Effect of the TNF-α inhibitor adalimumab in patients with recalcitrant sarcoidosis: a prospective observational study using FDG-PET

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Effect of the TNF-α inhibitor adalimumab in patients with recalcitrant sarcoidosis: a prospective observational study using FDG-PET. / Milman, Nils; Graudal, Niels; Loft, Annika; Mortensen, Jann; Larsen, Janni; Baslund, Bo.

I: Clinical Respiratory Journal, Bind 6, Nr. 4, 2012, s. 238-247.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Milman, N, Graudal, N, Loft, A, Mortensen, J, Larsen, J & Baslund, B 2012, 'Effect of the TNF-α inhibitor adalimumab in patients with recalcitrant sarcoidosis: a prospective observational study using FDG-PET', Clinical Respiratory Journal, bind 6, nr. 4, s. 238-247. https://doi.org/10.1111/j.1752-699X.2011.00276.x

APA

Milman, N., Graudal, N., Loft, A., Mortensen, J., Larsen, J., & Baslund, B. (2012). Effect of the TNF-α inhibitor adalimumab in patients with recalcitrant sarcoidosis: a prospective observational study using FDG-PET. Clinical Respiratory Journal, 6(4), 238-247. https://doi.org/10.1111/j.1752-699X.2011.00276.x

Vancouver

Milman N, Graudal N, Loft A, Mortensen J, Larsen J, Baslund B. Effect of the TNF-α inhibitor adalimumab in patients with recalcitrant sarcoidosis: a prospective observational study using FDG-PET. Clinical Respiratory Journal. 2012;6(4):238-247. https://doi.org/10.1111/j.1752-699X.2011.00276.x

Author

Milman, Nils ; Graudal, Niels ; Loft, Annika ; Mortensen, Jann ; Larsen, Janni ; Baslund, Bo. / Effect of the TNF-α inhibitor adalimumab in patients with recalcitrant sarcoidosis: a prospective observational study using FDG-PET. I: Clinical Respiratory Journal. 2012 ; Bind 6, Nr. 4. s. 238-247.

Bibtex

@article{63164d6221c143ec984421b45b9489a7,
title = "Effect of the TNF-α inhibitor adalimumab in patients with recalcitrant sarcoidosis: a prospective observational study using FDG-PET",
abstract = "Background: Tumour necrosis factor-alpha (TNF-a) plays a crucial role in sarcoidosis. In severe disease, treatment with TNF-a inhibitors may be effective. Objectives: Changes in sarcoid disease activity were assessed by fluorine-18-fluorodeoxyglucose positron emission tomography (FDG-PET) in patients with recalcitrant sarcoidosis treated with adalimumab. Methods: Prospective 24-week observational study. Patients continued medication with steroids and antimetabolites and received adalimumab 40 mg subcutaneously every other week. Ten patients with biopsy-proven sarcoidosis (two men) were included with a median age of 47 years (range 35-73). An FDG-PET showing uptake indicating sarcoid activity was required at inclusion and repeated at the end of the study. FDG-PET uptake was assessed by calculated standardised uptake value (SUV). Blood samples and lung function tests were performed regularly. Quality of life was assessed by the short-form health survey (SF-36) questionnaire. Results: Following treatment with adalimumab, FDG-PET uptake decreased in nine patients (P = 0.011) and increased in one patient. Maximum SUV fell from median 14.1 to 7.0 (P ",
author = "Nils Milman and Niels Graudal and Annika Loft and Jann Mortensen and Janni Larsen and Bo Baslund",
note = "{\textcopyright} 2011 Blackwell Publishing Ltd.",
year = "2012",
doi = "10.1111/j.1752-699X.2011.00276.x",
language = "English",
volume = "6",
pages = "238--247",
journal = "Clinical Respiratory Journal",
issn = "1752-6981",
publisher = "Wiley-Blackwell",
number = "4",

}

RIS

TY - JOUR

T1 - Effect of the TNF-α inhibitor adalimumab in patients with recalcitrant sarcoidosis: a prospective observational study using FDG-PET

AU - Milman, Nils

AU - Graudal, Niels

AU - Loft, Annika

AU - Mortensen, Jann

AU - Larsen, Janni

AU - Baslund, Bo

N1 - © 2011 Blackwell Publishing Ltd.

PY - 2012

Y1 - 2012

N2 - Background: Tumour necrosis factor-alpha (TNF-a) plays a crucial role in sarcoidosis. In severe disease, treatment with TNF-a inhibitors may be effective. Objectives: Changes in sarcoid disease activity were assessed by fluorine-18-fluorodeoxyglucose positron emission tomography (FDG-PET) in patients with recalcitrant sarcoidosis treated with adalimumab. Methods: Prospective 24-week observational study. Patients continued medication with steroids and antimetabolites and received adalimumab 40 mg subcutaneously every other week. Ten patients with biopsy-proven sarcoidosis (two men) were included with a median age of 47 years (range 35-73). An FDG-PET showing uptake indicating sarcoid activity was required at inclusion and repeated at the end of the study. FDG-PET uptake was assessed by calculated standardised uptake value (SUV). Blood samples and lung function tests were performed regularly. Quality of life was assessed by the short-form health survey (SF-36) questionnaire. Results: Following treatment with adalimumab, FDG-PET uptake decreased in nine patients (P = 0.011) and increased in one patient. Maximum SUV fell from median 14.1 to 7.0 (P

AB - Background: Tumour necrosis factor-alpha (TNF-a) plays a crucial role in sarcoidosis. In severe disease, treatment with TNF-a inhibitors may be effective. Objectives: Changes in sarcoid disease activity were assessed by fluorine-18-fluorodeoxyglucose positron emission tomography (FDG-PET) in patients with recalcitrant sarcoidosis treated with adalimumab. Methods: Prospective 24-week observational study. Patients continued medication with steroids and antimetabolites and received adalimumab 40 mg subcutaneously every other week. Ten patients with biopsy-proven sarcoidosis (two men) were included with a median age of 47 years (range 35-73). An FDG-PET showing uptake indicating sarcoid activity was required at inclusion and repeated at the end of the study. FDG-PET uptake was assessed by calculated standardised uptake value (SUV). Blood samples and lung function tests were performed regularly. Quality of life was assessed by the short-form health survey (SF-36) questionnaire. Results: Following treatment with adalimumab, FDG-PET uptake decreased in nine patients (P = 0.011) and increased in one patient. Maximum SUV fell from median 14.1 to 7.0 (P

U2 - 10.1111/j.1752-699X.2011.00276.x

DO - 10.1111/j.1752-699X.2011.00276.x

M3 - Journal article

VL - 6

SP - 238

EP - 247

JO - Clinical Respiratory Journal

JF - Clinical Respiratory Journal

SN - 1752-6981

IS - 4

ER -

ID: 40141620