2.2. Adipose tissue and skin sampling and plasma collection

LH LaTonya J. Hickson
LP Larissa G.P. Langhi Prata
SB Shane A. Bobart
TE Tamara K. Evans
NG Nino Giorgadze
SH Shahrukh K. Hashmi
SH Sandra M. Herrmann
MJ Michael D. Jensen
QJ Qingyi Jia
KJ Kyra L. Jordan
TK Todd A. Kellogg
SK Sundeep Khosla
DK Daniel M. Koerber
AL Anthony B. Lagnado
DL Donna K. Lawson
NL Nathan K. LeBrasseur
LL Lilach O. Lerman
KM Kathleen M. McDonald
TM Travis J. McKenzie
JP João F. Passos
RP Robert J. Pignolo
TP Tamar Pirtskhalava
IS Ishran M. Saadiq
KS Kalli K. Schaefer
ST Stephen C. Textor
SV Stella G. Victorelli
TV Tammie L. Volkman
AX Ailing Xue
MW Mark A. Wentworth
EG Erin O. Wissler Gerdes
YZ Yi Zhu
TT Tamara Tchkonia
JK James L. Kirkland
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To avoid sun-exposed areas of skin and to simultaneously obtain abdominal subcutaneous adipose tissue superficial to Scarpa's fascia, elliptical incisional biopsies of adipose tissue and attached skin were acquired from at a point to the right or left of, and 2–5 cm inferior to the navel. Abdominal subcutaneous adipose tissue (0·5–2 g) and attached skin were collected under sterile conditions through a 3–5 cm incision on Study Days 0 and 14. The site for the post-treatment biopsy was contralateral to that for the pre-treatment biopsy, with both the pre- and post-treatment biopsies being from the same dermatome. Skin attached to the adipose tissue biopsy was cut from the underlying adipose tissue. Also on Study Days 0 and 14, blood was collected. Blood samples were stored at −80 °C for subsequent analyses.

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