Experiences with

Antithyroglobulin antibody test

This study aimed to characterize the distinct metabolic profiles associated with thyroid peroxidase antibody (TPOAb) and thyroglobulin antibody (TgAb) positivity in female patients with HT.

The associations of the UIC and selenium intake with thyroid peroxidase antibody (TPOAb) positivity, thyroglobulin antibody (TgAb) positivity, and TAI were assessed via weighted multivariable logistic regression. Interaction and subgroup analyses were conducted.

I am still awaiting another test result for anti parietal cell antibody which my GP did last week.

3000iu vitamin D The dr has now put me on 100mcg for all days of the week: [u]Thyroid[/u] Free Thyroxine: 13.78 pmol/l [10.4 - 19.4] Thyroid Stimulating Hormone: 3.895 mIU/l [0.55 - 4.78] Free T3: 4.45 pmol/L [2.6 - 7.1] Thyroid Peroxidase Antibodies: > 1300 U/ml [<60 H] Thyroglobulin Antibody

Did I take the test correctly? (timing) And my blood test results have several categories so they don't always line up each test. For example, I have TSH, Thyroxine (T4), Triodothyronine (Free T3), Reverse T3 serum (do I need this?), Thyroid peroxidase TPO, thyroglobulin antibody.

Just wondering whether any members have had this test? I'm not really thinking about those who have had a B12 deficiency (or suspected Pernicious Anaemia) followed up by this test. Rather has anyone had done spontaneously as the link below [i]appears[/i] to imply.

My GP for some reason cannot give the MMA blood test or active B12. However, he did agree to give me the IFAB test and the parietal cell antibody test. He also retested my serum B12 and folate.

Blood test results from endocrinologist visit: Thyroid function: • TSH: 10.50 mU/l (range 0.27 – 4.20) • Free T4: 12.1 pmol/L (range 12 – 22) • Free T3: 4.6 pmol/L (range 3.1 – 6.8) • TPO: 95 IU/mL (<25) • Thyroglobulin Antibody: 103 IU/mL (<40) Vitamins: • Vit B12: 512 pg/ml (range 191-663)

The private Dr says that the biopsy results for the Autoimmune Gastrtis will be negative, as the parietal cell antibody test was negative. I would have thought that both the parietal cell antibody test and the biopsies would be positive if I had pernicious anaemia / autoimmune gastritis.

During that time I also had undiagnosed celiac disease so not sure if that could have caused the antibody level seen in my result . My TSH has always been in range .

Prior to starting any injections my parietal cell antibody test was positive but completely normal gastrin - I would assume gastrin would be high as my new dr suspects PA.

Anti-nuclear antibody (ANA), anti-mitochondrial antibody M2 sub-type (AMA-M2), anti-smooth muscle antibody (ASMA), anti-liver kidney microsomal antibody (LKM-1), anti-soluble liver antigen/liver-pancreatic antigen antibody (SLA/LP), and hepatocyte solute antigen (LC-1) tested negative.

I am awaiting the results of a Parietal cell antibody test. Do these tests reveal anything further especially the B12 active and MMA?

He recommended I get a parietal cell antibody test. Now for the confusion and uncertainty created in me. I requested a PCA antibody test from my GP who text me to inform me that the lab does not do it instead they do an Autoimmune Profile. This came back negative.

He recommended I get a parietal cell antibody test. Now for the confusion and uncertainty created in me. I requested a PCA antibody test from my GP who text me to inform me that the lab does not do it instead they do an Autoimmune Profile. This came back negative.

Thank you Zakiya levels tsh - <0.01 free thyroxine 35.9 free t3 11.5 thyroglobulin antibody 61.4 thyroid peroxidase antibodies >600.0 TSH receptor antibodies 6.16 Thank you for your support!

my neurologist said my ferritin level was little low. Told me to supplement iron. Went to Walmart and bought some iron. Is there a difference in iron supplements or can someone recommend one is best. Thanks in advance

I have had RLS for as long as I can remember. I am 66 now. About 4.5 years ago I was so miserable at night and even had daytime symptoms my GP put me on ropinerole 0.5 mg at night if I remember correctly. It was a wonder drug for me. At some point I had what was probably augmentation with more daytime

Had problems swallowing over a year or so finally got worse in 2023. Had camera and they found a t4 tumour. Lots of tests and finally started chemo had 4 lots of flot which was gruelling. Surgery was schedualed for march 2024. Had ivor lewis. A week later i was back in surgery my diaphram had ruptured

Hi everyone - can someone run past me again how much T4 you should take by Kg weight please. Thanks