nueva página del texto (beta)
Artículo en XML
Referencias del artículo
Traducción automática
Enviar artículo por email
Citado por SciELO 
Similares en
SciELO 
Permalink
INTRODUCTION
Chronic orthostatic intolerance (OI), a heterogeneous entity associated with the alteration of adaptive mechanisms during the orthostatic challenge, is manifested by the instability of blood pressure (BP) and heart rate (HR) when adopting the upright position. OI is characterized by symptoms such as dizziness, weakness, nausea, headache, palpitations, sweating, presyncope, or syncope, which are improved or resolved by lying down1,2. In most patients with OI, the disorder is mild and improves over time, but some of them have more severe symptoms that could be disabling3,4.
OI involves a sympathetic dysfunction because the autonomic nervous system regulation fails to maintain an adequate increase in HR, cardiac contractility, and peripheral vasoconstriction. Therefore, during upright posture, the gravitational pooling of blood in the lower body induces an excessive BP fall with a decrease of cardiac output (CO) and cerebral perfusion3-5.
Head-up tilt test (HUTT) permits to identify different types of OI according to hemodynamic cardiovascular, cerebrovascular, and autonomic responses1. According to an international consensus statement6, postural tachycardia syndrome (POTS) is characterized by a sustained HR increment ≥ 30 beats/min within 10 min of standing or head-up tilt in the absence of orthostatic hypotension. The standing HR for all subjects is often ≥ 120 beats/min. This condition is different from the classical reflex syncope in which there is a relatively sudden change in autonomic nervous system activity leading to a fall in BP, HR, and cerebral perfusion. Chronic OI without tachycardia is a distinct entity that shares many features with POTS without the excess upright tachycardia, with milder dysautonomia7.
Orthostatic cerebral hypoperfusion syndrome (OCHOs) was defined as symptomatic reduction in the cerebral blood flow velocity (CBFv) during the first 10 min of HUTT, without significant changes in HR, BP, and respiratory pattern8. Cerebral hypoperfusion has been observed during HUTT in adult patients with OI leading to reflex syncope9.
Syncope is the transient loss of consciousness and postural tone secondary to cardiovascular collapse and generalized cerebral hypoperfusion due to sympathetic efferent activity withdrawal1,10,11. Although the autonomic nervous system dysregulation precedes syncope in patients with OI, fainting is infrequently observed during HUTT3,12,13.
Continuous BP recordings during an orthostatic challenge allow dividing the sequence of hemodynamic events leading to vasovagal response (VVR) (presyncope/syncope) into four phases14. Phase 1, early stabilization of CO and mean blood pressure (mBP), is almost complete within 2-3 min after tilting, due to an increase of HR and/or systemic vascular resistance (SVR) resulting from increased efferent sympathetic activity. Phase 2 is characterized by circulatory instability with increased BP variability with or without a progressive fall in SVR, CO, or both. After a variable time-interval, Phase 3, manifested by terminal hypotension and syncope, may occur. This phase is not necessarily observed in all patients with OI. Cerebral hypoperfusion (e.g., dizziness, confusion, blurred vision, and presyncope/syncope) always occurs when the cerebral autoregulation fails to compensate for the BP fall9,14. However, during Phase 2, early cerebral hypoperfusion has been observed in some patients with OI, independently of BP, HR, and respiratory changes8.
To the best of our knowledge, it has not been determined if the early cerebral hypoperfusion observed in some patients with chronic OI without tachycardia is related to the final circulatory collapse (VVR) leading to reflex syncope. Therefore, the purpose of this study was to compare cardiovascular, cerebrovascular, and autonomic variables during the first 10 min of tilting in chronic OI patients with or without a VVR (presyncope/syncope with hypotension, with or without bradycardia)15. We hypothesized that those with a VVR have a greater cerebral hypoperfusion and higher sympathetic activity during Phase 2 compared to those without VVR.
METHODS
Subjects
Participants were selected from the database of the Department of Cardiovascular Dysautonomia at the National Institute of Cardiology in Mexico (Instituto Nacional de Cardiología Ignacio Chávez). The database comprises 370 subjects who underwent a drug-free HUTT. All were screened with a medical history and 12-lead electrocardiogram to exclude those with cardiac, neurologic, or metabolic causes of syncope. We selected 49 patients with suspected OI and orthostatic symptoms during HUTT, similar to the symptoms they had for at least 1 year before the study (Fig. 1). All of them had a previous history of symptoms during standing (lightheadedness, palpitations, tiredness, weakness, diminished concentration, tremulousness, nausea, visual changes, discomfort in head or neck, throbbing of the head, anxiety, chest discomfort, dyspnea, presyncope, or syncope), relieved by lying down. Patients with POTS, orthostatic hypotension, orthostatic hypertension, and HUTT without symptoms were excluded from the study. Subjects unable to complete at least 10 min of HUTT for any reason (including syncope), with evidence of hyperventilation (postural hyperpnea), or with artifacts during HUTT were eliminated. Patients were categorized in two groups: (1) with a VVR positive (VVR+, n = 24), and (2) without VVR negative (VVR−, n = 25). The VVR in VVR+ occurred at 19.3 ± 7.0 min after tilting, with Type 1 (mixed response, i.e., hypotension with bradycardia) observed in 13 (54%) patients and Type 3 (vasodepressor response, i.e., hypotension only) in 11 (46%) patients15.
Twenty-five asymptomatic healthy subjects (recruited in a previous study from a sample of volunteer medical students and hospital staff) with negative HUTT16 served as a control group. All subjects gave their informed consent for inclusion before participating in the study. The study was conducted in accordance with the Declaration of Helsinki, and the protocol was approved by the Research and Ethics Committee of the National Cardiology Institute Ignacio Chávez (protocol number 18-1052).
HUTT protocol
All subjects were instructed to discontinue caffeine, alcohol, and tobacco use, and medications with cardiovascular/autonomic effects 48 h before the study, and the daily intakes of water and salt were not restrained. All tilt tests were performed between 8:00 am and 10:00 am after an overnight fast. After 30 min of supine resting, baseline characteristics were assessed during the last 5 min in the supine position. Thereafter, subjects were tilted to a 70° upright position. HUTT was interrupted when a VVR was elicited with a fall in systolic BP (sBP) below 80 mmHg, or after 30 min of tilting.
BP was recorded continuously using finger arterial plethysmography, and periodically calibrated to brachial artery pressure with an oscillometer in the contralateral arm (Task Force Monitor, TFM: CNSystems, Graz, Austria)17. Hemodynamic variables were determined with thoracic bioimpedance cardiography. The variables of interest were obtained on a beat-to-beat basis: mean HR, mBP, sBP, diastolic BP (dBP), stroke index (SI), cardiac index (CI), and total peripheral resistance index (TPRI). The autonomic modulation was obtained by estimation of the power spectral density of HR and dBP variability with an autoregressive method. Artifacts and ectopic activity were eliminated. The absolute powers in the low-frequency band (0.04-0.15 Hz) and high-frequency band (0.15-0.4 Hz) were calculated in normalized units18. Indexes within the low-frequency band are indicators of sympathetic efferent traffic to the heart (LF), or the peripheral arteries (LFdBP), while the high-frequency index (HF) represents parasympathetic traffic to the heart. The ratio LF/HF, considered as an indicator of sympathovagal, was also obtained.
The CBFv was continuously measured throughout the HUTT with a transcranial Doppler ultrasound (EZ-Dop; DWL, Electronics, Sipplingen, Germany). Through a temporal bone window, the left middle cerebral artery was insonated with a 2 MHz probe. Beat-to-beat measurements were obtained of the following variables: systolic CBFv (sCBFv), diastolic CBFv (dCBFv), mean CBFv (mCBFv), and cerebrovascular resistance (CVR). The CVR was defined as mBP/mCBF. The cerebral blood flow category was determined by the mCBFv velocity according to Novak19.
All variables were averaged within the following time intervals: last 5 min of supine resting (baseline), 1st min after tilting (min 1), from min 2 to 6 after tilting (min 5), and from min 6 to 11 after tilting (min 10).
Statistical analysis
A Kolmogorov–Smirnov test was applied to all continuous variables to verify if they had a normal distribution; only two variables required a logarithmic transformation. Results are presented as mean and standard deviation or as mean and 95% confidence intervals. Categorical variables are shown as absolute frequency and percentage. Age and body mass index was compared between groups by one-way ANOVA. All other continuous variables were compared with ANOVA for repeated measures to make comparisons between the three groups (controls, VVR+, and VVR−) and within the four periods of time measurements (baseline, 1, 5, and 10 min of tilt). The p-values of the post hoc analyses were adjusted by the Bonferroni method. p ≤ 0.05 was considered statistically significant. All the analyses were performed with the program SPSS version 21.0 (IBM Statistics, Armonk N.Y).
RESULTS
The three studied groups had similar age and body mass index, with fewer women in the control group (Table 1).
Table 1 Patient's characteristics and percentage of change of mean cerebral blood flow velocity (mCBFv) evaluated during HUTT. Results are reported as mean ± standard deviation or absolute value (percentage)
| Variables | Groups | ||
|---|---|---|---|
| Control (n = 25) | VVR (−) (n = 25) | VVR (+) (n = 24) | |
| Age (years) | 33 ± 11 | 33 ± 14 | 31 ± 12 |
| Women, n (%) | 8 (32%) | 18 (72%)& | 17 (70.8%)& |
| Body Mass Index (kg/m2) | 25.5 ± 3 | 23.9 ± 4 | 24.3 ± 4 |
| Percentage of mCBFv change from baseline | |||
| 1 min | −4.4 ± 5.2 | −11.2 ± 9.9* | −13.4 ± 14.7*,& |
| 5 min | −11.3 ± 8.7* | −22.0 ± 17.2*,& | −21.7 ± 14.9*,& |
| 10 min | −16.5 ± 11.2* | −25.1 ± 13.5* | −31.2 ± 19.1*,& |
*p < 0.05 versus baseline (within same group).
&p < 0.05 versus control.
VVR (−): Vasovagal response negative.
VVR (+): Vasovagal response positive.
Cardiovascular hemodynamics
Figure 2 shows the mean values of BP and HR. At baseline, sBP was lower in the VVR+ group (108.6 ± 11.8 mmHg) compared to the control group (117.4 ± 11.3 mmHg), p = 0.032. On tilting, sBP, dBP, mBP, and HR increased in all groups and remained higher than baseline. At 10 min of tilting, VVR+ patients had lower sBP, dBP, and mBP compared to the other two groups.
Figure 2 Hemodynamic variables measured during the orthostatic challenge in the studied groups (Control, VVR−: vasovagal response negative; and VVR+: vasovagal response positive). sBP: systolic blood pressure; dBP: diastolic blood pressure; mBP: mean blood pressure; HR: heart rate. These values are reported as mean with 95% confidence intervals.
At baseline, CI, SI, and TPRI were similar in all groups (Fig. 3). After tilting, SI decreased, and TPRI increased in all groups, while the CI decreased after 5 min of tilt only in the control and VVR-groups.
Figure 3 Hemodynamic variables measured during the orthostatic challenge in the studied groups (Control, VVR−: vasovagal response negative; and VVR+: vasovagal response positive). CI: cardiac index; SI: stroke index; TPRI: total peripheral resistance index. These values are reported as mean with 95% confidence intervals.
Cerebrovascular hemodynamics
Since baseline and throughout the tilting, sCBFv and dCBFv were lower in VVR− and VVR+ than in the control group (Fig. 4). As for mCBFv during baseline, it was lower only in VVR+ compared to control. Since min 1 of tilting, mCBFv was lower than control in both VVR− and VVR+. Conversely, at baseline CVR was similar in groups, and after tilting, it increased in all groups, being higher in VVR− and VVR+ compared to the control group.
Figure 4 Changes in cerebrovascular variables of each group according to the responses during the orthostatic challenge. (Control, VVR−: vasovagal response negative; and VVR+: vasovagal response positive). sCBFv: systolic cerebral blood flow velocity; dCBFv: diastolic cerebral blood flow velocity; mCBFv: mean cerebral blood flow velocity; CVR: cerebrovascular resistance. These values are reported as mean with 95% confidence intervals.
Table 1 shows the percentage of change in mCBFv during the tilt test as compared to baseline in each group. The mCBFv dropped from baseline in VVR− and VVR + since min 1 of tilting, while in the control groups, the fall started later at min 5. Compared to controls, VVR+ had a greater drop in mCBFv since the min 1 of tilting, while the decrease in the VVR− group was greater only at the min 5 of tilting. The fall of mCBFv throughout the tilt was similar in VVR− and VVR+ patients.
The cerebral blood flow response to tilt was evaluated according to the OCHOs severity scale. The response in the control group was normal in 12 (48%) and mild to severe in 13 (53%) subjects. In the VVR−, the response was normal in only 4 (16%) and mild to severe in 21 (84%) patients, while the VVR+ had only 2 (8%) patients with normal response and 15 (92%) patients with mild to severe OCHOs, (p = 0.002).
Autonomic variables
Figure 5 shows that all autonomic variables were similar between groups during the tilt test. LF increased, and HF decreased since min 5 in the VVR+ group, and since min 10 in the three groups. The LF/HF increased versus baseline values since min 5 of tilting in all groups. LFdBP increased compared to baseline values at min 10 in the three groups.
Figure 5 Changes in autonomic variables of each group according to the responses during the orthostatic challenge. (Control, VVR−: vasovagal response negative; and VVR+: vasovagal response positive). LF: low-frequency of heart rate fluctuations in normalized units; LFdBP: low-frequency of diastolic blood pressure fluctuations in normalized units; HF: high-frequency of heart rate fluctuations in normalized units. These values are reported as mean with 95% confidence intervals.
DISCUSSION
The main findings of the present study are the following: (i) in patients with chronic OI without tachycardia, there are important changes in the cerebral hemodynamics consisting of significant reduction of CBFv observed since the baseline in supine position, which remained lower than in healthy controls during the first 10 min of HUTT; and (ii) this cerebral hypoperfusion is independent of the VVR observed during the tilt test in some patients with chronic OI. These findings agree with those reported by Novak et al. (2018), who described a distinct form of OI without tachycardia in patients with hypocapnic cerebral hypoperfusion during HUTT20.
Our study included patients with OI without tachycardia, one form of chronic OI not widely recognized, which has clinical and pathophysiological features similar to POTS7. Reduced CBFv with orthostasis precedes hypocapnic hyperpnea and sympathetic activation in POTS patients during orthostatic challenge21. It has been shown than in young, normocapnic POTS subjects, CBFv drops by 19.5% compared with only 10.3% in healthy controls during HUTT. A decrease in the perfusion of the brain may explain the symptoms of lightheadedness, dizziness, and mental confusion that are common in POTS patients. Our group22 and others23 have observed that increased oscillations in arterial pressure were evident in POTS patients during tilt and appeared to synchronize with increased oscillations in CBFv, which could be related to inefficient autoregulation and increased sympathetic activity. Nevertheless, the sympathetic-mediated cerebral vasoconstriction is controversial: while some studies have found little sympathetic vascular control in the brain24, others have found a large sympathetic contribution to cerebral blood flow regulation in humans and mammals25.
Bondar et al. stated that a sympathetic-mediated cerebral vasoconstriction could shift the autoregulatory curve to the right26. Thus, autoregulation would be efficient at high BP but inefficient at lower BP. If this occurred, the decrease in BP seen in POTS subjects during tilt would not be autoregulated, and CBFV would decrease with the decrease in mBP. Ocon et al.23 reported that normocapnic patients with POTS have decreased upright cerebral blood flow and cerebral autoregulation during an orthostatic challenge. We believe that the postural reduction in CBFv could be attributed, at least in part, to cerebral vasoconstriction related to an increase in the baroreflex-induced sympathetic outflow to the cerebral circulation. However, in this study, sympathetic nerve function was assessed using only spectral measures of both HR and BP variability's, which did not show higher sympathetic activity during the orthostatic challenge in subjects with OI without tachycardia as compared to healthy controls. Moreover, we failed to show that those with a VVR had greater cerebral hypoperfusion and higher sympathetic activity during Phase 2 of HUTT, compared to those without VVR.
The cerebral hypoperfusion in our patients with chronic OI without tachycardia could not be explained by an exaggerated initial central hypovolemia21, since they did not show an important fall in SI (i.e., central hypovolemia). Nevertheless, the group of patients with VVR (VVR+) exhibited lower sBP at baseline, and significantly lower sBP, dBP, and mBP at 10 min of tilting, which may represent an impaired peripheral vasoconstriction.
OCHOs are a condition associated with orthostatic hypoperfusion. Patients with OCHOs have stable orthostatic BP, HR, and respiratory pattern (normocapnia), and they still have reduced orthostatic CBFv8. The reduction of CBFv was enough to induce symptoms of cerebral hypoperfusion in 25% of our young patients with OI without tachycardia, similar to that reported previously by Novak et al.8,27 in older patients with OCHO without orthostatic hypotension (20%), and by Ocon et al. in POTS (19.5%)23. Our study suggests that OI without tachycardia is also associated with cerebral hypoperfusion and vasoconstriction. POTS and OI without tachycardia have similar OI symptoms, comparable orthostatic decline in CBFv, and are of similar age and gender20.
An autoimmune basis for POTS has been described28. These observations have led investigators to seek for autoantibodies that might play a role in the pathogenesis of OI. Vernino et al. found ganglionic-receptor-binding antibodies in 7% of patients with POTS and none in healthy controls29. Adrenergic antibodies (α1, β1, and β2) have been also found in patients with OI syndromes which would lead to a hyperadrenergic state and play a role in these disorders pathophysiology30. Fedorowski et al.31 demonstrated that serum from subjects with POTS contains autoantibodies, some with a direct stimulatory effect on adrenergic receptors. A majority also exerted an allosterically mediated positive modulatory effect upon β1AR and a negative modulatory effect on α1AR activity, which may explain different constellations of symptoms in POTS.
The study has some limitations; it was retrospective where the diagnostic criteria were applied to already acquired data. Therefore, gender distribution in the control group was different than in the vasovagal positive and negative groups, as there were only 32% women compared to 67% and 61% in both OI groups. It is well known that orthostatic tolerance is greater in men than in women32, which makes difficult to recruit young asymptomatic healthy women for the control group. Further studies are required to show whether early cerebral hypoperfusion during orthostasis is more prevalent in women.
Hypocapnia is well known to affect CBFv. In this study, we attempted to control for this factor by only using OI patients and control subjects who did not exhibit altered respiratory patterns during tilt. Moreover, elucidating the involvement of hypocapnia in the cerebral blood flow autoregulation of OI patients was beyond the scope of the present work. Although the assessment of the autonomic regulation was based on spectral indexes of HR and BP variability's according to the international recommendations18, such indirect method may be less sensitive than direct methods (such as microneurography) to elucidate the mechanisms of autonomic regulation in response to tilt33. The cerebral blood flow was assessed indirectly using CBFv. Transcranial Doppler measures CBFv instead of blood flow34.
OI represents an important health problem and remains poorly understood. The main significance of these results is the insight that they provide into the events occurring during orthostatic stress, particularly on the changes in CBFv in the period leading up to presyncope/syncope.
The symptoms in patients with chronic OI without tachycardia may be explained by early postural cerebral hypoperfusion without orthostatic hypotension. Its mechanism is unknown but seems to be due to sympathetic activation alone or combined with hypocapnia. OCHOs are independent of the VVR manifested in some patients by syncope/presyncope. The time lag between the onset of the VVR and the premonitory symptoms excludes the hypothesis that the VVR is dependent on abnormal cerebral hemodynamics.
In conclusion, chronic OI mechanisms are poorly understood. Many patients with OI without tachycardia remain undiagnosed by the tilt test if the CBFv are not measured. Patients with chronic OI without tachycardia have early postural cerebral hypoperfusion. This early postural cerebral hypoperfusion is not related to the final hypotensive response. Then, the question arises whether POTS, OI with VVR+ and VVR− represent different diagnostic entities, or they represent a spectrum of the same disorder of OI. Identification and treatment of these patients are important, with interventions that could improve their cerebral hemodynamics, and the treatment focused on improving symptoms during orthostasis and not only to prevent syncope.
