Skip main navigation

Contribution of the Lung to the Genesis of Cheyne‐Stokes Respiration in Heart Failure: Plant Gain Beyond Chemoreflex Gain and Circulation Time

Originally publishedhttps://doi.org/10.1161/JAHA.119.012419Journal of the American Heart Association. 2019;8:e012419

    Abstract

    Background

    The contribution of the lung or the plant gain (PG; ie, change in blood gases per unit change in ventilation) to Cheyne‐Stokes respiration (CSR) in heart failure has only been hypothesized by mathematical models, but never been directly evaluated.

    Methods and Results

    Twenty patients with systolic heart failure (age, 72.4±6.4 years; left ventricular ejection fraction, 31.5±5.8%), 10 with relevant CSR (24‐hour apnea‐hypopnea index [AHI] ≥10 events/h) and 10 without (AHI <10 events/h) at 24‐hour cardiorespiratory monitoring underwent evaluation of chemoreflex gain (CG) to hypoxia () and hypercapnia () by rebreathing technique, lung‐to‐finger circulation time, and PG assessment through a visual system. PG test was feasible and reproducible (intraclass correlation coefficient, 0.98; 95% CI, 0.91–0.99); the best‐fitting curve to express the PG was a hyperbola (R2≥0.98). Patients with CSR showed increased PG, (but not ), and lung‐to‐finger circulation time, compared with patients without CSR (all P<0.05). PG was the only predictor of the daytime AHI (R=0.56, P=0.01) and together with the also predicted the nighttime AHI (R=0.81, P=0.0003) and the 24‐hour AHI (R=0.71, P=0.001). Lung‐to‐finger circulation time was the only predictor of CSR cycle length (R=0.82, P=0.00006).

    Conclusions

    PG is a powerful contributor of CSR and should be evaluated together with the CG and circulation time to individualize treatments aimed at stabilizing breathing in heart failure.

    Clinical Perspective

    What Is New?

    • This is the first study to explore the contribution of the lung or the plant gain in the genesis of central apneas in patients with heart failure.

    What Are the Clinical Implications?

    • Understanding the plant gain may help to predict Cheyne‐Stokes respiration severity and to refine pathophysiological treatments aimed at stabilizing breathing in heart failure.

    Introduction

    Cheyne‐Stokes respiration (CSR) is a form of periodic breathing characterized by alternating phases of hyperventilation and central apneas, typical of severe chronic conditions, such as congestive heart failure (HF).1 This breathing pattern results in numerous repetitive fluctuations in blood gases and hemodynamics,1 causes chronic sympathetic overactivation,2 impedes exercise capacity,3 precipitates ventricular arrhythmias,4 and increases mortality in HF.5, 6 Current treatments of CSR have rarely considered its complex pathogenesis in HF or tried to interfere with its pathophysiological triggers, with consequent disappointing results of major clinical trials based on positive pressure ventilation.7, 8

    In the past decades, different mathematical models have been proposed to describe the pathophysiology of CSR.9, 10, 11, 12 The overall accepted hypothesis is that the respiratory system could be seen as a closed‐loop system, with a certain transit time in the feedback loop.13 The loop gain (LG) can be defined as the ratio between the power of the response to a disturbance/the disturbance itself. Generally, the system reacts vigorously to each perturbation with a high LG, and with weaker effect when the LG is low.13 The main determinants of LG are the controller gain and the plant gain (PG).

    The controller within the respiratory system is represented by the chemoreflex gain (CG; change in ventilation per unit change in pco2 or po2), whereas the PG is represented by the lungs (change in pco2 or po2 per unit change in ventilation). The connection between the controller and the plant is represented by the blood circulating between the lung and the chemoreceptors.14 If the LG is <1, the response to any respiratory disturbance does not overshoot by more than the size of the original disturbance, so that ventilation slowly returns to steady state. Conversely, if LG is ≥1, any respiratory disturbance produces a response, which is even larger, leading to growing cycles of oscillation.13

    With these premises, the chemoreflex has been thoroughly evaluated in patients with HF and CSR.15, 16, 17 Increased CG is associated with CSR,16, 17 adrenergic overactivation,16, 17 and arrhythmias16, 17 and has independent prognostic significance in HF.18, 19 However, there is extensive overlap in CG between patients with and without CSR.15

    Although a few studies have also evaluated the role of circulation time (Ct), showing mainly an association with CSR cycle length rather than CSR severity,20 the role of PG has never been investigated.

    We hypothesized that full evaluation of the global LG, including the CG, the PG, and the Ct, might increase the capability to correctly predict respiratory stability and to design future rational and effective strategies to stabilize breathing, on the basis of tailored pathophysiological approaches acting on CSR triggers. Therefore, we developed a novel method for direct evaluation of PG, and we tested it in healthy subjects and in patients with HF with and without CSR, beyond the evaluation of both the CG and the Ct.

    Methods

    The data that support the findings of this study are available from the corresponding author on reasonable request.

    Study Population

    Consecutive outpatients with chronic systolic HF (left ventricular ejection fraction <50%) on stable (by 3 months) and optimal guideline‐recommended medical and device treatment were enrolled in the study.21 Exclusion criteria were as follows: chronic obstructive pulmonary disease or respiratory failure22; obstructive sleep apnea syndrome; and therapy with drug‐influencing ventilation.

    The study was approved by our Institutional Review Committee, and all subjects gave informed consent.

    All patients underwent the following: 2‐dimensional echocardiography23, 24, 25; neurohormonal characterization, including plasma norepinephrine, renin, aldosterone, and B‐type natriuretic peptides26; arterial blood gas analysis; spirometry and diffusing lung capacity for carbon monoxide; 24‐hour cardiorespiratory monitoring (Somtè; Compumedics, Abbotsford, Australia),6, 27 from which the apnea‐hypopnea index (AHI), the central apnea index (CAI), the obstructive apnea index, the minimal oxygen saturation (SaO2), time spent with SaO2 <90%, and the lung‐to‐finger Ct (LFCt) were calculated, as previously described28, 29; chemoreflex sensitivity to hypoxia () and hypercapnia (), by the rebreathing technique17, 18, 30, 31 (as explained below); and PG assessment (as explained below).

    On the basis of pilot analysis (4 patients with CSR [PG mean, 2.2 mm Hg/L per minute; SD, 0.6 mm Hg/L per minute] and 4 patients without CSR [PG mean, 1.4 mm Hg/L per minute; SD, 0.5 mm Hg/L per minute]) using PG as the target variable and using a 1‐sided Mann‐Whitney U test (calculated effect size of 1.45) to obtain a P<0.05 and a power of 80%, we calculated a sample size of 7 subjects per group. To ensure robustness of our findings, we decided to recruit 10 subjects for each group. Considering that we evaluated CSR over the 24 hours and that the 24‐hour AHI has an independent prognostic value in HF,6 we used a threshold of 24‐hour AHI ≥10 events/h to differentiate patients with relevant CSR (n=10; 24‐hour AHI ≥10 events/h) from those without (n=10; AHI <10 events/h) in this series. A group of 10 healthy controls matched for age, sex, body mass index, and body surface area was also recruited and underwent PG and CG assessment.

    CG Assessment

    Chemoreflex sensitivity was assessed using the rebreathing technique, as previously explained.17, 18 In summary, subjects were examined in standardized conditions, while seated and connected to a rebreathing circuit through a mouthpiece. ECG, airway flow, and respiratory gases were recorded continuously through a breath‐by‐breath gas analyzer (Vmax; Sensormedics, CA), and SaO2 was recorded through a pulse oximeter (SET Radical; Masimo).

    A 4‐minute baseline recording was performed during spontaneous breathing. Then, the and the were performed in a random order.

    In the , an isocapnic hypoxia trial was done (from resting SaO2 values to 70%–80%, according to individual tolerance), with end‐tidal CO2 (etCO2) kept constant through a scrubbing circuit; the was then expressed by the linear regression slope between minute ventilation and SaO2.

    In the , a progressive normoxic hypercapnic trial was done (from resting etCO2 values until 50 mm Hg or an increase >10 mm Hg from the basal values, according to individual tolerance), with inspired partial pressure of oxygen kept at the baseline value by adding oxygen to the circuit; the was expressed by the linear regression slope between minute ventilation and the end‐tidal pressure of CO2.

    PG Assessment

    To estimate the PG, we developed a new test to guide and monitor patient's breath‐by‐breath imposed variations in minute ventilation and consequent changes in etCO2.

    It was possible to refer the etCO2 to the invasive arterial measure, excluding from the study pulmonary diseases with different alveolar emptying constants.

    To enable subjects to change ventilation to a predetermined value, the subject's signal from the pneumotachograph (Vmax) was monitored online by a dedicated computer, running custom‐designed software. The system was programmed to change subject's ventilation as a percentage of resting ventilation, increasing/decreasing tidal volume and respiratory rate by the same proportion.

    The system displayed a moving bar controlled by the subject's inspiration, which should reach a tidal volume target at a respiratory rate rhythm given by a dynamic cursor (Figure 1A and Video S1).

    Figure 1.

    Figure 1. Schematic representation of plant gain assessment. A, The patient/software interface showing patient's inspiratory bar, target tidal volume (TV), and respiratory rate (RR) dynamic cursor. B, TV target is moved away from resting TV and RR cursor changes velocity across the different respiratory maneuvers, to obtain a prefixed percentage change in baseline ventilation. C, The postprocessing software interface allows us to reliably select a 20‐second plateau in the end‐tidal CO2 (etCO2) signal, following imposed changes in minute ventilation (VE).

    The study subject was first trained to familiarize with the software interface. After a 5‐minute baseline recording to obtain resting ventilation and etCO2, each subject was asked to perform 5 maneuvers in random order: 2 hypoventilation maneuvers (a −20% and −10% decrease from baseline ventilation) and 3 hyperventilation maneuvers (a 20%, 40%, 60% increase from baseline ventilation) (Figure 1B).

    Each step was maintained for at least 5 minutes, until a plateau in etCO2 had been achieved and maintained for ≥20 seconds. Each step was separated by the following one by 5 minutes of recovery (Figure 1B). Data were then analyzed (Figure 1C).

    PG was calculated as the ratio between the variances of etCO2 and minute ventilation across the different respiratory maneuvers (Equation 1).

    ((1))

    The PG repeatability was assessed in 5 volunteers on 2 consecutive days.

    Statistical Analysis

    Statistical analysis was performed using SPSS (IBM Statistics, version 25.0; 2017). A 2‐tailed P<0.05 was considered significant. Values were expressed as mean±SD or median and interquartile range, according to a normal or skewed distribution, evaluated by Kolmogorov‐Smirnov test; or as percentages for categorical data. The χ2 goodness‐of‐fit test for modified hyperbolic function was used to verify the shape of the PG relationship, using GraphPad Prism, version 7.04 for Windows.

    For quantitative variables, comparison between 2 groups was performed using Mann‐Whitney U test, whereas comparison among >2 groups was performed using the Kruskal‐Wallis test, with Dunn post hoc correction. For qualitative variables, a χ2 or Fisher exact test was used.

    Before regression analysis, variables with a skewed distribution were logarithmically corrected. Univariable and multivariable linear regression analyses were implemented to identify predictors of CSR severity and CSR cycle length (dependent variables), entering the CG, the PG, and the LFCt (independent variables) into the multivariable regression only if they resulted in predictors at univariable analysis with P≤0.05; multicollinearity was excluded by calculation of variance inflation factor, considering a low risk of multicollinearity if the variance inflation factor was <10. Repeatability was measured with the intraclass correlation coefficient and its 95% confidence interval.

    Results

    The clinical characteristics of the HF population are shown in Table 1. Patients were mainly men, with mild symptoms (90% in New York Heart Association class I/II) confirming clinical stability, despite moderate‐severe left ventricular systolic and diastolic dysfunction and presence of relevant mitral regurgitation and atrial fibrillation in 50% and 40%, respectively. All patients were receiving optimal medical and device treatment. According to matching criteria, patients and healthy controls were similar ages (72.4±6.4 versus 69.2±2.7 years; P=0.14), had a similar proportion of men (95% versus 90%; P=0.28), and had a similar body mass index (26.3±3.3 versus 25.9±3.7 kg/m2; P=0.76) and body surface area (1.97±0.17 versus 1.90±0.18 m2; P=0.10).

    Table 1. Clinical Features of Patients With HF With or Without CSR

    FeaturePatients With HFPatients With HF With 24‐h AHI <10 events/hPatients With HF With 24‐h AHI ≥10 events/h
    Total no.201010
    Age, y72.4±6.471.4±7.373.4±5.6
    Men19 (95)9 (90)10 (100)
    BMI, kg/m226.3±3.326.1±4.126.6±2.5
    BSA, m21.97±0.171.97±0.181.98±0.16
    Plasma creatinine, mg/dL1.12±0.371.17±0.481.07±0.22
    eGFR, mL/min per 1.73 m267.7±20.667±23.566.5±18.1
    Hemoglobin, g/dL13.8±1.313.9±0.813.4±1.7
    Ischemic/idiopathic9/11 (45/55)5/5 (50/50)4/6 (40/60)
    NYHA class I/II/III6/12/2 (30/60/10)4/5/1 (40/50/10)2/7/1 (20/70/10)
    Atrial fibrillation11 (55)5 (50)6 (60)
    Ejection fraction, %31.5±5.832.9±6.130.2±5.5
    Diastolic disfunction II–III10 (50)5 (50)5 (50)
    Moderate‐to‐severe MR8 (40)3 (30)5 (50)
    sPAP, mm Hg40.4±10.041.9±6.439.2±12.4
    FAC, %40.1±9.036.3±7.443±9.5
    HS‐troponin T, ng/L18.4 (10.2–26.4)13.7 (8.7–25.3)21.5 (16.6–31.5)
    Norepinephrine, ng/L431.5 (326.8–690.5)400 (290.5–513.0)561 (352.0–804.8)
    Renin, μU/mL39.1 (11.7–81.6)42.1 (14.4–95.2)30.4 (4.1–77.0)
    Aldosterone, ng/L82.9 (56.2–127.0)82.3 (55.1–82.3)92.5 (67.0–127.0)
    BNP, ng/L240.0 (142.0–659.0)219.0 (80.0–303.0)449.5 (164.3–824.0)
    NT‐proBNP, ng/L981 (484.8–2353.5)580 (265.0–1187.8)1340 (772.3–3494.3)*
    β Blockers20 (100)10 (100)10 (100)
    ACEi‐ARB14 (70)7 (70)7 (70)
    ARNI 6 (30)3 (30)3 (30)
    MRA 17 (85)7 (70)10 (100)
    Furosemide 11 (55)6 (60)5 (50)
    Digoxin 1 (5)1 (10)0 (0)
    CRT‐D 7 (35)4 (40)3 (30)
    CRT‐P 1 (5)0 (0)1 (10)
    ICD 1 (5)0 (0)1 (10)

    Data are given as mean±SD, number (percentage), or median (interquartile range). ACEi indicates angiotensin‐converting enzyme inhibitor; AHI, apnea‐hypopnea index; ARB, angiotensin receptor blocker; ARNI, angiotensin receptor/neprilysin inhibitor; BMI, body mass index; BNP, brain natriuretic peptide; BSA, body surface area; CRT‐D, cardiac resynchronization therapy‐defibrillator; CRT‐P, CRT‐pacemaker; CSR, Cheyne‐Stokes respiration; eGFR, estimated glomerular filtration rate by Modification of Diet in Renal Disease equation; FAC, fractional area change; HF, heart failure; HS, high sensitivity; ICD, implantable cardioverter‐defibrillator; MR, mitral regurgitation; MRA, mineralocorticoid receptor antagonist; NT‐proBNP, N‐terminal pro‐B‐type natriuretic peptide; NYHA, New York Heart Association; sPAP, systolic pulmonary artery pressure.

    *P<0.05 vs patients with HF with 24‐h AHI <10 events/h.

    Patients with CSR showed a higher plasma value of NT‐proBNP (N‐terminal pro‐B‐type natriuretic peptide; P=0.03) compared with patients without CSR (Table 1). No differences in age, body mass index, body surface area, New York Heart Association class, renal function, left ventricular systolic and diastolic function, systolic pulmonary pressure, and right ventricular function were observed between patients with or without CSR (Table 1).

    Because of patient allocation, patients with CSR showed increased AHI and CAI at daytime, nighttime, and over 24 hours, as well as increased CSR cycle length, apnea and hyperpnea length, and time spent with SaO2 <90%, whereas no difference was found in the obstructive apnea index (Table 2).

    Table 2. Respiratory Profile of Patients With HF With or Without CSR

    VariablePatients With HFPatients With HF With 24‐h AHI <10 events/hPatients With HF With 24‐h AHI ≥10 events/h
    Daytime AHI, events/h5 (2.0–14.5)2 (0.8–5.3)13 (4.8–27.0)*
    Nighttime AHI, events/h18 (5–31)5 (2.8–11.8)31 (22.8–36.8)*
    24‐h AHI, events/h9 (4.3–17.8)4.5 (2.8–7.0)19.5 (15.8–31.3)*
    Daytime CAI, events/h0 (0–3)0 (0–0)3 (1.8–18.8)*
    Nighttime CAI, events/h2.5 (0–14.5)0 (0–1)14 (7.0–21.3)*
    24‐h CAI, events/h1.5 (0–8)0 (0–0)7.5 (3.8–17.3)*
    Daytime OAI, events/h000 (0–1)
    Nighttime OAI, events/h1 (0–2)0 (0–2)2 (0.8–2.5)
    24‐h OAI, events/h0.5 (0–1)0 (0–1)1 (0–1.3)
    Cycle length, s59.8±10.753.1±7.766.5±9.1*
    Apnea length, s20.3±3.817.4±2.923.2±1.8*
    Hyperpnea length, s39.6±7.935.8±6.243.4±7.8*
    SaO2 min, %86.1±3.386.7±3.885.5±2.7
    T‐90, min5 (2–12)4 (0.8–11)9 (2–13)*

    Data are given as median (interquartile range) or mean±SD. AHI indicates apnea‐hypopnea index; CAI, central apnea index; CSR, Cheyne‐Stokes respiration; HF, heart failure; OAI, obstructive apnea index; SaO2, oxygen saturation; T‐90, time spent with SaO2 <90%.

    *P<0.05 vs patients with HF with 24‐h AHI <10 events/h.

    Chemoreflex Sensitivity, PG, and Ct

    Patients with CSR showed higher compared with both patients without CSR (P=0.02) and healthy controls (P=0.01, Table 3 and Figure 2). Conversely, no difference was found in among the different groups (Table 3 and Figure 3). No difference in both and was found between patients without CSR and healthy controls.

    Table 3. CG, PG, and Ct Measurement in the Study Population

    Variable Healthy Controls (n=10)Patients With HF With 24‐h AHI <10 events/h (n=10)Patients With HF With 24‐h AHI ≥10 events/h (n=10)
    CG
    Baseline VE, L/min11.9±2.011.9±2.411.3±2.4
    Baseline etCO2, mm Hg33.6±3.431.9±3.231.8±3.4
    Baseline SaO2, %95.7±1.195.9±1.695.4±1.5
    etCO2, mm Hg32.5±5.731.5±3.131.4±3.5
    SaO2, %78.2±1.481.5±4.881.6±4.7
    VE, L/min19.6±8.017.6±5.122.6±7.7
    , L/min per %SaO20.19 (0.06–0.69)0.29 (0.14–0.60)0.42 (0.23–0.67)
    etCO2, mm Hg47.3±4.647.5±3.148.0±3.6
    SaO2, %95.8±1.295.5±1.496.3±1.2
    VE, L/min24.1±9.126.2±5.436.1±11.1
    , L/min per mm Hg0.82 (0.15–1.13)0.89 (0.48–1.01)1.45 (0.99–2.26)*
    PG
    Baseline VE, L/min11.9±2.011.9±2.411.3±2.4
    −10% VE, L/min10.3±3.910.6±2.29.9±2.2
    −20% VE, L/min9.5±2.09.8±2.48.6±1.8
    20% VE, L/min14.2±2.014.7±3.113.9±2.4
    40% VE, L/min17.3±2.317.3±3.216.2±2.1
    60% VE, L/min20.3±2.619.9±3.718.9±2.9
    Baseline etCO2, mm Hg33.8±3.531.4±3.432.2±3.1
    −10% etCO2, mm Hg34.2±3.332.7±3.233.7±2.9
    −20% etCO2, mm Hg35.2±3.432.8±3.035.3±3.2
    20% etCO2, mm Hg29.7±3.328.1±3.127.9±3.6
    40% etCO2, mm Hg26.6±3.425.2±2.524.5±2.3
    60% etCO2, mm Hg24.2±3.122.3±2.520.9±2.4
    PG, mm Hg/L per min1.15 (0.83–2.06)1.37 (1.09–1.88)2.19 (1.44–2.81)*
    Ct
    Daytime LFCt, s···26.7±2.833.4±6.9
    Nighttime LFCt, s···26.1±3.132.9±6.4*
    24‐h LFCt, s···26.4±3.634.0±6.2

    Data are given as mean±SD or median (interquartile range). and etCO2, SaO2, and VE are the values recorded and averaged in the last 10 seconds of the and maneuvers. AHI indicates apnea‐hypopnea index; CG, chemoreflex gain; , CG to hypercapnia; , CG to hypoxia; Ct, circulation time; etCO2, end‐tidal CO2; HF, heart failure; LFCt, lung‐to‐finger Ct; PG, plant gain; SaO2, oxygen saturation; VE, minute ventilation.

    *P<0.05 vs HF with 24‐hour AHI <10 events/h.

    P<0.05 vs healthy controls.

    P<0.01 vs HF with 24‐hour AHI <10 events/h.

    Figure 2.

    Figure 2. Chemoreflex gain to hypercapnia in healthy subjects and in patients with and without Cheyne‐Stokes respiration (CSR). A, Linear regression slopes expressing the chemoreflex gain to hypercapnia () in a sample subject of each study group. B, was increased in a patient with heart failure (HF) with CSR compared with patients with HF without CSR and healthy subjects. AHI indicates apnea‐hypopnea index; etCO2, end‐tidal CO2; VE, minute ventilation.

    Figure 3.

    Figure 3. Chemoreflex gain to hypoxia in healthy subjects and in patients with and without Cheyne‐Stokes respiration (CSR). A, Linear regression slopes expressing the chemoreflex gain to hypoxia () in a sample subject of each study group. B, No difference was found among healthy subjects and patients with heart failure (HF) with or without CSR in terms of . AHI indicates apnea‐hypopnea index; SaO2, oxygen saturation; VE, minute ventilation.

    Both healthy subjects and patients with HF were able to perform the PG test correctly (Table 3), with little deviation from target ventilation (3.1±1.4% in the whole population, 2.7±2.9% in healthy subjects, 2.9±1.4% in those with HF without CSR, and 3.6±1.1% in those with HF with CSR). The PG test showed a high repeatability: intraclass correlation coefficient, 0.98 (95% CI, 0.91–0.99). The best‐fitting curve to express the relationship between induced changes in etCO2 and changes in ventilation was a hyperbola (R2=0.99 for patients without CSR and healthy controls, and R2=0.98 for patients with CSR) (Figure 4A).

    Figure 4.

    Figure 4. Plant gain (PG) in healthy subjects and in patients with and without Cheyne‐Stokes respiration (CSR). A, PG respiratory hyperbola in a sample subject of each study group. B, PG was increased in a patient with heart failure (HF) with CSR compared with patients with HF without CSR and healthy subjects. AHI indicates apnea‐hypopnea index; etCO2, end‐tidal CO2; VE, minute ventilation.

    PG was higher in patients with CSR than in patients without CSR (P=0.02) and healthy controls (P=0.01, Table 3 and Figure 4B). No difference in PG was found between patients without CSR and healthy controls. No significant difference in spirometry, lung diffusion, and blood gas analysis was found between patients with normal and increased PG, apart from a trend toward an increase in the forced expiratory volume in the first second (P=0.06) and in the total lung capacity (% predicted; P=0.09) in patients with increased PG (Table 4).

    Table 4. Blood Gas Analysis, Spirometry, and Pulmonary Diffusion in Patients With HF With Low or High PG, According to Its Median Value (1.63 mm Hg/L per Minute)

    Variable Patients With HF (n=20)Patients With Low PG (n=10)Patients With High PG (n=10)
    Blood gas analysis
    Po2, mm Hg80.8±8.382.0±7.479.9±9.4
    Pco2, mm Hg36.8±3.437.6±4.436.1±2.6
    pH7.43±0.047.42±0.037.44±0.04
    , mmol/L25.2±2.124.8±1.025.5±2.6
    SaO2, %97.7±1.397.6±1.897.9±1.0
    Spirometry
    FEV1, L2.99±0.482.76±0.353.2±0.50
    FEV1, % predicted106.8±18.099.3±19.9113.4±14.0
    FEV1/FVC, %70.7±5.671.3±7.670.1±3.4
    FEV1/VC, % predicted92.0±8.592.6±11.391.5±5.6
    TLC, L6.4±1.06.0±1.06.8±0.9
    TLC, % predicted97.4±13.790.9±12.6103.2±12.5
    RV/TLC, %33.7±6.936.3±5.331.4±7.7
    DS/TV0.16±0.060.16±0.060.17±0.05
    Pulmonary diffusion
    DLCO, mL/min per mm Hg23.8±5.422.6±5.224.9±5.6
    DLCO, % predicted88.5±27.477.3±32.598.6±18.5
    AV, L6.2±0.95.8±0.46.7±0.9
    AV, % predicted95.7±12.689.1±11.4101.6±11.0
    KCO, mL min−1 mm Hg−1 L−13.8±0.73.9±0.83.8±0.6
    KCO, % predicted99.1±17.8101.0±20.697.3±16.0

    Data are given as mean±SD. AV indicates alveolar volume; DLCO, diffusion capacity of the lungs for CO; DS, dead space; FEV1, forced expiratory volume in the first second; FVC, forced VC; HF, heart failure; KCO, DLCO divided by AV; PG, plant gain; SaO2, oxygen saturation; RV, residual volume; TLC, total lung capacity; TV, tidal volume; VC, vital capacity.

    The 24‐hour, daytime, and nighttime LFCt values were all increased in patients with CSR compared with patients without CSR (all P<0.05, Figure 5). No significant differences were observed in the LFCt calculated at different time windows (daytime, nighttime, and 24‐hour period), within the same group of patients.

    Figure 5.

    Figure 5. Lung‐to‐finger circulation time (LFCt) in patients with and without Cheyne‐Stokes respiration (CSR). The LFCt was increased in patients with heart failure (HF) with Cheyne‐Stokes respiration (CSR) compared with patients without CSR, over the 24‐hour period (A), at daytime (B), and at nighttime (C). AHI indicates apnea‐hypopnea index.

    and LFCt were correlated (ρ=0.64, P=0.004), whereas no correlation was found between PG and or PG and LFCt.

    Prediction of CSR Severity and CSR Cycle Length

    The univariable and multivariable predictors of CSR severity in patients with HF are shown in Table 5, whereas linear regression plots (for each CSR predictor) are shown in Figure 6.

    Table 5. Univariable and Multivariable Models for Prediction of 24‐Hour AHI, Nighttime AHI, and Daytime AHI

    Variable Univariable ModelMultivariable Model
    β, Mean±SDRR2P Valueβ, Mean±SDRR2R2‐PenalizedP ValueVIF
    Prediction of 24‐h AHI
    6.9±3.30.460.210.048.3±2.70.710.510.440.0081.03
    PG8.3±3.10.540.290.028.9±2.90.0091.03
    LFCt0.7±0.40.380.140.10···
    Prediction of nighttime AHI
    11.4±3.70.610.360.00710.4±3.30.810.650.570.0071.24
    PG8.5±4.10.440.190.048.1±3.30.031.06
    LFCt1.1±0.50.490.240.03···
    Prediction of daytime AHI
    3.9±3.40.260.070.29···
    PG8.3±2.80.560.320.01
    LFCt0.41±0.380.250.060.29

    AHI indicates apnea‐hypopnea index; , chemoreflex gain to hypercapnia; LFCt, lung‐to‐finger circulation time; PG, plant gain; VIF, variance inflation factor.

    Figure 6.

    Figure 6. Linear regression plots relating loop gain components and Cheyne‐Stokes respiration (CSR) severity in different time windows. Linear regression plots relating chemoreflex gain to hypercapnia (), plant gain (PG), and lung‐to‐finger (LF) circulation time (LFCt) with CSR severity, as expressed by the apnea‐hypopnea index (AHI), over the 24‐hour period (A), at nighttime (B), and at daytime (C).

    At multivariable analysis, and PG were independent predictors of both the 24‐hour AHI (Figure 7A) and the nighttime AHI (Figure 7B), whereas PG was the only independent predictor of the daytime AHI (Figure 7C). LFCt was only a univariable predictor of nighttime AHI, but it lost its predictive value at multivariable analysis. Using CAI as the target variable, PG was the only predictor of 24‐hour (R=0.55, P=0.01) and daytime (R=0.59, P=0.006) CAI, whereas was the only predictor of nighttime CAI (R=0.56, P=0.01).

    Figure 7.

    Figure 7. Regression plots showing predictors of Cheyne‐Stokes respiration severity in different time windows. Chemoreflex gain to hypercapnia () and plant gain (PG) were independent predictors of apnea‐hypopnea index (AHI) over the 24‐hour period (A) and at nighttime (B), whereas only PG was an independent predictor of AHI at daytime (C).

    On the other hand, the LFCt was an independent predictor of CSR cycle length (Figure 8A), as well as of hyperventilation length (Figure 8B). Apnea length was predicted by both LFCt and the , with LFCt remaining the only independent predictor at multivariable analysis (Figure 8C).

    Figure 8.

    Figure 8. Regression plots showing predictors of Cheyne‐Stokes respiration (CSR) cycle and hyperpnea and apnea lengths. The lung‐to‐finger circulation time (LFCt) was the only independent predictor of CSR cycle length (A), hyperventilation length (B), and apnea length (C).

    Discussion

    This was the first study to assess the PG in patients with HF with and without CSR. Assessing the PG, instead of only CG and the Ct, allowed us to comprehensively test the instability loop hypothesis (Figure 9).13 Higher , PG, and Ct values were found in patients with CSR. Notably, both CG and PG were able to predict CSR severity during the 24‐hour period and at nighttime, whereas only PG was able to predict CSR severity at daytime. Ct showed no role in CSR severity prediction, but was strongly related to CSR cycle length and to hyperpnea and apnea length.

    Figure 9.

    Figure 9. Testing the instability loop hypothesis in patients with heart failure: an overview. In patients with heart failure, plant gain determines Cheyne‐Stokes respiration (CSR) severity at daytime and, together with chemoreflex gain to CO2, CSR severity at nighttime. On the contrary, circulation time has no role in prediction of CSR severity, but it is associated with CSR cycle length. VE, minute ventilation.

    The Instability Loop Hypothesis

    The pathophysiological characteristics of CSR in HF are complex and multifactorial. Despite much theoretical and experimental work, a thorough understanding of the mechanisms involved and their interactions has not been achieved. The strength of the pathophysiological model is key to guide experiments designed to challenge the model's assumption and to provide optimal treatments for patients with a disease.32 On the other hand, if a treatment is not strongly pathophysiologically based and referred to a solid model, the randomized controlled trial is likely to fail, as happened to mask‐based therapies based on positive airway pressure, derived from the treatment of obstructive apneas and applied to central apneas of HF.7, 8

    In this setting, a great contribution was provided by the use of mathematical models. Currently, the most accepted hypothesis is that the respiratory control system could be seen as a closed‐loop system, constituted by a controller (ie, the chemoreflex) and the plant (ie, the lung), with a transit time in the feedback loop (ie, Ct). In principle, therefore, increased CG, increased PG, and increased Ct have theoretical potential to increase the global LG and cause CSR.

    Testing the Instability Loop Hypothesis: CG

    Alteration in the gain of the chemoreceptors has been well documented in both experimental33 and clinical settings.15, 16, 17, 18, 19 The original observation by Javaheri15 that was strongly correlated with CSR severity was later confirmed by different research groups.16, 17, 18, 19, 34 In the current study, the was again confirmed to play a key role in the prediction of CSR severity. By contrast, no significant difference in the was found between patients with or without CSR, highlighting once more that CO2, rather than hypoxia, is the main driver of ventilation, especially at night when ventilation is under chemical control. Recent lines of evidence have shown that in animals with HF, the CG remains high throughout the 24 hours, including the biological night, differently from healthy animals in which the CG is known to decrease during the inactive phase.35 This may also justify why the difference between the eupneic CO2 and the CO2 at anaerobic threshold is decreased at night in patients with HF and CSR compared with patients with stable breathing.36 The reasons for this persistent overactivity of the CG at night is still unknown, but key differences in the chronobiological characteristics of neurohormonal activity and in cardiac hemodynamics (decreased cardiac output and increased filling pressure), together with a decrease in cerebrovascular reactivity to increased CO2 (decreased CO2 washout from chemoreceptors),37 at night might be involved.

    Testing the Instability Loop Hypothesis: PG

    Before this study, the PG had been only mathematically hypothesized9, 10, 11, 12 and evaluated in a single study by Miyamoto et al in healthy volunteers,38 but not in patients with HF. Similar to Miyamoto et al, we also used a visual system to drive subjects during PG execution, but we performed shorter ventilatory maneuvers, to increase the feasibility in patients with HF. Moreover, we calculated the PG as a ratio between the variances of etCO2 and ventilation, rather than using a linear slope obtained at the equilibrium set point,38 to more reliably express the PG behavior far from stationary conditions.

    The feasibility of the test was demonstrated by the reassuringly small discrepancy (<5%) between the target and recorded ventilation in each respiratory maneuver, not only in healthy subjects, but even in patients with HF with or without CSR. Furthermore, as predicted by mathematical models, the relationship between changes in ventilation and the resulting changes in etCO2 fitted a hyperbola (R2=0.99 for patients without CSR and healthy controls, and R2=0.98 for patients with CSR).

    Notably, we first observed that the PG is increased in patients with HF with CSR, being ≈60% higher than in patients with HF without CSR. Moreover, the PG was the only predictor of CSR severity at daytime, where the chemical control is overdriven by different stimuli, especially cortical influences. Furthermore, adding PG to CG resulted in a more accurate prediction of CSR severity at night (PG+R=0.81 versus alone R=0.61). To put into practice, this means that in patients with a high PG, whatever stimulus is able to change ventilation can make the system oscillate and cause CSR, such as exercise or a mental stress when the patient is awake or an arousal when the patient is sleeping. This should be accounted for when designing and testing novel treatments aimed at stabilizing breathing.

    Indeed, several therapeutic approaches have been thought to act on the PG to obtain ventilatory stability, such as CO2 administration (by increasing lung CO2 reserve),39, 40 increase of death space (thus decreasing the washout of CO2 from the lung),41 acetazolamide administration (causing a shift in the ventilatory equilibrium at a different set point),42, 43 and positive pressure ventilation (by altering lung anatomical characteristics and/or mechanics).12 The PG was recently measured in patients with obstructive sleep apnea (n=8) and matched controls (n=7), by using a pseudorandom binary stimulation (63 breaths alternating between room air and 4% CO2, switching frequencies of between 1 and 6 consecutive breaths of CO2).44 No difference was found between patients with obstructive sleep apnea and controls, and no effect on the PG was observed after 6 week of continuous positive airway pressure treatment.

    The main determinants of the PG remained still unknown. In contrast to the hypothesis that lung congestion and the gas‐diffusion impairment may increase the PG,45 in our population, no significant difference in spirometry, lung diffusion, and blood gas analysis parameters was found between patients with high PG (PG above the median) and low PG (Table 4). The only exception was a trend toward an increase in forced expiratory volume in the first second (P=0.06) and total lung capacity (P=0.09) in patients with high PG. These results should be interpreted with caution, and further investigations in a larger population are needed to address this key pathophysiological issue.

    Testing the Instability Loop Hypothesis: Ct

    The pathophysiological role of Ct delay in determining respiratory instability was supposed by mathematical modeling9, 10, 11, 12 and experimentally demonstrated in dogs by Crowell and coworkers already in 1956.14 However, the increase in Ct needed to make ventilation unstable in anesthetized dogs14 was much higher (from 40 seconds to 5 minutes) than that observed in patients with HF.20 Subsequent studies in humans have highlighted that Ct delay seems to be mainly associated with CSR cycle length and hyperventilation length, rather than CSR onset or severity.20

    In our population and differently from previous studies, the LFCt, besides cycle length and hyperpnea length, also predicted the apnea duration. This difference may be explained by the use of LFCt over the 24‐hour period in place of the lung‐to‐ear Ct, evaluated only in phase 2 non–rapid eye movement sleep in the article by Hall et al,20 or by the higher number of patients with HF recruited in the current study. Both methods (LFCt and lung‐to‐ear Ct) were inversely correlated with cardiac output.20, 28, 29

    Study Limitations

    The PG test requires patient cooperation, and so it is unsuitable when there is marked physical and/or cognitive impairment. Nonetheless, in our population, the feasibility was 100%, even in patients with unstable breathing. Although the LFCt is only an estimation of the true Ct, it has the advantage of being measurable directly from cardiorespiratory monitoring. However, being based on SaO2, LFCt may also be influenced by the lungs and hemoglobin levels, so that direct measurements of Ct are needed to further improve the precision of the model.

    The CG and the PG were only evaluated during the daytime, when the patient was awake, and this may decrease our capacity to predict the ventilatory behavior (stability/instability and CSR severity and length) throughout the 24 hours. Currently, there is no evidence in patients with HF about the potential changes in the CG and the PG from awake to sleep conditions. Although we can hypothesize that the CG would remain high at night in patients with unstable breathing, as observed in animals,35 the potential changes of the PG at night are less predictable. We believe that, at night, the change in body position may reduce lung volumes, and further potential influences on the PG may be also related to the typical rostral fluid shift of patients with HF.

    Finally, the relatively small sample size of the study seems to hardly support the development of multivariable models. However, having used only 3 variables (independent variables; namely, the CG, the PG, and the LFCt) with a strong pathophysiological relationship with CSR severity and length (dependent variables), together with the lack of any relationships between the independent variables, apart from that observed between and LFCt, has actually increased the power of analysis (in each multivariable regression model, the calculated power was always >98%). Furthermore, the variance inflation factor observed makes the risk of multicollinearity rather low.

    Conclusions and Perspectives

    Ct does not predict CSR severity, but it influences the CSR cycle and hyperpnea and apnea length. The PG can be easily measured in patients with HF and is increased in patients with HF presenting with unstable ventilation, as previously hypothesized by mathematical models. Its estimation may help in predicting the severity of CSR at daytime and in refining the prediction of CSR severity at nighttime, when evaluated together with the CG. Future treatment strategies should consider those triggers to tailor a rational and thus effective approach in individual patients with HF and CSR.

    Disclosures

    None.

    Footnotes

    *Correspondence to: Alberto Giannoni, MD, PhD, Fondazione Toscana Gabriele Monasterio, via Giuseppe Moruzzi 1, 56124 Pisa, Italy. E‐mail:

    Dr Giannoni and Dr Gentile contributed equally to this work.

    References

    • 1 Emdin MG, Giannoni A, Passino C. The Breathless Heart: Apneas in Heart Failure. Basel, Switzerland: Springer; 2017.CrossrefGoogle Scholar
    • 2 Floras JS. Sympathetic nervous system activation in human with heart failure: clinical implications of an updated model. J Am Coll Cardiol. 2009; 54:375–385.CrossrefMedlineGoogle Scholar
    • 3 Andreas S, Clemens C, Sandholzer H, Figulla HR, Kreuzer H. Improvement of exercise capacity with treatment of Cheyne‐Stokes respiration in patients with congestive heart failure. J Am Coll Cardiol. 1996; 27:1486–1490.CrossrefMedlineGoogle Scholar
    • 4 Bitter T, Westerheide N, Prinz C, Hossain MS, Vogt J, Langer C, Horstkotte D, Oldenburg O. Cheyne‐Stokes respiration and obstructive sleep apnoea are independent risk factors for malignant ventricular arrhythmias requiring appropriate cardioverter‐defibrillator therapies in patients with congestive heart failure. Eur Heart J. 2011; 32:61–74.CrossrefMedlineGoogle Scholar
    • 5 Oldenburg O, Wellmann B, Buchholz A, Bitter T, Fox H, Thiem U, Horstkotte D, Wegscheider K. Nocturnal hypoxaemia is associated with increased mortality in stable heart failure patients. Eur Heart J. 2016; 37:1695–1703.CrossrefMedlineGoogle Scholar
    • 6 Emdin M, Mirizzi G, Giannoni A, Poletti R, Iudice G, Bramanti F, Passino C. Prognostic significance of central apneas throughout a 24‐hour period in patients with heart failure. J Am Coll Cardiol. 2017; 70:1351–1364.CrossrefMedlineGoogle Scholar
    • 7 Bradley TD, Logan AG, Kimoff RJ, Sériès F, Morrison D, Ferguson K, Belenkie I, Pfeifer M, Fleetham J, Hanly P, Smilovitch M, Tomlinson G, Floras JS; CANPAP Investigators . Continuous positive airway pressure for central sleep apnea and heart failure. N Engl J Med. 2005; 353:2025–2033.CrossrefMedlineGoogle Scholar
    • 8 Cowie MR, Woehrle H, Wegscheider K, Angermann C, d'Ortho MP, Erdmann E, Levy P, Simonds AK, Somers VK, Zannad F, Teschler H. Adaptive servo‐ventilation for central sleep apnea in systolic heart failure. N Engl J Med. 2015; 373:1095–1105.CrossrefMedlineGoogle Scholar
    • 9 Longobardo GS, Cherniack NS. Cheyne‐Stokes breathing produced by a model of the human respiratory system. J Appl Physiol. 1966; 21:1839.CrossrefMedlineGoogle Scholar
    • 10 Carley DW, Shannon DC. A minimal mathematical model of human periodic breathing. J Appl Physiol. 1988; 65:1400–1409.CrossrefMedlineGoogle Scholar
    • 11 Khoo MCK. Determinants of ventilatory instability and variability. Respir Physiol. 2000; 122:167–182.CrossrefMedlineGoogle Scholar
    • 12 Francis D, Willson K, Davies LC, Coats A, Piepoli M. Quantitative general theory for periodic breathing in chronic heart failure and its clinical implications. Circulation. 2000; 102:2214–2221.LinkGoogle Scholar
    • 13 White DP. Pathogenesis of obstructive and central sleep apnea. Am J Respir Crit Care Med. 2005; 172:1363–1370.CrossrefMedlineGoogle Scholar
    • 14 Crowell JW, Guyton AC, Moore JW. Basic oscillating mechanism of Cheyne‐Stokes breathing. Am J Physiol. 1956; 187:395–398.CrossrefMedlineGoogle Scholar
    • 15 Javaheri S. A mechanism of central sleep apnea in patients with heart failure. N Engl J Med. 1999; 341:949–954.CrossrefMedlineGoogle Scholar
    • 16 Ponikowski P, Anker SD, Chua TP, Francis D, Banasiak W, Poole‐Wilson PA, Coats AJ, Piepoli M. Oscillatory breathing patterns during wakefulness in patients with chronic heart failure: clinical implications and role of augmented peripheral chemosensitivity. Circulation. 1999; 100:2418–2424.LinkGoogle Scholar
    • 17 Giannoni A, Emdin M, Poletti R, Bramanti F, Prontera C, Piepoli M, Passino C. Clinical significance of chemosensitivity in chronic heart failure: influence on neurohormonal derangement, Cheyne‐Stokes respiration and arrhythmias. Clin Sci (Lond). 2008; 114:489–497.CrossrefMedlineGoogle Scholar
    • 18 Giannoni A, Emdin M, Bramanti F, Iudice G, Francis DP, Barsotti A, Piepoli M, Passino C. Combined increased chemosensitivity to hypoxia and hypercapnia as a prognosticator in heart failure. J Am Coll Cardiol. 2009; 53:1975–1980.CrossrefMedlineGoogle Scholar
    • 19 Ponikowski P, Chua TP, Anker SD, Francis DP, Doehner W, Banasiak W, Poole‐Wilson PA, Piepoli MF, Coats AJ. Peripheral chemoreceptor hypersensitivity: an ominous sign in patients with chronic heart failure. Circulation. 2001; 104:544–549.LinkGoogle Scholar
    • 20 Hall MJ, Xie A, Rutherford R, Ando S, Floras JS, Bradley TD. Cycle length of periodic breathing in patients with and without heart failure. Am J Respir Crit Care Med. 1996; 154:376–381.CrossrefMedlineGoogle Scholar
    • 21 Ponikowski P, Voors AA, Anker SD, Bueno H, Cleland JGF, Coats AJS, Falk V, González‐Juanatey JR, Harjola VP, Jankowska EA, Jessup M, Linde C, Nihoyannopoulos P, Parissis JT, Pieske B, Riley JP, Rosano GMC, Ruilope LM, Ruschitzka F, Rutten FH, Van Der Meer P. 2016 ESC guidelines for the diagnosis and treatment of acute and chronic heart failure. Eur Heart J. 2016; 37:2129–2200.CrossrefMedlineGoogle Scholar
    • 22 Pauwels RA, Buist AS, Calverley PM, Jenkins CR, Hurd SS; GOLD Scientific Committee . Global strategy for the diagnosis, management, and prevention of chronic obstructive lung disease: NHLBI/WHO Global Initiative for Chronic Obstructive Lung Disease (GOLD) Workshop summary. Am J Respir Crit Care Med. 2001; 163:1256–1276.CrossrefMedlineGoogle Scholar
    • 23 Lang RM, Badano LP, Mor‐Avi V, Afilalo J, Armstrong A, Ernande L, Flachskampf FA, Foster E, Goldstein SA, Kuznetsova T, Lancellotti P, Muraru D, Picard MH, Rietzschel ER, Rudski L, Spencer KT, Tsang W, Voigt J‐UU. Recommendations for cardiac chamber quantification by echocardiography in adults: an update from the American Society of Echocardiography and the European Association of Cardiovascular Imaging. J Am Soc Echocardiogr. 2015; 28:1–39.CrossrefMedlineGoogle Scholar
    • 24 Nagueh SF, Smiseth OA, Appleton CP, Byrd BF, Dokainish H, Edvardsen T, Flachskampf FA, Gillebert TC, Klein AL, Lancellotti P, Marino P, Oh JK, Popescu BA, Waggoner AD. Recommendations for the evaluation of left ventricular diastolic function by echocardiography: an update from the American Society of Echocardiography and the European Association of Cardiovascular Imaging. J Am Soc Echocardiogr. 2016; 29:277–314.CrossrefMedlineGoogle Scholar
    • 25 Rudski LG, Lai WW, Afilalo J, Hua L, Handschumacher MD, Chandrasekaran K, Solomon SD, Louie EK, Schiller NB. Guidelines for the echocardiographic assessment of the right heart in adults: a report from the American Society of Echocardiography. J Am Soc Echocardiogr. 2010; 23:685–713.CrossrefMedlineGoogle Scholar
    • 26 Emdin M, Passino C, Prontera C, Iervasi A, Ripoli A, Masini S, Zucchelli GC, Clerico A. Cardiac natriuretic hormones, neuro‐hormones, thyroid hormones and cytokines in normal subjects and patients with heart failure. Clin Chem Lab Med. 2004; 42:627–636.CrossrefMedlineGoogle Scholar
    • 27 Somers VK, White DP, Amin R, Abraham WT, Costa F, Culebras A, Daniels S, Floras JS, Hunt CE, Olson LJ, Pickering TG, Russell R, Woo M, Young T; American Heart Association Council for High Blood Pressure Research Professional Education Committee, Council on Clinical Cardiology; American Heart Association Stroke Council; American Heart Association Council on Cardiovascular Nursing; American College of Cardiology Foundation . Sleep apnea and cardiovascular disease: an American Heart Association/American College of Cardiology Foundation Scientific Statement from the American Heart Association Council for High Blood Pressure Research Professional Education Committee, Council on Clinical Cardiology, Stroke Council, and Council on Cardiovascular Nursing: in collaboration with the National Heart, Lung, and Blood Institute National Center on Sleep Disorders Research (National Institutes of Health). Circulation. 2008; 118:1080–1111.LinkGoogle Scholar
    • 28 Hosokawa K, Ando SI, Tohyama T, Kiyokawa T, Tanaka Y, Otsubo H, Nakamura R, Kadokami T, Fukuyama T. Estimation of nocturnal cardiac output by automated analysis of circulation time derived from polysomnography. Int J Cardiol. 2015; 181:14–16.CrossrefMedlineGoogle Scholar
    • 29 Kwon Y, van't Hof J, Roy SS, Bache RJ, Das G. A novel method for assessing cardiac output with the use of oxygen circulation time. J Card Fail. 2016; 22:921–924.CrossrefMedlineGoogle Scholar
    • 30 Read DJ. A clinical method for assessing the ventilatory response to carbon dioxide. Australas Ann Med. 1967; 16:20–32.CrossrefMedlineGoogle Scholar
    • 31 Rebuck A, Campbell E. A clinical method for assessing the ventilatory response to hypoxia. Am Rev Respir Dis. 1973; 109:345–350.Google Scholar
    • 32 Packer M. The neurohormonal hypothesis: a theory to explain the mechanism of disease progression in heart failure. J Am Coll Cardiol. 1992; 20:248–254.CrossrefMedlineGoogle Scholar
    • 33 Schultz HD, Marcus NJ, Del Rio R. Role of the carotid body chemoreflex in the pathophysiology of heart failure: a perspective from animal studies. Adv Exp Med Biol. 2015; 860:167–185.CrossrefMedlineGoogle Scholar
    • 34 Solin P, Roebuck T, Johns DP, Walters EH, Naughton MT. Peripheral and central ventilatory responses in central sleep apnea with and without congestive heart failure. Am J Respir Crit Care Med. 2000; 162:2194–2200.CrossrefMedlineGoogle Scholar
    • 35 Lewis R, Hackfort BT, Schultz HD. Chronic heart failure abolishes circadian rhythms in resting and chemoreflex breathing. Adv Exp Med Biol. 2018; 1071:129–136.CrossrefMedlineGoogle Scholar
    • 36 Xie A, Skatrud JB, Puleo DS, Rahko PS, Dempsey JA. Apnea‐hypopnea threshold for CO2 in patients with congestive heart failure. Am J Respir Crit Care Med. 2002; 165:1245–1250.CrossrefMedlineGoogle Scholar
    • 37 Xie A, Skatrud JB, Barczi SR, Reichmuth K, Morgan BJ, Mont S, Dempsey JA. Influence of cerebral blood flow on breathing stability. J Appl Physiol (1985). 2009; 106:850–856.CrossrefMedlineGoogle Scholar
    • 38 Miyamoto T, Nakahara H, Ueda S, Manabe K, Kawai E, Inagaki M, Kawada T, Sugimachi M. Periodic breathing in heart failure explained by dynamic and static properties of respiratory control. Clin Med Insights Cardiol. 2015; 9:133–142.MedlineGoogle Scholar
    • 39 Andreas S, Weidel K, Hagenah G, Heindl S. Treatment of Cheyne‐Stokes respiration with nasal oxygen and carbon dioxide. Eur Respir J. 1998; 12:414–419.CrossrefMedlineGoogle Scholar
    • 40 Giannoni A, Baruah R, Willson K, Mebrate Y, Mayet J, Emdin M, Hughes AD, Manisty CH, Francis DP. Real‐time dynamic carbon dioxide administration: a novel treatment strategy for stabilization of periodic breathing with potential application to central sleep apnea. J Am Coll Cardiol. 2010; 56:1832–1837.CrossrefMedlineGoogle Scholar
    • 41 Khayat RN, Xie A, Patel AK, Kaminski A, Skatrud JB. Cardiorespiratory effects of added dead space in patients with heart failure and central sleep apnea. Chest. 2003; 123:1551–1560.CrossrefMedlineGoogle Scholar
    • 42 Javaheri S. Acetazolamide improves central sleep apnea in heart failure: a double‐blind, prospective study. Am J Respir Crit Care Med. 2006; 173:234–237.CrossrefMedlineGoogle Scholar
    • 43 Fontana M, Emdin M, Giannoni A, Iudice G, Baruah R, Passino C. Effect of acetazolamide on chemosensitivity, Cheyne‐Stokes respiration, and response to effort in patients with heart failure. Am J Cardiol. 2011; 107:1675–1680.CrossrefMedlineGoogle Scholar
    • 44 Deacon‐Diaz NL, Sands SA, McEvoy RD, Catcheside PG. Daytime loop gain is elevated in obstructive sleep apnea but not reduced by CPAP treatment. J Appl Physiol. 2018; 125:1490–1497.CrossrefMedlineGoogle Scholar
    • 45 Szollosi I, Thompson BR, Krum H, Kaye DM, Naughton MT. Impaired pulmonary diffusing capacity and hypoxia in heart failure correlates with central sleep apnea severity. Chest. 2008; 134:67–72.CrossrefMedlineGoogle Scholar

    eLetters(0)

    eLetters should relate to an article recently published in the journal and are not a forum for providing unpublished data. Comments are reviewed for appropriate use of tone and language. Comments are not peer-reviewed. Acceptable comments are posted to the journal website only. Comments are not published in an issue and are not indexed in PubMed. Comments should be no longer than 500 words and will only be posted online. References are limited to 10. Authors of the article cited in the comment will be invited to reply, as appropriate.

    Comments and feedback on AHA/ASA Scientific Statements and Guidelines should be directed to the AHA/ASA Manuscript Oversight Committee via its Correspondence page.