Movatterモバイル変換


[0]ホーム

URL:


CN101972148A - Disturbance elimination method of near infrared brain function detection based on empirical mode decomposition - Google Patents

Disturbance elimination method of near infrared brain function detection based on empirical mode decomposition
Download PDF

Info

Publication number
CN101972148A
CN101972148ACN 201010551128CN201010551128ACN101972148ACN 101972148 ACN101972148 ACN 101972148ACN 201010551128CN201010551128CN 201010551128CN 201010551128 ACN201010551128 ACN 201010551128ACN 101972148 ACN101972148 ACN 101972148A
Authority
CN
China
Prior art keywords
lambda
time series
hbo
epsiv
mode decomposition
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN 201010551128
Other languages
Chinese (zh)
Other versions
CN101972148B (en
Inventor
孙金玮
张岩
彼得·罗弗
刘丹
李清连
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Harbin Institute of Technology Shenzhen
Original Assignee
Harbin Institute of Technology Shenzhen
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Harbin Institute of Technology ShenzhenfiledCriticalHarbin Institute of Technology Shenzhen
Priority to CN2010105511289ApriorityCriticalpatent/CN101972148B/en
Publication of CN101972148ApublicationCriticalpatent/CN101972148A/en
Application grantedgrantedCritical
Publication of CN101972148BpublicationCriticalpatent/CN101972148B/en
Expired - Fee Relatedlegal-statusCriticalCurrent
Anticipated expirationlegal-statusCritical

Links

Images

Landscapes

Abstract

Translated fromChinese

基于经验模态分解的近红外脑功能检测的扰动消除方法,属于光学领域,本发明为解决采用低通滤波无法全面有效去除脑功能检测时生理扰动;采用自适应滤波技术存在需要借助额外的设备、结构复杂的问题。本发明方法包括以下步骤:一、在待测脑组织的头皮表面放置由双波长光源和检测器构成的近红外探头,获得光密度变化量时间序列:

Figure 201010551128.9_AB_0
Figure 201010551128.9_AB_1
;二、采用修正朗伯比尔定律获取氧合血红蛋白浓度变化量时间序列Δ[HbO2](t)和还原血红蛋白浓度变化量时间序列Δ[HHb](t);三、对Δ[HbO2](t)和Δ[HHb](t)分别进行经验模态分解,获得所有的IMF分量;四、对所有IMF分量进行希尔伯特变换,将瞬时频率处于正常人呼吸频率和心脏跳动频率范围内的IMF分量剔除,以消除近红外脑功能检测时的生理扰动。

Figure 201010551128

The disturbance elimination method of near-infrared brain function detection based on empirical mode decomposition belongs to the field of optics. The present invention solves the problem that low-pass filtering cannot fully and effectively remove physiological disturbances during brain function detection; the use of adaptive filtering technology requires the use of additional equipment , problems with complex structures. The method of the present invention comprises the following steps: 1. Place a near-infrared probe consisting of a dual-wavelength light source and a detector on the scalp surface of the brain tissue to be measured to obtain a time series of optical density changes:

Figure 201010551128.9_AB_0
and
Figure 201010551128.9_AB_1
; 2. Obtain the time series Δ[HbO2 ](t) of oxygenated hemoglobin concentration change and the time series Δ[HHb](t) of reduced hemoglobin concentration change by using amended Lambert-Beer's law; 3. For Δ[HbO2 ] (t) and Δ[HHb](t) are subjected to empirical mode decomposition to obtain all IMF components; 4. Hilbert transform is performed on all IMF components, and the instantaneous frequency is in the range of normal human breathing frequency and heart beating frequency The internal IMF component is eliminated to eliminate the physiological disturbance in near-infrared brain function detection.

Figure 201010551128

Description

The disturbance removing method of the Near-infrared Brain Function detection of decomposing based on empirical modal
Technical field
The present invention relates to disturbance removing method, belong to optical field based on the Near-infrared Brain Function detection of empirical modal decomposition.
Background technology
Near-infrared spectrum technique (NIRS) can provide the information of the cerebral cortex blood oxygen metabolism in the cerebration process---HbO2 Oxyhemoglobin concentration change (Δ [HbO2]) and reduced hemoglobin concentration change (Δ [HHb]), can be used for the detection of cerebration.With other the brain function detection method as: functional magnetic resonance resonance, magnetoencephalography, positron emission tomography and EECG are compared, easy to use, easy enforcement that near-infrared spectrum technique has, temporal resolution height, safety, advantage such as cheap.Yet, utilize near-infrared spectrum technique to bring out the detection of when excitation cerebration, can be subjected to the influence that the physiological activity such as the heart of human body are beated, breathed, be referred to as the physiology disturbance.This physiology disturbance not only appears in the outer cerebral tissue such as scalp, skull and cerebrospinal fluid, also appears in the deep layer cerebral tissue such as ectocinerea and alba, has had a strong impact on the accurate measurement of cerebration.
At the influence of physiology disturbance to the Near-infrared Brain Function detection, the most direct processing method is to utilize low-pass filtering technique.Low-pass filtering technique can filter the disturbance that heartbeat causes effectively, because the forcing frequency that heartbeat causes is apparently higher than the cerebration signal.But low-pass filtering technique can't effectively filter the disturbance that breathing causes, this is because the forcing frequency that breathing causes is very low, and low excessively cut-off frequency has also caused the distortion of cerebration signal in this type of turbulent while of elimination.Auto-adaptive filtering technique is as one of turbulent removing method of physiology, showed de-noising characteristic preferably, can reduce the influence that the physiology disturbance detects at brain function near-infrared spectrum technique, but adaptive technique need be by means of pulse blood oxygen instrument or extra path channels, complex structure.
Summary of the invention
The present invention seeks in order to solve the multiple physiology disturbance when adopting low-pass filtering can't remove brain function comprehensively and effectively to detect; The turbulent method of physiology when adopting auto-adaptive filtering technique to eliminate brain function to detect exists need be by extra equipment, baroque problem, and a kind of disturbance removing method of Near-infrared Brain Function detection of decomposing based on empirical modal is provided.
The inventive method may further comprise the steps:
Step 1, place the near-infrared probe that constitutes by double-wavelength light source and detector in the scalp surface of cerebral tissue to be measured, diffuse-reflectance light intensity under the detector recording brain rest state and brain are in the diffuse-reflectance light intensity of bringing out when excitation, the time series of the optical density variable quantity when obtaining two different wave lengths:
Figure BDA0000033241910000011
With
Figure BDA0000033241910000012
T is the time, t=1, and 2 ..., N;
The time series ofstep 2, the optical density variable quantity that obtains according tostep 1, and adopt and revise the time series Δ [HbO that langbobier law obtains HbO2 Oxyhemoglobin concentration change amount2] (t) and the time series Δ [HHb] of reduced hemoglobin concentration change amount (t);
Δ[HbO2](t)=(ϵHHb(λ1)ΔODλ2(t)/DPF)-(ϵHHb(λ2)ΔODλ1(t)/DPF)r(ϵHbO2(λ2)ϵHHb(λ1)-ϵHbO2(λ1)ϵHHb(λ2)),
Δ[HHb](t)=(ϵHbO2(λ2)ΔODλ1(t)/DPF)-(ϵHbO2(λ1)ΔODλ2(t)/DPF)r(ϵHbO2(λ2)ϵHHb(λ1)-ϵHbO2(λ1)ϵHHb(λ2)),
Wherein, εHHb1) for the wavelength of probe light source be λ1The time extinction coefficient,
For the wavelength of probe light source is λ2The time extinction coefficient,
R is the air line distance of light source to detector,
DPF is the differential path factor,
Time series Δ [the HbO of step 3, HbO2 Oxyhemoglobin concentration change amount thatstep 2 is obtained2] (t) and the time series Δ [HHb] of reduced hemoglobin concentration change amount (t) carry out empirical modal respectively and decompose, obtain all IMF (intrinsicmode function, in accumulate mode function) component;
Step 4, all IMF components that step 3 is obtained carry out Hilbert transform, ask for the instantaneous frequency of each IMF component, instantaneous frequency is in IMF component rejection in normal person's respiratory frequency and the heartbeat frequency range, the physiology disturbance when eliminating the Near-infrared Brain Function detection.
Advantage of the present invention: the inventive method only need utilize easy probe can realize effectively eliminating the physiology disturbance, the inventive method adopts empirical modal to decompose this time frequency analysis method, handle the non-stationary nonlinear properties, complicated original signal is resolved into limited simple component, be called the IMF component, it has good Hilbert transform characteristic, makes instantaneous frequency to calculate.This decomposition method makes instantaneous frequency have the actual physical meaning, thereby can determine effectively rejecting of physiology disturbance in conjunction with human body physiological parameter.Δ [HbO when empirical modal decomposition and Hilbert transform can be applicable to cerebration2] and the reconstruct of Δ [HHb], can eliminate more than 90% by the physiology disturbance of breathing and heartbeat causes.
Description of drawings
To be the present invention carry out the flow chart that decomposes based on empirical modal to the IMF component to Fig. 1.
The specific embodiment
The specific embodiment one: below in conjunction with Fig. 1 present embodiment is described, the present embodiment method may further comprise the steps:
Step 1, place the near-infrared probe that constitutes by double-wavelength light source and detector in the scalp surface of cerebral tissue to be measured, diffuse-reflectance light intensity under the detector recording brain rest state and brain are in the diffuse-reflectance light intensity of bringing out when excitation, the time series of the optical density variable quantity when obtaining two different wave lengths:
Figure BDA0000033241910000031
With
Figure BDA0000033241910000032
T is the time, t=1, and 2 ..., N;
The time series ofstep 2, the optical density variable quantity that obtains according tostep 1, and adopt and revise the time series Δ [HbO that langbobier law obtains HbO2 Oxyhemoglobin concentration change amount2] (t) and the time series Δ [HHb] of reduced hemoglobin concentration change amount (t);
Δ[HbO2](t)=(ϵHHb(λ1)ΔODλ2(t)/DPF)-(ϵHHb(λ2)ΔODλ1(t)/DPF)r(ϵHbO2(λ2)ϵHHb(λ1)-ϵHbO2(λ1)ϵHHb(λ2)),
Δ[HHb](t)=(ϵHbO2(λ2)ΔODλ1(t)/DPF)-(ϵHbO2(λ1)ΔODλ2(t)/DPF)r(ϵHbO2(λ2)ϵHHb(λ1)-ϵHbO2(λ1)ϵHHb(λ2)),
Wherein, εHHb1) for the wavelength of probe light source be λ1The time extinction coefficient, depend on wavelength and specific absorbing material, be constant,
Figure BDA0000033241910000035
For the wavelength of probe light source is λ2The time extinction coefficient,
R is the air line distance of light source to detector,
DPF is the differential path factor, DPF (differential pathlength factor,), can measure with frequency domain spectroscopy or time-resolved spectroscopy method, also can obtain by Monte Carlo simulation calculation, little with wavelength change, be constant, adult brain tissue value 5.6, child's value 4.3.
Time series Δ [the HbO of step 3, HbO2 Oxyhemoglobin concentration change amount thatstep 2 is obtained2] (t) and the time series Δ [HHb] of reduced hemoglobin concentration change amount (t) carry out empirical modal respectively and decompose, obtain all IMF components;
Step 4, all IMF components that step 3 is obtained carry out Hilbert transform, ask for the instantaneous frequency of each IMF component, instantaneous frequency is in IMF component rejection in normal person's respiratory frequency and the heartbeat frequency range, the physiology disturbance when eliminating the Near-infrared Brain Function detection.
The technical scheme of present embodiment is achieved in that the sonde configuration that utilizes single light source list detector, and light source adopts double-wavelength light source (λ1=750nm, λ2=830nm), light source is 45mm to the air line distance (light source detection device spacing) of detector.Light source detection device spacing is approximately the twice of near infrared light investigation depth, and investigation depth can reach 20-22mm when light source detection device spacing was 45mm, and setting can make near infrared light can effectively penetrate cerebral cortex like this.Change the optical density variation that obtains into HbO2 Oxyhemoglobin Δ [HbO by revising langbobier law2] and the concentration change amount Δ [HHb] of reduced hemoglobin, the Δ [HbO of this moment2] and Δ [HHb] doping physiology turbulent noise even flooded by turbulent noise.Utilize EMD (empirical modal decomposition) with Δ [HbO2] be decomposed into IMF component with Δ [HHb] with different local features, and the IMF component is carried out Hilbert transform ask for instantaneous frequency.Utilize the instantaneous frequency of all IMF components, the IMF component that can determine physiology disturbance correspondence in conjunction with normal person's breathing and heartbeat frequency.Reject the IMF component of physiology disturbance correspondence, reconstruct cerebration signal.
Wherein, two kinds of wavelength sending of the described double-wavelength light source ofstep 1 are respectively λ1=750nm, λ2=830nm.
The time series of optical density variable quantity in thestep 1
Figure BDA0000033241910000041
Obtain by following formula:
ΔODλ1(t)=logIbase(λ1)/Istim(λ1),
Wherein: IBase1) for the wavelength of probe light source be λ1The time, brain is in the rest state output intensity in following time, and in the initial moment, brain is under the rest state, and the diffuse-reflectance light intensity that the record detector receives is as test benchmark.
IStim1) for the wavelength of probe light source be λ1The time, brain is in the output intensity when bringing out excitation,
At near infrared band HbO2With HHb be main absorber, and there is significant difference in its absorption spectra.Therefore, based on the Near-infrared Brain Function detection of continuous spectrum technology, mainly be to measure HbO2 Oxyhemoglobin (HbO2) and the concentration change of reduced hemoglobin (HHb).
Detect for brain function, adopt dual wavelength continuous light near-infrared measuring system, the time series of optical density variable quantity
Figure BDA0000033241910000043
Obtain by following formula:
ΔODλ2(t)=logIbase(λ2)/Istim(λ2),
Wherein: IBase2) for the wavelength of probe light source be λ2The time, brain is in the rest state output intensity in following time,
IStim2) for the wavelength of probe light source be λ2The time, brain is in the output intensity when bringing out excitation.
In the step 3 to the time series Δ [HbO of HbO2 Oxyhemoglobin concentration change amount2] (t) (t) to carry out the process that empirical modal decomposes identical with the time series Δ [HHb] of reduced hemoglobin concentration change amount, it is a kind of analytical method of non-linear, nonstationary time series that empirical modal decomposes, it can carry out linearisation to original series, tranquilization is handled, and keeps the feature of original series self in catabolic process.The time scale feature of its basis signal itself, with signal decomposition is to contain the different time yardstick and satisfy in a group of following two definite conditions and accumulate mode function (IMF): 1. in whole data sequence, the number of signal extreme point must differ one identical or at most with the number of signal zero crossing; 2. at any time on, the average of signal local maximum envelope and signal local minimum envelope is zero.
Described optical density signal is converted to Δ [HbO2] (t) and Δ [HHb] (t) carry out EMD then and decompose, the effectiveness of EMD method is to decompose Δ [HbO2] (t) and Δ [HHb] (t) rather than directly decompose and comprise the turbulent signal that diffuses of physiology because diffuse signal and Δ [HbO2] (t) and Δ [HHb] be index relation (t), the EMD algorithm decomposes the signal that diffuses can't realize separating fully the IMF component of physiology disturbance correspondence, thereby can't eliminate the physiology disturbance.
Below with Δ [HbO2] (t) and Δ [HHb] (t) be referred to as CIj(t), which IMF component i is, i=1, and 2 ..., n, j is the estimation number of times, initialization i=1, j=1 is to time series CIj(t) carry out empirical modal and decompose the acquisition process that obtains all IMF components:
Step 1, employing local extremum method are determined the hunting time sequence CIj(t) all maximum and minimum make up time series C with cubic spline interpolation respectively to all maximum value minimums that obtainIj(t) coenvelope line eMax(t) and lower envelope line eMin(t);
Step 2, obtain the average of upper and lower envelope
e(t)‾=emax(t)+emin(t)2,
Estimate h the j time of step 3, i IMF component of acquisition time sequenceIj(t):
hij(t)=Cij(t)-e(t)‾,
Step 4, judge whether following formula is set up:
Figure BDA0000033241910000054
ε>0 wherein, and fully near 0,
Judged result is for being, execution in step 5,
Judged result makes j=j+1, C for notI (j+1)(t)=hIj(t), and return execution instep 1,
Step 5, obtain i IMF component: Ci(t)=hIjAnd obtain i residual error (t):
ri(t)=Cij(t)-hij(t),
Step 6, i residual error r of judgementi(t) whether be monotonic function,
Judged result makes i=i+1 for not, j=1, and return execution instep 1,
Judged result is for being to finish time series CIj(t) carry out the empirical modal decomposition and obtain all IMF components: Ci(t).
The acquisition methods of the instantaneous frequency of IMF component is in the step 4:
Step 41, acquisition IMF component Ci(t) Hilbert transform y (t):
y(t)=H[Ci(t)]=1πP∫-∞∞Ci(t′)t-t′dt′,
Wherein, P represents Cauchy's principal value,
Step 42, IMF component Ci(t) analytic signal is z (t)=C (t)+iy (t)=a (t) exp[i θ (t)], wherein, a (t) is an instantaneous amplitude, θ (t) is a phase function,
Step 43, obtain IMF component Ci(t) instantaneous frequency f (t) is:
Figure BDA0000033241910000062
Normal person's respiratory frequency scope is 0.15Hz~0.4Hz, and the heartbeat frequency range is 1.0Hz~1.7Hz.
The instantaneous frequency of IMF component has embodied the internal feature of IMF component, according to normal person's respiratory frequency and heartbeat frequency, determines the IMF component of physiology disturbance correspondence.With the IMF component rejection of physiology disturbance correspondence, utilize other IMF component reconstruct to obtain the turbulent cerebration signal of physiology.
Described optical density signal is converted to Δ [HbO2] (t) and Δ [HHb] (t) carry out EMD then and decompose, the effectiveness of EMD method is to decompose Δ [HbO2] (t) and Δ [HHb] (t) rather than directly decompose and comprise the turbulent signal that diffuses of physiology because diffuse signal and Δ [HbO2] (t) and Δ [HHb] be index relation (t), the EMD algorithm decomposes the signal that diffuses can't realize separating fully the IMF component of physiology disturbance correspondence, thereby can't eliminate the physiology disturbance.

Claims (6)

Translated fromChinese
1.基于经验模态分解的近红外脑功能检测的扰动消除方法,其特征在于,它包括以下步骤:1. the disturbance elimination method based on the near-infrared brain function detection of empirical mode decomposition, it is characterized in that, it comprises the following steps:步骤一、在待测脑组织的头皮表面放置由双波长光源和检测器构成的近红外探头,检测器记录大脑安静状态下的漫反射光强和大脑处于诱发激励时的漫反射光强,以获得两个不同波长时的光密度变化量的时间序列:
Figure FDA0000033241900000012
t为时间,t=1,2,...,N;Step 1. Place a near-infrared probe consisting of a dual-wavelength light source and a detector on the surface of the scalp of the brain tissue to be tested. The detector records the diffuse reflection light intensity of the brain in a quiet state and the diffuse reflection light intensity of the brain when it is in the evoked excitation. Obtain a time series of optical density changes at two different wavelengths: and
Figure FDA0000033241900000012
t is time, t=1, 2,..., N;步骤二、根据步骤一获得的光密度变化量的时间序列、并采用修正朗伯比尔定律获取氧合血红蛋白浓度变化量的时间序列Δ[HbO2](t)和还原血红蛋白浓度变化量的时间序列Δ[HHb](t);Step 2. According to the time series of optical density changes obtained in step 1, the time series Δ[HbO2 ](t) of oxygenated hemoglobin concentration changes and the time series of reduced hemoglobin concentration changes are obtained by using the amended Lambert-Beer's law Δ[HHb](t);ΔΔ[[HbOHbO22]]((tt))==((ϵϵHHbHb((λλ11))ΔΔODODλλ22((tt))//DPFDPF))--((ϵϵHHbHb((λλ22))ΔΔODODλλ11((tt))//DPFDPF))rr((ϵϵHbOHbO22((λλ22))ϵϵHHbHb((λλ11))--ϵϵHbOHbO22((λλ11))ϵϵHHbHb((λλ22)))),,ΔΔ[[HHbHb]]((tt))==((ϵϵHbOHbO22((λλ22))ΔΔODODλλ11((tt))//DPFDPF))--((ϵϵHbOHbO22((λλ11))ΔΔODODλλ22((tt))//DPFDPF))rr((ϵϵHbOHbO22((λλ22))ϵϵHHbHb((λλ11))--ϵϵHbOHbO22((λλ11))ϵϵHHbHb((λλ22)))),,其中,εHHb1)为探头光源的波长为λ1时的消光系数,Among them, εHHb1 ) is the extinction coefficient when the wavelength of the probe light source is λ1 ,
Figure FDA0000033241900000015
为探头光源的波长为λ2时的消光系数,
Figure FDA0000033241900000015
is the extinction coefficient when the wavelength of the probe light source isλ2 ,
r为光源到检测器的直线距离,r is the linear distance from the light source to the detector,DPF为差分路径因子,DPF is the differential path factor,步骤三、对步骤二获得的氧合血红蛋白浓度变化量的时间序列Δ[HbO2](t)和还原血红蛋白浓度变化量的时间序列Δ[HHb](t)分别进行经验模态分解,获得所有的IMF分量;Step 3: Carry out empirical mode decomposition on the time series Δ[HbO2 ](t) of oxyhemoglobin concentration changes obtained in step 2 and the time series Δ[HHb](t) of reduced hemoglobin concentration changes respectively, and obtain all The IMF component of步骤四、对步骤三获得的所有IMF分量进行希尔伯特变换,求取各个IMF分量的瞬时频率,将瞬时频率处于正常人呼吸频率和心脏跳动频率范围内的IMF分量剔除,以消除近红外脑功能检测时的生理扰动。Step 4. Perform Hilbert transform on all the IMF components obtained in step 3, obtain the instantaneous frequency of each IMF component, and remove the IMF components whose instantaneous frequency is within the range of normal human respiratory rate and heartbeat frequency to eliminate near-infrared Physiological perturbations during brain function testing.2.根据权利要求1所述的基于经验模态分解的近红外脑功能检测的扰动消除方法,其特征在于,步骤一所述的双波长光源发出的两种波长分别为λ1=750nm,λ2=830nm。2. the disturbance elimination method based on the near-infrared brain function detection of empirical mode decomposition according to claim 1, it is characterized in that, two kinds of wavelengths that the dual-wavelength light source described in step 1 sends are respectively λ1 =750nm, λ2 = 830nm.3.根据权利要求1所述的基于经验模态分解的近红外脑功能检测的扰动消除方法,其特征在于,步骤一中光密度变化量的时间序列
Figure FDA0000033241900000016
按如下公式获取:
3. the disturbance elimination method based on the near-infrared brain function detection of empirical mode decomposition according to claim 1, is characterized in that, the time series of optical density variation in step 1
Figure FDA0000033241900000016
Obtain according to the following formula:
ΔΔODODλλ11((tt))==loglogIIbasebase((λλ11))//IIstimstim((λλ11)),,其中:Ibase1)为探头光源的波长为λ1时,大脑处于安静状态下时的出射光强,Istim1)为探头光源的波长为λ1时,大脑处于诱发激励时的出射光强,光密度变化量的时间序列
Figure FDA0000033241900000021
按如下公式获取:
Among them: Ibase1 ) is the outgoing light intensity when the brain is in a quiet state when the wavelength of the probe light source is λ1 , and Istim1 ) is when the wavelength of the probe light source is λ1 and the brain is in evoked excitation The time series of the outgoing light intensity and optical density variation
Figure FDA0000033241900000021
Obtain according to the following formula:
ΔΔODODλλ22((tt))==loglogIIbasebase((λλ22))//IIstimstim((λλ22)),,其中:Ibase2)为探头光源的波长为λ2时,大脑处于安静状态下时的出射光强,Istim2)为探头光源的波长为λ2时,大脑处于诱发激励时的出射光强。Among them: Ibase2 ) is the outgoing light intensity when the brain is in a quiet state when the wavelength of the probe light source is λ2 , and Istim2 ) is when the wavelength of the probe light source is λ2 and the brain is in evoked excitation of the emitted light intensity.
4.根据权利要求1所述的基于经验模态分解的近红外脑功能检测的扰动消除方法,其特征在于,步骤三中对氧合血红蛋白浓度变化量的时间序列Δ[HbO2](t)和还原血红蛋白浓度变化量的时间序列Δ[HHb](t)进行经验模态分解的过程相同,以下将Δ[HbO2](t)和Δ[HHb](t)统称为Cij(t),i为第几个IMF分量,i=1,2,…,n,j为估计次数,初始化i=1,j=1,对时间序列Cij(t)进行经验模态分解获取所有的IMF分量的获取过程:4. The method for eliminating disturbance based on near-infrared brain function detection based on empirical mode decomposition according to claim 1, characterized in that, in step 3, the time series Δ[HbO2 ](t) of oxyhemoglobin concentration variation It is the same as the process of empirical mode decomposition of the time series Δ[HHb](t) of the reduced hemoglobin concentration variation. Hereinafter, Δ[HbO2 ](t) and Δ[HHb](t) are collectively referred to as Cij (t) , i is the number of IMF components, i=1, 2,..., n, j is the number of estimates, initialize i=1, j=1, perform empirical mode decomposition on time series Cij (t) to obtain all IMFs Component acquisition process:步骤1、采用区域极值法确定寻找时间序列Cij(t)的所有极大值和极小值,对获得的所有极大值、极小值分别用三次样条插值构建时间序列Cij(t)的上包络线emax(t)和下包络线emin(t);Step 1. Use the regional extremum method to determine and find all the maximum and minimum values of the time series Cij (t), and use cubic spline interpolation to construct the time series Cij ( t) the upper envelope emax (t) and the lower envelope emin (t);步骤2、获取上、下包络线的均值
Figure FDA0000033241900000023
Step 2. Obtain the mean value of the upper and lower envelopes
Figure FDA0000033241900000023
ee((tt))‾‾==eemaxmax((tt))++eeminmin((tt))22,,步骤3、获取时间序列第i个IMF分量的第j次估计hij(t):Step 3. Obtain the j-th estimate hij (t) of the i-th IMF component of the time series:hhijij((tt))==CCijij((tt))--ee((tt))‾‾,,步骤4、判断下式是否成立:
Figure FDA0000033241900000026
其中ε>0,且充分接近0,
Step 4. Determine whether the following formula is established:
Figure FDA0000033241900000026
Where ε>0, and sufficiently close to 0,
判断结果为是,执行步骤5,If the judgment result is yes, go to step 5,判断结果为否,令j=j+1,Ci(j+1)(t)=hij(t),并返回执行步骤1,If the judgment result is no, set j=j+1, Ci(j+1) (t)=hij (t), and return to step 1,步骤5、获取第i个IMF分量:Ci(t)=hij(t),并获得第i个残差:Step 5. Obtain the i-th IMF component: Ci (t)=hij (t), and obtain the i-th residual:ri(t)=Cij(t)-hij(t),ri (t)=Cij (t)-hij (t),步骤6、判断第i个残差ri(t)是否为单调函数,Step 6. Determine whether the i-th residual ri (t) is a monotone function,判断结果为否,令i=i+1,j=1,并返回执行步骤1,If the judgment result is no, let i=i+1, j=1, and return to execute step 1,判断结果为是,完成对时间序列Cij(t)进行经验模态分解获取所有的IMF分量:Ci(t)。If the judgment result is yes, the empirical mode decomposition of the time series Cij (t) is completed to obtain all IMF components: Ci (t).
5.根据权利要求1所述的基于经验模态分解的近红外脑功能检测的扰动消除方法,其特征在于,步骤四中IMF分量的瞬时频率的获取方法为:5. the disturbance elimination method based on the near-infrared brain function detection of empirical mode decomposition according to claim 1, is characterized in that, the acquisition method of the instantaneous frequency of IMF component in the step 4 is:步骤41、获得IMF分量Ci(t)的希尔伯特变换y(t):Step 41. Obtain the Hilbert transform y(t) of the IMF component Ci (t):ythe y((tt))==Hh[[CCii((tt))]]==11ππPP∫∫--∞∞∞∞CCii((tt′′))tt--tt′′ddtt′′,,其中,P表示柯西主值,Among them, P represents the Cauchy principal value,步骤42、IMF分量Ci(t)的解析信号为z(t)=C(t)+iy(t)=a(t)exp[iθ(t)],其中,a(t)为瞬时幅度,θ(t)为相位函数,Step 42, the analytical signal of the IMF component Ci (t) is z(t)=C(t)+iy(t)=a(t)exp[iθ(t)], where a(t) is the instantaneous amplitude , θ(t) is the phase function,步骤43、获取IMF分量Ci(t)的瞬时频率f(t)为:
Figure FDA0000033241900000032
Step 43, obtaining the instantaneous frequency f(t) of the IMF component Ci (t) is:
Figure FDA0000033241900000032
6.根据权利要求1所述的基于经验模态分解的近红外脑功能检测的扰动消除方法,其特征在于,正常人呼吸频率范围为0.15Hz~0.4Hz,心脏跳动频率范围为1.0Hz~1.7Hz。6. The disturbance elimination method of near-infrared brain function detection based on empirical mode decomposition according to claim 1, characterized in that the breathing frequency range of a normal person is 0.15 Hz to 0.4 Hz, and the heart beating frequency range is 1.0 Hz to 1.7 Hz. Hz.
CN2010105511289A2010-11-192010-11-19Disturbance elimination method of near infrared brain function detection based on empirical mode decompositionExpired - Fee RelatedCN101972148B (en)

Priority Applications (1)

Application NumberPriority DateFiling DateTitle
CN2010105511289ACN101972148B (en)2010-11-192010-11-19Disturbance elimination method of near infrared brain function detection based on empirical mode decomposition

Applications Claiming Priority (1)

Application NumberPriority DateFiling DateTitle
CN2010105511289ACN101972148B (en)2010-11-192010-11-19Disturbance elimination method of near infrared brain function detection based on empirical mode decomposition

Publications (2)

Publication NumberPublication Date
CN101972148Atrue CN101972148A (en)2011-02-16
CN101972148B CN101972148B (en)2011-11-16

Family

ID=43572080

Family Applications (1)

Application NumberTitlePriority DateFiling Date
CN2010105511289AExpired - Fee RelatedCN101972148B (en)2010-11-192010-11-19Disturbance elimination method of near infrared brain function detection based on empirical mode decomposition

Country Status (1)

CountryLink
CN (1)CN101972148B (en)

Cited By (16)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
CN102512142A (en)*2011-12-222012-06-27哈尔滨工业大学 Recursive Least Squares Adaptive Filtering Near-infrared Brain Functional Activity Signal Extraction Method Based on Multi-distance Measurement Method
CN102525422A (en)*2011-12-262012-07-04哈尔滨工业大学 Brain function signal extraction method based on empirical mode decomposition optimization algorithm of multi-distance measurement method
CN104182645A (en)*2014-09-012014-12-03黑龙江省计算中心Empirical mode decomposition and sliding time window weighted least square method based brain-computer interface extraction method
CN104224165A (en)*2014-09-172014-12-24哈尔滨工业大学Near-infrared brain function signal robust estimation method based on multi-distance measurement method and least absolute deviation criterion
CN105203495A (en)*2015-09-112015-12-30天津工业大学Spectrum signal denoising method based on Hilbert-Huang transformation
CN105748089A (en)*2016-02-012016-07-13刘进Method and device for monitoring oxygen supply parameters
CN105832289A (en)*2015-01-302016-08-10三星电子株式会社Method and equipment using Hilbert transform to estimate biophysiological rates
CN106725520A (en)*2016-12-312017-05-31中国科学院苏州生物医学工程技术研究所The signal processing method system of brain blood oxygen detection
CN107174204A (en)*2017-05-122017-09-19哈尔滨工业大学Near-infrared Brain function signal processing method based on total least square method
CN107239739A (en)*2017-05-052017-10-10北京化工大学A kind of scale parameter controls adjustable signal envelope extracting method
CN107280685A (en)*2017-07-212017-10-24国家康复辅具研究中心Top layer physiological noise minimizing technology and system
CN110547768A (en)*2019-08-302019-12-10北京师范大学Near-infrared brain function imaging quality control method and control system
CN112263242A (en)*2020-10-262021-01-26哈尔滨工业大学Respiration detection and mode classification method based on FMCW radar
CN112274144A (en)*2019-07-222021-01-29苏州布芮恩智能科技有限公司Method and device for processing near-infrared brain function imaging data and storage medium
CN112386253A (en)*2019-08-162021-02-23浙江象立医疗科技有限公司Near-infrared optical detection method for human body local venous blood flow parameters
CN119453944A (en)*2024-11-292025-02-18华南理工大学 A high-resolution portable near-infrared brain functional imaging system

Citations (6)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
CN1223844C (en)*2003-11-072005-10-19清华大学Tissue blood-oxygen parameter detection method capable of amending outer layer tissue influence
CN1223843C (en)*2003-11-142005-10-19清华大学Method for detecting newborn baby partial tissue oxygen saturation under oxygen absorption stimulation
CN1223858C (en)*2003-11-212005-10-19清华大学Near infrared tissue non-destructive testing method for blood transportation parameter of skeletal muscle metabolism
CN1298284C (en)*2002-02-142007-02-07加藤俊德Biological function diagnostic device
CN1946336A (en)*2004-03-092007-04-11内尔科尔普里坦贝内特公司Pulse oximetry motion artifact rejection using near infrared absorption by water
CN100518640C (en)*2006-08-252009-07-29清华大学Method for testing absolute volume of concentration of oxidized hemoglobin and reduced hemoglobin in human tissue

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
CN1298284C (en)*2002-02-142007-02-07加藤俊德Biological function diagnostic device
CN1223844C (en)*2003-11-072005-10-19清华大学Tissue blood-oxygen parameter detection method capable of amending outer layer tissue influence
CN1223843C (en)*2003-11-142005-10-19清华大学Method for detecting newborn baby partial tissue oxygen saturation under oxygen absorption stimulation
CN1223858C (en)*2003-11-212005-10-19清华大学Near infrared tissue non-destructive testing method for blood transportation parameter of skeletal muscle metabolism
CN1946336A (en)*2004-03-092007-04-11内尔科尔普里坦贝内特公司Pulse oximetry motion artifact rejection using near infrared absorption by water
CN100518640C (en)*2006-08-252009-07-29清华大学Method for testing absolute volume of concentration of oxidized hemoglobin and reduced hemoglobin in human tissue

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
《光学学报》 20070228 周振宇,杨宏宇,龚辉等 基于希尔伯特-黄变换的近红外脑功能成像信号分析 第307-312页 1-6 第27卷, 第2期 2*
《光谱学与光谱分析》 20060531 腾轶超,丁海曙,龚庆成等 近红外光谱监测体外循环手术中脑组织氧合状况的研究 第828-832页 1-6 第26卷, 第5期 2*
《医学生物力学》 20060630 孙仁,沈海 东,鲁传敬等 HHT方法在脉搏波信号分析中的应用 第87-93页 1-6 第21卷, 第2期 2*
《激光生物学报》 20060430 吴太虎,徐可欣,刘庆珍等 近红外光谱法无创测量人体血红蛋白浓度 第204-208页 1-6 第15卷, 第2期 2*
《红外与毫米波学报》 20031031 黄岚,田丰华,丁海曙等 用近红外光谱对组织氧测量方法的研究 第379-383页 1-6 第22卷, 第5期 2*

Cited By (23)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
CN102512142B (en)*2011-12-222013-10-23哈尔滨工业大学 Recursive Least Squares Adaptive Filtering Near-infrared Brain Functional Activity Signal Extraction Method Based on Multi-distance Measurement Method
CN102512142A (en)*2011-12-222012-06-27哈尔滨工业大学 Recursive Least Squares Adaptive Filtering Near-infrared Brain Functional Activity Signal Extraction Method Based on Multi-distance Measurement Method
CN102525422A (en)*2011-12-262012-07-04哈尔滨工业大学 Brain function signal extraction method based on empirical mode decomposition optimization algorithm of multi-distance measurement method
CN102525422B (en)*2011-12-262014-04-02哈尔滨工业大学Brain function signal extraction method based on empirical mode decomposition optimization algorithm of multi-distance measurement method
CN104182645A (en)*2014-09-012014-12-03黑龙江省计算中心Empirical mode decomposition and sliding time window weighted least square method based brain-computer interface extraction method
CN104224165A (en)*2014-09-172014-12-24哈尔滨工业大学Near-infrared brain function signal robust estimation method based on multi-distance measurement method and least absolute deviation criterion
CN105832289A (en)*2015-01-302016-08-10三星电子株式会社Method and equipment using Hilbert transform to estimate biophysiological rates
CN105203495A (en)*2015-09-112015-12-30天津工业大学Spectrum signal denoising method based on Hilbert-Huang transformation
CN105203495B (en)*2015-09-112018-05-29天津工业大学A kind of spectral signal denoising method based on Hilbert-Huang transform
CN105748089A (en)*2016-02-012016-07-13刘进Method and device for monitoring oxygen supply parameters
CN105748089B (en)*2016-02-012018-10-26刘进A kind of oxygen is for parameter monitoring method and monitoring device
CN106725520A (en)*2016-12-312017-05-31中国科学院苏州生物医学工程技术研究所The signal processing method system of brain blood oxygen detection
CN107239739A (en)*2017-05-052017-10-10北京化工大学A kind of scale parameter controls adjustable signal envelope extracting method
CN107239739B (en)*2017-05-052020-10-27北京化工大学Signal envelope extraction method with adjustable scale parameter control
CN107174204A (en)*2017-05-122017-09-19哈尔滨工业大学Near-infrared Brain function signal processing method based on total least square method
CN107280685B (en)*2017-07-212020-05-15国家康复辅具研究中心Surface layer physiological noise removing method and system
CN107280685A (en)*2017-07-212017-10-24国家康复辅具研究中心Top layer physiological noise minimizing technology and system
CN112274144A (en)*2019-07-222021-01-29苏州布芮恩智能科技有限公司Method and device for processing near-infrared brain function imaging data and storage medium
CN112386253A (en)*2019-08-162021-02-23浙江象立医疗科技有限公司Near-infrared optical detection method for human body local venous blood flow parameters
CN110547768A (en)*2019-08-302019-12-10北京师范大学Near-infrared brain function imaging quality control method and control system
CN110547768B (en)*2019-08-302020-07-28北京师范大学 A quality control method and control system for near-infrared brain functional imaging
CN112263242A (en)*2020-10-262021-01-26哈尔滨工业大学Respiration detection and mode classification method based on FMCW radar
CN119453944A (en)*2024-11-292025-02-18华南理工大学 A high-resolution portable near-infrared brain functional imaging system

Also Published As

Publication numberPublication date
CN101972148B (en)2011-11-16

Similar Documents

PublicationPublication DateTitle
CN101972148B (en)Disturbance elimination method of near infrared brain function detection based on empirical mode decomposition
CN102512142B (en) Recursive Least Squares Adaptive Filtering Near-infrared Brain Functional Activity Signal Extraction Method Based on Multi-distance Measurement Method
Virtanen et al.Comparison of principal and independent component analysis in removing extracerebral interference from near-infrared spectroscopy signals
CN104055524B (en)Brain function based near infrared spectrum connects detection method and system
JP4201876B2 (en) Component concentration determination method
Kohl et al.Determination of the wavelength dependence of the differential pathlength factor from near-infrared pulse signals
CN103027690B (en)Hypoperfusion oxyhemoglobin saturation measuring method based on self-correlation modeling method
CN102973279B (en)Near-infrared brain-machine interface signal detection method integrating independent component analysis
US20040122300A1 (en)Method for measuring venous oxygen saturation
KR20110095281A (en) Non-Invasive Measurement System and Apparatus of Glucose Level in Blood
CN102525422B (en)Brain function signal extraction method based on empirical mode decomposition optimization algorithm of multi-distance measurement method
Tian et al.Enhanced functional brain imaging by using adaptive filtering and a depth compensation algorithm in diffuse optical tomography
CN108185992B (en)Noninvasive optical brain tissue oxygen metabolism measurement method
CN104688234A (en)Noninvasive and disturbance-resistant detection method for ICG pigment concentration spectrum
CN107280685B (en)Surface layer physiological noise removing method and system
Ram et al.On the performance of Time Varying Step-size Least Mean Squares (TVS-LMS) adaptive filter for MA reduction from PPG signals
He et al.Spectral data quality assessment based on variability analysis: application to noninvasive hemoglobin measurement by dynamic spectrum
Addison et al.Secondary wavelet feature decoupling (SWFD) and its use in detecting patient respiration from the photoplethysmogram
CN105962950A (en) Near-infrared Brain Function Signal Extraction Method Based on Least Squares Support Vector Machine
CN107981869A (en)A kind of blood oxygen measuring method and device
Zhang et al.Reduction of global interference in functional multidistance near-infrared spectroscopy using empirical mode decomposition and recursive least squares: a Monte Carlo study
CN104182645A (en)Empirical mode decomposition and sliding time window weighted least square method based brain-computer interface extraction method
Colier et al.Detailed evidence of cerebral hemoglobin oxygenation changes in response to motor cortical activation revealed by a continuous-wave spectrophotometer with 10-Hz temporal resolution
Zhang et al.Monte Carlo study for physiological interference reduction in near-infrared spectroscopy based on empirical mode decomposition
Ram et al.Adaptive reduction of motion artifacts from PPG signals using a synthetic noise reference signal

Legal Events

DateCodeTitleDescription
C06Publication
PB01Publication
C10Entry into substantive examination
SE01Entry into force of request for substantive examination
C14Grant of patent or utility model
GR01Patent grant
C17Cessation of patent right
CF01Termination of patent right due to non-payment of annual fee

Granted publication date:20111116

Termination date:20121119


[8]ページ先頭

©2009-2025 Movatter.jp