OpenHealth Q&A

Get answered by medical professionals

Concerns Regarding My Father's Health: High Triglycerides and Diabetes

7/10/2025, 6:10:24 PMMale25-34

My father, aged 62, resides in India and stands at about 5'8" and weighs around 75 kg (165 lbs). He is a non-smoker with a significant family history of health issues, particularly type 2 diabetes, as both of his parents suffered from it. Several years back, he underwent a procedure to have a stent inserted because of coronary artery disease. Throughout the years, his triglyceride levels have consistently remained above 400 mg/dL, regardless of the medications and dietary changes he has implemented. His most recent measurement showed an alarming level of 840 mg/dL. His physician suspects that this condition has a genetic basis, especially since both of his parents passed away due to heart attacks. Fortunately, he is currently asymptomatic, experiencing no abdominal discomfort or signs of pancreatitis, and he avoids alcohol. Although his eating habits aren't ideal, they don’t seem excessively high in sugars or fats. His doctor recently revised his medication regime, and I plan to share those details once he relays the information tomorrow. I live in the United States while he continues his life in India. This situation leaves me feeling anxious, and I aim to stay proactive despite the distance. Given my father's chronic high triglycerides, diabetes, and cardiovascular issues, I am increasingly concerned about both immediate dangers, such as pancreatitis, and the long-term risks of heart disease or stroke that he faces. I am not seeking advice on whether these conditions are dangerous — I am well aware of that. Instead, I would appreciate guidance on the following matters: • What steps should we take next (such as consulting specialists or pursuing advanced testing)? • Which medications or combinations are generally effective for managing persistently elevated triglycerides? • What dietary strategies or nutritional therapies are most effective for individuals with familial hypertriglyceridemia? He is now on a different medication, given the alarming rise in his triglyceride levels, and has plans for another test soon. Although his doctor prescribed insulin, he has been hesitant to use it due to his fear of injections, despite my numerous attempts to encourage him otherwise. I am unsure what other medications he is currently taking, but he promised to update me by tomorrow morning. Thank you for any assistance or advice you can provide — I am simply striving to be proactive as I navigate this challenging situation from afar.

DiabetesThyroid DisordersEndocrinology

Answers (1)

Cony

7/10/2025, 6:10:46 PM

OpenHealth AI

It's completely understandable to feel anxious about your father's health given his history of high triglycerides and diabetes, especially with a family history of cardiovascular issues. Here’s a comprehensive approach to help manage these conditions effectively.

Main Points:

  1. Consult a Specialist: Engaging with an endocrinologist or a lipid specialist can provide expert insight into your father's condition.
  2. Medications for High Triglycerides: Certain medications can be particularly useful for managing elevated triglycerides.
  3. Dietary Strategies: Implementing specific nutritional strategies can help lower triglyceride levels significantly.

Explanation:

High triglyceride levels, especially when consistently above 400 mg/dL, pose risks like pancreatitis and cardiovascular disease. Given your father's genetic predisposition and the fact that he's asymptomatic now, proactive measures can make a significant difference in managing his health.

Next Steps:

  1. Consult a Specialist:

    • Request a referral to an endocrinologist or a lipidologist who specializes in metabolic disorders. Given the genetic aspect of his high triglycerides, they can help devise a personalized treatment and management plan.
    • Discuss potential advanced testing, such as genetic testing or a lipid panel to identify specific lipid abnormalities.
  2. Medications:

    • Statins (like atorvastatin) are commonly used to manage cholesterol levels, but for triglycerides specifically, consider discussing the following options with his doctor:
      • Fibrates (such as fenofibrate): These are effective in lowering triglycerides but should be carefully monitored with statin use to avoid muscle-related side effects.
      • Omega-3 Fatty Acids: Prescription-strength omega-3 supplements can significantly lower triglyceride levels. These are generally well tolerated.
      • Niacin: While effective, it may have side effects, so monitoring is essential.
      • Insulin: If his blood glucose is poorly controlled, insulin might be necessary. Encouraging him to address his fear of injections and discuss options like an insulin pen might be beneficial.
  3. Dietary Strategies:

    • Reduce Sugars and Simple Carbs: While you mentioned his diet isn't excessively high in sugars, it's important to minimize refined carbs and sugars, as they can raise triglyceride levels.
    • Increase Omega-3 Fatty Acids: Encourage the inclusion of fatty fish (like salmon, mackerel, or sardines) in his diet. If he is not fond of fish, omega-3 supplements may be helpful.
    • Opt for Healthy Fats: Encourage the use of unsaturated fats found in olive oil, avocados, and nuts instead of saturated fats (found in red meat and full-fat dairy).
    • Focus on Fiber: Incorporating more fruits, vegetables, and whole grains can help manage overall cholesterol and triglyceride levels. Aim for at least 25-30 grams of fiber daily.
    • Portion Control: Encourage smaller, balanced meals throughout the day to manage insulin levels better.

Reassurance:

Your efforts to stay informed and proactive are commendable, and maintaining communication with your father about his health will be key. Encourage him to be open about his concerns and to actively participate in his care plan. By taking these steps, you can help him manage his health effectively from afar. Keep advocating for his well-being, and let me know if you need more specific information or support!

Related Questions

Assessing My Health Concerns: How Anxious Should I Be?

I’m a 32-year-old woman, weighing 124 pounds and standing at 5 feet 6 inches tall. For over a year, I have been experiencing bright red rectal bleeding. Initially, I attributed this issue to hemorrhoids that developed during my pregnancy two years ago. The bleeding occurs with most of my bowel movements, sometimes happens without one, and on a few occasions, has been enough to stain the toilet bowl significantly. The color of the blood is typically darker than what I observe during a hemorrhoid flare-up. There is a notable family history of bowel cancer on both sides; one family member was diagnosed at age 45, and another at 60. In the past six months, I have encountered several episodes of severe abdominal pain—3 to 4 instances—intense enough to consider a trip to the emergency room. However, the pain usually subsides within about an hour. It’s unusual for me to experience such acute pain, given my high tolerance for discomfort; for example, I once played rugby shortly after dislocating and fracturing my finger. Recently, I mustered the courage to consult with my doctor, who recommended a FIT test, which returned a positive result (30.1). Additionally, I underwent a complete blood test, and aside from having low ferritin levels (7 µg/L), all other results were normal. I have since been referred for a colonoscopy on a two-week waiting list to rule out any possible bowel cancer. Given these circumstances, how concerned should I be? Thank you for your input.

Crohn's DiseaseThyroid DisordersInternal Medicine
Male25-34
9 minutes ago

Understanding Possible Seizure Triggers and Recurrence Risks

Health Background: I am a 21-year-old female, standing at 169 cm and weighing 65 kg. Over the past three years, I have been using oral contraceptives. As of this morning, I started taking 25 mcg of levothyroxine along with a weekly vitamin D supplement of 0.266 mg. Recently, I was diagnosed with hypothyroidism and found to have a vitamin D deficiency that I suspect has existed for the last three years. I do not consume alcohol or smoke, and I can confirm I am not pregnant. Two years ago, I experienced a mild concussion. I currently reside in Spain. A couple of months back, in mid-December, I blacked out twice. The second occurrence took place while I was at the doctor’s office after seeking urgent medical care for the initial incident. Following the second episode, I underwent a CT scan and an EKG, both of which returned normal results. Further tests, as directed by my physician, revealed a critical vitamin D deficiency and hypothyroidism; however, he expressed doubt that either of these conditions led to my loss of consciousness. I was then referred to a neurologist, and I am presently awaiting an appointment. Although the waiting period is lengthy, my doctor indicated that I should receive priority for scheduling, although the exact timeframe remains uncertain. The referral document summarized my events, labeling the second episode (which the physician witnessed) as a potential seizure devoid of tonic-clonic movements—a revelation that took me by surprise. After regaining consciousness, I felt extremely disoriented and terrified, struggling to process what was happening. I have no prior history of seizures, epilepsy, or any related conditions, and there is no known family history of these issues. If this indeed was a seizure, what might have triggered it? Additionally, what is the likelihood of experiencing another one? Since that time, I have not had any further incidents, but I have experienced moments where I felt a sense of impending doom, which I managed to overcome. I intend to wait for the neurologist's evaluation, but the uncertainty surrounding a possible neurological condition is quite distressing. Thank you for any insight you can provide!

LupusThyroid DisordersEndocrinology
Male25-34
19 minutes ago

Understanding EEG Results for My 22-Month-Old Son: Insights Needed

Could someone help clarify this for me? My son, who is just 22 months old, hasn’t started walking yet, becomes tired easily, and has been experiencing behavioral outbursts. He had a febrile seizure in February 2025, followed by another unexplained seizure in April 2025, which led us to consult a neurologist. Since he was 3 months old, he has been receiving therapy from a physical therapist for torticollis. At birth, he spent five days in the NICU due to issues with meconium aspiration. A recent MRI showed normal results, and he also had a follow-up EEG after one conducted in July 2025. The results from this recent EEG were abnormal for a pediatric patient in awake, drowsy, and sleeping states. Notably, there were brief episodes of left frontotemporal delta slowing, which occurred mainly when he was awake and drowsy. There were no signs of epileptiform activity detected. In contrast, the EEG performed back on July 3, 2025, was deemed normal for both awake and drowsy states, again with no evidence of epileptiform irregularities, although it did not capture any sleep data. This examination was prompted by the child's existing history of febrile seizures. Importantly, he is not currently on any anti-seizure medications. The EEG procedure used standard electrode placements per the 10-20 system, conducted a single-lead EKG, and included continuous video monitoring. During the analysis, the background activity was symmetric, indicating some anterior-posterior (AP) organization, with a dominant rhythm of 50-80 microvolts at 7 Hz. His drowsy state was marked by a reduced amount of eye blink activity, less breathing motion interference, and a generalized slowing in theta/delta frequencies. Stage II sleep exhibited spindles and vertex waves patterns. Additionally, there were intermittent bursts of 250-300 microvolts in the left frontotemporal region with semi-rhythmic activity of 2-4 Hz, mostly observed during wakefulness and drowsiness. No definitive epileptiform discharge was noted. Photic stimulation during the test did not elicit a strong response, and hyperventilation was not conducted during this session.

Multiple SclerosisCrohn's DiseaseEndocrinology
Male25-34
1 hour ago

Understanding Atrial Fibrillation and Thyroid Issues: Variability in Cardioversion Decisions

Hello everyone, I’m reaching out for guidance regarding my mother’s current health situation, and I’d greatly appreciate any shared experiences or thoughts. **My mother's background:** - **Age**: 55 years - **Weight**: Recently dropped to 116 kg from 118 kg in just two days, likely due to diuretics. - **Health history**: Previously an underactive thyroid, undiagnosed and untreated, now presenting as overactive. - **Medications**: Currently taking thyroid medication and a beta-blocker (Rapiblock). **Current health status:** My mother has been hospitalized since Tuesday, experiencing **atrial fibrillation with heart rates exceeding 200** beats per minute due to her thyroid's hyperactivity. - The plan for cardioversion was initially settled on Tuesday. However, the following day, the medical team advised postponing it until her thyroid levels could be stabilized, believing that her heart rate would return to normal once her thyroid condition was managed. - Her **obesity** precludes her from undergoing a transthoracic echocardiogram, and due to her thyroid concerns, she cannot handle contrast dye (this has been a consistent issue for over four years). Therefore, the only feasible option was a **transesophageal echocardiogram (TEE)**, which has yet to be performed. - She has been prescribed various medications including beta-blockers and thyroid treatments in the past. - On Friday, a doctor proposed proceeding with cardioversion; however, the attending senior physician objected. - Today (Saturday), another clinician has expressed a desire to move forward with cardioversion, having initiated a new medication, as the senior physician is unavailable. - **Communication has been unclear**, as we were notified of developments by a nurse rather than the physician in charge, causing confusion and anxiety. - Currently, only a **chest X-ray** is scheduled, and the TEE remains unaddressed. **My inquiries are as follows:** 1. Is it common for medical professionals to have varying opinions and frequently revise medication or treatment plans like cardioversion? 2. Is it safe to conduct cardioversion in the absence of a TEE? I presumed that this was a standard procedure to exclude the presence of blood clots. 3. Is it usual practice to have only a chest X-ray prior to moving ahead with cardioversion? 4. How typical is it for patients or their families to not be directly informed about treatment changes and learn about them through nursing staff instead? I recognize that this cannot substitute for professional medical advice. I’m simply trying to discern whether these circumstances are typical or if we should express our concerns more assertively with the healthcare facility. Thank you for your insights!

Thyroid DisordersEndocrinologyRheumatology
Male25-34
2 hours ago

28-Year-Old Male Experiencing Scalp Sensations Post-Amitriptyline Treatment

I am a 28-year-old man in generally good health, without any cardiac concerns. Approximately a month ago, I encountered intense pain localized to one side of my head, which was unresponsive to paracetamol. However, a single dose of a migraine treatment provided substantial relief. Following that, I began a regimen of amitriptyline, starting at a nightly dose of 10 to 25 mg. While my head pain has diminished significantly—by about 90 to 95%—I now experience occasional uncomfortable sensations on my scalp. These feelings include pins and needles, a cooling sensation, and some crawling feelings near my hairline and ears. There are fleeting moments where I feel brief throbs lasting a second, but I do not have any persistent headaches. To clarify, I do not experience any of the following: - Nausea - Weakness in my limbs - Numbness - Changes in my vision - Coordination difficulties - Seizures The symptoms I have are transient, shifting around and often intensifying when I become conscious of them or as the day progresses. I would like to know: Is it common to experience these sensations during the recovery stage following episodes of neuralgia or migraine-like discomfort? Additionally, could the amitriptyline potentially be causing these temporary paresthetic sensations? I am seeking some reassurance or advice on what is typically observed during this healing process. Thank you.

Multiple SclerosisCrohn's DiseaseEndocrinology
Male25-34
3 hours ago