2 Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, México City. Department of Ophthalmology.
Aim: To evaluate the effect of bromocriptine (BRC) or pentoxifylline (PTX) added to methimazole (MTZ) in proptosis, clinical activity, and quality of life in individuals with mild GO. Methods: Randomized, open, clinical trial. Forty-five patients with mild GO with an onset of less than one year were randomly assigned to MTZ, MTZ+BRC, or MTZ+PTX treatment during one year. Proptosis was measured with exophthalmometry, clinical activity was evaluated using the Clinical Activity Score (CAS), and the Graves’ Orbitopathy Quality Of Life (GO-QOL) questionnaire was also applied. Results: Thirty-five patients were analyzed, 13 assigned to MTZ, 9 to MTZ+BRC, and 13 to MTZ+PTX. After one year, a decrease in proptosis was documented in the MTZ+BRC group. Proptosis on right eye (OD) decreased from 20 [18-21] to 18 [16-18] mm (p= 0.006), and on left eye (OS) from 20 [19-20] to 18 [16-18] (p= 0.006). MTZ+PTX treatment also decreased proptosis. In OD from 19 [17.5-19] to 16.5 mm [16-19] (p= 0.120) and in OS from 19 [17.5-19] to 17 [16-20] (p= 0.025). No change was observed on the MTZ group. The CAS and GO-QOL scores significantly improved in all groups. Conclusions: BRC or PTX treatments added to MTZ improved proptosis in individuals with recent onset, mild GO. CAS and quality of life similarly improved in all groups.
Clinical Trial Registration Number: NCT01893450
Keywords: Hyperthyroidism; Graves’ ophthalmopathy; exophthalmos; bromocriptine; pentoxifylline
At present, available treatments are insufficient [4] and are focused on identifying patients with sight-threatening GO whom require aggressive intervention with glucocorticoids, orbital decompression, and/or radiotherapy. Patients with moderate to severe GO defined with lid retraction >2 mm, moderate or severe soft tissue involvement, exophthalmos >3 mm above normal, inconstant or constant diplopia, also qualify for immunosuppressive therapy [3].
For mild cases, management is restricted to hyperthyroidism correction and topical treatments [3]. However, patients with mild GO have a reduced quality of life [5] and 13.5% progress to moderate or severe manifestations without treatment [6]. Some studies evaluating agents for mild GO have shown promising results. Long-acting release octreotide showed a significant reduction in proptosis compared to placebo [7]. Colchicine demonstrated an amelioration of the clinical activity score (CAS) and improvement in the signal intensity ratio of the recti muscle in magnetic resonance imaging [8]. Allopurinol plus nicotinamide was associated with a decrease in soft tissue inflammation [9]. Diclofenac showed a significant reduction in the muscle restriction score and CAS [10]. A multicenter, randomized clinical trial showed utility of selenium improving quality of life, eye involvement, and reducing GO progression [11]. A small study using pentoxifylline (PTX) improved GO severity compared to placebo [12]. Lastly, case reports and small case series have shown improvement in GO activity with bromocriptine (BRC) [13-15]. The postulated mechanisms explaining the favorable effect of BRC are the inhibition of immune cells and dropping of TSH secretion [13].
Besides the well-known roles of prolactin (PRL) in reproduction and lactation, it also functions as a cytokine implicated in the immune response [16]. Lymphocytes and other immune cells express both PRL and the PRL receptor. PRL functions as a local regulator of the lymphocyte proliferation [17, 18], increases cytokine production [19] including interferon gamma [20, 21], among other immunological effects. Modulation of PRL may have an effect in the onset and progression of autoimmune diseases [22].
The primary aim of this study is to evaluate the effect of BRC and PTX added to methimazole (MTZ) on the proptosis and CAS in patients with mild GO, and secondarily to assess their effect on quality of life.
Patients attended for a monthly evaluation for the first four months, and thereafter every two months until the study ended. Each subject completed 10 visits over one year. A Hertel exophtalmometer was used to evaluate exophthalmos. Proptosis, in millimeters, was recorded in right eye (OD) and left eye (OS). The CAS was calculated as the sum of the following items: spontaneous retrobulbar pain, pain on attempted eye movements (upward, side-to-side, and downward gazes), conjunctival redness, redness of the eyelids, chemosis, swelling of the caruncle, and swelling of the eyelid [23]. Evaluations were performed by three trained and standardized Endocrinologists that were blinded for the assigned treatment. Concordance between Endocrinologists in proptosis measurements compared to an expert Ophthalmologist were satisfactory (kappa= 0.94, p< 0.001).
We evaluated the quality of life at baseline and at the end of the study with the Graves’ Orbitopathy Quality Of Life (GOQOL) questionnaire [24]. The questionnaire was not available in Spanish; therefore it was translated to Spanish and then translated back to English by a native English speaker to assure accuracy. The Spanish version is now available on the European Group of Graves’ Orbitopathy (EUGOGO) webpage: http://www. eugogo.eu/_downloads/clincial_evaluation/GO_QOL_ES.pdf. The questionnaire evaluates visual functioning and appearance. A score of 1, 2, or 3 is assigned to each question indicating the limitation as severe, mild, or absent, respectively. The scores are added to obtain a raw score and the final score is calculated as follows: (raw score – 8) /16 * 100. The final score ranges from a minimum of 0 (full limitation) to 100 (no limitation). An increase in the score indicates improvement and a decrease indicates worsening.
Blood samples were obtained to assess thyroid function. Side effects of medications were recorded at follow-up visits. Adherence to treatment was evaluated by pill count. The primary outcomes were the change in proptosis and in the CAS.
The study was approved by the Comité de Ética en Investigación del Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán (#1950). Written informed consent was obtained from all participants before enrollment.
Variables distribution was evaluated using the Shapiro- Wilk test. Variables are reported using mean ± SD or median [interquartile range], as appropriate. We evaluated differences in the basal characteristics between groups using one way ANOVA or Kruskal-Wallis test. To evaluate the change in proptosis we used the Wilcoxon signed-rank test. The change in proptosis, CAS, and GO-QOL scores between the three groups was assessed with the Kruskal-Wallis test. Individual comparisons between BRC + MTZ or PTX + MTZ vs MTZ were tested using Mann-Whitney U test. Adverse events reported in all visits between groups were compared using Chi-square or Fisher exact test as appropriate. A p value of less than 0.05 was considered to indicate statistical significance. Statistical analyses were performed with the SPSS version 21. Patients were included in final statistical analysis if they completed evaluations for at least 6 months. The results of the last evaluation were carried forward as the last visit.
Variable |
MTZ (n= 13) |
MTZ + BRC (n= 9) |
MTZ + PTX (n= 13) |
Age – years |
34.4 ± 11.2 |
37.4 ± 13.5 |
32.8 ± 8.7 |
Female - number (%) |
12 (92.3) |
7 (78.8) |
11 (84.6) |
Body mass index – kg/m2b |
22.6 [20.5-26.4] |
22.6 [20.4-25.2] |
23.2 [21.3-26.0] |
Heart rate – beats per minute |
95 [91-100] |
93 [80-101] |
92 [80-99] |
Proptosis OD – mm |
19 [18-20] |
20 [18-21] |
19 [17.5-19] |
Proptosis OS – mm |
18 [16-19] |
20 [19-20] |
19 [17.5-19] |
Diplopia– number (%) c |
|||
Absent |
8 (61.5) |
6 (66.7) |
5 (38.5) |
Intermittent |
5 (38.5) |
1 (11.1) |
6 (46.2) |
Inconstant |
0 |
2 (22.2) |
2 (15.3) |
Clinical activity score OD d |
3 [3-4] |
4 [3-4] |
4 [3-4] |
Clinical activity score OS |
3 [3-4] |
4 [3-4] |
4 [3-4] |
T3 Uptake - % f |
46 [43-51] |
47 [41-50] |
0.45 [0.41-0.48] |
Total T3 – nmol/l f |
5.63 [3.78-8.48] |
4.1 [3.14-5.74] |
4.36 [3.47-5.28] |
Total T4 – nmol/l f |
240 [185.9-283.5] |
254 [191.8-297.9] |
241.7 [164.7-280.6] |
TSH - µU/ml f |
0.017 ± 0.009 |
0.018 ± 0.008 |
0.024 ± 0.017 |
b Calculated as the weight in kilograms divided by the square of the height in meters
c Evaluated according to the subjective diplopia score as follows intermittent, i.e. diplopia in primary position of gaze, when tired or when first awakening; inconstant, i.e.diplopia at extremes of gaze; constant, i.e. continuous diplopia in primary or reading position. None individual had constant diplopia
d The clinical activity score (CAS) is the sum of all items present: spontaneous retro bulbar pain, pain on attempted up or down gaze, redness of the eyelids, redness of the conjunctiva, swelling of the eyelids, inflammation of the caruncle and/or plica, conjunctival edema. A CAS ≥3/7 indicates active GO
e Reference values for T3 uptake, total T3, total T4, and TSH are 32-48.4%, 1.34-2.73 nmol/l, 78.3-157.4 nmol/l, and 0.34-5.6 μU/ml, respectively p values obtained using One-way ANOVA, Kruskal-Wallis or Chi Square test, as appropriate
Variable |
Participants (n= 35) |
Not included in final analysis (n= 10) |
p |
Age – years |
34.6 ± 10.8 |
32.1 ± 9.2 |
0.516 |
Female - number (%) |
30 (85.7) |
9 (90) |
0.598 |
Body mass index – kg/m2‡ |
22.6 [21.0-25.7] |
23.6 [19.8-27.8] |
0.799 |
Systolic blood pressure – mmHg |
120 [110-130] |
115 [110-120] |
0.657 |
Diastolic blood pressure – mmHg |
70 [60-80] |
70 [70-80] |
0.799 |
Heart rate – beats per minute |
92 [81-100] |
93.5 [80-110] |
0.989 |
Proptosis OD – mm |
19 [17.7-20] |
19 [18.5-20.2] |
0.819 |
Proptosis OS – mm |
19 [17.5-20] |
19.5 [17-21] |
0.677 |
Diplopia OD – number (%) § |
0.735 |
||
Absent |
21 (60) |
7 (70) |
|
Intermittent |
10 (28.6) |
3 (30) |
|
Inconstant |
4 (11.2) |
2 (22.2) |
|
Diplopia– number (%) c |
0.766 |
||
Absent |
19 (54.3) |
7 (70) |
|
Intermittent |
12 (34.3) |
2 (20) |
|
Inconstant |
3 (8.6) |
1 (10) |
|
Clinical activity score OD d |
4 [3-4] |
3.5 [2.5-4] |
0.381 |
Clinical activity score OS |
3 [3-4] |
4 [3-4] |
0.819 |
T3 Uptake - % f |
46 [42-50] |
48 [45-51] |
0.302 |
Total T3 – nmol/l f |
4.61 [3.59-5.93] |
4.41 [3.59-8.41] |
0.842 |
Total T4 – nmol/l f |
241 [189.9-282.2] |
230 [191.6-294.9] |
0.866 |
TSH - µU/ml f |
0.020 ± 0.013 |
0.017 ± 0.010 |
0.616 |
c Calculated as the weight in kilograms divided by the square of the height in meters
d Evaluated according to the subjective diplopia score as follows intermittent, i.e. diplopia in primary position of gaze, when tired or when first awakening; inconstant, i.e. diplopia at extremes of gaze; constant, i.e. continuous diplopia in primary or reading position. None individual had constant diplopia
e The clinical activity score (CAS) is the sum of all items present: spontaneous retrobulbar pain, pain on attempted up or down gaze, redness of the eyelids, redness of the conjunctiva, swelling of the eyelids, inflammation of the caruncle and/or plica, conjunctival edema. A CAS ≥3/7 indicates active GO
f Reference values for T3 uptake, total T3, total T4, and TSH are 32-48.4%, 1.34-2.73 nmol/l, 78.3-157.4 nmol/l, and 0.34-5.6 μU/ ml, respectively
The change in proptosis, calculated as the baseline proptosis – final proptosis, was compared between groups. As shown in Table 2, proptosis decreased significantly in both eyes with BRC. The change in proptosis with PTX was significant only in OS.
Proptosis change (mm) |
MTZ (n=13) |
MTZ + BRC (n=9) |
MTZ + PTX (n=13) |
p† |
|
MTZ vs. BRC |
MTZ vs. PTX |
||||
OD |
0 [0 - 2] |
2 [2 - 2] |
1 [0 - 3] |
0.014 |
0.343 |
OS |
0 [-1 - 1] |
2 [2 - 2] |
1 [1 - 2] |
<0.001 |
0.015 |
† P values obtained from individual comparisons between BRC and PTX with MTZ treatments using Mann-Whitney U test
The pathophysiology of proptosis involves an increase in glycosaminoglycan production, adipose tissue hypertrophy, and edema of orbital tissues [26]. The fibroblasts are key cells involved in the development of GO [27], they can differentiate into mature adipocytes [28] with an increased expression of the thyroid stimulating hormone receptor [29]. Other fibroblasts are responsive to cytokines such as the transforming growth factor beta (TGF-β) and can differentiate into myofibroblasts, participating in processes such as inflammation, repair, and fibrosis [30,
MTZ(n= 13) |
MTZ + BRC (n= 9) |
MTZ + PXF (n= 13) |
P b |
||
Baseline CAS ODc |
3 [3-4] |
4 [3-4] |
4 [3-4] |
0.393 |
0.65 |
6-month CAS OD |
2 [1-2] |
1 [0-2] |
0 [0-1] |
0.262 |
0.034 |
Final CAS OD |
1[0-2] |
0 [0-1] |
0 [0-1] |
0.556 |
0.418 |
Baseline CAS OI |
3 [3-4] |
4 [3-4] |
4 [3-4] |
0.292 |
0.336 |
6-month CAS OI |
1 [1-2] |
1 [0-2] |
1 [0-2] |
0.965 |
0.287 |
Final CAS OI |
1 [0-2] |
0 [0-1] |
1 [0-1] |
0.357 |
0.614 |
Baseline visual functioning scored |
75 [43.7-96.9] |
56.2 [50.0-75.0] |
73.2 [43.7-78.6] |
0.651 |
0.497 |
Final visual functioning score |
96.9 [87.5-100] |
100 [83.3-100] |
100 [93.7-100] |
0.862 |
0.832 |
Baseline appearance score |
71.9 [43.7-84.4] |
75.0 [68.7-93.7] |
75.0 [56.2-87.5] |
0.382 |
0.314 |
Final appearance score |
93.7 [81.2-96.9] |
100 [93.7-100] |
96.9 [93.7-100] |
0.148 |
0.228 |
b p values obtained from individual comparisons between BRC or PTX with MTZ treatments using Mann-Whitney U test.
c The clinical activity score (CAS) is the sum of all items present: spontaneous retro bulbar pain, pain on attempted up or down gaze, redness of the eyelids, redness of the conjunctiva, swelling of the eyelids, inflammation of the caruncle and/or plica, conjunctival edema. A CAS ≥3/7 indicates active GO.
d The final score ranges from a minimum of 0 (full limitation) to 100 (no limitation). An increase in the score indicates improvement and a decrease indicates worsening.
Event |
MTZ (n= 13) |
MTZ + BRC (n= 9) |
MTZ + PTX (n= 13) |
P b |
Orthostatic hypotension |
0 |
3 (2) |
4 (3) |
0.12 |
Epistaxis |
5 (2) |
2 (2) |
7 (2) |
0.497 |
Skin reaction |
3 (2) |
4 (3) |
4 (4) |
0.67 |
Nausea and/or vomit |
9 (5) |
8 (5) |
13 (6) |
0.67 |
Diarrhea |
5 (4) |
2 (1) |
13 (6) |
0.026 |
Edema |
7 (4) |
2 (1) |
10 (6) |
0.212 |
Bronchospasm |
0 |
2 (1) |
1 |
0.211 |
Pharyngitis |
1 |
1 |
2 (2) |
0.843 |
Fever |
1 |
1 |
1 |
0.955 |
Anorexia |
1 |
2 (1) |
1 |
0.535 |
Pruritus |
2 (2) |
1 |
3 (2) |
0.783 |
Abdominal pain |
12 (5) |
10 (4) |
12 (4) |
0.874 |
Arthralgia |
1 |
1 |
0 |
0.523 |
Mild neutropenia |
1 |
0 |
0 |
0.428 |
Somnolence |
13 (5) |
14 (7) |
16 (7) |
0.467 |
Headache |
9 (4) |
11 (6) |
12 (6) |
0.407 |
b p values obtained from comparisons between the total events reported in all visits in each of the three treatment groups using Chi-square or Fisher exact test as appropriate
BRC is a dopamine 2 receptor agonist. It has direct effects on immune cells that seem to be independent of PRL levels [34]. However, there is evidence of an association between PRL levels and autoimmune disease. Reduction of PRL causes a decline of interferon gamma and IL-2 secretion by Th1 lymphocytes [20]. A possible mechanism explaining the improvement in GO is its anti-proliferative effect on T lymphocytes by blocking IL-2 production [13, 35]. Furthermore, BRC suppresses human B lymphocyte function along with immunoglobulin production [35]. Finally, an additional effect of dopaminergic agonists is inhibition of the vascular endothelial growth factor (VEGF) [36], which can be an additional mechanism involved in clinical improvement in proptosis in patients with mild GO of recent onset. Some reports have found increased serum levels of VEGF in individuals with GO in comparison with controls [32].
The particular effect of PTX in GO is the inhibition of tumor necrosis factor alpha synthesis [37]. Also, using fibroblast cell cultures and animal models, an anti-fibrotic effect has been reported [38]. These two mechanisms may contribute to the favorable effect in GO.
It is well known that MTZ improves the CAS [3]. Since the three groups in our study received MTZ, it is not unexpected the lack of statistical significance between CAS score between the three groups
Our results are consistent with previous case reports and small case series describing a possible beneficial effect of BRC in individuals with GO [13, 15].
It is important to emphasize that we treated patients with less than one year of GO onset. This fact decreases the possibility of development of fibrosis that could limit the improvement in proptosis.
This study has limitations that should be mentioned. First, we include a small number of patients. However, participants were carefully selected and followed, and sufficient statistical power was achieved to detect significant results with clinical relevance. Nevertheless, it can be also possible that lack of study power was the reason to find a non-significant effect of PTX treatment on proptosis on the OD. The results of this study cannot be generalized to patients with moderate or severe GO in whom other interventions are required. Finally, although we postulate potential mechanisms for the observed improvement in the proptosis, the confirmation of these mechanisms will be the subject of future studies.
Disclosure statement: The authors declare that no financial or other conflicts of interest exist in relation to the content of the article.
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