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1 monization, and not investigating factors at midlife.
2 high fat intake during both adolescence and midlife.
3 cognitive sequelae of these risk factors in midlife.
4 , the elderly report less pain than those in midlife.
5 father, and a sibling from childhood through midlife.
6 gain are associated with adult body size in midlife.
7 ly childhood growth with BMI in daughters at midlife.
8 associated with better cognitive function in midlife.
9 socioeconomic mobility between childhood and midlife.
10 al territory, and with increasing age during midlife.
11 edict more pronounced depressive symptoms in midlife.
12 ed ELS in relation to depressive symptoms in midlife.
13 with other physical health problems in early midlife.
14 nd measured coronary artery calcium (CAC) in midlife.
15 es (ACEs) are associated with elevated AL in midlife.
16 0.16-0.64) compared with men with low CRF in midlife.
17 fitness had higher cognitive test scores at midlife.
18 ve effect of cardiorespiratory fitness as of midlife.
19 nd striatal neurons, as well as morbidity in midlife.
20 sk of hyperproliferative disease (cancer) by midlife.
21 le to costly health and social problems into midlife.
22 evaluate men with above-median PSA levels in midlife.
23 o middle adulthood and cognitive function at midlife.
24 with worse gait and cognitive performance in midlife.
25 it scores and cardiovascular disease risk at midlife.
26 ines, was associated with worse cognition in midlife.
27 with intellectual decline from childhood to midlife.
28 midlife with gait and cognitive function in midlife.
29 ith worse indices of LV systolic function in midlife.
30 ith gait, but not with cognitive function in midlife.
31 uggested lower structural brain integrity in midlife.
32 hort study followed 516 young adults through midlife.
33 g adulthood may affect cognitive function in midlife.
34 several cases are still detectable well into midlife.
35 signs of cognitive decline from childhood to midlife.
36 ek to measure dementia-prevention efforts in midlife.
38 portance of monitoring women's health during midlife, a critical window for implementing early interv
41 later life with cardiorespiratory fitness in midlife after adjustment for cardiovascular risk factors
42 r mixed-effects models, elevated CHD risk in midlife (age 55 years) was associated with lower levels
45 urity and increases in deaths of despair and midlife all-cause mortality in US counties during 2000-2
47 ets and definitions of pain, we show today's midlife Americans have had more pain throughout adulthoo
48 mine whether better cognitive functioning at midlife among more physically fit individuals reflects n
49 cells with a rapid decline in population at midlife and a concomitant increase in peripheral blood b
50 k of developing type 2 diabetes (T2D) during midlife and an elevated risk of developing hypertension
51 oid-beta1-42 levels were already frequent in midlife and APOE genotype strongly affects the levels of
52 40% of variance in the same measure in late midlife and approximately 10% of variance in each of sev
55 n ICAD prevalence and the risk factors (both midlife and concurrent) associated with its development
56 mal / preclinical phase of LOAD for women in midlife and highlight therapeutic windows of opportunity
57 relation between habitual dietary intake at midlife and incident PAD over approximately 20 y of foll
58 ate or ideal level of behavioral CVH in both midlife and late life (versus poor level in both midlife
59 with intermediate global CVH metrics in both midlife and late life and 0.14 (0.02, 0.76; p = 0.024) f
60 ns of cardiovascular health (CVH) metrics in midlife and late life in relation to risk of dementia.
61 ife and late life (versus poor level in both midlife and late life) was significantly associated with
62 Compared with those who were normotensive in midlife and late life, only participants with midlife hy
63 ompared with poor global CVH metrics in both midlife and late life, the fully adjusted HR of dementia
66 95% CI, 1.69-2.32 per 100 person-years); for midlife and late-life hypertension (n = 1030), 2.83 (95%
68 ion and late-life hypotension, compared with midlife and late-life normal BP, were associated with in
69 between duration of elevated CHD risk during midlife and levels (but not trajectories) of later-life
70 post-intervention surveys for this sample of midlife and older adults new to smartphone technology.
72 , postmenopausal estrogen deprivation during midlife and older age has a detrimental impact on metabo
74 ress, diabetes, head trauma, hypertension in midlife and orthostatic hypotension) and 9 with Level B
75 tigated whether duration of diabetes in late midlife and poor glycaemic control were associated with
77 s Risk in Communities (ARIC) participants in midlife and to explore associations between midlife vasc
78 life and fish-oil consumption in early life, midlife, and late life with osteoporotic fracture risk.
79 ly recorded ELS, but not stressful events in midlife, and the mean BDI score (average of time 1 and t
80 panics; black non-Hispanics and Hispanics at midlife, and those aged 65 and above in every racial and
82 ow to moderate, and stable heavy drinking in midlife are not associated with lesser and greater cogni
83 0, as well as improvements in behaviors over midlife, are associated with a lower risk of frailty lat
84 nges in memory circuitry that occur in early midlife, as a function of sex and women's reproductive s
86 Our findings support an association between midlife atherosclerosis and development of vascular deme
87 mentia (CAIDE) study, who were followed from midlife (baseline from1972 to 1987; mean age 50.4 years;
88 rly and possibly reciprocally with age, with midlife being a critically vulnerable period in life.
95 dy aims to examine the relationships between midlife body mass index (BMI) and (1) AAO of AD (2) seve
99 w that induction of mitochondrial fission in midlife, but not in early life, extends the health and l
100 een apoB in young adults and the presence of midlife CAC independent of baseline traditional CVD risk
103 lifetime systolic blood pressure burden and midlife cognitive function was accounted for by LV mass
104 in childhood/adolescence is associated with midlife cognitive function, leveraging data from the Car
105 vities accounted for little variance in late midlife cognitive functioning in men age 56-66 (n = 1009
107 ntia risk by examining its associations with midlife cognitive performance and cognitive decline from
109 m childhood/adolescence associate with worse midlife cognitive performance independent of adulthood e
110 ood were independently associated with worse midlife cognitive performance, especially memory and lea
112 djusted MD = -0.03 (95% CI: -0.18, 0.11)) in midlife compared with stable never-drinking were not ass
116 implicated economic insecurity in increasing midlife death rates and "deaths of despair," including s
118 ning, and TPI identified an increased BTP in midlife depressed patients, suggesting early and subtle
126 rom demographics and the APOE genotype, only midlife dyslipidemia was associated with amyloid deposit
129 ere at higher risk of poor (lowest quartile) midlife episodic memory and associative learning (relati
130 he early phase of the study corresponding to midlife, even when chronic/recurring, do not increase th
133 cancer, exploring the influence of early and midlife exposures will further advance our understanding
134 ting Drp1-mediated mitochondrial fission, in midlife, facilitates mitophagy and improves both mitocho
138 lder with high midlife fitness than with low midlife fitness in both men($7,569 vs. $12,811; p < 0.00
140 articipants aged 65 years or older with high midlife fitness than with low midlife fitness in both me
141 ational and occupational attainment in early midlife for female respondents was not affected by their
144 The relations between body composition at midlife, health-related quality of life (HRQoL) in old a
146 able risk factors (less childhood education, midlife hearing loss, hypertension, and obesity, and lat
147 ut it is unclear whether flavonoid intake in midlife helps to maintain good health and wellbeing in a
148 lerance and slightly increased locomotion at midlife, however, only soma-specific knockdown of nsun-1
152 with late-life ICAD in blacks only, whereas midlife hypertension and hyperlipidemia were associated
153 CI, 1.68-2.54 per 100 person-years); and for midlife hypertension and late-life hypotension (n = 389)
154 o [HR], 1.49 [95% CI, 1.06-2.08]) and in the midlife hypertension and late-life hypotension group (HR
155 idlife and late life, only participants with midlife hypertension and late-life hypotension had highe
156 ion in midlife to late life and a pattern of midlife hypertension and late-life hypotension, compared
158 2) of several variables except job score and midlife hypertension in predicting exceptional aging wit
161 k factors (eg, physical inactivity, smoking, midlife hypertension, midlife obesity, and diabetes) and
162 f an association with the disease (diabetes, midlife hypertension, midlife obesity, physical inactivi
163 0.14 (0.02, 0.76; p = 0.024) for those with midlife ideal and late-life intermediate global CVH metr
165 option and mental health-related outcomes in midlife in 243,797 UK Biobank participants (n adopted =
166 were incrementally lower per MET achieved in midlife in men (6.8% decrease in costs per MET achieved;
167 ist actigraphy among 426 participants in the Midlife in the United States Study (31% AA; 69% EA; 61%
168 RIH2 mRNA levels significantly decrease from midlife in vastus lateralis muscles and highly correlate
171 preceding the imaging markers, and early to midlife intellectual enrichment to predict longitudinal
172 0.174) and 0.52 (0.29, 0.93; p = 0.027) for midlife intermediate and ideal levels (versus poor level
173 0.03 to 0.26; p < 0.05), whereas people with midlife intermediate and late-life ideal biological CVH
174 inAGE as a potential surrogate biomarker for midlife intervention studies that seek to measure dement
175 at impaired lung function or lung disease in midlife is associated with greater risk of incident deme
176 Exposure to higher BP levels from young to midlife is associated with worse gait and cognitive perf
178 e find that short-term induction of Drp1, in midlife, is sufficient to improve organismal health and
181 proportions of plasma phospholipid VLSFAs in midlife may be associated with less 20-y cognitive decli
183 clusion, maintaining healthy lifestyle since midlife may help reduce cognitive decline in aging.
184 usion, maintaining a healthy lifestyle since midlife may help reduce cognitive decline in aging.
185 Diabetes prevention and glucose control in midlife may protect against late-life cognitive decline.
186 he associations of overweight and obesity at midlife (mean age, 50 (standard deviation, 4.7) years) w
188 ogy and mortality in mammals when applied in midlife.Mitochondrial fission and fusion are important m
191 her rates of deaths of despair and all-cause midlife mortality at baseline but similar rates of incre
193 (95% confidence interval: 1.36, 1.47) higher midlife mortality rates at baseline and a rate of increa
201 e rate for participants with normotension in midlife (n = 833) and late life was 1.31 (95% CI, 1.00-1
204 95% CI, 1.00-1.72 per 100 person-years); for midlife normotension and late-life hypertension (n = 155
205 95% CI, 2.40-3.35 per 100 person-years); for midlife normotension and late-life hypotension (n = 927)
206 f these results, gathered in a population of midlife northeast American adults, hold in the general p
208 the disease (diabetes, midlife hypertension, midlife obesity, physical inactivity, depression, smokin
209 ocioeconomic markers (height, education, and midlife occupation categorized as low, intermediate, and
211 ic circumstances, early-adulthood education, midlife occupational stress, and late-life social networ
212 was strongly associated with baseline PSA in midlife: odds ratios (95% CIs) comparing PSA in the > 90
213 y extensive loss of striatal neurons and the midlife onset of debilitating and progressive chorea, de
214 functioning in healthy menopausal women with midlife onset of executive difficulties include modulati
215 , a neurodegenerative disorder with frequent midlife onset, encompasses developmental components.
216 Herein we describe Japanese siblings with a midlife-onset, slowly progressive type of cerebellar ata
217 l behavioral CVH metrics in particular, from midlife onwards is associated with a reduced risk of dem
220 -up of 26.2 (standard deviation, 4.9) years, midlife overweight and obesity were not associated with
224 s study include the lack of data on diet and midlife plasma glucose, high rate of attrition, as well
225 the memory pool early in life followed by a midlife plateau to the ease of learning salient features
226 Prostate-specific antigen (PSA) level in midlife predicted future prostate cancer (PCa) mortality
227 to determine if a baseline PSA level during midlife predicts lethal PCa in a US population with oppo
228 otein that promotes mitochondrial fission-in midlife, prolongs Drosophila lifespan and healthspan.
229 on-based sample of individuals with NAFLD in midlife, prospectively assessed alcohol use is not assoc
230 Risk-stratified screening on the basis of midlife PSA should be considered in men age 45 to 59 yea
231 is study, we investigated the association of midlife quality of close relationships with subsequent c
232 demographics, APOE, intellectual enrichment, midlife risk factors (physical inactivity, obesity, smok
234 1, and 134 had 2 or more; a higher number of midlife risk factors was associated with elevated amyloi
236 ing blood pressure from early adulthood into midlife seems to be associated with increased WMHV and s
237 ted biomechanical exposure and job strain in midlife separately and jointly predicted back and degene
238 l health and prolong lifespan, and observe a midlife shift toward a more elongated mitochondrial morp
241 ed linear models examined the association of midlife social contact between 45 and 55 years and cogni
245 alidated contributors: early life education, midlife substantive work complexity, late life leisure a
246 Further, ovariectomy unexpectedly promotes midlife survival of female mice lacking hepatic mTORC2,
247 eters, such as mitochondrial respiration and midlife survival, increases functional healthspan of the
250 , and physical activity between groups, from midlife through 1 year preceding the cognitive sub-study
251 , and physical activity between groups, from midlife through 1 year preceding the cognitive substudy.
254 nteract with the psychosocial environment of midlife to contribute to perimenopausal depression risk.
255 ng-term follow-up, sustained hypertension in midlife to late life and a pattern of midlife hypertensi
256 ents in, ideal cardiovascular health through midlife to late life are associated with lower CVD preva
257 al and primary prevention efforts throughout midlife to late life as a potential intervention to decr
258 that increasing weight loss per decade from midlife to late life is a marker for MCI and may help id
259 the relationship of CVHS attainment through midlife to late life with CVD prevalence and cardiovascu
260 e associations of composite CVH metrics from midlife to late life with risk of incident dementia.
262 percentile of education/occupation score and midlife to late-life cognitive activity), the onset of c
263 his, Apoe-deficient mice were exercised from midlife to old age and in contrast to wild-type (Apoe-su
264 Importantly, long-term aerobic exercise from midlife to old age prevented this age-related neurovascu
265 itive performance and cognitive decline from midlife to old age, including cognitive decline trajecto
266 n (SD) rate of weight change per decade from midlife to study entry was greater for participants who
267 rowth factors with adult BMI in daughters at midlife using quantile, linear, and logistic regression
268 midlife and to explore associations between midlife vascular risk factors and 25-year dementia incid
271 cipants without dementia and with nonmissing midlife vascular risk factors at baseline (mean age, 52
272 Place of birth, race, educational level, and midlife vascular risk factors data were collected betwee
276 t 3 life epochs (childhood, young adulthood, midlife) via questionnaire (2001-2002) and summarized in
277 hort study enrolled 4761 participants during midlife (visit 1, 1987-1989) and followed-up over 6 visi
278 terol, and smoking associated inversely with midlife visual and episodic memory and visuospatial asso
280 s having cancer at Medicare age, high CRF in midlife was associated with an adjusted 32% (HR, 0.68; 9
283 e of late-life BP, sustained hypertension in midlife was associated with dementia risk (HR, 1.41 [95%
284 years at baseline, 60% women), higher IMT in midlife was associated with development of small vessel
287 ithout an incident CV event, OSA assessed in midlife was independently associated with higher left ve
288 e cohort study, diet quality assessed during midlife was not significantly associated with subsequent
289 the AHEI-2010 (upper vs. lower quintiles) in midlife was related to 34% (95% CI, 9% to 66%; P for tre
290 cognitive function is limited, especially in midlife.We hypothesize that higher intake of these B vit
291 d 9 with Level B weaker evidence (obesity in midlife, weight loss in late life, physical exercise, sm
292 Intakes of 6 major flavonoid subclasses in midlife were ascertained on the basis of averaged intake
294 he most common neurodegenerative disorder of midlife, while Alzheimer's disease (AD) is the most comm
295 Increasing evidence of associations from midlife will guide the shift to interventional studies f
297 mulative BP exposure from young adulthood to midlife with gait and cognitive function in midlife.
299 pattern of decreasing depressive symptoms in midlife women, with higher risk before and lower risk af