz_tg{at}126.com

Abstract

Introduction Subjective cognitive decline (SCD) refers to individuals’ perceived decline in memory and/or other cognitive abilities relative to their previous level of performance, while objective neuropsychological deficits are not observed. SCD may represent a preclinical phase of Alzheimer’s disease. At this very early stage of decline, intervention could slow the rate of incipient decline to prolong and preserve cognitive and functional abilities. However, there is no effective treatment recommended for individuals with SCD. Acupuncture, as a non-pharmacological intervention, has been widely employed for patients with cognitive disorders.

Methods and analysis The proposed study is a randomised, assessor-blinded and placebo-controlled study that investigates the efficacy and mechanism of acupuncture in SCD. Sixty patients with SCD will be randomly allocated either into an acupuncture group or a sham acupuncture group. They will receive 24 sessions of real acupuncture treatment or identical treatment sessions using a placebo needle. Global cognitive changes based on a multidomain neuropsychological test battery will be evaluated to detect the clinical efficacy of acupuncture treatment at baseline and end of treatment. MRI scans will be used to explore acupuncture-related neuroplasticity changes. Correlation analyses will be performed to investigate the relationships between the changes in brain function and symptom improvement.

Ethics and dissemination The trial was approved by the research ethics committee. The results of the study will be published in a peer-reviewed academic journal and will also be disseminated electronically through conference presentations.

Trial registration number NCT03444896.

  • Subjective cognitive decline
  • Dementia
  • Acupuncture
  • Sham acupuncture
  • Magnetic Resonance Imaging
  • Clinical trial

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Strengths and limitations of this study

  • Compared with the neuropsychological tests alone as efficacy evaluations, the combination with in vivo measures of brain alterations in this study will be more sensitive in detecting acupuncture efficacy.

  • This study will first uncover the efficacy and neural mechanism of acupuncture treatment in older adults with subjective cognitive decline.

  • A multidomain neuropsychological test battery will be employed, which can assess multiple cognitive domains including executive function, attention, visuospatial function and language.

  • Sham needles and adhesive pads will be used for better patient blinding.

  • A potential limitation is that not a large sample size will be performed in this study.

Introduction

Dementia is the greatest global challenge for health and social care in the 21st century.1 Globally, about 47 million people were living with dementia in 2015, and this number is projected to triple by 2050, based on the World Alzheimer Report (2015). Alzheimer’s disease (AD) is the most common form of dementia.2 Currently, there is no effective cure for AD, and the available treatments have only moderately alleviated the symptoms.3 Therefore, prevention is essential to reduce the dementia epidemic.4 5 The long ‘preclinical’ phase of AD provides an opportunity for individuals to participate in treatment trials to delay or prevent cognitive decline.6–8

Subjective cognitive decline (SCD) usually occurs in older adults, and it refers to the self-perception of cognitive decline, when individuals perform cognitive tests within normal limits and have preserved activities of daily living.9 A review demonstrated that the prevalence of these complaints in persons aged 65 years or more varied from 25% to 50%.10 Actually, many older adults claim cognitive decline might be regarded as hypochondriacs by professional healthy carers. However, several lines of evidence from longitudinal ageing studies suggest that older adults with SCD are more likely to present AD biomarkers than their healthy peers. About 60% of SCD individuals will decline to mild cognitive impairment (MCI) and AD over a 15-year period.11 12 People with SCD have more brain abnormalities such as hippocampal volume loss and hypometabolism compared with healthy controls.13 Moreover, cerebrospinal amyloid β is strongly predictive of subsequent clinical progression in patients with SCD.14 This suggests that, for some older adults, SCD may represent a preclinical phase of AD.

There is still much plasticity in SCD. The patients in this stage may not progress to dementia or even revert to no cognitive impairment after effective treatment. Development of safe and effective interventions in early AD stages is important. Specific criteria to define SCD have been published,9 15 but clinical trials in SCD are in their infancy, and no pharmacological treatment or intervention is currently recommended for individuals with SCD. Despite these difficulties, the development of new treatments should be encouraged.16

The accumulated evidence suggests that non-pharmacological intervention may benefit cognitive function in older adults with SCD.17 Acupuncture, as a non-pharmacological intervention, has been widely used for patients with cognitive disorders. The WHO reports that acupuncture treatment can be beneficial for vascular dementia. A number of clinical studies have provided evidence that acupuncture is beneficial for the treatment of dementia or MCI.18 A systematic review supports the use of acupuncture for MCI.19 Animal studies showed that acupuncture elicits its effects by mediation of neural plasticity in pathological conditions.20 However, the efficacy of acupuncture in patients with SCD has not be investigated. An experimental study is needed to test this hypothesis.

By definition, individuals with SCD are within the normal range on clinical-neuropsychological tests. It will be difficult to detect response in this population compared with people who already have clinically manifested impairment (eg, MCI) due to a ceiling effect. As such, neuropsychological tests in conjunction with in vivo measures of brain function such as electroencephalography, or functional MRI (fMRI), may be a more sensitive alternative to neuropsychological tests.21–23 Brain alterations are subtle but measurable to identify individuals at risk for AD well before cognitive symptoms are manifested by using fMRI, allowing researchers to use neuroimaging to ascertain response after intervention sensitivity.24 For better ascertaining the clinical response and unveiling the mechanism, brain alterations measured by fMRI could also be used to evaluate the efficacy of acupuncture.

Objectives

This study is a randomised controlled functional brain imaging trial with 12 weeks of treatment, aiming at: (1) evaluating the effects of acupuncture treatment on cognitive function in older adults with SCD; (2) exploring the central mechanism of the long-lasting effect of acupuncture on SCD; and (3) investigating the safety of acupuncture treatment on SCD.

Methods

Design

The Consolidated Standards of Reporting Trials (CONSORT) statement for non-pharmacological interventions has been used as a framework for development of the methodology for this project.25 26

This trial is a 1:1 randomised single-blinded and placebo-controlled study with two parallel groups involving elderly adults. The study is designed to examine the effect and neural mechanism of acupuncture treatment on cognitive function before and after a 12-week intervention period. As shown in figure 1, the cognitive assessments and MRI scans will be performed at baseline and immediately after the completion of the intervention.

Participants

The study will mainly take place in Dongcheng, Fengtai and Shunyi districts in Beijing. People with SCD will be recruited from community-dwelling population in those districts. In order to have better insight into the trial for community residents, science popularisation lectures about dementia and advertisement of the trial will be given in community service centres. The brochures and posters will also be distributed. Besides, advertisement of the trial will be shared in the official account on WeChat (China’s most popular social media platform) of the Beijing Hospital of Traditional Chinese Medicine Affiliated to Capital Medical University and health website (www.39.net) or local newspaper for recruiting participants. Interested individuals will be screened in the clinic, community service centres or by phone using the inclusion/exclusion criteria. All those who meet the inclusion criteria will receive a study information sheet including the design, procedure, benefits and risks of the study. Before the study procedure started, the subjects will have to provide signed written informed consent forms. The diagnosis of SCD will be based on the published SCD research criteria proposed by the Subjective Cognitive Decline Initiative.9 In this study, the patients who answer ‘yes’ to the question ‘Do you have problem in memory?’ in the initial screening by phone or face-to-face interviews will be selected to the next step. Besides, the Subjective Cognitive Decline Questionnaire 9 (SCD-Q9) is further used for SCD screening. Only the patients with the SCD-Q9 score more than 5.0 will pass the screening.

Inclusion criteria

  • Male and female adults aged 55–75.

  • Native Chinese speakers who are right handed and have at least a primary school education.

  • Self-reported persistent memory decline compared with a previous normal status within the last 5 years, which is confirmed by caregivers.

  • Normal age and education-adjusted performance on neuropsychological test including the Chinese version of Mini-Mental State Examination,27 the Auditory Verbal Learning Test (AVLT; the short-term delayed free recall, the long-term delayed free recall and the recognition test),28 Trail Making Test (TMT)29 and Animal Fluency Test (AFT).30

  • No or minimal impairment in activities of daily living.

Exclusion criteria

  • Presence of a positive neurological history (eg, traumatic brain injury, stroke, Parkinson’s disease, multiple sclerosis).

  • Treatments that would affect cognitive function (eg, treatment for an acute psychiatric episode, therapy with memantine, rivastigmine and donepezil).

  • Presence of significant psychiatric history (eg, bipolar disorder, schizophrenia) and/or severe anxiety and depression.

  • Presence of serious heart, kidney, liver, gastrointestinal, infectious, endocrine disease or cancer.

  • History of alcohol or drug abuse/addiction.

  • Any contraindications for MRI scans (eg, aneurysm clip pacemaker).

  • Significant visual and/or auditory impairment uncorrected by aids, and unable to perform neuropsychological evaluations.

  • Currently enrolled in another research study.

  • Received acupuncture treatment in the preceding month.

During the trial period, patients with SCD who meet the following criteria will be excluded from the study:

  • Taking medication or receiving additional treatment that is expected to affect the cognitive function (eg, tranquillisers, antianxiolytics, hypnotics, nootropics and cholinomimetic agents).

  • Withdrawal of consent for study participation because the patient does not wish to continue.

  • Missing more than 5 of 24 acupuncture treatment sessions.

  • Occurrence of a serious adverse event that the doctors consider the treatment should be termination.

  • Critical protocol violation such as violation of eligibility criteria.

Intervention

Patients will receive 24 acupuncture treatment sessions over 12 weeks (twice a week). Hwato brand single-use acupuncture needles (size 0.35×25 mm or 0.35×40 mm), pragmatic placebo needles (size 0.30×25 mm) and SDZ-V electroacupuncture apparatuses will be used.

For the acupuncture group (figure 2), acupuncture needles will be placed at acupoints Baihui (DU20), Shengting (DU24), Fengfu (DU16), Fengchi (GB20), Danzhong (RN17), Zhongwan (RN12), Qihai (RN6), Neiguan (PC6), Tongli (HT5), Xuehai (SP10), Zusanli (ST36), Zhaohai (KI6), Xinshu (BL15) and Yixi (BL45). After skin disinfection in patients in the supine position, the adhesive pads are pasted on the acupoints surface except for Baihui (DU20) and Shengting (DU24). Then, the acupuncture needles will be inserted through the adhesive pads into the skin depending on the location of the needle. The locations are shown in table 1. Manual acupuncture by acupuncturists using small, equal manipulations of twirling, lifting and thrusting will be performed on all needles to reach deqi. The patients will feel the deqi sensation, such as soreness, numbness, distention, heaviness and other sensations. Paired electrodes from the electroacupuncture apparatus will be attached to the needle holders of the DU20 and DU24. A dilatational wave of 2–100 Hz and a current intensity of 1–5 mA will be performed according to the degree of needle handle shivering, ignoring the patients’ feelings. The needles will be extracted after 20 min for each treatment. The acupoints of DU16, BL15 and BL45 will achieve deqi in patients in a sitting position without retaining the needle.

Table 1

Location of acupoints used in the acupuncture group

Figure 2

Location of acupoints or sham acupoints in the trial. BL15, Xinshu; BL45, Yixi; DU16, Fengfu; DU20, Baihui; DU24, Shengting; GB20, Fengchi; HT5, Tongli; KI6, Zhaohai; PC6, Neiguan; RN6, Qihai; RN12, Zhongwan; RN17, Danzhong; SA, sham acupoint; SP10, Xuehai; ST36, Zusanli.

For the sham acupuncture group, sham acupoints at locations away from known acupuncture points will be used to minimise physiological effects, and the locations of sham acupoints are shown in table 2. Patients will receive non-insertive acupuncture using the pragmatic placebo needles (Hwato brand, size 0.35×25 mm; online supplementary figure 1). Similar to the acupuncture group, the adhesive pads are initially pasted on the sham acupoints surface except for sham acupoint 1. The pragmatic placebo needles with a blunt tip will be placed on the adhesive pads. In order to minimise the physiological effect, acupuncturists will be instructed to lightly place the sham needles with a blunt tip on the adhesive pads with no manipulation. The acupuncture needle will be inserted to a shallow depth at the sham acupoint 1, which does not penetrate below the skin, and needle manipulation for deqi. Sham acupoint 11 and sham acupoint 12 will be inserted with sham needles without retaining the needle. Paired electrodes will be attached to the needle holders of the bilateral sham acupoint 2 but with no electricity output.

Table 2

Location of sham acupoints used in the sham acupuncture group

MRI protocol

Patients will undergo brain MRI at baseline and after treatments. The MRI scan will be performed with a 3.0 Tesla superconductor (Skyra, Siemens, Erlangen, Germany) in the Beijing Hospital of Traditional Chinese Medicine Affiliated to Capital Medical University. The parameters of sequences employed in this study are provided by China Association of Brain Imaging (www.abimaging.org). Sagittal structural images will be acquired using a magnetisation prepared rapid gradient-echo three-dimensional (3D) T1-weighted sequence with the following parameters: repetition time (TR)/echo time (TE)=2530/2.98 ms, flip angle=7°, inversion time=1100 ms, matrix=256×256, 1 mm slice thickness without slice gap. T2*-weighted functional images will be collected using a gradient-echo echo-planar imaging (EPI) sequence with the following parameters: TR=3200 ms, TE=407 ms, flip angle=120°.

Resting state fMRI and task fMRI will be performed using an EPI sequence with the following parameters: TR/TE=2000/30 ms, flip angle=90°, matrix=64×64, slice thickness=3.5 mm with 1 mm slice gap. Diffusion tensor imaging (DTI) will use a double spin-echo EPI sequence (TR/TE=12 000/77 ms, flip angle=90°, volume interval=12, 2 mm thick axial slices). Arterial spin labelling (ASL) imaging of the whole brain is performed by use of a 3D pseudocontinuous ASL sequence (TR/TE=5000/15.92 ms, flip angle=180°, slice thickness=3.5 mm; labelling duration, number of slices=40).

All scans will be reviewed qualitatively by two radiologists to screen for possible brain lesions or structural abnormalities. DTI images will be analysed using the PANDA package.31 fMRI data were collected during the memory task and at rest. ASL data will be performed with the resting state fMRI (DPARSF) toolbox and SPM8 (http://www.fil.ion.ucl.ac.uk/spm/software/spm8) for MATLAB. Brain activation, connectivity changes and cerebral blood flow will be compared between the two groups before and after treatment.

Outcome measures

Clinical outcome assessments

Global cognitive function based on a composite score will be used to evaluate the clinical efficacy of acupuncture treatment at baseline, and at the end of the 12-week treatment period. It will be computed by averaging z scores from a multidomain neuropsychological test battery that includes eight tests. AFT assesses the language and executive function by examining categorical verbal fluency.30 TMT part A and B examines graphomotor speed, attention and executive function.32 Digit Symbol Substitution Test is used to assess processing speed, attention and concentration.33 Clock Drawing Test can assess multiple cognitive functions, including verbal understanding, memory, abstract thinking and executive functions.34 Digit Span Test is used to measure working memory’s number storage capacity. Stroop Color and Word Test is a classic instrument for the assessment of selective attention, cognitive flexibility, cognitive inhibition and information processing speed.35 AVLT is a powerful neuropsychological test that assesses episodic memory.36 37

All patients will fill out an SCD-Q38 to assess their degree of SCD. The Face Recognition Questionnaire and the Santa Barbara Sense of Direction Scale39 will be used to measure the ability for facial recognition and direction. Depressive symptoms and sleep quality will be measured by Geriatric Depression Scale and Pittsburgh Sleep Quality Index.40

Neuroplasticity assessments

In this study, neuroplasticity changes between the two groups will be measured by fMRI. Before the acupuncture treatment, patients will complete the fMRI scan within 3 days. They will also have the follow-up fMRI scan within 3 days after the completion of their intervention (figure 3). Brain activity and functional connectivity will be assessed under a resting state and a memory task. Group difference on cerebral blood flow and white matter integrity will be assessed by means of ASL or DTI.

Figure 3

MRI experimental paradigm and an illustrative diagram of the memory task. ASL, arterial spin labelling; DTI, diffusion tensor imaging.

Memory task

The patients will be trained before entering the fMRI scanner. They will complete a practice version of the memory task paradigm in computer. This practice mock test will show the correct number, and they need to perform the tasks with an accuracy criterion of 80% to ensure that the patients understand how to do the memory task in the scanner. A blocked periodic design that incorporated alternating 1-back and 2-back tasks will be used. Patients will view facial pictures, scene pictures or single digits (0–9, black on a white background). In the 1-back task, the patients are required to press a button when a facial picture, scene picture or a digit appears the same as the one before. In the 2-back task, the patients are asked to press a response button if the current facial picture, scene picture or the digit is the same as the one which was presented two trials before. The stimuli consist of 17 blocks for 236 s and are presented on a computer using MATLAB V.8.6 (MathWorks, Natick, MA, USA) for 1 s, with an interstimulus interval of 1 s. Trial types within blocks are presented in pseudorandomised order.

Once in the scanner, anatomical and functional scans will be performed. During the scanning, all patients are asked to lie quietly in the scanner with their eyes open, trying to avoid thinking systematically, and moving as little as possible. In resting state fMRI scanning, the patients are instructed to view centrally placed fixation cross (+), and try to not think of anything. Two memory task runs will be conducted after T1 and resting state scans.

Apolipoprotein E genotyping

A TIANamp Blood DNA Kit (Tiangen Biotech, Beijing, China) will be used to isolate high-molecular-weight DNA. The genotype of apolipoprotein E (APOE) will be detected by APOE Gene Detection Kit (Wuhan YZY Biopharma, Wuhan, China) with E2 and E4 reaction liquid. Genomic DNA and reaction liquid will be placed on a 7500 HT Fast Real-Time PCR (Applied Biosystems, Foster City, USA) with the following conditions: uracil-N-glycosylase treatment at 37°C for 10 min, denaturation at 95°C for 5 min, followed by 40 cycles at 95°C for 15 s and annealing at 60°C for 60 s (acquiring the fluorescence signal in this step). According to the amplification plot, the genotype of APOE will be determined.

Safety and monitoring

Treatment-related adverse events, including haematoma, bleeding, subcutaneous haemorrhage, serious pain, local infection and fatigue, will be compared among patients in the acupuncture group and the sham acupuncture group, and will be documented at each treatment session. In order to ensure consistency, the neuropsychological tests and other assessment scales will be performed by the same researcher at baseline and the end of treatment. A professional staff will check the imaging data for quality and protocol conformity after each scanning session. Patients will undergo blood routine test and blood biochemical tests including blood glucose, homocysteine, total cholesterol, and so on, before randomisation and at the end of treatment.

Sample size and blinding

Task fMRI studies characteristically include small sample size41 and thus have a low statistical power. The statistically underpowered study by definition means that a study will have less of a chance for detecting significant effects.42 Therefore, power-based sample size will be calculated prior to fMRI data collection.43 Fortunately, approaches for sample size calculations in studies using fMRI have been developed.

By using the non-central random field theory, Hayasaka et al estimated that at least 12 subjects would be required to detect signals in either of the auditory cortices with at least 80% power.44 They also found that approximately 13 subjects would be required to detect signals in the auditory cortices with 80% power, when generated a sample size map based on the mock pilot analysis.44 Adopting a simulation-based method to calculate statistical power for group-level fMRI studies, Desmond and Glover found a minimum of 12 subjects are required to achieve 80% power at α=0.05 at the single voxel level.45 For a more realistic threshold, twice as many subjects are recommended to maintain this level of power after correcting for multiple comparisons. For a stricter alpha of 0.000002, approximately 25 subjects are needed. Mumford and Nichols recommended 20 subjects and a type I error of α=0.005 should probably be used, and this power calculation is based on a non-central T or F distribution.46 We used the largest sample size of 25 for each group with an estimated dropout rate and loss of data due to head motion, then we planned to enrol 60 participants in the two groups.

Eligible patients will be randomly assigned into either the acupuncture or sham acupuncture group after signing written informed consent forms via a randomisation digital table with a 1:1 ratio. Blocked randomisation with a block size of 6 will be employed to ensure balance within the two groups. The randomisation sequence will be generated by a third-party professional statistician using computer-generated randomisation digital table by using SAS V.9.2 (SAS Institute). The randomisation list will be stored by a non-involved investigator and out of reach and sight of the involved investigators. The allocation schedule will be using a telephone randomisation procedure. The randomisation list was restricted to this research coordinator and was concealed from other study personnel. The patients, outcome assessors and statisticians will be blinded to treatment allocation. Patients are told that they will receive one of two effective interventions randomised after enrolment. During the acupuncture treatment, the adhesive pads are pasted on the acupoints or sham acupoints after skin disinfection. The true or sham needles with a blunt tip will be placed in the adhesive pads. Patients in different groups will be assigned into separate cubicles to refrain from communication.

Data collection and management

At baseline, information of patients about age, sex, education, dominant hand and medical history will be collected (figure 4). For all patients who met the inclusion criteria, the neuropsychological tests will be performed before and after treatment in a quiet room by evaluators, who have been trained by the organisation of Alliance of early AD. All of the MRI scans will be conducted in the same machine, and the operators have been technically trained by a professional engineer from the China Association of Brain Imaging. Blood samples will be collected in the morning and handled by two persons. After each treatment session, adverse events will be recorded in a participant’s diary card by acupuncturists.

Figure 4

Standard Protocol Items: Recommendations for Interventional Trials (SPIRIT) and the schedule of the trial. AFT, Animal Fluency Test; AVLT, Auditory Verbal Learning Test; DSST, Digit Symbol Substitution Test; SBSDS,Santa Barbara Sense of Direction Scale; HAMD, Hamilton Rating Scale forDepression; HAMA, Hamilton Rating Scale for Anxiety; PSQI, Pittsburgh Sleep Quality Index; SCDQ, Subjective Cognitive Decline Questionnaire; SCWT, Stroop Color and Word Test; TMT, Trail Making Test.

A case report form (CRF) will be used to collect the clinical data for each patient, labelled by unique numeric identifier and recorded by a trained graduate student. The data in the CRF will be verified for accuracy, missing data and data consistency by a clinical research associate. Paper-based research data will be entered into an EpiData electronic database. For reducing errors in data entry, data will be entered independently twice by two independent people, and value pairs will then be compared for discordances, followed by resolution of discordances by referral to the original data source. The EpiData will export data in a Microsoft Excel spreadsheet format. The data will be entered in an electronic statistical package SPSS software (SPSS V.12.0 KO for Windows) for ease of statistical analysis.

Statistical analysis

Clinical data analysis

In this study, intent-to-treat analysis and per-protocol analysis will be used. In this study, the intent-to-treat population consisted of all randomised patients who received at least one dose of treatment and had a complete baseline assessment. The per-protocol population defined as all randomised patients who did not discontinue prematurely completed the 12 weeks’ treatment and had MRI scans before and after treatment. Observation of histograms and normal probability plots and a Shapiro-Wilk test will be performed to determine whether the data followed a normal distribution. Distributed data will be described using means, SDs and 95% CIs. Clinical outcome analyses will be done with SPSS software (SPSS V.22.0 KO for Windows), with a significance level of 0.05, and all hypothesis tests are two tailed.

Baseline demographic characteristics between the two groups will be analysed with χ² test or Fisher’s exact test for categorical measures, and with the t-test or Wilcoxon rank-sum test for continuous measures. The clinical outcome of the global cognitive function based on composite scores will be compared between the acupuncture group and the sham acupuncture group. The composite scores will be created by converting all individual cognitive scores to standardised z scores. As previously described,47 we computed z scores by subtracting the baseline group mean and dividing the baseline group SD, and then averaging the standardised z scores across all tests. The general linear model will be used to examine change in cognitive scores. For the other outcomes, if it agreed with normal distribution, an independent t-test will be used. Otherwise, for abnormal distribution, the data will be analysed with Wilcoxon test. The statisticians who analysed the data are blinded to the test settings.

MRI data analysis

For imaging, data will be analysed using DPABI toolkit performing on MATLAB V.8.6 (MathWorks) to detect any changes in brain function due to acupuncture treatment. After data preprocessing, some graph theory-based or data-driven approaches will be performed to investigate neuroplasticity between the two groups, such as regional homogeneity, amplitude of the low-frequency fluctuation and voxel-wise degree centrality. A two-sample t-test will be conducted to investigate the differences in brain regions between the acupuncture group and the sham acupuncture group in the DPARSF software. Multiple comparisons will be used in order to better control for a highly inflated false positivity rate. Pearson’s correlation analysis will be performed to examine the association between the fMRI image data and clinical variables.

Ethics and dissemination

The CONSORT statement and the CONSORT statement for non-pharmacological interventions have been used as a framework for development of the methodology for this project.24 25

If any modifications or decision are made, amendments will be reviewed and approved by the ethics committee, and new protocols would be uploaded to ClinicalTrials.gov. The results of the study will be published in a peer-reviewed academic journal and will also be disseminated electronically through conference presentations.

Patient and public involvement

Currently, this trial is at the recruitment phase with no patient involved in. The participants will be able to view the study results via social media.

Discussion

SCD may be the initial phase of AD, and could serve as a window of opportunity for interventions at an early disease stage.23 This study is planned as a randomised, assessor-blinded, placebo-controlled trial to evaluate the efficacy and central mechanism of acupuncture treatment on SCD compared with a sham acupuncture group. To our knowledge, this trial is also the first study to investigate the effect of acupuncture in patients with SCD.

This study has several strengths. First, we will assess patients with SCD on multiple levels, including multidomain neuropsychological tests, functional brain alterations, cerebrovascular risk factors and APOE genotyping. This multidomain assessment will be used to identify possible biomarkers involved in the effects of acupuncture in SCD.

Second, the neuropsychological assessment in the present study is a multidomain neuropsychological test battery that included eight tests, which can assess multiple cognitive domains including executive functions, attention, visuospatial functioning and language. Memory decline associated with AD risk factors,48 49 and then most instruments were used previously to measure SCD focus on memory.50 However, it might be too restrictive to limit the SCD assessment to memory, in particular for atypical forms of AD.9 51 In this study, multidomain cognitive function will be assessed.

Additionally, functional brain alterations will be used as outcome measures. Compared with the neuropsychological tests alone, the combination of in vivo measures of brain alterations in this study will be more sensitive in detecting acupuncture efficacy. A smaller training effect and ceiling effect may be found when using MRI.52 Furthermore, it can be used as a tool to understand the mechanism of the acupuncture’s effects. fMRI can identify whether neural efficiency is improved or the brain connectome is reorganised to achieve cognitive enhancement.53

A potential limitation is that the patients in this study will be recruited from the community. Considering the research environment, individuals recruited from a memory clinic may have a higher probability of having preclinical AD. They had specific concerns sufficient to prompt a medical visit.15 However, community-based studies have shown some predictive value of SCD for cognitive decline and dementia.10 54 Another potential limitation of our study is that it will not include a large sample size, and this may lead to the need for a future study. The main feature of our study is to systemically investigate and analyse the central mechanisms of acupuncture treatment in patients with SCD. The findings may provide deeper insight into the benefits and mechanisms of acupuncture for patients with SCD.

Trial status

This trial is currently in the recruitment phase.

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View Abstract

Footnotes

  • Contributors CZL and JWH conceived and designed the experiments. PZ, ZYW, SQH, CQY, GXS, JQL and YNZ performed the experiments. XW, JW and JFT analysed the data. CQY, XW and CZL wrote the paper. All authors approved the final manuscript.

  • Funding This work was supported by the National Natural Science Foundation of China (Grant No 81674055) and supported by the Fundamental Research Funds for the Central Universities (2017-JYB-JS-018).

  • Disclaimer We declared the study was only supported by the governmental funding, and the study did not receive funding/assistance from a commercial organisation.

  • Competing interests None declared.

  • Patient consent for publication Not required.

  • Ethics approval Ethics Committee of the Beijing Hospital of Traditional Chinese Medicine Affiliated to Capital Medical University (Ref: 2017BL-061-02).

  • Provenance and peer review Not commissioned; externally peer reviewed.

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