OpenHealth Q&A

Get answered by medical professionals

Seeking Guidance on Secondary Hypertension from Unknown Causes

2/3/2026, 4:10:40 AMMale25-34

Hello everyone! I want to start by saying that I’m not very familiar with how to post on Reddit, so I hope I’m doing this correctly. As noted in the title, I’m a 21-year-old woman attending college, and I’ve been diagnosed with secondary hypertension linked to unexplained hyperaldosteronism. The troubling part is that the origin of my hyperaldosteronism remains a mystery to my healthcare providers. To give some background, my health concerns began about two years ago during a routine dental cleaning when my hygienist measured my blood pressure and noted that my diastolic reading was in the 100s. I didn’t get the exact figures at that moment, but I found out later that my pressure was consistently elevated. What initially seemed like typical white coat syndrome turned out to be more serious, as my blood pressure readings were often at 150s/100s with a heart rate of around 130 bpm. Following numerous doctor visits, tests, and various medications, the results revealed that while my aldosterone levels were elevated, my renin levels fell within the normal range, and other laboratory tests showed normal findings. CT scans showed no abnormalities in the adrenal glands, and ultrasonography indicated no renal artery stenosis. Ultimately, I was diagnosed with idiopathic secondary hyperaldosteronism, and unfortunately, no further clarity has emerged since my diagnosis. Currently, I’m taking 25 mg of Spironolactone, 25 mg of Metoprolol, and using an oral contraceptive, which is not thought to influence my blood pressure. Although my blood pressure readings have improved slightly, a recent check showed 140/94 while at rest. The biggest issue I’m facing is that the lack of actionable options from doctors is leaving me frustrated—endocrinologists won’t intervene due to it being a secondary issue connected to my normal renin levels, while cardiologists are hesitant because my hypertension is driven by endocrine factors, and there are no other logical tests to perform. I am in dire need of solutions. My OB-GYN has expressed concern over my elevated blood pressure potentially increasing the risk of clotting from my birth control, and discontinuing it is not feasible for me at this time. It's crucial that I get a grasp on this situation before experiencing any severe health event. Additionally, I’ve learned that my aldosterone levels can’t be reassessed until I stop taking Spironolactone for six weeks, which is daunting since I often feel unwell even if I miss a single dose. I would greatly appreciate any suggestions on additional conditions I should explore for testing, steps to take during this medical journey, or any general advice you might have from a healthcare perspective. If you need more details about my medical background, please let me know—I am truly in search of answers (this has been quite challenging for me)! Thank you all for your help and support!

HypertensionCrohn's DiseaseEndocrinology

Answers (1)

Cony

2/3/2026, 4:11:01 AM

OpenHealth AI

It sounds like you're facing a challenging situation with your secondary hypertension due to unexplained hyperaldosteronism. Managing a condition like yours requires a blend of effective self-care strategies, ongoing monitoring, and a proactive approach to communication with your healthcare team. Here’s a breakdown of key points and actionable steps you can take:

Main Points:

  1. Your hypertension is linked to elevated aldosterone levels, but the cause remains unclear.
  2. Current medications have slightly improved your blood pressure but aren’t fully controlling it.
  3. The complexity of your situation may benefit from a multi-faceted approach in collaboration with your healthcare providers.

Explanation:

Secondary hypertension, as you know, can arise from various underlying conditions, and hyperaldosteronism typically leads to fluid retention and increased blood pressure. Since your aldosterone levels are elevated without corresponding renin levels, and you've ruled out common causes with imaging and lab tests, it’s understandable to feel frustrated by the lack of concrete answers.

Actionable Steps:

  1. Monitor Your Blood Pressure Regularly: Keep a daily log of your blood pressure readings, noting the time of day and any symptoms you experience. This documentation can be incredibly helpful when discussing your condition with healthcare providers.

  2. Lifestyle Adjustments:

    • Diet: Focus on a low-sodium diet, which can help decrease blood pressure. Aim for less than 2,300 mg of sodium per day. Including potassium-rich foods (like bananas, potatoes, and spinach) can also help balance your electrolytes.
    • Physical Activity: Engage in regular, moderate exercise, such as walking or cycling, for at least 150 minutes weekly. This can support heart health and blood pressure regulation.
    • Stress Management: Incorporate stress-reducing practices like yoga, meditation, or deep-breathing exercises, as stress can elevate blood pressure.
  3. Communicate with Your Healthcare Providers:

    • Endocrinologist: If you haven’t already, ask about genetic testing or rare causes of hyperaldosteronism that have not been considered. An evaluation for conditions like Conn's syndrome may still be worth revisiting, even if initial tests were negative.
    • Cardiologist: Discuss your ongoing symptoms and concerns about blood pressure and potential medication interactions with your oral contraceptives. Exploring alternative methods of birth control that may have a lower risk could be another option.
    • Team Collaboration: Consider asking your primary care doctor to help coordinate care between specialists so that everyone is aligned on your treatment plan.
  4. Reassess Medications: Since it seems that Spironolactone is a critical part of your treatment, discuss the timing and necessity of stopping this medication for aldosterone testing. Ensure any decision is made with a clear understanding of potential risks.

  5. Consider Support Groups or Therapy: Engaging with others who face similar challenges in managing chronic conditions can provide emotional support and coping strategies.

Your journey may feel daunting, but taking these steps can empower you to better navigate your health situation. Remember to prioritize your well-being and advocate for your health with persistence during your appointments. If you need more personalized advice or further details, feel free to reach out. You're doing the right thing by seeking help and understanding.

Related Questions

Understanding Prolonged Headaches: When to Seek Help

I’m a 24-year-old female with no significant health issues aside from being on birth control. For almost two weeks now, I’ve been struggling with persistent headaches that last all day and night. Over-the-counter pain medications have proven ineffective, and I find that eating and staying hydrated do little to alleviate my discomfort. Surprisingly, sleep seems to exacerbate my condition, as I often awaken to find the headache even more intense than before. I haven’t experienced any fever, sensitivity to light, nausea, or blurry vision. However, I do have mild stiffness in my neck, a runny nose, and occasionally, I feel a bit dizzy. These other symptoms are quite minimal, though. The pain intensifies with movement or deeper breaths, and I notice it worsens significantly when I transition from lying down to standing. Activities that involve bending my neck forward are particularly distressing. Initially, the headache was localized at the back of my head, but now the discomfort has shifted toward the center. I haven't been ill recently, so I’m uncertain about the cause. I've never suffered from migraines before, making it harder to gauge what I’m dealing with.

Crohn's DiseaseCOPDInternal Medicine
Male25-34
10 minutes ago

Considering HGH at 18: What You Should Know

I'm interested in starting HGH, but I'm somewhat in the dark about the whole process. I would appreciate a detailed, step-by-step guide on how to approach this safely. Currently, my stats are 5'9" at 145 pounds, possibly around 15% body fat or slightly less. I work out consistently, hitting the gym six to seven times a week, maintain a clean diet, and don't consume alcohol or smoke. I suspect my growth plates are still open, and they might close in a year or two; my goal is to see if I can increase my height. While I'm hoping to grow taller, I certainly wouldn't oppose experiencing some muscle gains during this process. I have a few queries about HGH: What side effects should I be aware of? Is it a concern to start treatment at such a young age? What would be a suitable duration and dosage for the cycle? Are there any necessary assessments I need to perform beforehand? I'd greatly appreciate any additional tips or insights you could share.

Thyroid DisordersInternal MedicineEndocrinology
Male25-34
2 hours ago

Understanding the Prevalence of Neuropathy with Uncertain Origins

A 46-year-old male, who has been on a stable regimen of various psychiatric medications for several years, along with pregabalin and oxycodone, has been diagnosed with neuropathy not otherwise specified (NOS), as well as experiencing migraines and bipolar disorder type 1. Approximately nine years prior, he began suffering from intense joint pain that was only present during the colder months. Although he experimented with Volarin Gel for relief, it proved ineffective, leading him to endure the discomfort since it was fleeting. Fast forward sixteen months, after contracting COVID-19, he began experiencing widespread joint pain, followed by muscle aches predominantly in his legs, as well as a painful burning sensation in his extremities. The severity of this pain has rendered him unable to work. He has explored numerous remedies including hot baths, heated showers, heating pads, blankets, patches, lidocaine patches, various herbal treatments, a supplement advised by his pain specialist, and an array of pain relief sprays and topical ointments. His pain specialist has indicated that this condition is likely a form of peripheral neuropathy worsened by the COVID infection. The neurologist, however, has advised that due to the lack of definitive testing linking his symptoms to COVID, he must classify the diagnosis as neuropathy of unknown origin. He is left questioning how seriously healthcare providers will regard his diagnosis considering the vague nature of the term. He has pursued every non-opioid treatment available and is diligently managing considerable pain. It's worth noting that both his pain specialist and pharmacist approach his situation with a great deal of seriousness, extending respect and compassion to him throughout his treatment journey.

Multiple SclerosisFibromyalgiaCrohn's Disease
Male25-34
2 hours ago

Seeking Answers for My Mother's Persistent Itching in Eyes and Ears

Hello everyone, My mother, who is 65 years old, stands about 5 feet 7 inches tall and weighs in the mid to upper 200-pound range, has been suffering from severe itching in her eyes and ears (particularly within the ear canal) since June 2025. The constant irritation has led to her losing nearly all of her eyelashes, which is adding to her difficulties. I've observed that her lower eyelids have also become quite droopy, revealing the entire eyelid margin and a noticeable portion of the dark pink inner eyelid. Additionally, she is experiencing hearing issues due to significant swelling in her ear canals. Here's a summary of our journey so far: Her general practitioner (GP) conducted blood tests, but the results for autoimmune markers were normal. An ophthalmologist was consulted, yet they couldn't provide any insights into her condition. We then visited a dermatologist who prescribed hydrocortisone cream, which unfortunately cannot be applied near the eyes or inside the ears. They also suggested we see an ear, nose, and throat (ENT) specialist because of some white spots they observed, suspecting a possible fungal infection. The ENT performed an ear wax extraction and prescribed steroid drops, but the sponges intended to hold the drops in place kept dislodging due to swelling. The drops provided only minimal relief. The GP subsequently ordered thyroid tests, which came back normal, and recommended an allergist. The first allergist we saw was quite unhelpful and rude, claiming the cause was contact dermatitis from her shampoo. We changed to a gentle, fragrance-free shampoo, but unfortunately, that did not bring any improvement. The second allergist, while agreeing with the first one regarding the absence of allergy symptoms like hives, was at least open to conducting tests. Today, we underwent patch testing, which returned negative results for the top 14 common environmental allergens (and just to note, we do not have pets in our home). Currently, my mom is taking metformin for borderline diabetes and Lumingan for managing glaucoma. Given the limited medical knowledge I possess, I feel it might be beneficial to return to the GP and ask for a referral to an endocrinologist. This seems to be the only branch of medicine that might not show symptoms in various other body areas, in contrast to cardiology or gastrointestinal issues. Is there any other medical specialty that anyone could recommend we explore? It would be fantastic to resolve this situation before she retires at the end of March when we would lose her valuable BCBS insurance coverage.

Thyroid DisordersInternal MedicineEndocrinology
Male25-34
3 hours ago

Navigating Symptoms of a Hyperkinetic Gallbladder

At the age of 23, I find myself dealing with persistent discomfort in my upper right abdomen, coupled with nausea, excessive gas, disrupted sleep, acid reflux, and ongoing fatigue. Initially, I suspected it might simply be gastritis or a similar condition, largely due to my unhealthy and greasy eating habits during my time in college. However, after conducting some online research, I began to consider that these symptoms might be related to gallbladder issues. So far, I’ve undergone a series of tests, including an ultrasound, a comprehensive CT scan of my chest, abdomen, and pelvis, along with laboratory tests and a physical examination conducted by my primary care physician. While I have yet to have an endoscopy due to its high cost, the only irregularities identified thus far have been mild tenderness in the upper right quadrant from the physical evaluation, and a gallbladder ejection fraction of 93 percent from a HIDA scan, which unfortunately led to significant diarrhea and gas the following day. My parents, who both work in medicine, advise against surgery. They believe that at my age, undergoing such a procedure could lead to various uncontrolled side effects affecting my gastrointestinal system and metabolism, which might even be long-lasting. It seems I’m in for a tough journey in seeking surgical intervention. In the meantime, I'm left wondering if there are any alternative treatments available to alleviate my symptoms without resorting to surgery. Currently, I'm taking Protonix for reflux, Zofran to combat nausea, and I plan to start Bentyl tomorrow to see if it can provide any relief. I would greatly appreciate any insights or shared experiences regarding hyperkinetic gallbladder issues, or any relevant studies that could assist in my situation. Thank you in advance for your help!

Crohn's DiseaseInternal MedicineEndocrinology
Male25-34
3 hours ago