# Postural Orthostatic Tachycardia Syndrome, Menopause and Hormone Replacement Therapy: Clinical Decisions in Times of Uncertainty

**Authors:** Svetlana Blitshteyn

PMC · DOI: 10.3390/jcm15041477 · 2026-02-13

## TL;DR

This paper reviews how menopause and hormone therapy affect women with POTS, offering guidance on managing symptoms and treatment decisions.

## Contribution

The paper provides a narrative review on the use of HRT in women with POTS during menopause, offering clinical decision-making insights.

## Key findings

- HRT may be considered for POTS patients with menopausal symptoms, considering comorbidities and cardiovascular risk.
- Vaginal estrogen is generally safe, while transdermal estrogen and micronized progesterone can help with significant menopausal symptoms.
- Long-term outcomes of HRT in POTS patients remain unknown and require further study.

## Abstract

Postural orthostatic tachycardia syndrome (POTS), characterized by a rise in heart rate of at least 30 beats per minute from supine to standing position without accompanying orthostatic hypotension, is one of the most common autonomic disorders with disabling cardiovascular and neurologic manifestations. Hormonal influence has been long recognized by the disorder predominantly affecting women of reproductive age, with frequent onset around menarche, exacerbation of symptoms before or during menses, and pregnancy being one of POTS triggers. Hormone replacement therapy (HRT) and menopause in women with POTS have not been studied, but issues surrounding HRT are highly relevant as women with POTS transition from reproductive age to menopause. Given a rising prevalence of POTS due to post-COVID onset and the US Food and Drug Administration recently removing the black box warning on estrogen-containing HRT formulations, informed decisions and risk assessments regarding HRT use in women with POTS are warranted. In this narrative review, existing studies on hormones and POTS and its common comorbidities are reviewed, and key points in decision-making on the use of HRT in women with POTS are discussed. In summary, for women with significant menopausal symptoms and/or exacerbation of POTS during the peri- or postmenopausal period, using some forms of HRT for treatment of menopausal symptoms may be considered, accounting for comorbidities, cardiovascular risk and other factors. Vaginal estrogen appears to be safe for most women while transdermal estrogen and micronized progesterone can be utilized for significant menopausal symptoms, although outcomes of their long-term use are unknown.

## Linked entities

- **Diseases:** Postural orthostatic tachycardia syndrome (MONDO:0011479), POTS (MONDO:0011479)

## Full-text entities

- **Genes:** IGHE (immunoglobulin heavy constant epsilon) [NCBI Gene 3497] {aka IgE}, AGTR1 (angiotensin II receptor type 1) [NCBI Gene 185] {aka AG2S, AGTR1B, AT1, AT1AR, AT1B, AT1BR}, IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}, OGA (O-GlcNAcase) [NCBI Gene 10724] {aka MEA5, MGEA5, NCOAT}, ESR1 (estrogen receptor 1) [NCBI Gene 2099] {aka ER, ESR, ESRA, ESTRR, Era, NR3A1}
- **Diseases:** anemia (MESH:D000740), POI (MESH:D016649), neurologic conditions (MESH:D019636), orthostatic intolerance (MESH:D054971), injury to (MESH:D014947), Ovarian cysts (MESH:D010048), headache (MESH:D006261), Ehlers-Danlos syndrome (MESH:D004535), inflammation (MESH:D007249), exercise intolerance (MESH:C564972), cerebral hypoperfusion (MESH:D002547), sympathetic (MESH:D006732), RA (MESH:D001172), small fiber neuropathy (MESH:D000071075), partum (MESH:D050032), tissue abnormalities (MESH:D000014), metabolic syndrome (MESH:D024821), Orthostatic Tachycardia Syndrome (MESH:D054972), thrombosis (MESH:D013927), flushing (MESH:D005483), clotting disorders (MESH:D020141), blood pressure dysregulation (MESH:D006973), sleep disturbance (MESH:D012893), PCOS (MESH:D011085), pain (MESH:D010146), autoimmune or connective tissue disorders (MESH:D003240), venous thromboembolism (MESH:D054556), hot flashes (MESH:D019584), mitochondrial dysfunction (MESH:D028361), endometriosis (MESH:D004715), dysmenorrhea (MESH:D004412), infection (MESH:D007239), vascular aneurysms (MESH:D000783), overactive bladder (MESH:D053201), insomnia (MESH:D007319), hypoactive sexual desire disorder (MESH:D020018), hyperhidrosis (MESH:D006945), Cardiovascular Disease (MESH:D002318), diabetes (MESH:D003920), sexual dysfunction (MESH:D012735), eclampsia (MESH:D004461), immunologic dysregulation (MESH:D007154), post (MESH:D000094025), endothelial dysfunction (MESH:D014652), orthostatic hypotension (MESH:D007024), SjD (MESH:D012859), ischemic stroke (MESH:D002544), cancers (MESH:D009369), pre-eclampsia (MESH:D011225), joint pain (MESH:D018771), dehydration (MESH:D003681), urinary track infections (MESH:D014552), hepatic coagulation factors (MESH:D020147), osteoporosis (MESH:D010024), anorexia (MESH:D000855), chronic kidney or liver disease (MESH:D051436), mast cell hyperactivity (MESH:D000090362), blood pressure spikes (MESH:D031261), hypovolemia (MESH:D020896), lightheadedness (MESH:D004244)
- **Chemicals:** elinzanetant (-), Clonidine (MESH:D003000), leukotriene C4 (MESH:D017997), medroxyprogesterone acetate (MESH:D017258), 17-beta-estradiol (MESH:D004958), lipid (MESH:D008055), testosterone (MESH:D013739), progesterone (MESH:D011374), Fezolinetant (MESH:C000608808), glucose (MESH:D005947), calcium (MESH:D002118)
- **Species:** Homo sapiens (human, species) [taxon 9606]

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Source: https://tomesphere.com/paper/PMC12941859