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11 citation(s) found for "Ma, Xiaojuan".

Bone Shape Feature Differences in Single and Recurrent Patellar Dislocations via Statistical Shape Modeling
Yang, Mingrui , Elias, John J. , Li, Mei, Ma, Jin , Çolak, Ceylan , Winalski, Carl S. , Farrow, Lutul, Li, X, Li, Mei , Farrow, Lutul D. , Li, Xiaojuan

Journal of Orthopaedic Research | July 17, 2026 | Volume: 44 | Issue: 7 | Pages: No page available

10.1002/jor.70243 | PMID 42464872 Get It

ABSTRACT This study aims to develop MRI‐based 3D statistical shape models for patellar dislocation patients and investigate bone shape features that distinguish between single and recurrent dislocation populations, as well as control and patellar dislocation populations. MRIs from 16 single dislocation patients, 17 recurrent dislocation patients, and 20 control subjects were used to build statistical shape models for femur and patella bones. Bone shape features were extracted and tested for statistical significance ( p < 0.05) for distinguishing the single dislocation group from the recurrent dislocation groups, and the control group from the dislocation group. Statistically significant shape features distinguishing the three groups were identified for both bones. A shallower trochlear groove and smaller patellar ridge told the dislocation groups apart from the control group. A prolonged lateral condyle in femur and a laterally shifted ridge and hood shaped lateral facet in patella distinguished the recurrent dislocation group from the single dislocation group. The study's findings from 3D statistical shape modeling of the femur and patella reveal distinct anatomical differences across control, single dislocation, and recurrent patellar dislocation groups. This advanced understanding aids in identifying individuals at higher risk for initial or recurring patellar dislocations, enabling clinicians to tailor treatment and management strategies more effectively to prevent further dislocations and mitigate potential patellofemoral joint damage.
Leveraging the Capabilities of the FDA’s Sentinel System To Improve Kidney Care
Adimadhyam, Sruthi , Frazee, Erin N. , Cocoros, Noelle M. , Brown, Jeffrey S. , Maro, Judith C. , Corrigan‐Curay, Jacqueline , Martin, David , Nguyen, Michael , Platt, Richard , Li, Xiaojuan , Maro, Judith C , Li, Xiaojuan , Toh, Sengwee , Pan, Gerald J. Dal , Ball, Robert

Journal of the American Society of Nephrology | October 19, 2020 | Volume: 31 | Issue: 11 | Pages: 2506-2516

10.1681/asn.2020040526 | PMID 33077615 Get It

The Sentinel System is a national electronic postmarketing resource established by the US Food and Drug Administration to support assessment of the safety and effectiveness of marketed medical products. It has built a large, multi-institutional, distributed data network that contains comprehensive electronic health data, covering about 700 million person-years of longitudinal observation time nationwide. With its sophisticated infrastructure and a large selection of flexible analytic tools, the Sentinel System permits rapid and secure analyses, while preserving patient privacy and health-system autonomy. The Sentinel System also offers enhanced capabilities, including accessing full-text medical records, supporting randomized clinical trials embedded in healthcare delivery systems, and facilitating effective collection of patient-reported data using mobile devices, among many other research programs. The nephrology research community can use the infrastructure, tools, and data that this national resource offers for evidence generation. This review summarizes the Sentinel System and its ability to rapidly generate high-quality, real-world evidence; discusses the program’s experience in, and potential for, addressing gaps in kidney care; and outlines avenues for conducting research, leveraging this national resource in collaboration with Sentinel investigators.
Influence of Cardiovascular Risk Communication Tools and Presentation Formats on Patient Perceptions and Preferences
Wang, Tracy Y , Mi, Xiaojuan, Robinson, Jennifer G. , Roger, Véronique L. , Goldberg, Anne C. , Návar, Ann Marie , Virani, Salim S. , Wilson, Peter W.F. , Peterson, Eric D.

JAMA Cardiology | November 12, 2018 | Volume: 3 | Issue: 12 | Pages: 1192

10.1001/jamacardio.2018.3680 | PMID 30419113 Get It

Statin Use and Adverse Effects Among Adults >75 Years of Age: Insights From the Patient and Provider Assessment of Lipid Management (PALM) Registry
Wang, Tracy Y., Mi, Xiaojuan, Louie, Michael J. , Lee, L. Veronica, Goldberg, Anne C. , Roger, Véronique L. , Robinson, Jennifer G. , Nanna, Michael G. , Návar, Ann Marie , Virani, Salim S. , Peterson, Eric D.

Journal of the American Heart Association | May 8, 2018 | Volume: 7 | Issue: 10 | Pages: No page available

10.1161/jaha.118.008546 | PMID 29739801 Get It

Background Current statin use and symptoms among older adults in routine community practice have not been well characterized since the release of the 2013 American College of Cardiology/American Heart Association guideline. Methods and Results We compared statin use and dosing between adults >75 and ≤75 years old who were eligible for primary or secondary prevention statin use without considering guideline‐recommended age criteria. The patients were treated at 138 US practices in the Patient and Provider Assessment of Lipid Management (PALM) registry in 2015. Patient surveys also evaluated reported symptoms while taking statins. Multivariable logistic regression models examined the association between older age and statin use and dosing. Among 6717 people enrolled, 1704 (25%) were >75 years old. For primary prevention, use of any statin or high‐dose statin did not vary by age group: any statin, 62.6% in those >75 years old versus 63.1% in those ≤75 years old ( P =0.83); high‐dose statin, 10.2% versus 12.3% in the same groups ( P =0.14). For secondary prevention, older patients were slightly less likely to receive any statin (80.1% versus 84.2% [ P =0.003]; adjusted odds ratio, 0.81; 95% confidence interval, 0.66–1.01 [ P =0.06]), but were much less likely to receive a high‐intensity statin (23.5% versus 36.2% [ P <0.0001]; adjusted odds ratio, 0.54; 95% confidence interval, 0.45–0.65 [ P =0.0001]). Among current statin users, older patients were slightly less likely to report any symptoms (41.3% versus 46.6%; P =0.003) or myalgias (27.3% versus 33.3%; P <0.001). Conclusions Overall use of statins was similar for primary prevention in those aged >75 years versus younger patients, yet older patients were less likely to receive high‐intensity statins for secondary prevention. Statins appear to be similarly tolerated in older and younger adults.
Effects of Surgical Factors on Cartilage Can Be Detected Using Quantitative Magnetic Resonance Imaging After Anterior Cruciate Ligament Reconstruction
Amano, Keiko , Li, Alan , Pedoia, Valentina , Krych, Aaron J. , Li, Xiaojuan , Benjamin, C. , Goldring, Steven R., Hannafin, Jo A., Marx, Robert G. , Nawabi, Danyal H. , Shah, Parina, Warren, Russell F. , Amrami, Kimberly K. , Felmlee, Joel P. , Frick, Matthew A., Williams, Steven L. , Kretzchmar, Martin, Okazaki, Narihiro , Russell, Colin, Savic, Dragana , Schwaiger, Benedikt J. , Cheong, Maxwell, Hardin, John , Koff, Matthew F. , Link, Thomas M. , Potter, Hollis G. , Rodeo, Scott A. , Majumdar, Sharmila , Goldring, Mary B. , Otero, Miguel , Stuart, Michael James , Lansdown, Drew Anderson , Russell, Colin, Su, Favian , Wyatt, Cory R. , Krych, Aaron J

The American Journal of Sports Medicine | January 28, 2017 | Volume: 45 | Issue: 5 | Pages: 1075-1084

10.1177/0363546516677794 | PMID 28768432 Get It

Background: Quantitative magnetic resonance (qMR) can be used to measure macromolecules in tissues and is a potential method of observing early cartilage changes in the development of posttraumatic osteoarthritis. Hypothesis/Purpose: We hypothesized that specific patient and surgical factors affecting cartilage matrix composition after anterior cruciate ligament (ACL) reconstruction (ACLR) can be detected using T1ρ and T2 relaxation times. Our purpose was to demonstrate this ability in a multicenter feasibility study. Study Design: Case series; Level of evidence, 4. Methods: A total of 54 patients who underwent ACLR underwent bilateral MRI at baseline before surgery and 6 months postoperatively. Operative findings were recorded. T1ρ and T2 relaxation times were calculated for 6 cartilage regions: the medial femur, lateral femur, medial tibia, lateral tibia, patella, and trochlea. A paired t test compared relaxation times at baseline and 6 months, univariate regression identified regions that influenced patient-reported outcome measures, and analysis of covariance was used to determine the surgical factors that resulted in elevated relaxation times at 6 months. Results: The injured knee had significantly prolonged T1ρ and T2 relaxation times in the tibiofemoral compartment at baseline and 6 months but had shorter values in the patellofemoral compartment compared with the uninjured knee. Prolonged T1ρ and T2 times at 6 months were noted for both the injured and uninjured knees. At 6 months, prolongation of T1ρ and T2 times in the tibial region was associated with lower patient-reported outcome measures. ACLR performed within 30 days of injury had significantly shorter T1ρ times in the tibial regions, and lateral meniscal tears treated with repair had significantly shorter T1ρ times than those treated with excision. Conclusion: Prolonged relaxation times in multiple regions demonstrate how the injury affects the entire joint after an ACL tear. Changes observed in the uninjured knee may be caused by increased loading during rehabilitation, especially in the patellofemoral articular cartilage and distal femur. Relaxation times in the tibial regions may be predictive of patient symptoms at 6 months. These same regions are affected by surgical timing as early as 30 days after injury, but this may partially be reflective of the severity of the preoperative injury and the choice of treatment of meniscal tears.
Liposomal bortezomib is active against chronic myeloid leukemia by disrupting the Sp1-BCR/ABL axis
Pang, Jiuxia, Yan, Fei , Wu, Lai‐Chu , Al‐Kali, Aref , Litzow, Mark R. , Liu, Shujun , Yang, Xiaojuan, Yang, Xiaojuan, Shen, Na , Peng, Yong , Lee, Robert J.

Oncotarget | April 22, 2016 | Volume: 7 | Issue: 24 | Pages: 36382-36394

10.18632/oncotarget.8871 | PMID 27144331 Get It

Comparative Effectiveness of Cardiac Resynchronization Therapy With an Implantable Cardioverter-Defibrillator Versus Defibrillator Therapy Alone
Masoudi, Frederick A. , Mi, Xiaojuan, Curtis, Lesley H. , Curtis, Jeptha P. , Fonarow, Gregg C. , Hammill, Stephen C., Heidenreich, Paul A. , Piccini, Jonathan P. , Qualls, Laura G., Hernandez, Adrian F. , Peterson, Pamela N. , Al‐Khatib, Sana M. , Qualls, Laura G. , Hernandez, Adrian

Annals of Internal Medicine | May 5, 2014 | Volume: 160 | Issue: 9 | Pages: 603-611

10.7326/m13-1879 | PMID 24798523 Get It

The Oxysterol, 27-Hydroxycholesterol, Links Cholesterol Metabolism to Bone Homeostasis Through Its Actions on the Estrogen and Liver X Receptors
Nelson, Erik R. , DuSell, Carolyn D., Howe, Matthew K., Evans, Glenda L., Michalek, Ryan D., Umetani, Michihisa , Rathmell, Jeffrey C. , Khosla, Sundeep , Gesty‐Palmer, Diane, McDonnell, Donald P. , Wang, Xiaojuan , Khosla, Sundeep

Endocrinology | September 21, 2011 | Volume: 152 | Issue: 12 | Pages: 4691-4705

10.1210/en.2011-1298 | PMID 21933863 Get It

Osteoporosis and age-related bone loss are important public health concerns. Therefore, there is a high level of interest in the development of medical interventions and lifestyle changes that reduce the incidence of osteoporosis and age-related bone loss. Decreased bone mineral density is associated with high cholesterol, and patients on statins have increased bone mineral densities, strongly implicating cholesterol as a negative regulator of bone homeostasis. In this study, using both molecular and pharmacological approaches, we have been able to demonstrate that the primary cholesterol metabolite, 27-hydroxycholesterol, through its actions on both estrogen receptors and liver X receptors, decreases osteoblast differentiation and enhances osteoclastogenesis, resulting in increased bone resorbtion in mice. Induction of the short heterodimer partner protein by estrogens in osteoblasts can attenuate the liver X receptor-mediated actions of 27-hydroxycholesterol in bone. These data establish a mechanistic link between cholesterol and bone quality, highlight an unexpected target of estrogens in osteoblasts, and define a signaling axis, the therapeutic exploitation of which is likely to yield novel antiosteoporotic drugs.
HOXB13 May Predict Response to Neoadjuvant Letrozole in Patients with Estrogen Receptor-Positive Breast Cancer.
Ma, Xiaojuan , Bandaru, Ravi , Letzkus, Martin, Philips, Prejesh, Barrett, J. Carl , Erlander, Mark G. , Sgroi, Dennis C. , Gardner, Humphrey, Baselga, José , Goetz, Matthew P.

Cancer Research | December 30, 2010 | Volume: 69 | Issue: 24_Supplement | Pages: 2120-2120

10.1158/0008-5472.sabcs-09-2120 Get It

Abstract Background. Third generation aromatase inhibitors (AIs) have been shown to be superior to tamoxifen in multiple randomized clinical trials and become the new standard of treatment for postmenopausal women with early or advanced endocrine-sensitive breast cancer. It is thus important to identify biomarkers predicting resistance to AIs so that alternative therapeutic options can be employed. A two gene expression index, HOXB13:IL17BR, and HOXB13 in particular, has been shown to be a negative predictor of clinical benefit from tamoxifen. It is unclear whether HOXB13:IL17BR or HOXB13 is also predictive of AI therapy.Methods. We performed a retrospective analysis of a phase II randomized neoadjuvant study of everolimus+letrozole vs. placebo+letrozole in patients with estrogen receptor-positive breast cancer. Total RNA was extracted from frozen tissue biopsies taken either prior to treatment or after 15 days of treatment. HOXB13:IL13BR and a molecular grade index (MGI) were measured in 107 pre-treatment samples and 111 samples after 15 days of treatment. Antiproliferative response as defined by a ln[Ki767] &lt;1 at day 15 in the samples analyzed was correlated with these gene expression indices.Results. In the placebo+letrozole treatment arm, the antiproliferative response rate was 30% (14/47). Using a pre-specified cutpoint of 0.06, the response rate was 40% for low HOXB13:IL17BR patients, compared to 12% for high HOXB13:IL17BR patients (p=0.05). In the everolimus+letrozole arm, the antiproliferative response rate in the samples analyzed was 55% (33/60), and the response rates for low and high HOXB13:Il17BR patients were 70% and 37% (p=0.02), respectively. When examined separately, high HOXB13 expression was significantly associated with nonresponse to therapy (everolimus+letrozole arm, p=0.02; placebo+letrozle arm, p=0.03), but IL17BR was not (everolimus+letrozole arm, p=0.6; placebo+letrozle arm, p=0.88). As expected, we observed a significant correlation between MGI and Ki67 staining (Spearman r=0.67, p&lt;0.0001).Conclusions. High HOXB13:IL17BR index and high HOXB13 expression may identify a possible subset of patients with estrogen receptor-positive tumor that could be less responsive to aromatase inhibitors such as letrozole. Furthermore, use of MGI may enable rapid assessment of antiproliferative response by fine needle aspiration. Citation Information: Cancer Res 2009;69(24 Suppl):Abstract nr 2120.