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What is the difference between dihydropyridine and nondihydropyridine CCB?

4 min read

In 2020, dihydropyridine (DHP) calcium channel blockers were prescribed to an estimated 55 million people in the United States, highlighting their widespread use in treating cardiovascular conditions. Understanding what is the difference between dihydropyridine and nondihydropyridine CCB is crucial, as their distinct effects on the heart and blood vessels determine their medical application and side effect profiles.

Quick Summary

Dihydropyridine CCBs primarily cause vasodilation by acting on blood vessels, while nondihydropyridine CCBs predominantly affect heart rate and contractility. This fundamental difference dictates their clinical applications for various heart and vascular conditions.

Key Points

  • Primary Site of Action: Dihydropyridines act mainly on blood vessels to cause vasodilation, while nondihydropyridines primarily affect the heart muscle and its conduction system.

  • Heart Rate Effects: DHPs can cause a reflex increase in heart rate (tachycardia) due to potent vasodilation, whereas non-DHPs directly decrease heart rate and conduction speed.

  • Common Indications: DHPs are widely used for hypertension and vasospastic angina. Non-DHPs are used for rate control in arrhythmias like atrial fibrillation and for treating angina.

  • Side Effect Profiles: Common DHP side effects include peripheral edema and headache, while non-DHPs can cause bradycardia and constipation.

  • Contraindications: Non-DHPs are generally not recommended for patients with heart failure with reduced ejection fraction or certain heart blocks due to their cardiodepressant effects.

  • Drug Examples: Amlodipine and nifedipine are common DHPs; verapamil and diltiazem are the most recognized non-DHPs.

In This Article

Understanding Calcium Channel Blockers

Calcium channel blockers (CCBs) are a class of medications used to treat conditions like hypertension, angina, and cardiac arrhythmias by blocking the influx of calcium ions into heart and smooth muscle cells. Calcium plays a vital role in muscle contraction, so inhibiting its entry causes relaxation. However, CCBs are not a homogenous group and are categorized into two main subclasses based on their chemical structure and primary site of action: dihydropyridines (DHPs) and nondihydropyridines (non-DHPs).

The Dihydropyridine (DHP) Class

Dihydropyridine CCBs are primarily vascular-selective, meaning their main target is the calcium channels found in the smooth muscle cells of blood vessels. By blocking these L-type calcium channels, DHPs cause peripheral arteries to relax and widen, a process known as vasodilation. This leads to a decrease in systemic vascular resistance and, consequently, a drop in blood pressure. DHPs have minimal direct effects on the heart's contractility or conduction, although the resulting drop in blood pressure can sometimes trigger a reflex increase in heart rate (reflex tachycardia).

Common Dihydropyridine CCBs

  • Amlodipine (Norvasc): A long-acting DHP commonly used for hypertension and stable angina.
  • Nifedipine (Procardia, Adalat): Available in both short-acting and extended-release formulations, used for hypertension and vasospastic angina.
  • Felodipine (Plendil): Primarily used for hypertension.
  • Nicardipine (Cardene): Used for hypertension and sometimes for vasospasm after intracranial hemorrhage.
  • Nimodipine (Nymalize): Uniquely, this DHP is used for preventing cerebral vasospasm following a subarachnoid hemorrhage.

Common Side Effects of DHPs

The side effects of DHPs are largely a result of their potent vasodilatory effects. They include:

  • Peripheral edema (swelling of ankles and feet)
  • Headache
  • Flushing (redness and warmth of the skin)
  • Dizziness
  • Reflex tachycardia (an increase in heart rate)

The Non-Dihydropyridine (Non-DHP) Class

In contrast to DHPs, nondihydropyridine CCBs are cardiac-selective. They primarily target calcium channels in the heart muscle (myocardium) and the conduction system, particularly the sinoatrial (SA) and atrioventricular (AV) nodes. By blocking calcium influx in these areas, non-DHPs have several key effects:

  • Negative chronotropy: They slow the heart rate.
  • Negative dromotropy: They slow the conduction velocity through the AV node.
  • Negative inotropy: They decrease the force of myocardial contraction.

Because of their action on the heart, non-DHPs are useful for treating conditions where slowing the heart rate is beneficial, such as certain arrhythmias. They also cause vasodilation but to a much lesser extent than DHPs.

Common Non-Dihydropyridine CCBs

  • Verapamil (Calan, Isoptin): A phenylalkylamine that is relatively more selective for the myocardium and less effective as a systemic vasodilator.
  • Diltiazem (Cardizem): A benzothiazepine that is intermediate in its selectivity, with both significant cardiac and moderate vasodilatory effects.

Common Side Effects of Non-DHPs

Side effects of non-DHPs stem from their cardiac depressant effects and are distinct from DHPs. They include:

  • Bradycardia (abnormally slow heart rate)
  • Constipation, especially with verapamil
  • Impaired AV nodal conduction
  • Dizziness
  • Worsening heart failure in patients with reduced ejection fraction

Key Differences: A Comparison Table

Feature Dihydropyridine (DHP) CCB Nondihydropyridine (Non-DHP) CCB
Primary Site of Action Vascular smooth muscle (arteries) Cardiac muscle and conduction system
Main Physiological Effect Potent vasodilation; lowers blood pressure Decreases heart rate and contractility
Examples Amlodipine, Nifedipine, Nicardipine Verapamil, Diltiazem
Key Indications Hypertension, vasospastic angina, Raynaud's phenomenon Atrial fibrillation/flutter, PSVT, angina, hypertension
Effect on Heart Rate Can cause reflex tachycardia Decreases heart rate (bradycardia)
Most Common Side Effects Peripheral edema, flushing, headache Bradycardia, constipation, AV block

Which CCB is Right for You?

Choosing between a DHP and a non-DHP CCB depends on a patient's specific cardiovascular condition and other health factors. For instance, a DHP might be a better choice for someone with uncomplicated hypertension who needs powerful blood pressure lowering, especially if they have a slow heart rate. Conversely, a non-DHP is preferable for patients who have both hypertension and a coexisting heart rhythm issue, like atrial fibrillation, that requires rate control.

It is critical to note that non-DHPs are generally contraindicated in patients with heart failure with reduced ejection fraction (HFrEF) or certain types of heart block, as their negative inotropic and dromotropic effects can worsen these conditions. Additionally, non-DHPs should not be used in combination with beta-blockers without careful consideration, as the combination can lead to dangerously low heart rates.

Conclusion

While all calcium channel blockers inhibit the movement of calcium, the distinct chemical properties of dihydropyridine and nondihydropyridine subclasses lead to fundamentally different therapeutic actions and side effect profiles. The primary difference lies in their tissue selectivity: DHPs are more vascular-selective, leading to potent vasodilation, whereas non-DHPs are more cardiac-selective, leading to a reduction in heart rate and contractility. This foundational distinction guides healthcare providers in selecting the most appropriate medication for a patient's specific needs, whether it be for managing hypertension, angina, or cardiac arrhythmias, while avoiding potential contraindications. For more detailed information on specific medications, consult authoritative sources such as the National Institutes of Health.

Frequently Asked Questions

Both dihydropyridine and nondihydropyridine CCBs can effectively lower blood pressure. However, DHPs are typically preferred as a first-line treatment for uncomplicated hypertension due to their potent vasodilatory effects.

It is not recommended to take a nondihydropyridine CCB (like verapamil or diltiazem) with a beta-blocker due to the risk of dangerously low heart rate and conduction problems. A DHP CCB can often be safely combined with a beta-blocker for enhanced blood pressure control.

Dihydropyridine CCBs, due to their powerful vasodilatory action, are significantly more likely to cause peripheral edema, or swelling of the ankles and feet.

Non-dihydropyridine CCBs, particularly verapamil, can cause constipation by blocking calcium channels in the smooth muscles of the gastrointestinal tract, leading to decreased muscle tone and motility.

Non-dihydropyridine CCBs, such as diltiazem and verapamil, slow the heart rate and conduction by inhibiting calcium channels in the heart's electrical nodes, making them effective for controlling certain fast heart rhythms like atrial fibrillation.

Both classes of CCBs have specific safety considerations. Non-DHPs can worsen heart failure in some patients and should not be combined with beta-blockers. DHPs can cause reflex tachycardia, particularly in short-acting forms. A doctor will assess a patient's overall health to determine the safest and most effective option.

Vascular-selective drugs, like dihydropyridine CCBs, have a stronger effect on the blood vessels than on the heart. Their primary purpose is to relax and widen arteries to lower blood pressure.

Dihydropyridine drugs typically have names that end with '-dipine', such as amlodipine and nifedipine. Non-dihydropyridines (verapamil and diltiazem) do not follow this naming convention.

References

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Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.