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Tytuł pozycji:

Inflammation and breast density among female Chinese immigrants: exploring variations across neighborhoods.

Tytuł:
Inflammation and breast density among female Chinese immigrants: exploring variations across neighborhoods.
Autorzy:
Fang CY; Cancer Prevention and Control Program, Fox Chase Cancer Center, 333 Cottman Ave., Philadelphia, PA, 19111, USA. .
Egleston BL; Biostatistics and Bioinformatics Facility, Fox Chase Cancer Center, 333 Cottman Ave., Philadelphia, PA, 19111, USA.
Byrne C; Department of Preventive Medicine & Biostatistics, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, MD, 20814, USA.
Bohr GS; Social Sciences Department, California Polytechnic State University, 1 Grand Avenue, San Luis Obispo, CA, 93407-0329, USA.
Pathak HB; Department of Pathology & Laboratory Medicine, University of Kansas Medical Center, Kansas City, KS, 66160, USA.
Godwin AK; Department of Pathology & Laboratory Medicine, University of Kansas Medical Center, Kansas City, KS, 66160, USA.; University of Kansas Cancer Center, 3901 Rainbow Boulevard, Kansas City, KS, 66160, USA.
Siu PT; Chinatown Medical Services, Greater Philadelphia Health Action, Inc., 930 Washington Avenue, Philadelphia, PA, 19147, USA.
Tseng M; Department of Kinesiology and Public Health, California Polytechnic State University, 1 Grand Avenue, San Luis Obispo, CA, 93407, USA.
Źródło:
Cancer causes & control : CCC [Cancer Causes Control] 2019 Oct; Vol. 30 (10), pp. 1113-1126. Date of Electronic Publication: 2019 Aug 07.
Typ publikacji:
Journal Article
Język:
English
Imprint Name(s):
Publication: Dordrecht : Kluwer Academic Publishers
Original Publication: Oxford, UK : Rapid Communications of Oxford Ltd., 1990-
MeSH Terms:
Asian People*
Breast Density*
Emigrants and Immigrants*
Residence Characteristics*
Inflammation/*blood
Adult ; Breast/diagnostic imaging ; C-Reactive Protein/analysis ; Female ; Humans ; Middle Aged ; Receptors, Tumor Necrosis Factor, Type II/blood
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Grant Information:
R01 CA106606 United States CA NCI NIH HHS; R01CA106606 United States CA NCI NIH HHS; R01MD012621 United States MD NIMHD NIH HHS; P30 CA006927 United States CA NCI NIH HHS; R01 MD012621 United States MD NIMHD NIH HHS; P20 GM130423 United States GM NIGMS NIH HHS
Contributed Indexing:
Keywords: Acculturation; Asian; Breast density; Immigrant; Inflammation; Neighborhood
Substance Nomenclature:
0 (Receptors, Tumor Necrosis Factor, Type II)
9007-41-4 (C-Reactive Protein)
Entry Date(s):
Date Created: 20190809 Date Completed: 20191111 Latest Revision: 20230825
Update Code:
20240104
PubMed Central ID:
PMC6745706
DOI:
10.1007/s10552-019-01206-x
PMID:
31392546
Czasopismo naukowe
Purpose: We examined associations of inflammation with breast density, a marker of breast cancer risk, among female Chinese immigrants and explored whether associations varied by neighborhood environment.
Methods: Assessments of serum C-reactive protein (CRP), soluble tumor necrosis factor receptor 2 (sTNFR2), and breast density were performed among 401 Chinese immigrants across the Philadelphia region. Participant addresses were geocoded, with the majority residing in areas representing traditional urban enclaves (i.e., Chinatown and South Philadelphia) or an emerging enclave with a smaller, but rapidly growing Chinese immigrant population (i.e., the Near Northeast). The remainder was classified as residing in non-enclaves.
Results: In multivariable adjusted regression models, CRP was inversely associated with dense breast area (p = 0.01). Levels of sTNFR2 were also inversely associated with dense breast area, but these associations varied by neighborhood (interaction p = 0.01); specifically, inverse associations were observed among women residing in the emerging enclave (p = 0.03), but not other neighborhoods.
Conclusions: Among Chinese immigrant women, aggregate analyses that do not take neighborhood context into consideration can mask potential variations in association of inflammatory markers with breast density. Future studies should consider how neighborhood contextual factors may contribute to differential risk pathways.

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