02516nas a2200325 4500008004100000022001400041245014100055210006900196260001300265300000900278490000600287520149900293653001801792653003101810653002401841653002201865653002801887653002301915100001901938700002301957700002101980700002002001700002002021700002402041700002202065700002002087700002402107700002302131856003602154 2023 eng d a2398-923800aCirculating differentiated and senescent lymphocyte subsets and incident diabetes risk in older adults: The Cardiovascular Health Study.0 aCirculating differentiated and senescent lymphocyte subsets and c2023 Jan ae3840 v63 a
INTRODUCTION: Cellular senescence is a feature of aging implicated in the pathophysiology of diabetes mellitus (DM). Whether senescent lymphocytes are associated with the future occurrence of DM is uncertain.
METHODS: We used cryopreserved peripheral blood mononuclear cells collected from 1860 Cardiovascular Health Study participants (average age 80.2 years) and flow cytometry immunophenotyping to evaluate the longitudinal relationships of naive (CD45RA ), memory (CD45RO ), senescent (CD28 ), and T effector memory RA (TEMRA) (CD28 CD57 CD45RA ) CD4 and CD8 T cells, and memory B cells (CD19 CD27 ), with the risk of incident DM. In exploratory analyses we evaluated the relationships of 13 additional innate lymphocyte and CD4 and CD8 subsets with incident DM risk.
RESULTS: Over a median follow-up time of 8.9 years, 155 cases of incident DM occurred. In Cox models adjusted for demographic variables (age, sex, race, study site and flow cytometry analytical batch) or diabetes risk factors (demographic variables plus education, body mass index, smoking status, alcohol use, systolic blood pressure, hypertension medication use and physical activity), no significant associations were observed for any CD4 , CD8 or CD19 cell phenotypes with incident DM.
CONCLUSIONS: These results suggest the frequencies of naive, memory and senescent T cells and memory B cells are not strongly associated with incident DM risk in older adults.
10aCD28 Antigens10aCD8-Positive T-Lymphocytes10aCellular Senescence10aDiabetes Mellitus10aLeukocytes, Mononuclear10aLymphocyte Subsets1 aOlson, Nels, C1 aDoyle, Margaret, F1 aBůzková, Petra1 aHuber, Sally, A1 ade Boer, Ian, H1 aSitlani, Colleen, M1 aTracy, Russell, P1 aPsaty, Bruce, M1 aMukamal, Kenneth, J1 aDelaney, Joseph, A uhttps://chs-nhlbi.org/node/9240