Click Here to Download this Blog Post – Orthostatic Hypotension: Part 4 Of 6
By Dr. Nicholas L. DePace, M..D., F.A.C.C – Cardiologist specializing in autonomic dysfunction, Ehlers-Danlos syndrome and POTS.
This is Part 4 of a 6 Part Series about Orthostatic-Hypotension
The first thing when a person presents with orthostatic hypotension is to determine if there is a volume depletion issue or if there is truly an autonomic (baroreflex) failure.
Neurogenic autonomic hypotension, which means not related to dehydration, volume depletion, or a drug effect, can be classified into disorders with either a primary or secondary cause of autonomic failure.
It is estimated that up to 40% of people have no definite cause of orthostatic hypotension, and therefore, it is idiopathic.
About a quarter can have underlying neurodegenerative disorders, a third autonomic failure to diabetic neuropathy or paraneoplastic syndromes (cancer-related neuropathies).
The use of antidepressant drugs is often the cause of orthostatic hypotension if really sought for.
Secondary causes of autonomic dysfunction include peripheral neuropathies that affect the peripheral small fibers, which include the autonomic nerves.
The most common is diabetes mellitus.
However, usually, before this occurs in diabetes, one will have sensory abnormalities of the hands and feet, such as numbness and tingling, and then autonomic neuropathy will follow with drops in blood pressure.
Amyloidosis is not an uncommon cause of a peripheral neuropathy that can leave a person with orthostatic hypotension.
We will do an amyloid workup on patients who present with orthostatic hypotension and also a diabetic workup, including a hemoglobin A1c.
The amyloid workup may include genetic testing and blood and urine workup, especially to look for special types of proteins and immunoglobulins.
About the Author
Nicholas L. DePace, MD, FACC is a board-certified cardiologist and Medical Director of Franklin Cardiovascular Associates. A graduate of the Mount Sinai School of Medicine, Dr. DePace has decades of clinical, academic, and research experience and has held faculty appointments as a Clinical Professor of Medicine, becoming one of the youngest full professors in Philadelphia at the time of his appointment.
Dr. DePace specializes in the diagnosis and treatment of autonomic nervous system dysfunction (dysautonomia), including POTS, autonomic dysfunction associated with Ehlers-Danlos syndrome (EDS), chronic fatigue, and anxiety-like conditions that are frequently misdiagnosed. He is nationally recognized for his work on parasympathetic and sympathetic (P&S) nervous system imbalance, a core mechanism underlying many complex chronic disorders.
In addition to treating patients from across the United States, Dr. DePace is a prolific clinical researcher and author of multiple nationally distributed medical textbooks published by Springer and W.W. Norton, focusing on autonomic dysfunction, mitochondrial disorders, cardiovascular disease, and mind–body medicine.
👉 View Dr. DePace’s professional profile
👉 View medical books by Dr. DePace

