G. Neumann
Brigham and Women's Hospital
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Featured researches published by G. Neumann.
Arthritis Care and Research | 2010
Jeffrey Duryea; G. Neumann; Jingbo Niu; Saara Totterman; J. Tamez; Christine Dabrowski; Marie-Pierre Hellio Le Graverand; Monica Luchi; Chan Beals; David J. Hunter
Magnetic resonance imaging (MRI) and radiography are established imaging modalities for the assessment of knee osteoarthritis (OA). The objective of our study was to compare the responsiveness of radiographic joint space width (JSW) with MRI‐derived measures of cartilage morphometry for OA progression in participants from the Osteoarthritis Initiative (OAI).
Osteoarthritis and Cartilage | 2009
G. Neumann; David J. Hunter; Michael C. Nevitt; Lori B. Chibnik; K. Kwoh; Hepei Chen; T. B. Harris; Suzanne Satterfield; Jeffrey Duryea
OBJECTIVE To establish the performance of location specific computer measures of radiographic joint space width (JSW) compared to measurements of minimum joint space width (mJSW) for the assessment of medial compartment knee osteoarthritis (OA). The study also investigated the most disease-responsive location for measuring medial compartment JSW. METHODS Serial bilateral Posterior Anterior (PA) conventional radiographs acquired with a fixed flexion protocol were obtained 36 months apart in 118 persons with knee OA participating in the Health, Aging and Body Composition (Health ABC) Study. Measurements of medial compartment mJSW and JSW at seven fixed locations were facilitated by the use of semi-automated software that delineated the femoral and tibial margins of the joint. A human reader operated custom software to verify and correct the software-drawn margins where necessary. Paired images were displayed with the reader blinded to the chronological order. The amount of joint space narrowing was measured and the standardized response mean (SRM) was used as a metric to quantify performance. RESULTS For all subjects, the mJSW SRM value was 0.42 while, for the most responsive location specific measure of JSW, it was SRM=0.46. For subjects with a Kellgren-Lawrence (KL) score less than or equal to 1, mJSW (SRM=0.40) was more responsive than the new measures (Maximum SRM=0.30). For KL=2or3, SRM=0.49 for mJSW, and SRM=0.74 for the most responsive location specific measure of JSW. Improved responsiveness was observed in the more central portion of the joint on the more diseased knees. CONCLUSIONS Location specific computer measures of JSW are feasible and potentially provide a superior method to assess radiographic OA for more diseased subjects. This new measure has the potential to improve the power of clinical studies that use a fixed flexion protocol.
Arthritis Care and Research | 2011
G. Neumann; Paola dePablo; Axel Finckh; Lori B. Chibnik; Fred Wolfe; Jeffrey Duryea
Computer‐based methods to measure radiographic joint space width (JSW) have the potential to improve the longitudinal assessment of rheumatoid arthritis (RA). The purpose of this report was to measure the long‐term patient repositioning reproducibility of software‐measured radiographic JSW.
BMC Musculoskeletal Disorders | 2009
Dennis S. Meredith; Elena Losina; G. Neumann; Hiroshi Yoshioka; Philipp Lang; Jeffrey N. Katz
BackgroundIn this cross-sectional study, we conducted a comprehensive assessment of all articular elements that could be measured using knee MRI. We assessed the association of pathological change in multiple articular structures involved in the pathoanatomy of osteoarthritis.MethodsKnee MRI scans from patients over 45 years old were assessed using a semi-quantitative knee MRI assessment form. The form included six distinct elements: cartilage, bone marrow lesions, osteophytes, subchondral sclerosis, joint effusion and synovitis. Each type of pathology was graded using an ordinal scale with a value of zero indicating no pathology and higher values indicating increasingly severe levels of pathology. The principal dependent variable for comparison was the mean cartilage disease score (CDS), which captured the aggregate extent of involvement of articular cartilage. The distribution of CDS was compared to the individual and cumulative distributions of each articular element using the Chi-squared test. The correlations between pathological change in the various articular structures were assessed in a Spearman correlation table.ResultsData from 140 patients were available for review. The cohort had a median age of 61 years (range 45-89) and was 61% female. The cohort included a wide spectrum of OA severity. Our analysis showed a statistically significant trend towards pathological change involving more articular elements as CDS worsened (p-value for trend < 0.0001). Comparison of CDS to change in the severity of pathology of individual articular elements showed statistically significant trends towards more severe pathology as CDS worsened for osteophytes (p-value for trend < 0.0001), bone marrow lesions (p = 0.0003), and subchondral sclerosis (p = 0.009), but not joint effusion or synovitis. There was a moderate correlation between cartilage damage, osteophytes and BMLs as well as a moderate correlation between joint effusion and synovitis. However, cartilage damage and osteophytes were only weakly associated with synovitis or joint effusion.ConclusionOur results support an inter-relationship of multiple articular elements in the pathoanatomy of knee OA. Prospective studies of OA pathogenesis in humans are needed to correlate these findings to clinically relevant outcomes such as pain and function.
Osteoarthritis and Cartilage | 2006
M. H. Brem; P. M. Schlechtweg; G. Neumann; Rebecca D. Jackson; Joseph S. Yu; Charles B. Eaton; Hiroshi Yoshioka; Philipp Lang; J. Duryea
M.H. Brem1, P.M. Schlechtweg2, G. Neumann2, R. Jackson3, J. Yu3, C. Eaton4, H. Yoshioka2, P. Lang2, J. Duryea2 1Friedrich Alexander University Erlangen-Nuremberg, Dept. of Surgery/Orthopedic Surgery, Erlangen, Germany, 2Brigham and Womens’ Hospital, Dept. of Radiology, Boston, MA, Boston, MA, 3The Ohio State University, Dept. Endocrinology, Diabetes and Metabolism and Radiology, Columbus, OH, 4Memorial Hospital of Rhode Island, Center for Primary Care and Prevention and Brown Medical School, Providence, RI
Medical Imaging 2004: Physics of Medical Imaging | 2004
Jeffrey Duryea; G. Neumann; Hiroshi Yoshioka; James T. Dobbins
PURPOSE: Rheumatoid arthritis (RA) of the hand is a significant healthcare problem. Techniques to accurately quantity the structural changes from RA are crucial for the development and prescription of therapies. Analysis of radiographic joint space width (JSW) is widely used and has demonstrated promise. However, radiography presents a 2D view of the joint. In this study we performed tomosynthesis reconstructions of proximal interphalangeal (PIP), and metacarpophalangeal (MCP) joints to measure the 3D joint structure. METHODS: We performed a reader study using simulated radiographs of 12 MCP and 12 PIP joints from skeletal specimens imaged with micro-CT. The tomosynthesis technique provided images of reconstructed planes with 0.75 mm spacing, which were presented to 2 readers with a computer tool. The readers were instructed to delineate the joint surfaces on tomosynthetic slices where they could visualize the margins. We performed a quantitative analysis of 5 slices surrounding the central portion of each joint. Reader-determined JSW was compared to a gold standard. As a figure of merit we calculated the average root-mean square deviation (RMSD). RESULTS: RMSD was 0.22 mm for both joints. For the individual joints, RMSD was 0.18 mm (MCP), and 0.26 mm (PIP). The reduced performance for the smaller PIP joints suggests that a slice spacing less than 0.75 mm may be more appropriate. CONCLUSIONS: We have demonstrated the capability of limited 3D rendering of joint surfaces using digital tomosynthesis. This technique promises to provide an improved method to visualize the structural changes of RA.
Osteoarthritis and Cartilage | 2007
G. Neumann; A.D. Mendicuti; K.H. Zou; T. Minas; Jonathan S. Coblyn; Carl S. Winalski; Philipp Lang
American Journal of Roentgenology | 2003
Kathryn J. Stevens; Caroline Tao; Shi-Uk Lee; Natalie Salem; Jan E. Vandevenne; Calise Cheng; G. Neumann; Alexandre Valentin-Opran; Philipp Lang
Osteoarthritis and Cartilage | 2007
Jeffrey Duryea; G. Neumann; M. H. Brem; W. Koh; F. Noorbakhsh; Rebecca D. Jackson; Joseph S. Yu; Charles B. Eaton; Philipp Lang
Arthritis & Rheumatism | 2006
Axel Finckh; Paola de Pablo; Jeffrey N. Katz; G. Neumann; Ying Lu; Frederick Wolfe; Jeffrey Duryea