Skip to main content
NCBI home page
PLOS One logoLink to PLOS One
. 2020 Jan 10;15(1):e0227651. doi: 10.1371/journal.pone.0227651

Assessment of dynamic cerebral autoregulation in humans: Is reproducibility dependent on blood pressure variability?

Jan Willem Elting 1,*, Marit L Sanders 2, Ronney B Panerai 3, Marcel Aries 4, Edson Bor-Seng-Shu 5, Alexander Caicedo 6, Max Chacon 7, Erik D Gommer 8, Sabine Van Huffel 9, José L Jara 7, Kyriaki Kostoglou 10, Adam Mahdi 11, Vasilis Z Marmarelis 12, Georgios D Mitsis 13, Martin Müller 14, Dragana Nikolic 15, Ricardo C Nogueira 5, Stephen J Payne 11, Corina Puppo 16, Dae C Shin 12, David M Simpson 15, Takashi Tarumi 17, Bernardo Yelicich 16, Rong Zhang 17, Jurgen A H R Claassen 1
Editor: Tatsuo Shimosawa18
PMCID: PMC6954074  PMID: 31923919

Abstract

We tested the influence of blood pressure variability on the reproducibility of dynamic cerebral autoregulation (DCA) estimates. Data were analyzed from the 2nd CARNet bootstrap initiative, where mean arterial blood pressure (MABP), cerebral blood flow velocity (CBFV) and end tidal CO2 were measured twice in 75 healthy subjects. DCA was analyzed by 14 different centers with a variety of different analysis methods. Intraclass Correlation (ICC) values increased significantly when subjects with low power spectral density MABP (PSD-MABP) values were removed from the analysis for all gain, phase and autoregulation index (ARI) parameters. Gain in the low frequency band (LF) had the highest ICC, followed by phase LF and gain in the very low frequency band. No significant differences were found between analysis methods for gain parameters, but for phase and ARI parameters, significant differences between the analysis methods were found. Alternatively, the Spearman-Brown prediction formula indicated that prolongation of the measurement duration up to 35 minutes may be needed to achieve good reproducibility for some DCA parameters. We conclude that poor DCA reproducibility (ICC<0.4) can improve to good (ICC > 0.6) values when cases with low PSD-MABP are removed, and probably also when measurement duration is increased.

Introduction

Dynamic cerebral autoregulation (DCA) is a key mechanism in cerebral homeostasis and protects the brain from alterations in blood pressure by arteriolar vasodilatation or constriction[1],[2]. Through this process, cerebral blood flow is preserved at a relatively constant level. Abnormal DCA status has been found in many pathological conditions such as stroke and traumatic brain injury[3],[4],[5],[6]. Despite detectable differences between healthy controls and patient groups, high variability is present which reduces the reliability of individual estimates[1]. Distributions of patient and healthy subject groups overlap considerably which results in poor diagnostic properties. This hampers implementation of DCA measurements as a diagnostic or monitoring tool in clinical practice.

The causes of variability in DCA measurements can be categorized as physiological or methodological. Physiological causes of DCA variability include the influence of confounders such as PaCO2, autonomic nerve activity, and the amount of blood pressure variability[7],[8],[9]. Non stationarity of cerebral autoregulation suggests that DCA activity is not always constant over time, and can also be thought of as physiological variability[10],[11]. Non stationarity may be linked to variations in blood pressure variability or absolute blood pressure; if no change is present in blood pressure, no change in arteriolar diameter is needed to keep cerebral blood flow constant. Methodological causes of variability include measurement conditions and analytical techniques used to estimate DCA metrics. The influence of measurement conditions has been demonstrated previously: time of day, use of caffeine, amount of rest before measurement, body position, and external influences are all important to consider[12]. Recommendations for optimal settings of these components have been published in the 1st CARNet bootstrap initiative[12]. Many different analysis strategies for DCA assessment have been developed, some of which try to model and account for physiological causes of variability, such as PaCO2. For example, Transfer Function Analysis (TFA) based on multiple inputs (MABP, CO2) allows for correction of CO2 influences[13],[14], while Volterra Kernels[7],[15] or Multi-model Pressure Flow Modeling[16],[17] try to capture the non-linear aspects of cerebral autoregulation. Time varying autoregressive moving average models (ARMA models) and multiple-input finite impulse response models have been used to model the non-stationary aspects of cerebral autoregulation[18],[19],[20]. However, at present it is not clear if any of these methods is superior to others in terms of variability and reproducibility of the DCA estimates.

The second CARNet bootstrap initiative was started in 2015 to gain further insight into the problem of variability of DCA estimates. Specifically, reproducibility was assessed to quantify variability between repeated measurements. The main focus of this study was to evaluate any differences in reproducibility between the different analysis strategies that have been developed. Initially, surrogate data were used to isolate the separate effects of modelling method from physiological variability[21]. In the second analysis, physiological data were used to quantify reproducibility of several DCA analysis methods on physiological data[22]. The third analysis is described in this study, focusing on the effect of blood pressure variability, quantified as power spectral density of mean arterial blood pressure (PSD-MABP), on DCA reproducibility. Some studies have shown that DCA parameters are more stable if PSD-MABP is high, and can become variable if PSD-MABP is low[23],[24]. A number of techniques to increase PSD-MABP variability have been described, and in some of these studies reproducibility of the DCA estimates have been shown to improve[23],[25],[26],[27].

The specific hypothesis that were tested are:

  1. DCA Reproducibility will increase if subjects with low PSD-MABP are left out of the analysis.

  2. DCA Reproducibility after PSD-MABP based case removal is similar for different analysis methods.

  3. DCA Reproducibility after PSD-MABP based case removal is similar for different DCA parameters.

Materials and methods

Subjects and centers

S1 and S2 Tables summarize the participating centers, their roles and the analysis methods. Measurements from 75 subjects were collected from 6 participating centers. A formal sample size calculation was not possible before the study was performed, due to the lack of information about inter-subject variability for the majority of autoregulation indices. In a previous study, Brodie et al. provided estimates for the sample size in studies using the ARI index, but similar information was not available for the other indices in our study. From the information provided, with n = 75 subjects in our case, we can estimate that a difference of ARI = 0.77 could be detected with 80% power at α = 0.05, which should be very satisfactory to detect intra-subject differences [28].

Subjects were 18 years or older, male or female, and were in good health. Exclusion criteria included a history of uncontrolled hypertension, smoking, diabetes, irregular heart rhythm, cardiovascular disease, TIA/stroke or significant pulmonary disease. The study has been carried out in accordance with the Code of Ethics of the World Medical Association (Declaration of Helsinki). Written informed consent was obtained from all subjects. A study flowchart is presented in Fig 1.

Fig 1. Study flowchart.

Fig 1

Open in a new tab

Measurements

Measurement data had to consist of transcranial Doppler ultrasound (TCD) derived cerebral blood flow velocity in the middle cerebral artery (CBFV) data and MABP as well as end tidal CO2 (EtCO2) data. TCD recordings could be unilateral or bilateral. Beat to beat data had to be resampled at 10 Hz. For each subject, 2 periods of at least 5 minutes of continuous, good quality, artifact free data were required. The interval between the measurements could not exceed 3 months. Subjects were measured supine at rest. No MABP oscillation inducing maneuvers were performed.

Pre-analysis data validation

Data validation was performed using the following criteria:

Mean CBFV > 30 cm/s, EtCO2 > 3 kPA and < 7 kPA, and mean MABP >40 and < 160 mmHg at all times. Further visual inspection of all data consisted of checking for step artifacts, and other artifacts such as large slow drifts. Based on these criteria, 6 subjects were excluded from the analysis, and were replaced with good quality backup data from 1 center. Missing data from one hemisphere (CBFV), were replaced with artificially generated data. This procedure resulted in N = 55 left sides, N = 71 right sides, and N = 22 artificial sides. The results for the artificial and physiological data have been presented elsewhere, and will not be reported here[21]. Since there were no significant differences between left and right sided values for all DCA variables examined in this study, left and right sides were averaged in case of bilateral measurement, or were used singly in case of unilateral missing data.

Analysis methods

S1 Table summarizes the analysis methods that were used by each center. The full details of all analysis methods will not be presented here, instead references for each method are provided. Each method was categorized into one of three possible broad categories of methods: 1. Transfer function like methods: those that produce at least some form of phase and/or gain estimates. 2. Autoregulation index like methods: Those that produce an autoregulation index which ranges from 0–9. 3. Correlation index like methods: Those that produce a correlation like index. These categories were created from the perspective of similar output parameters, not because the analysis is similar on mathematical grounds.

PSD-MABP based case removal

Power spectra were created by calculating power spectral density (PSD) of the mean arterial blood pressure (MABP) signals. This was not part of the analysis of the individual centers, instead it was performed centrally. A Hanning window was applied, and segments of 100 seconds with 50% overlap were used, according to the Welch method of spectral estimation. Mean PSD-MABP estimates were calculated in VLF (0.02–0.07 Hz) and LF (0.07–0.2 Hz). Histograms of the PSD-MABP estimates were created and 10 cut-off levels were defined, which reflected the 0, 10, 20, 30, 40, 50, 60, 70, 80 and 90th percentiles of the PSD-MABP distribution. Each cut-off level was used to remove cases with PSD-MABP levels below these values. The same cut-off levels were used for all analysis methods, which results in the same number of cases for each analysis method for each cut-off level. For DCA variables, cases were removed based on the corresponding frequency band PSD-MABP (DCA-VLF vs PSD-MABP-VLF and DCA-LF vs PSD-MABP-LF) but for DCA variables in the LF band cases were also removed using PSD-MABP in the VLF.

Statistical analysis

To evaluate the possible impact of PSD-MABP levels on DCA variables, the relation between the absolute difference of the duplicate DCA variable measurements and the lowest PSD value of the PSD-MABP signal of both measurements was analyzed using Spearman rank correlation for each method. We used the absolute difference for this analysis, since it is irrelevant which of the two measurement has the higher or lower value of the DCA variable. The lowest PSD value was used, since this will assure that when using PSD-MABP as a filter variable based on threshold levels, both PSD-MABP values will be above the threshold. To investigate main effects, the Spearman correlation coefficients were used as a summary measure and were tested against the null hypothesis value of zero using a one sample T test.

To assess reproducibility, one way Intraclass Correlation Coefficient (ICC) analysis was performed on all available data, and for each subgroup created through case removal based on PSD-MABP. The one way setting in SPSS, version 22, was used to calculate the ICC. To meet the prerequisite of bivariate normal distributions, data were transformed using Box-Cox transformations[29]. Within one analysis method, the same transformation was applied to both the first and second measurement, but different transformations could be used for different methods and DCA variables. To quantify the effect of case removal based on PSD-MABP on ICC values for different DCA variables within the main method groups, a repeated measurements ANOVA was used, entering the ICC values at the 10 PSD levels as repeated measurements and DCA variable type as the group variable. Gain VLF, Gain LF, Phase VLF, Phase LF and ARI were the possible values for the group variable. Post Hoc tests were performed to assess differences between the DCA variable groups.

To test for differences in ICC values between different analysis methods, Monte Carlo simulations were conducted using correlated random data with an inhouse written script in LabVIEW 2014[30]. The details of the Monte Carlo simulations can be found in S1 File.

A final analysis consisted of extrapolating the ICC result to a longer measurement period. The Spearman-Brown prophecy formula was used to predict the length of time needed for a DCA variable to reach a good ICC value of at least 0.6[31]. The estimated longer durations involve the assumption that autoregulation would remain stable when the measurement duration is extended. The Spearman-Brown calculated ICC (ICCSB) is calculated as:

ICCSB = nICC1+(n−1)ICC where ICC is the ICC value based on 2 measurements of 5 minutes and n is the factor by which the measurement duration will be extended.

Results

Subject characteristics

Thirty-three subjects (44%) were female and 42 were male. Mean age was 47.8 ± 18.6 years (range 20–80). Five subjects had a history of asymptomatic hypertension, which was well controlled by medication at the time of measurement. Median lowest PSD-MABP was comparable between those that used vasoactive medication and those without any medication (S1 Fig) Four older subjects had a history of mild cognitive impairment, but not dementia. Another 4 subjects used NSAIDs regularly, without any history of vascular disease.

Correlation between DCA variables and PSD-MABP

Fig 2 shows the correlation between the absolute difference of DCA variables between the first and second measurement and the lowest PSD-MABP value of both measurements. High absolute differences tend to occur at low PSD-MABP values, especially for gain variables, and to a lesser degree also for phase variables. For ARI and correlation like variables, this dependency is less clear or absent. Results of the Spearman rank correlation analysis can be found in Table 1. For individual methods, differences in gain in the VLF had a strong relation to the PSD-MABP estimates; for other variables, this relationship was less strong. When all Spearman correlation coefficients were used as summary measures, mean gain (VLF: -0.25 ± 0.1, p<0.001; LF: -0.19 ± 0.06, p<0.001) and phase (VLF: -0.13 ± 0.09, p<0.001; LF: -0.11 ± 0.08, p<0.001) coefficients were significantly different from zero. However, for ARI (0.00 ± 0.11, p = 0.98) and correlation like indices (0.05 ± 0.02, p = 0.10), no significant correlation was found.

Fig 2. Absolute between measurement differences vs the lowest PSD-MABP of repeated measurements.

Fig 2

Open in a new tab

Table 1. Spearman correlation coefficients for the absolute DCA variable difference between the two measurements and the lowest PSD-MABP value of both measurements.

Method Category Gain VLF Gain LF Phase VLF Phase LF ARI Cor
1.1:TFA 1 -0.33* -0.08 -0.13 -0.18
1.2:ARI 2 -0.00
2.1:V.Kernels.SISO 1 -0.17 -0.23* -0.19 -0.13
2.2:V.Kernels.MISO 1 -0.08 -0.23* -0.28* -0.03
3.1:TFA 1 -0.28* -0.12 -0.03 -0.09
3.2:TFA 1 -0.25 -0.15
4.1:ARI:FFT 2 -0.02
4.2:ARI:MA1 2 0.13
4.3:ARI:MA2 2 0.15
5.1:TFA 1 -0.39* -0.19 -0.25* -0.19
5.2: SIDE-ObSP 3 0.06
6.1:TFA 1 -0.1 -0.15 -0.06 -0.27*
7.1:TFA 1 -0.21 -0.18 -0.24* -0.14
8.1:ARX 2 -0.11
8.2:Wavelets 1 -0.05 -0.16
9.1:TFA 1 -0.29* -0.25* -0.15 -0.16
9.2:CCM 3 0.03
11.1:TFA 1 -0.28* -0.13 -0.15 -0.04
11.2:TFA 1 -0.25* -0.17 -0.15 -0.04
11.3:TFA 1 -0.21 -0.15
11.4:TFA 1 -0.17 0.03
11.5:IR coeff 2 -0.19
11.6:TFA:MISO 1 -0.15 -0.06
12.1:TFA 1 -0.42* -0.22 -0.09 -0.15
12.2:ARI 2 -0.04
12.3:Wavelets 1 -0.25* -0.22 0.04 -0.05
13.1:TFA 1 -0.27* -0.06 -0.10 -0.17
14.1:ARX:SISO 1 -0.25* -0.22 -0.09 0.02
14.2:ARX:MISO 1 -0.36* -0.25* -0.24* -0.03
14.3:FIR:SISO 1 -0.07 -0.30* -0.12 -0.10
14.4:FIR:MISO 1 -0.2 -0.32* -0.03 -0.06
14.5:TFA 1 -0.34* -0.15 -0.19 -0.26*
Mean ± SD -0.25 ± 0.1 -0.19 ± 0.06 -0.13 ± 0.09 -0.11 ± 0.08 0.00 ± 0.11 0.05 ± 0.02
Probability = 0 < 0.001 < 0.001 < 0.001 < 0.001 0.98 NA
Open in a new tab

* = Significant correlation, p<0.05.

VLF = Very low Frequency, LF = Low Frequency. Category: 1 = TFA, 2 = ARI, 3 = correlation. SISO = Single Input (MABP), Single Output (CBFV). MISO = Multiple Input (MABP, EtCO2), Single Output (CBFV). Note that especially gain in the VLF is strongly correlated with PSD-MABP. For ARI and correlation like indices, no significant correlation was found. The last two rows show the mean of all Spearman coefficients, and the result of the one sample T test vs value 0.

Reproducibility: ICC analysis for incremental case removal

Figs 3–5, and S2–S4 Figs summarize the main findings of the ICC analysis for different levels of PSD-MABP based case removal. For gain, phase and ARI, mild to moderate increases in ICC can be seen, while for correlation like indices, no clear change in ICC is present. There was a significant linear increase in ICC with increasing numbers of cases removed based on PSD-MABP for gain (VLF: F = 34.3 p<0.001, LF: F = 8.6 p = 0.008) and phase (VLF: F = 15.2 p = 0.001, LF: F = 112.4 p<0.001), but not for ARI (F = 0.2 p = 0.68). For ARI, the absence was mainly due to a sudden decrease in ICC at the highest PSD-MABP cut-off level; when repeating the analysis without the last level, a significant linear increase in ICC was found (F = 9.7 p = 0.014). For gain LF, the increase in ICC was highest when removing cases with PSD-MABP-VLF, and not with PSD-MABP-LF. For all other DCA variables, the ICC increase was always higher when removing cases using the corresponding PSD-MABP frequency band. Viewed from the level of group averages, gain LF had significantly higher ICCs compared to all other DCA variable groups (p<0.001 for all comparisons), while gain VLF and phase LF had higher ICCs compared to phase VLF (both p<0.001). A significant interaction between PSD-MABP based case removal and DCA variable group was found (F = 4.1 p = 0.004).

Fig 3. ICC values for gain LF and gain VLF.

Fig 3

Open in a new tab

Beeswarm boxplot with ICC values for gain LF (upper figure) and gain VLF (lower figure) for different cut-off levels of PSD-MABP. Each grey dot represents an analysis method. No significant differences between methods were found. The increase in ICC with increasing cut-off levels was significant for both gain LF and gain VLF.

Fig 5. ICC values for ARI and correlation like indices.

Fig 5

Open in a new tab

Beeswarm boxplot with ICC values for ARI and correlation like indices for different cut-off levels of PSD-MABP. Each grey dot represents an analysis method. ! : indicates cut-off level at which significant differences between the methods were found. * indicates correlation like indices, which were not included in calculation of the boxplot. The increase in ICC with increasing cut-off levels was significant for ARI like indices, when the highest cut-off level (110) was excluded.

Fig 4. ICC values for phase LF and phase VLF.

Fig 4

Open in a new tab

Beeswarm boxplot with ICC values for phase LF (upper figure) and phase VLF (lower figure) for different cut-off levels of PSD-MABP. Each grey dot represents an analysis method. ! : indicates cut-off level at which significant differences in ICC values between the methods were found. The increase in ICC with increasing cut-off levels was significant for both phase LF and phase VLF.

Within each main method group, Monte Carlo simulations indicated significant differences between individual methods for phase VLF, phase LF and ARI, but not for gain VLF and LF. S2–S4 Figs show beeswarm letter-box graphs with post-hoc sum-scores for each individual method. For phase VLF, methods 14.1 and 14.2 (S1 Table, both ARX (autoregression) models with 1 and 2 inputs (MABP, MABP and CO2) respectively) were the methods that showed the clearest increase in ICC, with ICC values compatible with moderate to good reproducibility. For phase LF, multiple methods had ICC values in the moderate range, while some had very low ICC values. For ARI, method 11.5 (impulse response filter coefficient) had the highest reproducibility, with ICC values showing good reproducibility at low PSD-MABP cut-off levels.

Spearman-Brown prediction of ICC values

Fig 6 shows the Spearman-Brown predicted ICC values for the median DCA variable values without PSD-MABP based case removal. To achieve a good ICC value of at least 0.6, the recording length must be increased to 10 minutes for median phase LF, 15 minutes for gain VLF, 20 minutes for ARI and 35 minutes for phase VLF. For gain LF, 5 minutes is sufficient.

Fig 6. Results of the Spearman-Brown analysis.

Fig 6

Open in a new tab

Spearman-Brown predicted ICC values based on single measures ICC values calculated on 2 measurement periods of 5 minutes. The assumption is that autoregulation would remain stable when the measurement duration is extended. The observed median ICC values for DCA variables based on all cases (n = 75) are projected onto the predicted ICC = 0.6 line. The first intersecting curve on the left represents the recording time that is needed to achieve an ICC of at least 0.6. To achieve an ICC value of ≥ 0.6 the recording length must be increased to 10 minutes for median phase LF, 15 minutes for gain VLF, 20 minutes for ARI and 35 minutes for phase VLF. For gain LF, 5 minutes is sufficient.

Discussion

In this study, the effect of PSD-MABP on DCA reproducibility was investigated. In the first step, a dependency of reproducibility on PSD-MABP was established by correlating the absolute within subject difference of DCA variable values with the lowest PSD-MABP value of the two measurements. Significant correlations were exclusively found for TFA like DCA variables, with the highest correlations for gain. For ARI and correlation like methods, no significant correlations were found. This means that the effect of any case removal based on PSD-MABP levels on reproducibility can be expected to be higher in TFA like methods. However, absence of significant correlations does not mean that there can be no benefit in reproducibility following case removals: if only a few outliers exist at low PSD-MABP power, there may not be a significant correlation, but reproducibility statistics such as ICC values can still be significantly affected, as they are quite sensitive to even a few outliers. In line with this reasoning, increases in ICC after incremental case removal were most pronounced in DCA variables whose difference values were significantly correlated to PSD-MABP (gain and phase), but were also found in ARI like methods. For most DCA variables, case removal based on PSD-MABP within the corresponding frequency band yielded the highest increases in ICC, except for gain LF where case removal based on PSD-MAPB-VLF (instead of PSD-MABP-LF) resulted in the highest increases in ICC. The reason for this is not clear from these results, but we speculate that the higher MABP oscillations in the VLF occur simultaneously with lower oscillations in the LF band, which may create a cross-dependency between LF band DCA parameters and PSD-MABP-VLF.

When interpreting the absolute and maximal values of ICC, and comparing the values with often quoted guidelines for the interpretation of ICC values (less than 0.40: poor, between 0.40 and 0.59: fair, between 0.60 and 0.74: good, between 0.75 and 1.00: excellent)[32], it is clear that for most DCA variables ICC is in the poor to fair range without any PSD-MABP based case removal, with the exception of gain LF. On average, gain LF was clearly the most reproducible DCA parameter, with significantly higher ICCs compared to all other DCA variables, followed by gain VLF and phase LF. With case removal, maximal ICC’s can be in the range regarded as ‘good’ (>0.6), especially for TFA like variables such as gain, and to a lesser degree also phase. However, the maximum level of reproducibility that can be reached depends on the method that was used, as there were significant differences between the methods, mostly for phase and ARI. Noteworthy in this regard, is that for phase in the VLF, there does seem to be some benefit in using linear auto-regressive models, as methods 14.1 and 14.2 (S1 Table) have the highest ICCs in the VLF. Furthermore, for ARI like indices, the use of impulse response FIR filters seems advisable, given the high reproducibility for method 11.5 (impulse response filter coefficient).

What can be advised for the analysis of DCA in practical terms given these results? The answer to this question is not straightforward due to the variety of methods that were employed in this study, but will also depend highly on the type of clinical problem that is being addressed. As has been stated previously, it is unlikely that a single analysis method will prove to be satisfactory for all possible clinical situations[33,34]. Reproducibility by itself is not sufficient for good diagnostic properties of DCA variables, but it can be viewed as a necessary precondition for any diagnostic test. Therefore, the variable with the highest reproducibility (Gain LF), may not be necessarily the best variable to detect disease states, so we cannot recommend a preferred analysis method or DCA variable based on this study alone. However, it is unlikely that those methods with low reproducibility will be clinically useful. Increases in ICC after PSD-MABP based case removal are clearly present, but they are only achieved at the cost of leaving out a substantial amount of cases. These positive and negative aspects need to be carefully balanced in each clinical situation. One way to avoid the negative effects is to put further effort in investigating the influence of maneuvers that induce MABP oscillations[33]. The other option is to increase the duration of measurement in order to obtain more stable DCA estimates. Both from the viewpoint of DCA variables themselves and from the viewpoint of reproducibility statistics this may lead to more reliable results. For example, with TFA, it is known that the confidence limits of the estimates depend on the level of coherence, and on the number of degrees of freedom used in the estimate which is determined by measurement duration and spectral smoothing[35],[36]. With increasing measurement duration, confidence limits of DCA estimates will be reduced, leading to less variability and higher reproducibility. From the viewpoint of ICC, the Spearman-Brown formula was used to visualize that 5 minutes of measurement duration is not enough for most DCA metrics, except for gain LF. It is estimated that for some methods, extending the measurement duration to beyond 30 minutes will be required to achieve acceptable reproducibility. It needs to be emphasized that this is only a prediction based on the assumption of stable and stationary autoregulation, which may not always be realistic. Ideally, the prediction results should be verified in measurements of longer duration, for example the study of Zhang and colleagues have used measurement durations of up to 2 hours[37].

Clinical perspectives and recommendations:

Based on the results in this study, it seems advisable to calculate PSD-MABP in the VLF and LF bands during data acquisition, so that one can evaluate if sufficient power is present in the MABP signal. It is advisable to have at least 29 mmHg2/Hz PSD in the VLF when analyzing gain and phase and also ARI, so that at least moderate reproducibility can be achieved for some methods, with good reproducibility for the best performing methods. This will be accompanied by a 20% loss of analyzable cases, if one extrapolates from the relatively large sample adopted in this study. When phase LF is of interest, at least 10 mmHg2/Hz PSD is advisable, which will lead to 30% loss of cases, but these estimates need further confirmation in different measurement conditions and patient sub-groups. If not sufficient, recordings may be extended while selectively leaving out data segments with low PSD-MABP. Alternatively, oscillation inducing maneuvers can be attempted. In clinical situations, longer measurement duration without loss of data quality may sometimes be difficult, for example in acute stroke patients who may suffer from delirium and restlessness. On the other hand, in the intensive care setting when patients are sedated and intubated, a longer measurement duration may be more easily obtained.

A number of limitations need to be mentioned. First, this was a retrospective study, with highly selected measurements that were further inspected and checked for quality issues, and if necessary were replaced. The results that were found here may not always apply in situations where optimal recordings are not easily achieved. Secondly, some of the subjects were using medication during the time of the measurement, most often for hypertension. We cannot exclude the possibility that low PSD-MABP power was in part due to the use of medication, but suspect that it is likely that this is not a major cause, since median lowest PSD-MABP was comparable between those that used vasoactive medication and those without any medication (S1 Fig). Third, subjects of all ages were included, and this may have contributed to increased variability in some of the parameters. For DCA variables on the other hand, no clear influence of age has been established so far[38], therefore a major influence of age variability on the results seems unlikely. Fourth, only two centers employed correlation based methods in this study, therefore these methods could not be analyzed with the same level of detail as other methods. Lastly, we did not consider the influence of time between the two measurements, which could be up to 3 months in this study. We cannot exclude the possibility that a longer interval between the two measurements will introduce extra variability in the DCA estimates.

To conclude, the reproducibility of DCA parameters, derived from spontaneous fluctuations in MABP, is poor to moderate when all cases were used for the analysis, except for gain LF which has good reproducibility with TFA-like methods in some centers. By removing cases with low PSD-MABP power, reproducibility can increase to levels generally accepted as ‘good’, but only for a limited number of analysis methods. Future research should perform a similar assessment of reproducibility using protocols that induce PSD-MABP oscillations or use longer measurement durations at rest. Studies of short term reproducibility in patient-groups or induced pathological states would also be highly relevant to allow further progress with translation of assessment of dynamic CA methods to clinical practice.

Supporting information

S1 Table. Analysis methods with references and corresponding output variables per center.

Category: 1 = TFA-like methods, 2 = ARI-like methods, 3 = correlation-like methods, Method group: 1 = TFA, 2 = Laguerre expansions, 3 = Wavelets, 4 = IR-filter, 5 = ARX, 6 = ARI, 7 = ARMA-ARI/ARX, 9 = IR-filter, 10 = correlation coefficient; VLF: very low frequency; LF: low frequency; BP: blood pressure; FFT: fast Fourier transform; ARI: autoregulation index; ARX: autoregressive model with exogenous input; Centre names are listed in S2 Table.

(DOCX)

Click here for additional data file. (44.9KB, docx)
S2 Table. Participating centers and their roles.

(DOCX)

Click here for additional data file. (14.9KB, docx)
S1 File. Monte Carlo simulation details.

(DOCX)

Click here for additional data file. (15.9KB, docx)
S1 Fig. PSD-MABP comparison between subjects with and without vasoactive medication.

Median lowest PSD-MABP levels for subjects with and without vasoactive medication, in all frequency bands (VLF, LF and HF). No significant differences were found between the two groups.

(DOCX)

Click here for additional data file. (33.8KB, docx)
S2 Fig. ICC values for gain LF and gain VLF.

Beeswarm letter-boxplot with ICC values for Gain LF (upper figure) and Gain VLF (lower figure) for different cut-off levels of PSD-MABP. Each analysis method is represented by a letter. No significant differences between methods were found.

(DOCX)

Click here for additional data file. (89.1KB, docx)
S3 Fig. ICC values for phase LF and phase VLF.

Beeswarm letter-boxplot with ICC values for Phase LF (upper figure) and Phase VLF (lower figure) for different cut-off levels of PSD-MABP. Each analysis method is represented by a letter. ! :indicates cut-off level at which significant differences between the methods were found. Post hoc sum-scores for each cut-off level with significant differences between the methods are indicated in the legend, from left to right. For each method, a significant positive ICC difference with another method is scored as +1, no difference as 0, and a negative difference as -1. The sum of all the scores in the post-hoc sum-score. Negative ICC values do not appear in this plot.

(DOCX)

Click here for additional data file. (106KB, docx)
S4 Fig. ICC values for ARI and correlation like indices.

Beeswarm letter-boxplot with ICC values for ARI and correlation like indices for different cut-off levels of PSD-MABP. Each analysis method is represented by a letter. ! :indicates cut-off level at which significant differences between the methods were found. Post hoc sum-scores for each cut-off level with significant differences between the methods are indicated in the legend, from left to right. For each method, a significant positive ICC difference with another method is scored as +1, no difference as 0, and a negative difference as -1. The sum of all the scores in the post-hoc sum-score. Negative ICC values do not appear in this plot. H and I indicate correlation like indices, which were not included in calculation of the boxplot or in the statistical analysis.

(DOCX)

Click here for additional data file. (51.8KB, docx)
S1 Dataset. All_measurment_files_anonymized.zip: Contains all the anonymized measurement files named 1 through 150.txt.

Allcenters_DCAoutput_andotherdata.xlsx: contains the DCA analysis output data off all participating centers, Power Spectral Density data for Mean Arterial Blood Pressure, and means and standard deviations for all variables in the measurement files.

CARNETanonymization.xlsx: contains the anonymization key used for this study.

(ZIP)

Click here for additional data file. (6.5MB, zip)

Acknowledgments

The authors wish to thank all participating centers for their efforts and support.

Data Availability

All relevant data are available within the paper and its Supporting Information files.

Funding Statement

The author(s) received no specific funding for this work.

References

  • 1.Panerai RB. Transcranial Doppler for evaluation of cerebral autoregulation. Clin Auton Res. 2009;19: 197–211. 10.1007/s10286-009-0011-8 [DOI] [PubMed] [Google Scholar]
  • 2.Aaslid R, Lindegaard KF, Sorteberg W, Nornes H. Cerebral autoregulation dynamics in humans. Stroke. 1989;20: 45–52. 10.1161/01.str.20.1.45 [DOI] [PubMed] [Google Scholar]
  • 3.Aries MJH, Elting JW, De Keyser J, Kremer BPH, Vroomen PCAJ. Cerebral autoregulation in stroke: A review of transcranial doppler studies. Stroke. 2010;41: 2697–2704. 10.1161/STROKEAHA.110.594168 [DOI] [PubMed] [Google Scholar]
  • 4.Reinhard M, Roth M, Guschlbauer B, Harloff A, Timmer J, Czosnyka M, et al. Dynamic cerebral autoregulation in acute ischemic stroke assessed from spontaneous blood pressure fluctuations. Stroke. 2005;36: 1684–1689. 10.1161/01.STR.0000173183.36331.ee [DOI] [PubMed] [Google Scholar]
  • 5.Aries MJH, Van Der Naalt J, van den Bergh WB, van Dijk M, Elting JWJ, Czosnyka M, et al. Neuromonitoring of patients with severe traumatic brain injury at the bedside. Netherlands J Crit Care. 2015;20: 6–12. [Google Scholar]
  • 6.Aries MJH, Wesselink R, Elting JWJ, Donnelly J, Czosnyka M, Ercole A, et al. Enhanced Visualization of Optimal Cerebral Perfusion Pressure over Time to Support Clinical Decision Making. Crit Care Med. 2016;44: e996–e999. 10.1097/CCM.0000000000001816 [DOI] [PubMed] [Google Scholar]
  • 7.Mitsis GD, Poulin MJ, Robbins PA, Marmarelis VZ. Nonlinear modeling of the dynamic effects of arterial pressure and CO 2 variations on cerebral blood flow in healthy humans. IEEE Trans Biomed Eng. 2004;51: 1932–1943. 10.1109/TBME.2004.834272 [DOI] [PubMed] [Google Scholar]
  • 8.Panerai RB, Deverson ST, Mahony P, Hayes P, Evans DH. Effect of CO 2 on dynamic cerebral autoregulation measurement. Physiol Meas. 1999;20: 265–275. 10.1088/0967-3334/20/3/304 [DOI] [PubMed] [Google Scholar]
  • 9.van Lieshout JJ, Secher NH. Point:Counterpoint: Sympathetic activity does/does not influence cerebral blood flow. Point: Sympathetic activity does influence cerebral blood flow. J Appl Physiol. 2008;105: 1364–6. 10.1152/japplphysiol.90597.2008 [DOI] [PubMed] [Google Scholar]
  • 10.Panerai RB. Nonstationarity of dynamic cerebral autoregulation. Med Eng Phys. 2014;36: 576–584. 10.1016/j.medengphy.2013.09.004 [DOI] [PubMed] [Google Scholar]
  • 11.Marmarelis VZ, Shin DC, Orme M, Zhang R. Time-varying modeling of cerebral hemodynamics. IEEE Trans Biomed Eng. 2014;61: 694–704. 10.1109/TBME.2013.2287120 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Claassen JA, Meel-Van Den Abeelen AS, Simpson DM, Panerai RB, Alexander Caicedo Dorado, Mitsis GD, et al. Transfer function analysis of dynamic cerebral autoregulation: A white paper from the International Cerebral Autoregulation Research Network. J Cereb Blood Flow Metab. 2015;36: 665–680. 10.1177/0271678X15626425 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Peng T, Rowley AB, Ainslie PN, Poulin MJ, Payne SJ. Multivariate system identification for cerebral autoregulation. Ann Biomed Eng. 2008;36: 308–320. 10.1007/s10439-007-9412-9 [DOI] [PubMed] [Google Scholar]
  • 14.Marmarelis VZ, Mitsis GD, Shin DC, Zhang R. Multiple-input nonlinear modelling of cerebral haemodynamics using spontaneous arterial blood pressure, end-tidal CO 2 and heart rate measurements. Philos Trans R Soc A Math Phys Eng Sci. 2016;374 10.1098/rsta.2015.0180 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Mitsis GD, Poulin MJ, Robbins PA, Marmarelis VZ. Nonlinear modeling of the dynamic effects of arterial pressure and CO 2 variations on cerebral blood flow in healthy humans. IEEE Trans Biomed Eng. 2004;51: 1932–1943. 10.1109/TBME.2004.834272 [DOI] [PubMed] [Google Scholar]
  • 16.Novak V, Yang ACC, Lepicovsky L, Goldberger AL, Lipsitz LA, Peng CK. Multimodal pressure-flow method to assess dynamics of cerebral autoregulation in stroke and hypertension. Biomed Eng Online. 2004;3 10.1186/1475-925X-3-3 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Lo MT, Hu K, Liu Y, Peng CK, Novak V. Multimodal pressure-flow analysis: Application of Hilbert Huang transform in cerebral blood flow regulation. EURASIP J Adv Signal Process. 2008;2008 10.1155/2008/785243 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.System R.B. P. identification of human cerebral blood flow regulatory mechanisms. Cardiovasc Eng. 2004;4: 59–71. Available: http://www.embase.com/search/results?subaction=viewrecord&from=export&id=L39127634%5Cn [DOI] [Google Scholar]
  • 19.Panerai RB, Eames PJ, Potter JF. Variability of time-domain indices of dynamic cerebral autoregulation. Physiological Measurement. 2003. pp. 367–381. 10.1088/0967-3334/24/2/312 [DOI] [PubMed] [Google Scholar]
  • 20.Kostoglou K, Debert CT, Poulin MJ, Mitsis GD. Nonstationary multivariate modeling of cerebral autoregulation during hypercapnia. Med Eng Phys. 2014;36: 592–600. 10.1016/j.medengphy.2013.10.011 [DOI] [PubMed] [Google Scholar]
  • 21.Sanders ML, Claassen JAHR, Aries M, Bor-Seng-Shu E, Caicedo A, Chacon M, et al. Reproducibility of dynamic cerebral autoregulation parameters: A multi-centre, multi-method study. Physiol Meas. 2018;39 10.1088/1361-6579/aae9fd [DOI] [PubMed] [Google Scholar]
  • 22.Sanders ML, Claassen JAHR, Aries M, Bor-Seng-Shu E, Caicedo A, Chacon M, et al. Dynamic cerebral autoregulation reproducibility is affected by physiological variability. Front Physiol. 2019;in press. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Reinhard M, Müller T, Guschlbauer B, Timmer J, Hetzel a. Transfer function analysis for clinical evaluation of dynamic cerebral autoregulation—a comparison between spontaneous and respiratory-induced oscillations. Physiol Meas. 2003;24: 27–43. 10.1088/0967-3334/24/1/303 [DOI] [PubMed] [Google Scholar]
  • 24.Liu J, Simpson DM, Allen R. High spontaneous fluctuation in arterial blood pressure improves the assessment of cerebral autoregulation. Physiol Meas. 2005;26: 725–741. 10.1088/0967-3334/26/5/012 [DOI] [PubMed] [Google Scholar]
  • 25.Elting JW, Aries MJH, van der Hoeven JH, Vroomen PCAJ, Maurits NM. Reproducibility and variability of dynamic cerebral autoregulation during passive cyclic leg raising. Med Eng Phys. 2014;36: 585–591. 10.1016/j.medengphy.2013.09.012 [DOI] [PubMed] [Google Scholar]
  • 26.Claassen JAHR, Levine BD, Zhang R. Dynamic cerebral autoregulation during repeated squat-stand maneuvers. J Appl Physiol. 2008;106: 153–160. 10.1152/japplphysiol.90822.2008 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Birch AA, Neil-Dwyer G, Murrills AJ. The repeatability of cerebral autoregulation assessment using sinusoidal lower body negative pressure. Physiol Meas. 2002;23: 73–83. 10.1088/0967-3334/23/1/307 [DOI] [PubMed] [Google Scholar]
  • 28.Brodie FG, Atkins ER, Robinson TG, Panerai RB. Reliability of dynamic cerebral autoregulation measurement using spontaneous fluctuations in blood pressure. Clin Sci. 2009;116: 513–520. 10.1042/CS20080236 [DOI] [PubMed] [Google Scholar]
  • 29.Box GEP, Cox DR. An Analysis of Transformations. J R Stat Soc Ser B. 1964;26: 211–243. 10.1111/j.2517-6161.1964.tb00553.x [DOI] [Google Scholar]
  • 30.McCrary S. Implementing a Monte Carlo Simulation: Correlation, Skew, and Kurtosis. In: Ssrn: https://papers.ssrn.com/sol3/papers.cfm?abstract_id=2665147 [Internet]. 2015 pp. 1–20. 10.2139/ssrn.2665147 [DOI]
  • 31.de Vet HCW, Mokkink LB, Mosmuller DG, Terwee CB. Spearman–Brown prophecy formula and Cronbach’s alpha: different faces of reliability and opportunities for new applications. J Clin Epidemiol. Elsevier Inc; 2017;85: 45–49. 10.1016/j.jclinepi.2017.01.013 [DOI] [PubMed] [Google Scholar]
  • 32.Cicchetti D V. Guidelines, Criteria, and Rules of Thumb for Evaluating Normed and Standardized Assessment Instruments in Psychology. Psychol Assess. 1994;6: 284–290. 10.1037/1040-3590.6.4.284 [DOI] [Google Scholar]
  • 33.Simpson D, Claassen J. CrossTalk opposing view: dynamic cerebral autoregulation should be quantified using induced (rather than spontaneous) blood pressure fluctuations. J Physiol. 2018;596: 7–9. 10.1113/JP273900 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Tzeng YC, Panerai RB. CrossTalk proposal: dynamic cerebral autoregulation should be quantified using spontaneous blood pressure fluctuations. J Physiol. 2018;596: 3–5. 10.1113/JP273899 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Halliday DM, Rosenberg JR, Amjad AM, Breeze P, Conway BA, Farmer SF. A framework for the analysis of mixed time series/point process data-Theory and application to the study of physiological tremor, single motor unit discharges and electromyograms. Prog Biophys Mol Biol. 1995;64: 237–278. 10.1016/s0079-6107(96)00009-0 [DOI] [PubMed] [Google Scholar]
  • 36.Bendat J, Piersol A. Random Data Analysis and Measurement Procedures 4th ed Measurement Science and Technology. John Wiley And Sons Ltd; 2010. [Google Scholar]
  • 37.Zhang R, Zuckerman JH, Levine BD. Spontaneous fluctuations in cerebral blood flow: insights from extended-duration recordings in humans. Am J Physiol Circ Physiol. 2017;278: H1848–H1855. 10.1152/ajpheart.2000.278.6.h1848 [DOI] [PubMed] [Google Scholar]
  • 38.Carey BJ, Eames PJ, Blake MJ, Panerai RB, Potter JF. Dynamic cerebral autoregulation is unaffected by aging. Stroke. 2000;31: 2895–2900. 10.1161/01.str.31.12.2895 [DOI] [PubMed] [Google Scholar]

Decision Letter 0

Tatsuo Shimosawa

7 Nov 2019

PONE-D-19-25218

Assessment of dynamic cerebral autoregulation in humans: is reproducibility dependent on blood pressure variability?

PLOS ONE

Dear Dr. Elting,

Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

Three experts raised independent concerns. In the revision all the concerns should be clarified.  Specially clinical implication should be refined.

We would appreciate receiving your revised manuscript by Dec 22 2019 11:59PM. When you are ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter.

To enhance the reproducibility of your results, we recommend that if applicable you deposit your laboratory protocols in protocols.io, where a protocol can be assigned its own identifier (DOI) such that it can be cited independently in the future. For instructions see: http://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols

Please include the following items when submitting your revised manuscript:

  • A rebuttal letter that responds to each point raised by the academic editor and reviewer(s). This letter should be uploaded as separate file and labeled 'Response to Reviewers'.

  • A marked-up copy of your manuscript that highlights changes made to the original version. This file should be uploaded as separate file and labeled 'Revised Manuscript with Track Changes'.

  • An unmarked version of your revised paper without tracked changes. This file should be uploaded as separate file and labeled 'Manuscript'.

Please note while forming your response, if your article is accepted, you may have the opportunity to make the peer review history publicly available. The record will include editor decision letters (with reviews) and your responses to reviewer comments. If eligible, we will contact you to opt in or out.

We look forward to receiving your revised manuscript.

Kind regards,

Tatsuo Shimosawa, M.D., Ph.D.

Academic Editor

PLOS ONE

Journal Requirements:

1. When submitting your revision, we need you to address these additional requirements. Please ensure that your manuscript meets PLOS ONE's style requirements, including those for file naming. The PLOS ONE style templates can be found at http://www.journals.plos.org/plosone/s/file?id=wjVg/PLOSOne_formatting_sample_main_body.pdf and http://www.journals.plos.org/plosone/s/file?id=ba62/PLOSOne_formatting_sample_title_authors_affiliations.pdf

2. We note that you have indicated that data from this study are available upon request. PLOS only allows data to be available upon request if there are legal or ethical restrictions on sharing data publicly. For information on unacceptable data access restrictions, please see http://journals.plos.org/plosone/s/data-availability#loc-unacceptable-data-access-restrictions.

In your revised cover letter, please address the following prompts:

a) If there are ethical or legal restrictions on sharing a de-identified data set, please explain them in detail (e.g., data contain potentially identifying or sensitive patient information) and who has imposed them (e.g., an ethics committee). Please also provide contact information for a data access committee, ethics committee, or other institutional body to which data requests may be sent.

b) If there are no restrictions, please upload the minimal anonymized data set necessary to replicate your study findings as either Supporting Information files or to a stable, public repository and provide us with the relevant URLs, DOIs, or accession numbers. Please see http://www.bmj.com/content/340/bmj.c181.long for guidelines on how to de-identify and prepare clinical data for publication. For a list of acceptable repositories, please see http://journals.plos.org/plosone/s/data-availability#loc-recommended-repositories.

We will update your Data Availability statement on your behalf to reflect the information you provide.

3. PLOS requires an ORCID iD for the corresponding author in Editorial Manager on papers submitted after December 6th, 2016. Please ensure that you have an ORCID iD and that it is validated in Editorial Manager. To do this, go to ‘Update my Information’ (in the upper left-hand corner of the main menu), and click on the Fetch/Validate link next to the ORCID field. This will take you to the ORCID site and allow you to create a new iD or authenticate a pre-existing iD in Editorial Manager. Please see the following video for instructions on linking an ORCID iD to your Editorial Manager account: https://www.youtube.com/watch?v=_xcclfuvtxQ

[Note: HTML markup is below. Please do not edit.]

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

Reviewer #2: Yes

Reviewer #3: Yes

**********

2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

Reviewer #2: Yes

Reviewer #3: Yes

**********

3. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: Yes

Reviewer #3: Yes

**********

4. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

Reviewer #2: Yes

Reviewer #3: Yes

**********

5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: This manuscript provides us the novel clinical implications in the assessment of cerebral circulation. The methods were reasonable, and discussion is quite scientific.

To strength the manuscript I would like to ask several minor questions to the authors.

1) How did you calculate the sample size (75 healthy subjects)?

2) As described in the limitation, I also afraid the effects of hypertensive agents to your results. Your discussion about this issue in the limitation paragraph was quite reasonable. If possible, it will be helpful to us that the subjects with hypertensive agents would be excluded or showed in separate table.

3) I would like you to show more concrete clinical perspectives.

Reviewer #2: The reproducibility of dynamic cerebral autoregulation assessment is an important step for its clinical use. The authors found that the assessment was not reproducible unless MAP variations during the measurement window are significant. I found the analysis in the paper is sound. I have the following suggested revisions:

1. The authors mention that reproducibility will probably improve if measurement duration is increased. This is based on their use of the Spearman-Brown prophecy formula. The authors cite a reference for this, but they should also write what the formula is in the manuscript to make it easier to understand Fig. 5. Are longer durations more likely to be reproducible because there are more likely to be significant spontaneous MAP variations?

2. I would appreciate practical recommendations in the manuscript about what the power spectral density MABP levels need to be for reproducible results.

Reviewer #3: The article "Assesment of dynamic cerebral autoregulation in humans: is reproducibility dependent on blood pressure variability?" by Elting et. al. is an interesting and potentially significant article on the intra-sibject variability of cerebral autoregulation measurements. The authors have performed a retrospective analysis of data from several sites, comprising of recordings of mean arterial blood pressure and cerebral blood flow velocity (derived from TCD). The goal of the analysis is to quantify the variability in autoregulation indices specifically with respect to blood pressure variability. The analysis methods, statistical techniques used are rigorous, with instructive and explanative figures. The conclusions drawn by the authors are appropriate. However, a few minor details reduce the clarity and readabilty of the article. Those and other comments are listed below.

1. The organization of the data sources is somewhat difficult to understand. The authors provide a list of data sources and analysis performed therein in supplementary tables S1 and S2. While the text states that data was derived form 5 participating centers, the tables seem to suggest 6 data sources. Furthermore, it is evident that the tables that each data source is used more than once. However, it is difficult for the reader to ascertain if the same class of analysis (e.g., transfer function) is performed more than once on the same data set. Furthermore, are all three categories of analysis avaibale for all data sources? Some clarity on this, perhaps in the form of a supplementary table that lists the data source and associated analysis, will help.

2. One of the goals of the analysis is to look at the variabilities of autoregulatory responses at different time points. However, the authors do not specifiy the range of time pioints from which dual ratings were derived for analysis (besides from an upper bound of 3 months). The time between measurements may be a significant factor in the variablity - this is not considered here.

3. For the surrogate data used to replace data of poor quality, the authors performed simulatons absed on the Tiecks model. How did the authors know which ARI to use, if the data was of poor quality to perform analysis in the first place? Also, please include a citaiton for the model.

4. It might help to describe the outecome variables from the three autoregulation measurement classes.

5. The authors describe the PSD based case removal approach, but do not provide sufficient justification for why the authors considered PSD as a measure of variability. Similarly, what is the rationale for using the 'lowest' PSD-MABP as the independent variable for correlation analyses?

**********

6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: Yes: Takuya Kishi

Reviewer #2: No

Reviewer #3: No

[NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files to be viewed.]

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email us at figures@plos.org. Please note that Supporting Information files do not need this step.

Decision Letter 1

Tatsuo Shimosawa

26 Dec 2019

Assessment of dynamic cerebral autoregulation in humans: is reproducibility dependent on blood pressure variability?

PONE-D-19-25218R1

Dear Dr. Elting,

We are pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it complies with all outstanding technical requirements.

Within one week, you will receive an e-mail containing information on the amendments required prior to publication. When all required modifications have been addressed, you will receive a formal acceptance letter and your manuscript will proceed to our production department and be scheduled for publication.

Shortly after the formal acceptance letter is sent, an invoice for payment will follow. To ensure an efficient production and billing process, please log into Editorial Manager at https://www.editorialmanager.com/pone/, click the "Update My Information" link at the top of the page, and update your user information. If you have any billing related questions, please contact our Author Billing department directly at authorbilling@plos.org.

If your institution or institutions have a press office, please notify them about your upcoming paper to enable them to help maximize its impact. If they will be preparing press materials for this manuscript, you must inform our press team as soon as possible and no later than 48 hours after receiving the formal acceptance. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact onepress@plos.org.

With kind regards,

Tatsuo Shimosawa, M.D., Ph.D.

Academic Editor

PLOS ONE

Additional Editor Comments (optional):

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.

Reviewer #1: All comments have been addressed

Reviewer #2: All comments have been addressed

Reviewer #3: All comments have been addressed

**********

2. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

Reviewer #2: Yes

Reviewer #3: Yes

**********

3. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

Reviewer #2: Yes

Reviewer #3: Yes

**********

4. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: Yes

Reviewer #3: Yes

**********

5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

Reviewer #2: Yes

Reviewer #3: Yes

**********

6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: (No Response)

Reviewer #2: (No Response)

Reviewer #3: (No Response)

**********

7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: Yes: TAKUYA KISHI

Reviewer #2: No

Reviewer #3: No

Acceptance letter

Tatsuo Shimosawa

30 Dec 2019

PONE-D-19-25218R1

Assessment of dynamic cerebral autoregulation in humans:  is reproducibility dependent on blood pressure variability?

Dear Dr. Elting:

I am pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department.

If your institution or institutions have a press office, please notify them about your upcoming paper at this point, to enable them to help maximize its impact. If they will be preparing press materials for this manuscript, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org.

For any other questions or concerns, please email plosone@plos.org.

Thank you for submitting your work to PLOS ONE.

With kind regards,

PLOS ONE Editorial Office Staff

on behalf of

Prof. Tatsuo Shimosawa

Academic Editor

PLOS ONE

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Supplementary Materials

    S1 Table. Analysis methods with references and corresponding output variables per center.

    Category: 1 = TFA-like methods, 2 = ARI-like methods, 3 = correlation-like methods, Method group: 1 = TFA, 2 = Laguerre expansions, 3 = Wavelets, 4 = IR-filter, 5 = ARX, 6 = ARI, 7 = ARMA-ARI/ARX, 9 = IR-filter, 10 = correlation coefficient; VLF: very low frequency; LF: low frequency; BP: blood pressure; FFT: fast Fourier transform; ARI: autoregulation index; ARX: autoregressive model with exogenous input; Centre names are listed in S2 Table.

    (DOCX)

    Click here for additional data file. (44.9KB, docx)
    S2 Table. Participating centers and their roles.

    (DOCX)

    Click here for additional data file. (14.9KB, docx)
    S1 File. Monte Carlo simulation details.

    (DOCX)

    Click here for additional data file. (15.9KB, docx)
    S1 Fig. PSD-MABP comparison between subjects with and without vasoactive medication.

    Median lowest PSD-MABP levels for subjects with and without vasoactive medication, in all frequency bands (VLF, LF and HF). No significant differences were found between the two groups.

    (DOCX)

    Click here for additional data file. (33.8KB, docx)
    S2 Fig. ICC values for gain LF and gain VLF.

    Beeswarm letter-boxplot with ICC values for Gain LF (upper figure) and Gain VLF (lower figure) for different cut-off levels of PSD-MABP. Each analysis method is represented by a letter. No significant differences between methods were found.

    (DOCX)

    Click here for additional data file. (89.1KB, docx)
    S3 Fig. ICC values for phase LF and phase VLF.

    Beeswarm letter-boxplot with ICC values for Phase LF (upper figure) and Phase VLF (lower figure) for different cut-off levels of PSD-MABP. Each analysis method is represented by a letter. ! :indicates cut-off level at which significant differences between the methods were found. Post hoc sum-scores for each cut-off level with significant differences between the methods are indicated in the legend, from left to right. For each method, a significant positive ICC difference with another method is scored as +1, no difference as 0, and a negative difference as -1. The sum of all the scores in the post-hoc sum-score. Negative ICC values do not appear in this plot.

    (DOCX)

    Click here for additional data file. (106KB, docx)
    S4 Fig. ICC values for ARI and correlation like indices.

    Beeswarm letter-boxplot with ICC values for ARI and correlation like indices for different cut-off levels of PSD-MABP. Each analysis method is represented by a letter. ! :indicates cut-off level at which significant differences between the methods were found. Post hoc sum-scores for each cut-off level with significant differences between the methods are indicated in the legend, from left to right. For each method, a significant positive ICC difference with another method is scored as +1, no difference as 0, and a negative difference as -1. The sum of all the scores in the post-hoc sum-score. Negative ICC values do not appear in this plot. H and I indicate correlation like indices, which were not included in calculation of the boxplot or in the statistical analysis.

    (DOCX)

    Click here for additional data file. (51.8KB, docx)
    S1 Dataset. All_measurment_files_anonymized.zip: Contains all the anonymized measurement files named 1 through 150.txt.

    Allcenters_DCAoutput_andotherdata.xlsx: contains the DCA analysis output data off all participating centers, Power Spectral Density data for Mean Arterial Blood Pressure, and means and standard deviations for all variables in the measurement files.

    CARNETanonymization.xlsx: contains the anonymization key used for this study.

    (ZIP)

    Click here for additional data file. (6.5MB, zip)
    Attachment

    Submitted filename: Reply_reviewers_Elting_et_al.docx

    Click here for additional data file. (30.6KB, docx)

    Data Availability Statement

    All relevant data are available within the paper and its Supporting Information files.

    Articles from PLoS ONE are provided here courtesy of PLOS

    RESOURCES