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Completed

NCT Number: NCT04495231

Sympathetic Activity and Cardiometabolic Complications

Recent studies on catecholamine physiology have shown a direct correlation with arterial hypertension, overcoming the exclusive role in the diagnosis and follow-up of chromaffin tumors.

Nevertheless, in literature, few studies explore and reveal the utility of testing metanephrines for the evaluation of sympathetic activity and its associated cardiometabolic complications in patients with essential hypertension.

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Key information

About this study

Catecholamines (noradrenaline, adrenaline and dopamine) are adaptive and maladaptive stress hormones.

In the classic "fight or flight" mechanism, they activate behavioral and physiological processes that facilitate the overcoming of stress; for instance, challenged by a physical stressor, an organism responds to the threat either fighting and prevailing or accepting defeat and fleeing in avoidance.

In the pathological context, an excessive catecholamine secretion is typical of the chromaffin tissue tumors, determining a clinical picture characterized by blood pressure elevation, tachycardia, anxiety, pallor, sweating and headache.

COMT enzyme catalyzes the O-methylation of the 3-hydroxyl group of catecholamines. The O-methylated derivatives of noradrenaline, adrenaline and dopamine are normetanephrine, metanephrine and 3-methoxytyramine, respectively. The term "metanephrines" is generally used to collectively refer to the first two compounds.

Compared to catecholamines, metanephrines are characterized by longer half-life and more stable levels over time. Their superior accuracy for the diagnosis and follow-up of pheochromocytoma and paraganglioma (PPGL) has been widely proved.

Excluding patients with PPGL, however, metanephrines can be more broadly considered as reliable markers of the whole sympathetic system activity; therefore, their levels may be hypothesized to be associated to a higher rate of concurrent cardiometabolic complications and, if so, could be useful for the stratification of cardiovascular risk.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Measurement of 24h urinary metanephrines at the laboratory of "City of Health and Science" hospital in Turin between 2007 and 2015
  • Availability of contextual clinical patient data as collected in prospective registries of Piedmont region

Exclusion criteria

  • Diagnosis of pheochromocytoma or paraganglioma (at the time of urinary metanephrines collection or within the following 5 years)
  • Diagnosis of other forms of secondary hypertension
  • Previous cardiovascular or cerebrovascular event
  • Chronic heart failure
  • eGFR < 50 ml/min (according to CKD-EPI)
  • Liver cirrhosis
  • Acute conditions and/or hospitalization in ICU (at the time of urinary metanephrines collection)
  • Assumption of acetaminophen during the day before the 24-hour urine collection
  • Therapy with labetalol
  • Therapy with sotalol
  • Therapy with alpha-methyldopa
  • Therapy with MAO inhibitors
  • Therapy with tricyclic antidepressants
  • Therapy with buspirone
  • Therapy with phenoxybenzamine
  • Therapy with sulfasalazine
  • Therapy with L-Dopa
  • Therapy with sympathomimetic drugs or other vasopressors
  • Alcohol abuse
  • Cocaine abuse

Treatment and study plan

Primary outcomes

  1. Presence of left ventricular hypertrophy

    Time frame: At baseline

    The value of urinary metanephrines will be evaluated as a possible predictor of the presence of left ventricular hypertrophy

  2. Presence of chronic kidney disease

    Time frame: At baseline

    The value of urinary metanephrines will be evaluated as a possible predictor of the presence of chronic kidney disease

  3. Presence of type 2 diabetes mellitus

    Time frame: At baseline

    The value of urinary metanephrines will be evaluated as a possible predictor of the presence of type 2 diabetes mellitus

  4. Presence of metabolic syndrome

    Time frame: At baseline

    The value of urinary metanephrines will be evaluated as a possible predictor of the presence of metabolic syndrome

Secondary outcomes

  1. Systolic blood pressure (SBP)

    Time frame: At baseline

    The value of urinary metanephrines will be evaluated as a possible predictor of systolic blood pressure values (mmHg)

  2. Diastolic blood pressure (DBP)

    Time frame: At baseline

    The value of urinary metanephrines will be evaluated as a possible predictor of diastolic blood pressure values (mmHg)

  3. Resting heart rate

    Time frame: At baseline

    The value of urinary metanephrines will be evaluated as a possible predictor of resting heart rate (bpm)

  4. eGFR

    Time frame: At baseline

    The value of urinary metanephrines will be evaluated as a possible predictor of eGFR values (ml/min, as estimated by CKD-EPI formula)

  5. Urinary albumin/creatinine ratio

    Time frame: At baseline

    The value of urinary metanephrines will be evaluated as a possible predictor of albumin/creatinine ratio values (mg/mmol)

  6. Fasting glucose

    Time frame: At baseline

    The value of urinary metanephrines will be evaluated as a possible predictor of fasting glucose values (mg/dl)

  7. Total cholesterol

    Time frame: At baseline

    The value of urinary metanephrines will be evaluated as a possible predictor of total cholesterol values (mg/dl)

  8. HDL cholesterol

    Time frame: At baseline

    The value of urinary metanephrines will be evaluated as a possible predictor of HDL cholesterol values (mg/dl)

  9. LDL cholesterol

    Time frame: At baseline

    The value of urinary metanephrines will be evaluated as a possible predictor of LDL cholesterol values (mg/dl, as estimated by Friedewald formula)

  10. Triglycerides

    Time frame: At baseline

    The value of urinary metanephrines will be evaluated as a possible predictor of triglycerides values (mg/dl)

  11. Body Mass Index (BMI)

    Time frame: At baseline

    The value of urinary metanephrines will be evaluated as a possible predictor of BMI values (kg/m2)

  12. Cardiovascular risk as estimated by Framingham Risk Score (FRS)

    Time frame: At baseline

    The value of urinary metanephrines will be evaluated as a possible predictor of cardiovascular risk as estimated by FRS; FRS is expressed as a percentage, with higher values indicating higher risk; patients in which the risk estimation is not applicable will be excluded from the analysis

  13. Cardiovascular risk as estimated by Systematic COronary Risk Evaluation (SCORE)

    Time frame: At baseline

    The value of urinary metanephrines will be evaluated as a possible predictor of cardiovascular risk as estimated by SCORE; SCORE is expressed as a percentage, with higher values indicating higher risk; patients in which the risk estimation is not applicable will be excluded from the analysis

  14. Cardiovascular risk as estimated by Progetto Cuore Score (english translation: "Heart Project Score")

    Time frame: At baseline

    The value of urinary metanephrines will be evaluated as a possible predictor of cardiovascular risk as estimated by Progetto Cuore Score; Progetto Cuore Score is expressed as a percentage, with higher values indicating higher risk; patients in which the risk estimation is not applicable will be excluded from the analysis

Sponsors and collaborators

Lead sponsor

University of Turin, Italy

Other

Registry information

Official study title

Association Between Enhanced Sympathetic Activity and Cardiometabolic Complications: a Cross-sectional Study on Predictive Power of 24-hour Urinary Metanephrines (SYMPACT)

Acronym: SYMPACT

Important dates

Study start
2007
Primary completion
2015
Study completion
2020
First posted
Jul 31, 2020
Registry last updated
Jul 31, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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