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Departments of 1Pediatrics and 2Physiology, New York Medical College, Valhalla, New York; and Departments of 3Medicine and 4Neurosciences, University of Medicine and Dentistry of New Jersey-New Jersey Medical School, Newark, New Jersey
Submitted 22 December 2005 ; accepted in final form 10 March 2006
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ABSTRACT |
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 TOP ABSTRACT MATERIALS AND METHODSRESULTSDISCUSSIONGRANTSREFERENCES |
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vasoconstriction; hypocapnia; orthostatic intolerance
40 mmHg to an upright value of 36 mmHg, which is similar to our general experience (28). Much larger postural decrements in PCO2 below 30 mmHg and often reaching <25 mmHg have been reported in diverse forms of orthostatic intolerance where they are associated with an increase in ventilation (19, 22, 24) although this finding remains controversial (27). Such hypocapnia does not appear to be achieved through simple physical or physiological processes but rather requires some form of greatly activated central and peripheral chemoreflex function and operating set point (22). In particular, postural tachycardia syndrome (POTS) has been associated with hyperventilation and decreased PETCO2 that may occur in a majority of patients (22, 27, 36). Hypocapnia accounts for documented reduction of cerebral blood flow in these patients (22, 27, 36). Decreased cerebral blood flow may account for certain symptoms of orthostatic intolerance, including dizziness, headache, neurocognitive deficit, fatigue, visual loss, or impaired consciousness. Interestingly, voluntary hyperventilation fails to induce similar symptomatology (22). One possible explanation for the posturally related hyperventilation is that it might benefit venous return and thus thoracic blood volume and cardiac preload. However, this hypothesis remains unsubstantiated during voluntary or spontaneous hyperventilation (Fig. 1), in which reduced rather than increased thoracic blood volume has been found.
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In contrast, available data support an intimate relation with heightened sympathetic activity: LeLorier et al. (14) produced consistent and uniformly large reductions in PETCO2 by using combined upright tilt and lower-body negative pressure in healthy volunteers. This same group demonstrated a close relation between increased peroneal muscle sympathetic nerve activity and experimentally controlled PETCO2 in another group of healthy subjects (31).
In our own POTS patients, postural hyperventilation and reduced PETCO2 have been confined to a subgroup of patients we have denoted "normal- flow POTS." These patients are characterized by blood volume, cardiac output, and peripheral resistance similar to healthy control subjects but in whom splanchnic blood flow is increased and peripheral blood flow is decreased during upright tilt (33) and during phase II of the Valsalva maneuver (34).
In the present work we hypothesize that sympathetic activation, increased by upright tilt, drives hyperventilation and hypocapnia in POTS patients. On the basis of this hypothesis, we predict that peripheral vasoconstriction, blood pressure (BP) variability, and low frequency (LF)-to-high frequency (HF) ratio, as surrogate measures of sympathetic activity, are significantly increased in those patients with hypocapnic hyperventilation. Results confirm widespread orthostatic peripheral sympathetic activation in hypocapnic POTS patients. Marked peripheral vasoconstriction balances enhanced splanchnic dilation to yield unchanged thoracic blood flow in these patients.
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MATERIALS AND METHODS |
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TOPABSTRACTMATERIALS AND METHODSRESULTSDISCUSSIONGRANTSREFERENCES |
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We studied 20 POTS patients and 10 healthy volunteer control subjects. The POTS patient data were collected from consecutive subjects fulfilling criteria for normal-flow POTS (see below).
POTS patients were referred for >6 mo of orthostatic intolerance defined by the symptoms of lightheadedness, fatigue, exercise intolerance, headache, neurocognitive deficits, tremulousness, nausea and abdominal pain, altered vision, and sometimes shortness of breath when upright with no other medical explanation for the symptoms. All patients with self-described dyspnea had been evaluated by a pulmonary physician with normal outcome. In all patients, POTS was confirmed on a screening upright tilt-table test at 70°. POTS was diagnosed by symptoms of orthostatic intolerance during the screening tilt test associated with an increase in sinus heart rate of >30 beats/min or to a rate of >120 beats/min during the first 10 min of tilt as defined in adult subjects in the literature (16, 26). We used occlusion cuffs placed around the midthigh above a mercury-in-Silastic strain gauge (Hokanson) placed at midcalf to measure supine calf blood flow by venous occlusion strain-gauge plethysmography (SPG). Measurements were made supine at the beginning of experiments after a 30-min resting period. Blood flow was measured while supine by standard venous occlusion methods (6). We subdivided the POTS patients after the tilt test on the basis of calf blood flow by using calf blood flow data collected from >60 healthy volunteer subjects evaluated during prior research protocols. For purposes of this study, only "normal" calf blood flow subjects were retained. Normal flow was defined as >1.2 ml·min–1·100 ml tissue–1, which is the smallest calf blood flow that we have measured in volunteer subjects, and <3.6 ml·min–1·100 ml tissue–1, which is the largest calf blood flow we have measured in volunteer subjects. We defined normal-flow POTS as those POTS patients with calf blood flow falling between these limits.
There were 20 normal flow POTS patients, 14–23 yr of age, identified in this manner (median = 16.8 yr; 6 male, 14 female). There were 10 healthy volunteers who were 14–22 yr of age (median = 17.4 yr; 3 male, 7 female). All subjects (POTS and control subjects) were free from systemic illnesses, and all subjects refrained from taking medications for at least 2 wk before testing. There were no tobacco users. Caffeine was withheld for at least 24 h. All subjects had normal electrocardiograms and echocardiograms. We excluded healthy volunteers with a history of syncope or orthostatic intolerance. There were no trained competitive athletes or bedridden subjects. Informed consent was obtained from subjects or from parents and subjects in those <18 yr old. All protocols were approved by the Committee for the Protection of Human Subjects (Institutional Review Board) of New York Medical College.
Laboratory Evaluation
We assessed BP, heart rate, tidal volume, respiratory rate, and PETCO2 and estimated changes in thoracic, splanchnic, pelvic, and calf segmental blood volumes and blood flows by impedance plethysmography and forearm and calf blood flow by venous occlusion plethysmography while supine and throughout upright tilt as explained below.
Protocol
Tests began after an overnight fast. After a 30-min acclimatization period, we assessed heart rate, BP, respiratory rate, respiratory volumes, and PETCO2 during a supine baseline period of at least 5 min. We then measured blood flow in the arms and legs by using strain-gauge venous occlusion plethysmography. Supine impedance plethysmography (IPG) was employed continuously to measure resistance (R0) and beat-to-beat change in resistance (
R) of thoracic, splanchnic, pelvic, and leg segments.
After supine data collections were complete, the patients were tilted upright to an angle of 70° with the horizontal for maximum of 10 min to obtain steady-state changes in splanchnic and thoracic impedance. Impedance flows and volumes were determined from electrical resistance measurements made while patients gently held their breath in half inspiration. In some POTS subjects, 10 min of tilt could not be sustained, in which cases measurements were made at the longest time upright (see below). The minimum sustained PETCO2, maximum sustained respiratory rate, and maximum sustained minute volume averaged over 30-s epochs were tabulated during tilt. Segmental flow data were tabulated before tilt and at their minima during tilt.
Details of Method
Heart rate, PETCO2, and respiratory and BP monitoring.
ECG.
The ECG was assessed throughout by a microamplifier.
END-TIDAL PARTIAL PRESSURE OF CARBON DIOXIDE.
PETCO2 was measured by using both the analog waveform and the recorded numeric values of PETCO2 obtained from a CapnoCheck II capnograph. Before and during tilt procedures, patients were provided with a nasal cannula and instructed in its use. Side-stream capnography was performed by continuous infrared spectrography at the selective wavelength for carbon absorption (4.3 nm).
RESPIRATORY VOLUMES.
Relative respiratory volumes were obtained by respiratory inductance plethysmograph (Respitrace, NIMS Scientific) as follows: on startup, Respitrace volumes were normalized to an internal scale; once normalization was complete and with the subjects remaining supine, we calibrated normalized Respitrace volumes against a pneumotachograph (Grass Telefactor, West Warwick, RI), which also yielded resting tidal volumes recorded for POTS patients and control subjects alike. This enabled the unobtrusive use of the Respitrace as a comparative quantitative measure of relative changes in tidal volume throughout supine and upright testing. Data for assessment of relative changes in ventilation were obtained offline. After taking absolute values of Respitrace excursions, we integrated these values to obtain a quantity linearly related to total ventilation (Fig. 2).
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ECG, respiratory, PETCO2, and Finometer data were interfaced to a personal computer through an analog-to-digital converter (DI-720 DataQ Ind, Milwaukee, WI). All data were multiplexed with strain-gauge and impedance data and were thereby synchronized.
Heart rate and BP variability, and coherence analysis. At least 5 min of heart beats were acquired during baseline supine continuous recordings of heart rate and BP after a 30-min resting period in all subjects. Beats were again acquired for 3–5 min after a 1- to 2-min BP stabilization period after upright tilt. We used custom software to collect digital sequences containing RR interval, and systolic, diastolic, and mean BPs for each heart beat, although continuous BP and electrocardiographic data were digitized as well (see above). Ectopy was corrected by removing the ectopic beat and interpolating with a cubic spline for five beats in either direction. This was rarely necessary. Beat epochs were linear detrended. For the current analysis, only frequency domain analyses were employed. An autoregressive model was used to calculate the RR interval spectrum, BP power spectrum, and cross spectrum (13–15). In brief, RR intervals and BP, acquired as a sequence of discrete point events, were transformed into an impulse train in which pulses were arranged at equal intervals (equal to the mean RR interval) with impulse heights equal to the RR intervals or BP as appropriate. Autoregression was performed, and digital power spectra were calculated by using the extended Yule-Walker equations (11). The final order of the model was chosen to minimize Akaike's final prediction error (11). This yields the interval spectrum, which is converted to the spectrum of counts by dividing by the mean RR interval of the sequence. The spectral power within a given band was computed by taking the power in the actual frequency band. Spectral power could be partitioned into ultra-low-frequency (ULF, <0.01 Hz), very low-frequency (VLF, 0.01–0.04 Hz), low-frequency (LF, 0.04–0.15 Hz), and high-frequency (HF, 0.15–0.40 Hz) power bands. However, for current purposes, only LF and HF data and total power (TP) were retained for both heart rate and BP. The LF systolic BP power band represents periodic oscillations, which may reflect intrinsic arteriolar vasomotion (17). The LF RR power band reflects small contributions directly from the sympathetic nervous system (13, 14) plus dominant vagal-efferent baroreceptor-mediated changes originating in the pressure trace; it therefore contains both sympathetic and parasympathetic contributions. The HF band represents effects of parasympathetic modulation of heart rate and BP and also mechanical effects of respiration on cardiac filling. The LF-to-HF ratio was calculated to represent overall sympathovagal balance (14). The normalized cross-spectrum between RR and systolic BP was used to calculate the magnitude and phase of the transfer function between systolic BP and RR interval as an index of baroreceptor gain when coherence exceeded 0.5 (15, 17).
Forearm and calf blood flow by SPG. We used venous occlusion SPG in all subjects to measure forearm and calf blood flow. Occlusion cuffs were placed at midbiceps and midthigh. Appropriate-sized mercury-in-Silastic strain gauges (Hokanson) were placed at the maximum dimension of the forearm and calf. Measurements were made in standard fashion by suddenly inflating cuffs to a pressure of 45 mmHg and then computing the slope of time-dependent increase in limb cross section. Measurements of forearm and calf blood flows were made at the beginning of experiments. Measurements of forearm flow were made during upright tilt as indicated. We also estimated supine forearm and calf venous pressures (Pv) by gradually increasing occlusion cuff pressure until a change in SPG deflection was noted. We have used this technique before (32).
IPG to measure changes in segmental blood volumes and blood flows.
We used a Tetrapolar high-resolution impedance monitor (THRIM) four-channel digital impedance plethysmograph (UFI, Morro Bay, Ca) to detect shifts in blood volume and changes in blood flow. These quantities were obtained within four anatomic segments operationally defined by electrode placement on anatomic landmarks. These were designated the thoracic segment (supraclavicular area to xyphoid process), the splanchnic segment (xyphoid process to iliac crest), the pelvic segment incorporating lower pelvis to the knee (iliac crest to knee), and the leg or calf segment (upper calf just below the knee to the ankle). Ag/AgCl ECG electrodes were attached at these segmental boundaries and also to the left foot and left hand, where they served as current injectors. Electrical resistance values were measured by using the segmental pairs as sampling electrodes. The midline distance between the sampling electrodes (L) was measured with a tape measure. We also measured the circumferences of calf, thigh, hips, waist, and chest to obtain approximate volume contents of each anatomic segment. We estimated postural changes in blood volume in each segment during upright tilt from the formula (3)
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is electrical conductivity of blood estimated as 53.2 x exp(hematocrit x 0.022) given by Geddes and Kidder (4). We measured hematocrit from a venous sample taken from the antecubital vein. R0 is the resistance of a specific segment before change in tilt angle, R1 is the resistance after change in the tilt angle, and R is the change in resistance (R1 – R0) in a specific segment during the each incremental tilt step; was regarded as constant during the maneuver. We also used this calculation to quantitate changes in thoracic blood volume during voluntary hyperventilation as shown in Fig. 1.
IPG was also used to measure segmental blood flows (20). Methods have recently been validated in our laboratory for the detection of leg, thoracic, and splanchnic blood flow (33, 34). Pulsatile changes in electrical resistance for each segment were employed to compute the time derivative 
R/t, which we used to obtain the blood flow responses of each body segment during tilt.
Blood flow was estimated for an entire anatomic segment from the formula (3)
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IPG flows were expressed in milliliters per minute for anatomic segment and could be normalized by dividing by estimated segmental volume.
Tilt-table testing. An electrically driven tilt table (Colin Medical, San Antonio, TX) with a footboard was used. After supine measurements were complete, the subjects underwent tilt to 70° for a maximum of 10 min as explained above. Steady state was defined by a stable splanchnic blood volume which could be determined in real time. Typically, splanchnic blood volume steady state was associated with stable splanchnic and thoracic blood flows.
Statistics
All tabular and graphic results are reported as means ± SE. Forearm and calf blood flows and peripheral resistances by SPG, resting tidal volume, PETCO2, impedance estimates of blood flow, and relative change in ventilation were compared by one-way ANOVA comparing control, POTS subjects who demonstrated significant hyperventilation and hypocapnia (POTSHC subjects) and POTS subjects who were normocapnic (POTSNC subjects). We used two-way ANOVA for comparisons of heart rate, mean and systolic BPs, heart rate, and BP variability indexes, IPG blood flow, and blood volume responses to tilt. Results were calculated by using SPSS (Statistical Package for the Social Sciences) software version 11.0.
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RESULTS |
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Lightheadedness was uniformly reported by POTS patients along with other symptoms of orthostatic intolerance during tilt. Two POTS subjects required the tilt to be discontinued before 10 min had elapsed but not before splanchnic steady state was complete. These data were preserved for analysis. No patient fainted. Volunteer control subjects tolerated upright tilt without symptoms.
Resting Supine Hemodynamics and Size Measurements
As shown in Table 1, age, weight, height, and body surface area were similar for all groups.
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SPG forearm and calf flows were not different among the groups, nor were calculated peripheral resistances.
Total power for RR variability and BP variability over the frequency range from 0.001 to 0.6 Hz was not different for the groups, nor was LF-to-HF ratio and transfer function gain. There was a trend toward lower transfer gain (P = 0.12) in the POTSHC group.
As we reported previously (33), splanchnic blood flow was increased in POTS patients compared with control. This held true for both POTSHC (P = 0.035) and POTSNC (P = 0.027) subgroups. There were no significant differences for thoracic, pelvic, or leg (calf) regional segmental circulations.
Changes During Upright Tilt
Heart rate and BP with upright tilt. Referring to Fig. 4, heart rate increased in all subjects at 70° of upright tilt and was further increased compared with control subjects in all POTS patients. Heart rate was most increased in POTSHC (P = 0.001) and significantly less increased in POTSNC (P = 0.045) in the latter compared with the POTSHC subgroup.
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Respiratory indexes with upright tilt. Respiratory rate did not significantly change with upright tilt. Changes in PETCO2 and relative minute ventilation are shown in Fig. 5. PETCO2 decreased significantly for all groups with tilt but was significantly (P < 0.001) reduced in the POTSHC group compared with both of the other groups. This is an expected result based on the definition of the subgroups. Figure 6 shows the degree of inverse correlation (r2 = 0.68) between percent change in minute volume and percent change in PETCO2.
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SPLANCHNIC.
Splanchnic blood volume increased in all subjects, but this increase was significantly greater in all POTS patients (P = 0.009) and was similar for POTSNC and POTSHC. Splanchnic blood flow was markedly decreased in control compared with baseline (P < 0.001). The decrease in splanchnic blood flow was significantly blunted in POTSNC (P = 0.046) compared with control. The decrease was eliminated in POTSHC (P = 0.006). Also, splanchnic blood flow was increased in POTSHC compared with POTSNC (P < 0.05).
PERIPHERAL BLOOD FLOW (PELVIC, CALF, AND FOREARM).
Pelvic and calf blood volume increased in all subjects with tilt (P < 0.001), but the increase was blunted in POTS patients particularly POTSHC. Forearm, pelvic, and calf blood flows decreased in all subjects with tilt (P < 0.001). This decrease in blood flow was significantly accentuated in POTSHC (P = .0045). Forearm, calf, and pelvic blood flows were reduced compared with control subjects in POTSHC only (P = 0.017), indicating increased peripheral vasoconstriction in POTSHC.
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DISCUSSION |
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TOPABSTRACTMATERIALS AND METHODSRESULTSDISCUSSIONGRANTSREFERENCES |
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We have previously demonstrated on orthostatic challenge that despite being normovolemic, normal-flow POTS patients preferentially redistribute extra blood to the splanchnic circulation when upright compared with control subjects (33).
We have since noted that this was often associated with hyperventilation, that is, an increase in tidal volume, and hypocapnia, defined here as a PETCO2 of <30 mmHg. Although hyperventilation has been offered as a theoretical mechanism by which reduced thoracic blood volume may be in part compensated (30), such compensation does not occur in practice. Instead, hyperventilating POTSHC patients demonstrate significantly decreased orthostatic peripheral blood flow in arms, legs, and pelvic areas (which primarily comprise the buttocks and upper legs) compared with control subjects or POTSNC. One might speculate that extreme peripheral vasoconstriction compensated for selective splanchnic vasodilation in these subjects such that thoracic blood flow remained unchanged.
Sympathetic Vasoconstriction May Increase in POTSHC
While our study is limited by the absence of recorded sympathetic neural impulses (see below), the data suggest that marked peripheral vasoconstriction during orthostasis may reflect increased sympathetic activity. This interpretation is supported by heart rate and BP variability data acquired before and during upright tilt. These data show that BP variability and LF-to-HF ratio are significantly increased for POTSHC compared with control subjects, and thus there is enhanced cardiovascular modulation by sympathetic tone.
Does Sympathetic Activation Produce Hyperventilation in POTSHC?
This suggests a possible mechanism by which enhanced sympathetic activation and associated parasympathetic withdrawal alter peripheral and central chemoreflex activity, provoking hyperventilation and hypocapnia. Rapid autonomic modulation of the peripheral chemoreflexes, particularly the carotid chemoreflex, is known (18) and may account in part for ventilatory enhancement during physical and emotional stress (10). This represents one form of cross-talk between the baroreflexes and the chemoreflexes (7). While it is tempting to ascribe significance to reduced blood flow to the glomus in forms of orthostatic intolerance, blood flow alterations do not seem to exert much influence on carotid chemoreflex activity, and there is little evidence for reduced carotid blood flow in POTS patients anyway until cerebral blood flow is diminished.
Alternatively, Does Hyperventilation Produce Sympathetic Activation in POTSHC?
However, an entirely different interpretation could explain our results. Rather than sympathoexcitation and vagal withdrawal producing hyperventilation, could hyperventilation result in sympathoexcitation? Quantitative investigations into the cardiovascular as well as cerebrovascular effects of hyperventilation and hypocapnia date at least to the work of Kety and Schmidt (12). These early studies noted a small increase in cardiac output and reduction in systolic BP with a small increase in mean arterial pressure and heart rate during voluntary or active hyperventilation. Similar findings were found later by Richardson et al. (25), who examined voluntary hyperventilation over a 7-min time period. Those investigators concluded that the peripheral cardiovascular effect of hyperventilation was vasodilation, not vasoconstriction, and that this was primarily the result of respiratory alkalosis and unrelated to mechanical factors. Subsequent work by Van de Borne et al. (37) also indicates a reduction in baroreflex modulation of RR interval (i.e., reduced RR-BP baroreflex gain, such as we measured) but usually associated with sympathoexcitation during isocapnic hyperventilation. [There is an ancient literature on sympathetic activation as evidenced by increased heart rate with hyperventilation.]
Do Hyperventilation and Attendant Cerebral Vasoconstriction Cause POTS Symptoms?
Hyperventilation and hypocapnia are reported in a spectrum of orthostatic intolerance syndromes, specifically reported in chronic orthostatic intolerance (POTS), chronic fatigue syndrome (CFS), and postural faint (19, 21, 22). In these, respiratory changes have been related to decreased cerebral blood flow. Recent data indicate that respiratory changes are not entirely responsible for reduced cerebral blood flow (29). Moreover, there is no evidence of abnormal beat-to-beat cerebral autoregulation in the patients (27). Nor is there evidence that cerebral vasoconstriction alone can produce syncope (15) although complex cardiorespiratory interactions may play an active role (13). Data from Shoemaker's laboratory indicate that actual rather than simulated orthostasis is required for hyperventilation to occur (9). Our data are entirely consistent with prior publications that view hyperventilation as physiologically driven and regard reduced cerebral blood flow as the result of these physiological changes.
Where does this Fit in the Spectrum of "Hyperventilation Syndromes"?
One could also look at patients primarily from the standpoint of a hyperventilation syndrome as it may integrate into a wider scheme of panic disorders. A panic attack is defined symptomatically by the Diagnostic and Statistical Manual IV and the American Psychiatric Association by accelerated heartbeat, difficulty breathing or choking, terror that is almost paralyzing, dizziness or lightheadedness, nausea or abdominal distress, trembling, derealization, sweating, shaking, chest pains, hot flashes, sudden chills, tingling fingers or toes, and fear of losing control or imminent death (1). Many of these symptoms closely resemble findings in POTS and symptoms of orthostatic intolerance.
Limitations
Direct measurement of sympathetic activity such as muscle sympathetic nerve activity would better justify our claim that peripheral sympathetic vasoconstriction is increased in normal-flow POTS patients who are hypocapnic. Such instrumentation is difficult in young subjects and was not pursued. However, indirect measures of arm and leg peripheral vasoconstriction are at least consistent with the claim of sympathoexcitation, as are observed heart rate and BP variability data. Prior published work indicates exaggerated vasoconstriction in comparable normal-flow POTS patients during phase II of the Valsalva maneuver (34).
Respiratory pneumotachography was not performed during orthostatic stress because of feasibility issues and difficulty with simultaneous capnography. Instead, a pneumotachograph was used to calibrate a Respitrace inductance respiratory plethysmograph while the subject remained at supine rest, and the Respitrace alone was used during tilt procedures. This calibration gave highly linear and predictable results over a wide range of inspired volumes. However, the Respitrace provides only relative changes in tidal volume. Therefore while supine minute ventilation and tidal volume could be reported, we could only report relative changes in these quantities while the subject remained upright.
We cannot make statements concerning the impact of hypocapnia on cerebral blood flow because this was not measured while supine or during upright tilt. Results concerning the impact of hypocapnia and reduced cerebral blood flow on POTS remain controversial (22, 27).
We reported changes in segmental blood flow. It might be more useful to report changes in segmental arterial resistance. In past work, we demonstrated that peripheral arterial resistance is related to flow by the relation R = (MAP – Pv)/flow, where Pv is the local venous pressure and MAP is mean arterial pressure. While Pv could be measured supine, it could not be accurately measured during upright tilt, and therefore computed resistance was not reported. However, if it is assumed, as have others (23), that Pv during tilt is not different among various subjects, an assumption that is supported by prior work (32), then it is reasonable to assume that decreased flow predicts increased peripheral resistance.
The majority of subjects were females with regular menstrual cycles, and none was menstruating at the time of testing. Past studies have demonstrated hormonal fluctuations and potentially altered autonomic regulation throughout the menstrual cycle and in response to environmental stimuli (35). There is no apparent effect on orthostatic tolerance (8). Nonetheless, controlling for menstrual cycle will be important to future work.
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ACKNOWLEDGMENTS |
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FOOTNOTES |
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The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.
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REFERENCES |
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TOPABSTRACTMATERIALS AND METHODSRESULTSDISCUSSIONGRANTSREFERENCES |
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CO2) inversely affects MSNA response to orthostatic stress. Am J Physiol Heart Circ Physiol 281: H1040–H1046, 2001.This article has been cited by other articles:
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  A. J. Ocon, M. S. Medow, I. Taneja, D. Clarke, and J. M. Stewart Decreased upright cerebral blood flow and cerebral autoregulation in normocapnic postural tachycardia syndrome Am J Physiol Heart Circ Physiol, August 1, 2009; 297(2): H664 - H673. [Abstract] [Full Text] [PDF]
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 S. Masuki, J. H. Eisenach, W. G. Schrage, N. M. Dietz, C. P. Johnson, B. W. Wilkins, R. A. Dierkhising, P. Sandroni, P. A. Low, and M. J. Joyner Arterial baroreflex control of heart rate during exercise in postural tachycardia syndrome J Appl Physiol, October 1, 2007; 103(4): 1136 - 1142. [Abstract] [Full Text] [PDF]
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J. M. Stewart, I. Taneja, and M. S. Medow Reduced central blood volume and cardiac output and increased vascular resistance during static handgrip exercise in postural tachycardia syndrome Am J Physiol Heart Circ Physiol, September 1, 2007; 293(3): H1908 - H1917. [Abstract] [Full Text] [PDF]
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K. D. Reesink, E. Hermeling, M. C. Hoeberigs, R. S. Reneman, and A. P. G. Hoeks Carotid artery pulse wave time characteristics to quantify ventriculoarterial responses to orthostatic challenge J Appl Physiol, June 1, 2007; 102(6): 2128 - 2134. [Abstract] [Full Text] [PDF]
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P < 0.05 compared with POTSNC.
