Browsing by Author "Bartalena, L. (7102317749)"
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Publication Antithyroid drugs in Graves’ hyperthyroidism: differences between “block and replace” and “titration” regimes in frequency of euthyroidism and Graves’ orbitopathy during treatment(2021) ;Žarković, M. (7003498546) ;Wiersinga, W. (7101819215) ;Perros, P. (7006707944) ;Bartalena, L. (7102317749) ;Donati, S. (55236626100) ;Okosieme, O. (6506743718) ;Morris, D. (16203319800) ;Fichter, N. (6603189201) ;Lareida, J. (57199562074) ;Daumerie, C. (7003840029) ;Burlacu, M.-C. (23018289900) ;Kahaly, G.J. (7005506174) ;Pitz, S. (7003508414) ;Beleslin, B. (6701355427) ;Ćirić, J. (6601995819) ;Ayvaz, G. (6602696412) ;Konuk, O. (56180435400) ;Törüner, F.B. (6602398288) ;Salvi, M. (7006487887) ;Covelli, D. (26024659100) ;Curro, N. (23979561200) ;Hegedüs, L. (7102638527)Brix, T. (15070407400)Purpose: Whereas antithyroid drugs (ATD) are the preferred treatment modality for Graves’ hyperthyroidism (GH), there is still controversy about the optimal regimen for delivering ATD. To evaluate whether ‘Block and Replace’ (B + R) and ‘Titration’ (T) regimes are equivalent in terms of frequency of euthyroidism and Graves’ Orbitopathy (GO) during ATD therapy. Methods: A prospective multicentre observational cohort study of 344 patients with GH but no GO at baseline. Patients were treated with ATD for 18 months according to B + R or T regimen in line with their institution’s policy. Results: Baseline characteristics were similar in both groups. In the treatment period between 6 and 18 months thyrotropin (TSH) slightly increased in both groups, but TSH was on average 0.59 mU/L (95% CI 0.27–0.85) lower in the B + R group at all time points (p = 0.026). Serum free thyroxine (FT4) remained stable during the same interval, with a tendency to higher values in the B + R group. The point-prevalence of euthyroidism (TSH and FT4 within their reference ranges) increased with longer duration of ATD in both groups; it was always higher in the T group than in the B + R group: 48 and 24%, respectively, at 6 months, 81 and 58% at 12 months, and 87 and 63% at 18 months (p < 0.002). There were no significant differences between the B + R and T regimens with respect to the fall in thyrotropin binding inhibiting immunoglobulins (TBII) or thyroid peroxidase antibodies (TPO-Ab). GO developed in 15.9% of all patients: 9.1 and 17.8% in B + R group and T group, respectively, (p = 0.096). GO was mild in 13% and moderate-to-severe in 2%. Conclusion: The prevalence of biochemical euthyroidism during treatment with antithyroid drugs is higher during T compared to B + R regimen. De novo development of GO did not differ significantly between the two regimens, although it tended to be higher in the T group. Whether one regimen is clinically more advantageous than the other remains unclear. © 2020, Italian Society of Endocrinology (SIE). - Some of the metrics are blocked by yourconsent settings
Publication Antithyroid drugs in Graves’ hyperthyroidism: differences between “block and replace” and “titration” regimes in frequency of euthyroidism and Graves’ orbitopathy during treatment(2021) ;Žarković, M. (7003498546) ;Wiersinga, W. (7101819215) ;Perros, P. (7006707944) ;Bartalena, L. (7102317749) ;Donati, S. (55236626100) ;Okosieme, O. (6506743718) ;Morris, D. (16203319800) ;Fichter, N. (6603189201) ;Lareida, J. (57199562074) ;Daumerie, C. (7003840029) ;Burlacu, M.-C. (23018289900) ;Kahaly, G.J. (7005506174) ;Pitz, S. (7003508414) ;Beleslin, B. (6701355427) ;Ćirić, J. (6601995819) ;Ayvaz, G. (6602696412) ;Konuk, O. (56180435400) ;Törüner, F.B. (6602398288) ;Salvi, M. (7006487887) ;Covelli, D. (26024659100) ;Curro, N. (23979561200) ;Hegedüs, L. (7102638527)Brix, T. (15070407400)Purpose: Whereas antithyroid drugs (ATD) are the preferred treatment modality for Graves’ hyperthyroidism (GH), there is still controversy about the optimal regimen for delivering ATD. To evaluate whether ‘Block and Replace’ (B + R) and ‘Titration’ (T) regimes are equivalent in terms of frequency of euthyroidism and Graves’ Orbitopathy (GO) during ATD therapy. Methods: A prospective multicentre observational cohort study of 344 patients with GH but no GO at baseline. Patients were treated with ATD for 18 months according to B + R or T regimen in line with their institution’s policy. Results: Baseline characteristics were similar in both groups. In the treatment period between 6 and 18 months thyrotropin (TSH) slightly increased in both groups, but TSH was on average 0.59 mU/L (95% CI 0.27–0.85) lower in the B + R group at all time points (p = 0.026). Serum free thyroxine (FT4) remained stable during the same interval, with a tendency to higher values in the B + R group. The point-prevalence of euthyroidism (TSH and FT4 within their reference ranges) increased with longer duration of ATD in both groups; it was always higher in the T group than in the B + R group: 48 and 24%, respectively, at 6 months, 81 and 58% at 12 months, and 87 and 63% at 18 months (p < 0.002). There were no significant differences between the B + R and T regimens with respect to the fall in thyrotropin binding inhibiting immunoglobulins (TBII) or thyroid peroxidase antibodies (TPO-Ab). GO developed in 15.9% of all patients: 9.1 and 17.8% in B + R group and T group, respectively, (p = 0.096). GO was mild in 13% and moderate-to-severe in 2%. Conclusion: The prevalence of biochemical euthyroidism during treatment with antithyroid drugs is higher during T compared to B + R regimen. De novo development of GO did not differ significantly between the two regimens, although it tended to be higher in the T group. Whether one regimen is clinically more advantageous than the other remains unclear. © 2020, Italian Society of Endocrinology (SIE). - Some of the metrics are blocked by yourconsent settings
Publication Asymmetry indicates more severe and active disease in Graves’ orbitopathy: results from a prospective cross-sectional multicentre study(2020) ;Perros, P. (7006707944) ;Žarković, M.P. (7003498546) ;Panagiotou, G.C. (55362746900) ;Azzolini, C. (36127411000) ;Ayvaz, G. (6602696412) ;Baldeschi, L. (6602585043) ;Bartalena, L. (7102317749) ;Boschi, A.M. (7006668224) ;Nardi, M. (55550143000) ;Brix, T.H. (15070407400) ;Covelli, D. (26024659100) ;Daumerie, C. (7003840029) ;Eckstein, A.K. (7003932063) ;Fichter, N. (6603189201) ;Ćirić, S. (57079927600) ;Hegedüs, L. (7102638527) ;Kahaly, G.J. (7005506174) ;Konuk, O. (56180435400) ;Lareida, J.J. (57199562074) ;Okosieme, O.E. (6506743718) ;Leo, M. (18037556900) ;Mathiopoulou, L. (15519735200) ;Clarke, L. (56313122000) ;Menconi, F. (6603101916) ;Morris, D.S. (16203319800) ;Orgiazzi, J. (7006062635) ;Pitz, S. (7003508414) ;Salvi, M. (7006487887) ;Muller, I. (23052085100) ;Knežević, M. (36192212000) ;Wiersinga, W.M. (7101819215) ;Currò, N. (23979561200) ;Dayan, C.M. (55161416500) ;Marcocci, C. (7006557829) ;Marinò, M. (7201365908) ;Möller, L. (6602822748) ;Pearce, S.H. (7102959910) ;Törüner, F. (6602398288)Bernard, M. (7202666194)Purpose: Patients with Graves’ orbitopathy can present with asymmetric disease. The aim of this study was to identify clinical characteristics that distinguish asymmetric from unilateral and symmetric Graves’ orbitopathy. Methods: This was a multi-centre study of new referrals to 13 European Group on Graves’ Orbitopathy (EUGOGO) tertiary centres. New patients presenting over a 4 month period with a diagnosis of Graves’ orbitopathy were included. Patient demographics were collected and a clinical examination was performed based on a previously published protocol. Patients were categorized as having asymmetric, symmetric, and unilateral Graves’ orbitopathy. The distribution of clinical characteristics among the three groups was documented. Results: The asymmetric group (n = 83), was older than the symmetric (n = 157) group [mean age 50.9 years (SD 13.9) vs 45.8 (SD 13.5), p = 0.019], had a lower female to male ratio than the symmetric and unilateral (n = 29) groups (1.6 vs 5.0 vs 8.7, p < 0.001), had more active disease than the symmetric and unilateral groups [mean linical Activity Score 3.0 (SD 1.6) vs 1.7 (SD 1.7), p < 0.001 vs 1.3 (SD 1.4), p < 0.001] and significantly more severe disease than the symmetric and unilateral groups, as measured by the Total Eye Score [mean 8.8 (SD 6.6) vs 5.3 (SD 4.4), p < 0.001, vs 2.7 (SD 2.1), p < 0.001]. Conclusion: Older age, lower female to male ratio, more severe, and more active disease cluster around asymmetric Graves’ orbitopathy. Asymmetry appears to be a marker of more severe and more active disease than other presentations. This simple clinical parameter present at first presentation to tertiary centres may be valuable to clinicians who manage such patients. © 2020, The Author(s). - Some of the metrics are blocked by yourconsent settings
Publication Asymmetry indicates more severe and active disease in Graves’ orbitopathy: results from a prospective cross-sectional multicentre study(2020) ;Perros, P. (7006707944) ;Žarković, M.P. (7003498546) ;Panagiotou, G.C. (55362746900) ;Azzolini, C. (36127411000) ;Ayvaz, G. (6602696412) ;Baldeschi, L. (6602585043) ;Bartalena, L. (7102317749) ;Boschi, A.M. (7006668224) ;Nardi, M. (55550143000) ;Brix, T.H. (15070407400) ;Covelli, D. (26024659100) ;Daumerie, C. (7003840029) ;Eckstein, A.K. (7003932063) ;Fichter, N. (6603189201) ;Ćirić, S. (57079927600) ;Hegedüs, L. (7102638527) ;Kahaly, G.J. (7005506174) ;Konuk, O. (56180435400) ;Lareida, J.J. (57199562074) ;Okosieme, O.E. (6506743718) ;Leo, M. (18037556900) ;Mathiopoulou, L. (15519735200) ;Clarke, L. (56313122000) ;Menconi, F. (6603101916) ;Morris, D.S. (16203319800) ;Orgiazzi, J. (7006062635) ;Pitz, S. (7003508414) ;Salvi, M. (7006487887) ;Muller, I. (23052085100) ;Knežević, M. (36192212000) ;Wiersinga, W.M. (7101819215) ;Currò, N. (23979561200) ;Dayan, C.M. (55161416500) ;Marcocci, C. (7006557829) ;Marinò, M. (7201365908) ;Möller, L. (6602822748) ;Pearce, S.H. (7102959910) ;Törüner, F. (6602398288)Bernard, M. (7202666194)Purpose: Patients with Graves’ orbitopathy can present with asymmetric disease. The aim of this study was to identify clinical characteristics that distinguish asymmetric from unilateral and symmetric Graves’ orbitopathy. Methods: This was a multi-centre study of new referrals to 13 European Group on Graves’ Orbitopathy (EUGOGO) tertiary centres. New patients presenting over a 4 month period with a diagnosis of Graves’ orbitopathy were included. Patient demographics were collected and a clinical examination was performed based on a previously published protocol. Patients were categorized as having asymmetric, symmetric, and unilateral Graves’ orbitopathy. The distribution of clinical characteristics among the three groups was documented. Results: The asymmetric group (n = 83), was older than the symmetric (n = 157) group [mean age 50.9 years (SD 13.9) vs 45.8 (SD 13.5), p = 0.019], had a lower female to male ratio than the symmetric and unilateral (n = 29) groups (1.6 vs 5.0 vs 8.7, p < 0.001), had more active disease than the symmetric and unilateral groups [mean linical Activity Score 3.0 (SD 1.6) vs 1.7 (SD 1.7), p < 0.001 vs 1.3 (SD 1.4), p < 0.001] and significantly more severe disease than the symmetric and unilateral groups, as measured by the Total Eye Score [mean 8.8 (SD 6.6) vs 5.3 (SD 4.4), p < 0.001, vs 2.7 (SD 2.1), p < 0.001]. Conclusion: Older age, lower female to male ratio, more severe, and more active disease cluster around asymmetric Graves’ orbitopathy. Asymmetry appears to be a marker of more severe and more active disease than other presentations. This simple clinical parameter present at first presentation to tertiary centres may be valuable to clinicians who manage such patients. © 2020, The Author(s). - Some of the metrics are blocked by yourconsent settings
Publication Graves’ orbitopathy as a rare disease in Europe: a European Group on Graves’ Orbitopathy (EUGOGO) position statement(2017) ;Perros, P. (7006707944) ;Hegedüs, L. (7102638527) ;Bartalena, L. (7102317749) ;Marcocci, C. (7006557829) ;Kahaly, G.J. (7005506174) ;Baldeschi, L. (6602585043) ;Salvi, M. (7006487887) ;Lazarus, J.H. (7103203566) ;Eckstein, A. (7003932063) ;Pitz, S. (7003508414) ;Boboridis, K. (55872796000) ;Anagnostis, P. (23974640600) ;Ayvaz, G. (6602696412) ;Boschi, A. (7006668224) ;Brix, T.H. (15070407400) ;Currò, N. (23979561200) ;Konuk, O. (56180435400) ;Marinò, M. (7201365908) ;Mitchell, A.L. (55584797277) ;Stankovic, B. (16205536900) ;Törüner, F.B. (6602398288) ;Von Arx, G. (6602439374) ;Zarković, M. (7003498546)Wiersinga, W.M. (7101819215)Background: Graves’ orbitopathy (GO) is an autoimmune condition, which is associated with poor clinical outcomes including impaired quality of life and socio-economic status. Current evidence suggests that the incidence of GO in Europe may be declining, however data on the prevalence of this disease are sparse. Several clinical variants of GO exist, including euthyroid GO, recently listed as a rare disease in Europe (ORPHA466682). The objective was to estimate the prevalence of GO and its clinical variants in Europe, based on available literature, and to consider whether they may potentially qualify as rare. Recent published data on the incidence of GO and Graves’ hyperthyroidism in Europe were used to estimate the prevalence of GO. The position statement was developed by a series of reviews of drafts and electronic discussions by members of the European Group on Graves’ Orbitopathy. The prevalence of GO in Europe is about 10/10,000 persons. The prevalence of other clinical variants is also low: hypothyroid GO 0.02-1.10/10,000; GO associated with dermopathy 0.15/10,000; GO associated with acropachy 0.03/10,000; asymmetrical GO 1.00-5.00/10,000; unilateral GO 0.50-1.50/10,000. Conclusion: GO has a prevalence that is clearly above the threshold for rarity in Europe. However, each of its clinical variants have a low prevalence and could potentially qualify for being considered as a rare condition, providing that future research establishes that they have a distinct pathophysiology. EUGOGO considers this area of academic activity a priority. © 2017 The Author(s).