I-123 Uptake

Procedures

RAIU preparation begins with limiting the patients' intake of iodine and avoiding interfering medications to maximize I-123 uptake by thyroid tissue.[4] For RAIU alone, 3.7 MBq (100 µCi) of Sodium Iodide I-123 is administered orally. An uptake probe (2-inch diameter), with non-radioactive thallium, activated sodium iodide (NaI (Tl)) crystal (approximately 2 inches thick), a flat field collimator, photomultiplier tube detector, and multi-channel analyzer are used for counting of the 159 keV gamma peak. If rapid iodine turnover is suspected in hyperthyroidism, RAIU may be done at 4-6 hours in addition to the routine 24 hours delay. The radioactive dose is initially placed in a lucite neck phantom with the same geometry as the patient's neck and counted prior to administration. A second nearly identical Standard dose, which is not administered to the patient, may also be used in the phantom when subsequent counts of the neck are taken. The patient is positioned either sitting or supine with neck extended, and the probe positioned at a constant distance of 20 cm to 30 cm. Counts are also obtained of room background and of the patient's mid-thigh away from the urinary bladder for the patient background.

If no second standard dose is used, decay corrected 24 hours (24h) RAIU is calculated:

RAIU (in %) = {(24h Neck - 24h Thigh) / ([Initial Dose in Phantom counts - Initial Room Background] x I-123 decay correction factor for 24h)} x 100%

If a second nearly identical standard dose is used, the 24h calculation RAIU is calculated factoring in the standard dose:

RAIU (in %) = {(24h Neck - 24h Thigh) / (|Correction factor to adjust for difference in activity between initial patient dose and initial Standard dose| x [24h Standard in Phantom - 24h Room Background])} x 100%

In the absence of an uptake probe, a nuclear scintillation gamma camera with a low energy parallel hole collimator can be used if validated by comparison with a reliable standard.[5][6] For the perchlorate discharge test in neonatal hypothyroidism, RAIU is performed before and after perchlorate administration.[7]

For combined thyroid RAIU uptake and scan, the oral dose is 7.4 to 14.8 MBq (200 to 400 µCi). RAIU is done as above, while for the scan, the thyroid is imaged using either a conventional or small field gamma camera with a pin-hole or parallel-hole collimator centered at 159 KeV after 24 hrs. Imaging is captured with the patient lying supine with the neck extended.

Thyroid radioactive uptake can also be measured using intravenous technetium-99m (Tc-99m) pertechnetate. However, Tc-99m pertechnetate is trapped, but not organified, and may not always reflect true overall thyroid function. RAIU can also be measured using I-131 sodium iodide, which, like I-123 sodium iodide, is both trapped and organified. I-131 has a half-life of 8 days and has both a beta minus emission and a principal 364 keV gamma photon emission; thus, patient ionizing radiation exposure is much higher with I-131. RAIU with I-123 sodium iodide is much more popular, if available.[6][5]

Indications

RAIU with I-123 is used to measure overall thyroid function in hyperthyroidism, to help differentiate among differential causes, including productive thyrotoxicosis, destructive thyrotoxicosis, and factitious thyrotoxicosis. It can also be used to help calculate the dose for I-131 therapy. I-123 RAIU and scan may be helpful in the evaluation of thyroid nodules if the TSH is subnormal to low. I-123 RAIU’s value is limited in evaluating hypothyroidism but can be used as part of the perchlorate discharge test to identify an iodine organification defect in neonatal hypothyroidism.[8][9][10][7]

Potential Diagnosis

Normal thyroid metabolism, increased thyroid metabolism, and decreased thyroid metabolism are potential diagnoses from the RAIU I-123 test.

Normal and Critical Findings

The normal reference range for RAIU will vary by laboratory, partly depending on local geographic dietary iodine intake. Sample normal RAIU ranges could be 6-18% at 4 hours and 10 to 35% at 24 hours.

Thyrotoxicosis can be defined as a clinical state in response to an elevated thyroid hormone, which may be due to inappropriately elevated secretion or synthesis of thyroid hormone. Many disease states can cause an abnormally elevated thyroid hormone level. Regarding nodules, hyperfunctioning nodules or nodules that have increased radiotracer uptake are rarely malignant, and no cytologic evaluation is indicated.[8] 

Graves Disease

Graves disease classically presents as hyperthyroidism with a suppressed TSH. Graves disease is an autoimmune disease caused by an antibody targeted at the TSH receptor. This antibody mimics TSH, causing excessive stimulation of the thyroid gland. The I-123 exam would demonstrate a diffusely enlarged thyroid gland with increased RAIU.[10] The pyramidal lobe, which is often not visualized, may be seen just superior to the isthmus due to diffuse increased radiotracer uptake of the thyroid in Graves disease.

Occasionally, the 24 hours radiotracer uptake of the thyroid gland will be normal in a patient with Graves disease. This finding is due to the rapid turnover of the thyroid hormone, which depletes the radiotracer taken up by the thyroid gland. RAIU at 4-6 hours will demonstrate increased radiotracer, which can help diagnose Graves disease with rapid iodine turnover.[11]

A variant of Graves disease, termed Marine-Lenhart syndrome, can be seen when cold thyroid nodules are also present in the setting of Graves disease.[11][12] This presentation can also be described as Graves disease with multinodular goiter and appears as cold nodular areas in a thyroid gland with overall increased radiotracer uptake. RAIU is increased in Graves disease and Marine-Lenhart syndrome.

Toxic Autonomous Nodule

A thyroid nodule may act independently of TSH and continually excrete the thyroid hormone. This thyroid nodule will demonstrate increased radiotracer uptake, while the remaining thyroid may demonstrate normal or decreased radiotracer uptake depending on the extent of excretion from the toxic autonomous nodule. The toxic nodules are histologically adenomas and oftentimes demonstrate mutated TSH receptors, which are perpetually activated.[11] The toxic autonomous nodule is also referred to as Plummer disease. Overall, thyroid gland RAIU may be mildly decreased, regular, or mildly elevated in a toxic autonomous nodule.

Toxic Multinodular Goiter

Multinodular goiter is usually a diagnosis initially found on physical exam or ultrasound of an enlarged thyroid with multiple nodules. These nodules can eventually progress to hyperplasia and possibly become autonomous. There is often low to subnormal TSH, and the radiotracer uptake is heterogeneous with areas of increased uptake representing hot nodules along with areas of decreased uptake representing cold nodules. The extent of thyrotoxicosis is usually milder when compared to Graves' disease. Overall, thyroid gland RAIU may be mildly decreased, normal, or mildly elevated in toxic multinodular goiter.[11][12]

Iodine-induced Hyperthyroidism

The body's natural mechanism to prevent excess thyroid hormone production is known as the Wolff-Chaikoff effect, which works by preventing the organification of thyroglobulin to T3 or T4. The Wolff-Chaikoff effect regulates thyroid hormone production when an excess amount of iodine is administered, which can be seen with iodine-containing medications (most commonly amiodarone), iodine-containing contrast administration, or even excess dietary intake, more prominently seen in areas of iodine deficiency. Occasionally, the thyroid may develop autonomous nodules, which are able to bypass the Wolff-Chaikoff effect and induce hyperthyroidism in the setting of iodine repletion. This effect, called the Jod-Basedow phenomenon, is more commonly seen in regions of iodine deficiency. I-123 scans demonstrate uniformly low radiotracer uptake, and the RAIU is decreased.[11]

Subacute Thyroiditis

Subacute thyroiditis, also known as giant cell thyroiditis or de Quervain thyroiditis, is classically characterized as thyrotoxicosis with neck pain and fever, which is often preceded by a viral upper respiratory infection. The post-infectious inflammatory response leads to giant cell invasion of the thyroid tissue, causing disruption and leakage of thyroid hormone. As the thyroid hormone is no longer concentrated in the thyroid tissue, the RAIU is diminished. Clinically, the patient will have a suppressed TSH.[12]

Silent Thyroiditis

Silent thyroiditis, an autoimmune disease, is characterized by lymphocytes infiltrating the thyroid gland, causing disruption of the thyroid gland and subsequent release of thyroid hormone. Thyroid peroxidase (TPO) is also classically elevated in silent thyroiditis. Unlike subacute thyroiditis, silent thyroiditis is painless. Silent thyroiditis can also be seen postpartum, where symptoms may be seen 2-6 months following delivery and are usually self-limiting, lasting 2-6 weeks. The elevated released thyroid hormone causes a low TSH. The thyroid gland demonstrates reduced RAIU, similar to subacute thyroiditis.[12][13][11]

Hashimoto Thyroiditis

Hashimoto thyroiditis is an autoimmune disease in which there is lymphocytic infiltration of the thyroid tissue with autoimmunity to thyroid antigens. These antibodies may include antithyroglobulin (seen in 55-90%) and antibodies to TPO (seen in 90-95%). Lymphocytic and plasma cell infiltration eventually lead to the destruction of the thyroid follicles followed by fibrosis. The fibrosis leads to enlargement of the thyroid gland. As the disease progresses, more thyroid tissue is replaced with fibrosis, leading to depressed thyroid hormone production and a hypothyroid state. Radiotracer uptake is dependent on the phase of disease imaged. During the early disease, there is an increased release of thyroid hormone due to the destruction of the thyroid follicles, and RAIU is increased. With the progression of the disease, the body eventually becomes hypothyroid with consistent scintigraphy findings of decreased RAIU and an elevated TSH. The decreased radiotracer uptake is nonuniform as areas of fibrosis do not uptake radiotracer.[13]

Thyrotoxicosis of Extrathyroidal Origin

There are multiple sources of extrathyroidal thyroid hormone, including exogenous thyroid hormone ingestion seen in factitious hyperthyroidism, thyroid hormone-producing metastatic thyroid cancer, and struma ovarii, a teratomatous ovarian mass that contains functional thyroid tissue. Another extrathyroidal cause of thyrotoxicosis includes TSH-induced thyrotoxicosis, which is caused by an autonomous TSH secreting pituitary adenoma, the only extrathyroidal cause associated with an elevated RAIU. Clinically, patients can have varying levels of thyrotoxicosis, depending on the level of excretion the exogenous source releases. Factitious hyperthyroidism can often be difficult to diagnose as the patients rarely disclose exogenous thyroid ingestion. Oftentimes the ingested thyroid hormone is T4, which may yield a higher than normal T4 to T3 ratio. Thyroid hormone production from metastatic thyroid malignancy is not very common as it requires a well-differentiated metastatic malignancy, which is usually less efficient at producing and excreting thyroid hormone. These metastases are usually seen in the setting of known thyroid cancer on I-131 imaging. Similar to metastasis, struma ovarii does not efficiently excrete thyroid hormone and rarely produces significant amounts of thyroid hormone. Struma ovarii is often found incidentally when pathology of an ovarian mass returns with thyroid tissue. RAIU of the overall thyroid gland in the neck is decreased, while the lesion may have elevated RAIU.[11]

Neonatal Hypothyroidism

If RAIU is reduced by at least 10% after administration of sodium perchlorate, an iodine organification defect is identified as the cause of neonatal hypothyroidism.[7]

Interfering Factors

Iodine intake should be limited prior to an I-123 RAIU or RAIU uptake and scan. If the patient is exposed to too much iodine prior to scanning, the thyroid gland uptakes less iodine, decreasing the sensitivity of the RAIU and scan. Potential sources of iodine include iodine contrast agents, iodine-containing medications, including amiodarone, and an iodine-rich diet, including kelp and seaweed.[2] Iodinated intravenous contrast should be avoided for 4-8 weeks prior to an I-123 uptake scan.[4][2] Interestingly, iodinated contrast material acts to reduce radiotracer uptake by reducing the number of NIS symporters independent of iodinated contrast’s free iodine.[4] Amiodarone should be avoided for 3-6 months prior to an I-123 RAIU or uptake and scan.[2] Additional medications to hold include anti-thyroid medications, including methimazole, carbimazole, propylthiouracil and thyroid hormone replacement, including levothyroxine (LT4) and liothyronine (LT3).

Complications

No serious complications are known for the I-123 exam, aside from the factors that may decrease the sensitivity of the I-123 uptake scan or the contraindications of exposing a pregnancy or newborn to radiation through the placenta or breastfeeding. Because iodide freely passes through the placenta and is concentrated and excreted by lactating breast, I-123 administration is relatively contraindicated in pregnant patients and nursing mothers. In order for the radiotracer to be administered and absorbed, the patient must be able to tolerate orally ingesting the I-123 capsule or liquid.

To avoid errors, routine nuclear medicine quality control of the uptake probe, including sensitivity and energy spectrum, constancy, background, peaking, energy resolution, efficiency, and minimum detectable activity, should be performed and documented. Other error sources include incorrect positioning of patient or phantom or patient background (which should be mid-thigh, not near urinary bladder), substernal thyroid gland, contamination of phantom, malabsorption of the dose, high background activity, recent iodinated contrast administration, and patient radioactivity from another radiopharmaceutical. Renal failure can elevate RAIU, while illness such as euthyroid sick syndrome can reduce RAIU.[2][5][6]

Patient Safety and Education

Patient Safety

I-123 is relatively safe as a gamma emitter except in pregnant patients and nursing mothers. The effective dose equivalent for a 3.7 MBq (100 µCi) I-123 RAIU is estimated at 0.74 mSv (74 mrem).[2][14][15] Dosing of I-123 in children should be adjusted for patient weight, as low as reasonably achievable while maintaining test accuracy.

Patient Education

I-123 is a radioisotope of iodine used for a thyroid uptake scan. By measuring the amount of radiotracer uptake, the RAIU study is able to identify the activity of the overall thyroid gland. In conjunction with clinical symptoms, blood work, and other imaging findings (such as ultrasound), and I-123 RAIU, or RAIU and thyroid scan, can create a better picture of the thyroid pathology and help provide a diagnosis.

Clinical Significance

RAIU with I-123 scintigraphy is a useful thyroid test, which provides overall functional information about the thyroid gland, including its activity. In conjunction with laboratory findings, such as the thyroid hormone levels and thyroid-stimulating hormone, and physical examination, and other imaging tests, I-123 RAIU can aid in diagnosing causes of thyrotoxicosis, help in the calculation of I-131 therapy doses, and detect an iodine organification defect in neonatal hypothyroidism.