With emerge of NCDs, maintenance of health conditions may require continuous drug(s) administration or causing another disease in order to treat the original disease (
3). Physicians named this form of care “cure of the disease”, despite the fact that the status of the human body has not returned completely to like it was before the illness. On the other hand, such patients may be asymptomatic and feel well, but their body composition as well as cellular and humoral factors differ from unaffected individual. In addition, an unhealthy condition will return upon the discontinuation of any therapeutic approach, which the physician has prescribed. Nowadays, this concept of cure is employed for all relapse-free conditions, although the disease may relapse and may cause morbidity or mortality in the future (
4). To distinguish these concepts, we may use “restitutio ad integrum” as a cure and controlled status.
Regarding thyroid diseases, most conditions are managed as “controlled; and only in few diseases, the status of thyroid returns to the complete cured condition.
Table 1 shows a classification of cure into complete and controlled cure; In fact, a complete cure is defined as return to complete health. While, controlled cure is defined as a condition that the patient becomes asymptomatic and complications of the original disease are controlled; However, the health status of the patient is different from what it was before. Interestingly, hypothyroidism management rarely results in a complete cure. To better words, there are transient hypothyroidisms such as the recovery phase of subacute thyroiditis in which thyroid structure and function return to a healthy condition. The same may happen in < 50% of women who experience postpartum thyroiditis, in which after 12 months, serum level of TSH returns to the normal range without levothyroxine treatment (
5). In this line, patients with primary hypothyroidism and secondary form, which induced by ablative doses of radioiodine as well as total thyroidectomy, require lifelong levothyroxine medication for maintaining euthyroidism and therefore, are classified as under controlled hypothyroidisms (
6).
In patients with nodular goiter, benign or malignant, who are euthyroid or toxic multinodular goiter, only those who undergo lobectomy or radioiodine therapy and have no need to take levothyroxine would be categorized in complete cure group. All other patients with nodular goiter who are treated with levothyroxine following total thyroidectomy or radioiodine are categorized into the control treatment modality.
Graves’ hyperthyroidism is a rather common disease with a prevalence of 1% - 1.5% (
7). The majority of patients have a prolonged course of treatment with relapsing and remitting episodes over the years (
8). The strategy for Graves’ hyperthyroidism treatment is not straightforward and requires complex decision making. None of the three forms of current therapeutic approaches, i.e., radioiodine (RAI), surgery or anti-thyroid drugs (ATD), have been able to re-establish continuous normal thyroid function in all patients (
9). According to the guidelines, the aim of thyroidectomy should be induction of permanent hypothyroidism (
6,
9). This is due to the subtotal thyroidectomy which may be accompanied by 29% persistent or recurrent hyperthyroidism and 50% hypothyroidism; in this respect, only 19% of patients may remain euthyroid after 6 years of follow-up (
10). To note, the recurrence rate after sub-ablative doses of RAI is 61% - 69% (
11). In addition, one year following ablative RAI treatment, 77%, 17%, and 6% of patients were hypo-, hyper-and euthyroid, respectively; which 14% of patients might require the second RAI therapy. In this case, the rate of hypo-, hyper and euthyroidism were 86, 3.2 and 3.3%, respectively with 6.4% death after 80 months follow-up (
12). Notably, both total thyroidectomy and ablative RAI therapy cause permanent hypothyroidism in the majority of patients as well as causing another disorder and requiring lifelong levothyroxine treatment for maintaining euthyroidism. Therefore, both methods fulfill criteria of controlled management. Levothyroxine replacement may cause disruption in psychological condition, lower resting energy expenditure, lower T3:T4 ratio, higher body mass index (BMI) and increased levels of serum cholesterol and LDL compared with normal controls (
13-
17). Some of these findings have also been reported in RAI treated Graves’ patients on levothyroxine as compared to euthyroid Graves’ patients (
18). The main drawback of ATD therapy has been the high rate of hyperthyroidism relapse, mostly up to 4 years after drug withdrawal (
19). The rate of recurrence has been also reported between 20% - 70% with an average of about 50% after conventional 1 - 2 years of ATD treatment (
6). Recently, it has also been reported that long-term ATD treatment induces higher remission rates than conventional therapy (< 2 years) (
20,
21), and two meta-analyses have shown efficacy (
22) and safety (
23) of continuous long-term treatment with ATD. In addition, a randomized trial in 302 patients with Graves’ hyperthyroidism has demonstrated a relapse rate of 16% in those treated with methimazole (MMI) for 60 - 120 months, as compared to 51% of patients who received conventional MMI therapy four years after discontinuation of medication (
24).
Table 2 shows the remission possibility of Graves’ hyperthyroidism after a course of long-term ATD treatment. Between 12 - 22 years after treatment, only 27% of those treated with ATD for 2 years or less, remain euthyroid. 62% have recurrence, 80% have subclinical hypothyroidism, and 3% overt hypothyroidism (
25). Moreover, long-term treatment with MMI for 5 - 10 years (on average, 8 years) results in only 16% recurrence 4 years after discontinuation of MMI (
24). There are no data regarding the longer follow up rate of recurrence of overt hyperthyroidism, the rates of subclinical hyperthyroidism, and overt hyperthyroidism in patients who treated with long-term MMI. Given that the statistics results regarding in long-follow up of those patients who were in remission after the conventional therapy (
25), if the same rate of 40% reduction in euthyroidism occurs in long-term MMI treated patients, by fulfilling the criteria for complete cure, approximately 50% of them remain euthyroid 22 years after onset of treatment.