Abstract
Cerebrovascular diseases represent 2nd leading cause of death worldwide. Understanding how genetic predispositions and their interaction with environmental factors affect cerebrovascular diseases is fundamental for prevention, diagnosis and for the development of safe and efficient therapies. Cerebrovascular diseases have not only a very high mortality rate, but also results in debilitating neurological impairments or permanent disability in survivors associated with huge economic losses. Among the women and men individuals with a low-risk lifestyle (smoking, exercising daily, consuming a prudent diet including moderate alcohol and having a healthy weight during mid-life) had a significantly lower risk of stroke than individuals without a low-risk lifestyle. Current review focuses on determining the relationship between diet, as an important component of ‘life style’, aging and cerebrovascular diseases.This review may help to unravel biological mechanisms linking lifestyle, diet-induced, metabolic inflammation, aging and cerebral hypoperfusion to development of cerebrovascular diseases, a prerequisite for development of science-based preventive strategies needed to combat the major public health challenges like obesity and stroke.
Keywords: Inflammation, aging, depression, perfusion deficits, obesity, stroke
1. Introduction: the global burden of cerebrovascular diseasesroduction: the global burden of cerebrovascular diseases
Cerebrovascular diseases are among the most prevalent health care problems in Europe. Total European cost of brain disorders in 2010 was 798 billion € of which 64.1 billion € was related to stroke alone1. In many cases, the result of cerebrovascular disorders is a loss of independent living and secondary health problems affecting not only patients but also their families. The number of elderly people is increasing with a number of co-morbidities increasing the risk of cerebrovascular diseases (CVD)2. Thus, strategies in guiding patient selection and novel preventive and neuroprotective therapies are urgently needed. Emerging evidence suggest that several diseases show overlapping pathology with neuroinflammation as one possible common mechanism leading to increased risk of cerebrovascular disorders.
In demographically developed countries, the average age at which stroke occurs is around 73 years reflecting the older age structure of these countries. The probability of a first stroke or first transitory ischemic attack is around 1.6 per 1,000 and 0.42 per 1,000, respectively. In less developed regions, the average age of stroke will be younger due to the different population age structure resulting from higher mortality rates and competing causes of death (The World Health Report, 2002).
Stroke patients are at highest risk of death in the first weeks after the event, and between 20% to 50% die within the first month depending on type, severity, age, co- morbidity and effectiveness of treatment of complications. Patients who survive may be left with no disability or with mild, moderate or severe disability. Considerable spontaneous recovery occurs up to about six months3. However, patients with a history of stroke are at risk of a subsequent event of around 10% in the first year and 5% per year there after4.
The negative consequences of stroke extend well beyond the victims themselves, ultimately including families, caregivers, social networks and employers. The proportion of patients achieving independence in self-care by one year after a stroke ranges from around 60% to 83%. This wide variation relates to whether the studies are community based or hospital based, which activities are considered in estimating independence, and the methods used to rate ability. In established marked economies (EMEs), depending on the organization of hospital services, between 10% and 15% of survivors are resident in an institution at one year5.
Worldwide stroke incidence is increasing in parallel with modernization, changes in lifestyle, and the growing elderly population. In particular, rates in Eastern Europe have been increasing, such that currently the highest rates are found in countries such as Bulgaria, Romania, and Hungary. Among the women and men individuals with a low-risk lifestyle (no smoking, exercising daily, consuming a prudent diet including moderate alcohol and having a healthy weight during mid-life) had a significantly lower risk of stroke than individuals without a low-risk lifestyle. Therefore the relatively high incidence of stroke may be due in part to the impact of numerous known risk factors in these populations6: arterial hypertension, diabetes, high cholesterol, smoking, alcoholism, obesity, stress, and a sedentary lifestyle.
New methods of diagnosis and treatment have improved the management of known risk factors (such as hypercholesterolemia and high blood pressure) as well as the sequelae of stroke, such that decreases both in stroke incidence (by 20% in the 1980’s), and in mortality induced by stroke (by about 3-5% per year in Europe between the years 1970 and 1985) have been recorded7. At the same time, however, those vulnerable to stroke will become more numerous as the elderly population rapidly increases around the world, and many risk factors remain either unknown or beyond the reach of current therapies (as in the case of old age, the most important, and growing, risk factor for stroke).
2. Mechanisms linking lifestyle, diet-induced, metabolic inflammation to development of cerebrovascular diseases
Although CVDs to some extent are predictable through anthropometric, lifestyle, and clinical factors, the metabolic pathways underlying the progression of disease are only poorly understood.
Fuelled by rapid urbanization, westernised diet and an increasingly sedentary lifestyle, the Type2 Diabetes Mellitus epidemic has grown in parallel with the worldwide rise in obesity. For several decades, the diet-heart paradigm that high intake of saturated fat and cholesterol increases the risk of atherosclerosis and CVDs has been the driving force behind national and international dietary recommendations for prevention of CVD8.
Bad nutritional habits can lead to metabolic disorders, triggered by a system-wide chronic inflammation, also called metaflammation, metabolic inflammation9. A metaflammation state can lead to a series of disorders and diseases, including hypertension, metabolic syndrome, CVD, stroke, insulin resistance and type 2 diabetes mellitus (T2DM). It is postulated that lipid hormones including sphingolipids and eicosanoids in concert with cytokines and adipokines play an important role in this process by inducing adverse regulatory responses in target cells such as macrophages. The role of genetics in driving metabolic disease development is strongly indicated by the higher concordance rate of T2DM in monozygotic than in dizygotic twins. It has been estimated that 30% to 70% of T2DM risk can be attributed to genetics10. The investigation of gene-environment interactions through large collaborative efforts holds promise in furthering our understanding of the interplay between genetic and environmental factors11.
Since the completion of the HapMap project and the availability of whole genome single nucleotide polymorphisms (SNP) assays, genome-wide analysis of correlations between genetic variants and phenotypes has become an important approach to find disease-causative genes. Genome wide SNP typing is often performed in very large groups of human individuals (cohorts), and a large number of loci underlying disease have now been catalogued12 including variants that increase susceptibility to T2DM. However, these loci confer effects of only modest size and do not add to the clinical prediction of diabetes beyond that of traditional risk factors, such as obesity, physical inactivity, family history of diabetes, and certain clinical parameter. Furthermore, our contribution to identifying the genomic SNP pattern providing insights to biological basis of obesity13 and the identification of new genetic loci linking adipocyte and insulin biology to body fat distribution14, will enable differentiation between genetics and lifestyle factors. The combination of genome wide- association studies (GWAS) with metabolomics is now breaking new grounds15, as it allows making associations between SNPs and so-called intermediate phenotypes that can be obtained through exact measurements. Metabolomics facilitates the exact quantitative measurement of large sets of lipid molecules and other metabolites, and GWAS has allowed the mapping of numerous metabolic phenotypes on the genome, as demonstrated by the discovery of substantial numbers of loci with relative strong effects16-19.
3. Obesity, inflammation and rehabilitation odds in stroke patients
The “obesity paradox” has been reported in many articles as a inverse relationship between the body mass index (BMI) and mortality in stroke patients. The relationship between BMI and functional recovery in post stroke patients has not been well described20-25.
In a cohort study from the China National Stroke Registry war analysed the relationship between the body mass index (BMI) , mortality and post stroke functional recovery at 3 months after disease onset. This study enrolled and analyzed 10,905 patients with eligible acute ischemic stroke. Favourable functional recovery was seen in 52,4 % of underweight (BMI 18,5 kg/m2) , 55,0% of normal weight (BMI 18,5-22,9 kg/m2), 61% of overweight (BMI 23-27,4 kg/m2) , 59,2% of obese (27,5-32,4 km/m2) and 60,3% of severe obese (BMI > 32,5 kg/m2) stroke survivors. The overweight AIS survivors had better 3-month functional recovery and obesity not severe obesity showed a protective trend. Second, severe obesity was associated with higher mortality and overweight/obesity was not a protective factor of survival at 3 months after stroke26.
In a study on the effect of BMI on stroke rehabilitation that included 819 patients admitted to an acute rehabilitation hospital for stroke rehabilitation, overweighted patients had, paradoxically, better functional progression than did patients in other weight categories27.
In still another study on the “Obesity Paradox” that included 510 with transient ischemic attack survivors showed that the excess of adiposity increases the chance of severe disability after ischemic stroke. Since BMI reflects also total lean mass, it is risky to conclude that there is a protective effect of obesity alone in the functional recovery after stroke. Nevertheless, it is possible that a certain magnitude of body mass is necessary to prevent severe disability in stroke survivors28.
Contradictory results were reported in a study from 2007 that showed that the functional improvement in normal weighted patients was better than that in overweight/obese patients29.
In a large retrospective cohort study from the Danish Stroke Register, 53812 patients were analyzed for BMI, age, sex, civil status, stroke severity, stroke subtype, a predefined cardiovascular profile, and the socioeconomic status. There was no evidence of an “obesity paradox” in patients with reported stroke. However, stroke occurred at a significantly younger age in patients with higher BMI.
Another study analyzed 451 patients hospitalized for ischemic stroke and found that BMI on admission had no relationship to functional recovery on discharge30. The association between higher BMI and favorable functional recovery might be influenced by stroke severity because patients with high BMI seemed to have had less severe strokes25 and more lacunar infarctions31.
4. Perfusion deficits in the elderly, inflammation and depression
Recent work suggest that perfusion deficits in the elderly can trigger microglial activation and subsequent neuroinflammation32,33 ultimately resulting in demyelination and neurodegeneration34.
Previous studies in rodents indicate that aging and preclinical neurodegenerative disease processes promote proinflammatory states in older individuals and leads to the development of a primed and immune-reactive population of microglia35-41. Further, immune activation can be a characteristic of depression42,43 and precipitate depressive symptoms44,45. Moreover, recent work suggest that perfusion deficits in the elderly can trigger microglial activation and subsequent neuroinflammation and shifts the central nervous system (CNS) into a proinflammatory state32,33,41 ultimately resulting in demyelination and neurodegeneration34. This was particularly evident in middle aged rodents as compared to the young counterparts46.
Recent research suggests that the inflammatory process is potentially intricately linked with multiple neurodegenerative pathways for depression and pro-inflammatory cytokines47 and plays a central role in the pathophysiology of both depression and dementia48-51. There is strong evidence that in humans vascular disease vascular Abeta deposition in the brain promotes development of depression and increases the risk of dementia by causing loss of vascular autoregulation associated with rigidity of arterioles, leading to infarction in the territory of their branching vessels in the temporal cortex of patients with cerebral angiopathy (CAA). This is associated with marked vascular/perivascular infiltration of inflammatory cells, a condition mimicked in mice subjected to chronic cerebral hypoperfusion52,53.
5. Life style, co-morbidities and depression
It is becoming well established that lifestyle, especially dietary habits, greatly affect metabolic health. This model which promotes diets that are typically low in fat and high in carbohydrates (the ‘Western’ diet), has led to a substantial decline in the percentage of energy intake from total and saturated fats. At the same time, it has spurred a compensatory increase in consumption of refined carbohydrates and added sugars, a dietary shift that may be contributing to the current twin epidemics of obesity and diabetes: both metabolic diseases and identified as risk factors for CVD. The changed landscape in obesity and dietary patterns suggests a need to reassess the strategy of replacing total and saturated fats with carbohydrates.
Diabetes mellitus and depression and are two of the most common illnesses in the elderly. Both depression and diabetes increase reciprocally the risk of dementia. Recent reviews suggest that approximately 20% of adult patients with T2DM meet criteria for comorbid major depression. A systematically review aimed to estimate the prevalence of depression in adults with T2DM found that a personal history of depression are more likely to develop dementia and cognitive decline later in life. Recently, in a prospective study in patients with type 2 diabetes, 20% of the patients with diabetes met criteria for depression. Furthermore, patients with comorbid depression had a 100% increased risk of developing dementia during the 3 to 5 years study period54-58.
CONCLUSIONS:
♦ Worldwide cerebrovascular diseases are increasing in parallel with modernization, changes in lifestyle, and the growing elderly population.
♦ Understanding how aging and life style precipitate the development of cerebrovascular diseases is fundamental for prevention, diagnosis and for the development of safe and efficient therapies.
♦ Genetic findings, once unambiguously identified, have the potential to predict an individual’s disease risk, phenotype, and possibly progression. They also may contribute to clinical management by prompting heightened surveillance, providing indication for preventive intervention, and guiding treatment selection.
♦ Recent work suggests that perfusion deficits in the elderly can trigger microglial activation and subsequent neuroinflammation, and shifts the CNS into a proinflammatory state, ultimately resulting in demyelination and neurodegeneration (Figure 1).
Figure 1. Life style, aging, hypoperfusion and neuroinflammation precipitate neuropsychiatric diseases as shown in art images.
Brain neuroinflammation is illustrated by Iba1 immunoreactivity (red) in an aged subject (Popa-Wagner, unpublished data).
Acknowledgments
RES was supported by a grant from the European Social Found, Human Resources Development Operational Programme 2007-2013, project no. POSDRU/159/1.5/S/136893. APW was supported by a grant of the Romanian National Authority for Scientific Research, CNCS-UEFISCDI, project number PN-II-PT-PCCA-2011-3, No 80/2012.
Footnotes
Conflict of interests: The authors declare no conflict of interest.
Cerebrovascular diseases (CVD); type 2 diabetes mellitus (T2DM); single nucleotide polymorphisms (SNP); genome-wide association studies (GWAS); body mass index (BMI); central nervous system (CNS); cerebral angiopathy (CAA)
DISCOVERIES is a peer-reviewed, open access, online, multidisciplinary and integrative journal, publishing high impact and innovative manuscripts from all areas related to MEDICINE, BIOLOGY and CHEMISTRY
References
- 1.The economic cost of brain disorders in Europe. Olesen J, Gustavsson A, Svensson M, Wittchen H-U, Jönsson B. European journal of neurology. 2012;19(1):155–62. doi: 10.1111/j.1468-1331.2011.03590.x. [DOI] [PubMed] [Google Scholar]
- 2.Modelling the burden of stroke in Finland until 2030. Sivenius J, Torppa J, Tuomilehto J, Immonen-Räihä P, Kaarisalo M, Sarti C, Kuulasmaa K, Mähönen M, Lehtonen A, Salomaa V. International journal of stroke : official journal of the International Stroke Society. 2009;4(5):340–5. doi: 10.1111/j.1747-4949.2009.00330.x. [DOI] [PubMed] [Google Scholar]
- 3.Recovery of motor function after stroke. Bonita R., Beaglehole R. Stroke. 1988;19(12):1497-1500. doi: 10.1161/01.str.19.12.1497. [DOI] [PubMed] [Google Scholar]
- 4.Long-term risk of recurrent stroke after a first-ever stroke. The Oxfordshire Community Stroke Project. Burn J, Dennis M, Bamford J, Sandercock P, Wade D, Warlow C. Stroke. 1994;25(2):333–7. doi: 10.1161/01.str.25.2.333. [DOI] [PubMed] [Google Scholar]
- 5.Poor outcome after first-ever stroke: predictors for death, dependency, and recurrent stroke within the first year. Appelros Peter, Nydevik Ingegerd, Viitanen Matti. Stroke. 2003;34(1):122–6. doi: 10.1161/01.str.0000047852.05842.3c. [DOI] [PubMed] [Google Scholar]
- 6.Breaking the 3 h barrier for treatment of acute ischaemic stroke. Donnan Geoffrey A, Davis Stephen M. The Lancet. Neurology. 2008;7(11):981–2. doi: 10.1016/S1474-4422(08)70230-8. [DOI] [PubMed] [Google Scholar]
- 7.International trends in mortality from stroke, 1968 to 1994. Sarti C, Rastenyte D, Cepaitis Z, Tuomilehto J. Stroke. 2000;31(7):1588–601. doi: 10.1161/01.str.31.7.1588. [DOI] [PubMed] [Google Scholar]
- 8.Optimal diets for prevention of coronary heart disease. Hu Frank B, Willett Walter C. JAMA. 2002;288(20):2569–78. doi: 10.1001/jama.288.20.2569. [DOI] [PubMed] [Google Scholar]
- 9.Macrophages, inflammation, and insulin resistance. Olefsky Jerrold M, Glass Christopher K. Annual review of physiology. 2010;72:219–46. doi: 10.1146/annurev-physiol-021909-135846. [DOI] [PubMed] [Google Scholar]
- 10.Heritability of type II (non-insulin-dependent) diabetes mellitus and abnormal glucose tolerance--a population-based twin study. Poulsen P, Kyvik K O, Vaag A, Beck-Nielsen H. Diabetologia. 1999;42(2):139–45. doi: 10.1007/s001250051131. [DOI] [PubMed] [Google Scholar]
- 11.Gene-environment interactions in the development of type 2 diabetes: recent progress and continuing challenges. Cornelis Marilyn C, Hu Frank B. Annual review of nutrition. 2012;32:245–59. doi: 10.1146/annurev-nutr-071811-150648. [DOI] [PubMed] [Google Scholar]
- 12.A Catalog of Published Genome-Wide Association Studies; https://www.genome.gov/gwastudies/ National Human Genome Institute - Division of Genomic Medicine. 2015. https://www.genome.gov/gwastudies/ https://www.genome.gov/gwastudies/
- 13.Genetic studies of body mass index yield new insights for obesity biology. Locke Adam E, Kahali Bratati, Berndt Sonja I, Justice Anne E, Pers Tune H, Day Felix R, Powell Corey, Vedantam Sailaja, Buchkovich Martin L, Yang Jian, Croteau-Chonka Damien C, Esko Tonu, Fall Tove, Ferreira Teresa, Gustafsson Stefan, Kutalik Zoltán, Luan Jian'an, Mägi Reedik, Randall Joshua C, Winkler Thomas W, Wood Andrew R, Workalemahu Tsegaselassie, Faul Jessica D, Smith Jennifer A, Zhao Jing Hua, Zhao Wei, Chen Jin, Fehrmann Rudolf, Hedman Åsa K, Karjalainen Juha, Schmidt Ellen M, Absher Devin, Amin Najaf, Anderson Denise, Beekman Marian, Bolton Jennifer L, Bragg-Gresham Jennifer L, Buyske Steven, Demirkan Ayse, Deng Guohong, Ehret Georg B, Feenstra Bjarke, Feitosa Mary F, Fischer Krista, Goel Anuj, Gong Jian, Jackson Anne U, Kanoni Stavroula, Kleber Marcus E, Kristiansson Kati, Lim Unhee, Lotay Vaneet, Mangino Massimo, Leach Irene Mateo, Medina-Gomez Carolina, Medland Sarah E, Nalls Michael A, Palmer Cameron D, Pasko Dorota, Pechlivanis Sonali, Peters Marjolein J, Prokopenko Inga, Shungin Dmitry, Stančáková Alena, Strawbridge Rona J, Sung Yun Ju, Tanaka Toshiko, Teumer Alexander, Trompet Stella, van der Laan Sander W, van Setten Jessica, Van Vliet-Ostaptchouk Jana V, Wang Zhaoming, Yengo Loïc, Zhang Weihua, Isaacs Aaron, Albrecht Eva, Ärnlöv Johan, Arscott Gillian M, Attwood Antony P, Bandinelli Stefania, Barrett Amy, Bas Isabelita N, Bellis Claire, Bennett Amanda J, Berne Christian, Blagieva Roza, Blüher Matthias, Böhringer Stefan, Bonnycastle Lori L, Böttcher Yvonne, Boyd Heather A, Bruinenberg Marcel, Caspersen Ida H, Chen Yii-Der Ida, Clarke Robert, Daw E Warwick, de Craen Anton J M, Delgado Graciela, Dimitriou Maria, Doney Alex S F, Eklund Niina, Estrada Karol, Eury Elodie, Folkersen Lasse, Fraser Ross M, Garcia Melissa E, Geller Frank, Giedraitis Vilmantas, Gigante Bruna, Go Alan S, Golay Alain, Goodall Alison H, Gordon Scott D, Gorski Mathias, Grabe Hans-Jörgen, Grallert Harald, Grammer Tanja B, Gräßler Jürgen, Grönberg Henrik, Groves Christopher J, Gusto Gaëlle, Haessler Jeffrey, Hall Per, Haller Toomas, Hallmans Goran, Hartman Catharina A, Hassinen Maija, Hayward Caroline, Heard-Costa Nancy L, Helmer Quinta, Hengstenberg Christian, Holmen Oddgeir, Hottenga Jouke-Jan, James Alan L, Jeff Janina M, Johansson Åsa, Jolley Jennifer, Juliusdottir Thorhildur, Kinnunen Leena, Koenig Wolfgang, Koskenvuo Markku, Kratzer Wolfgang, Laitinen Jaana, Lamina Claudia, Leander Karin, Lee Nanette R, Lichtner Peter, Lind Lars, Lindström Jaana, Lo Ken Sin, Lobbens Stéphane, Lorbeer Roberto, Lu Yingchang, Mach François, Magnusson Patrik K E, Mahajan Anubha, McArdle Wendy L, McLachlan Stela, Menni Cristina, Merger Sigrun, Mihailov Evelin, Milani Lili, Moayyeri Alireza, Monda Keri L, Morken Mario A, Mulas Antonella, Müller Gabriele, Müller-Nurasyid Martina, Musk Arthur W, Nagaraja Ramaiah, Nöthen Markus M, Nolte Ilja M, Pilz Stefan, Rayner Nigel W, Renstrom Frida, Rettig Rainer, Ried Janina S, Ripke Stephan, Robertson Neil R, Rose Lynda M, Sanna Serena, Scharnagl Hubert, Scholtens Salome, Schumacher Fredrick R, Scott William R, Seufferlein Thomas, Shi Jianxin, Smith Albert Vernon, Smolonska Joanna, Stanton Alice V, Steinthorsdottir Valgerdur, Stirrups Kathleen, Stringham Heather M, Sundström Johan, Swertz Morris A, Swift Amy J, Syvänen Ann-Christine, Tan Sian-Tsung, Tayo Bamidele O, Thorand Barbara, Thorleifsson Gudmar, Tyrer Jonathan P, Uh Hae-Won, Vandenput Liesbeth, Verhulst Frank C, Vermeulen Sita H, Verweij Niek, Vonk Judith M, Waite Lindsay L, Warren Helen R, Waterworth Dawn, Weedon Michael N, Wilkens Lynne R, Willenborg Christina, Wilsgaard Tom, Wojczynski Mary K, Wong Andrew, Wright Alan F, Zhang Qunyuan, Brennan Eoin P, Choi Murim, Dastani Zari, Drong Alexander W, Eriksson Per, Franco-Cereceda Anders, Gådin Jesper R, Gharavi Ali G, Goddard Michael E, Handsaker Robert E, Huang Jinyan, Karpe Fredrik, Kathiresan Sekar, Keildson Sarah, Kiryluk Krzysztof, Kubo Michiaki, Lee Jong-Young, Liang Liming, Lifton Richard P, Ma Baoshan, McCarroll Steven A, McKnight Amy J, Min Josine L, Moffatt Miriam F, Montgomery Grant W, Murabito Joanne M, Nicholson George, Nyholt Dale R, Okada Yukinori, Perry John R B, Dorajoo Rajkumar, Reinmaa Eva, Salem Rany M, Sandholm Niina, Scott Robert A, Stolk Lisette, Takahashi Atsushi, Tanaka Toshihiro, van 't Hooft Ferdinand M, Vinkhuyzen Anna A E, Westra Harm-Jan, Zheng Wei, Zondervan Krina T, Heath Andrew C, Arveiler Dominique, Bakker Stephan J L, Beilby John, Bergman Richard N, Blangero John, Bovet Pascal, Campbell Harry, Caulfield Mark J, Cesana Giancarlo, Chakravarti Aravinda, Chasman Daniel I, Chines Peter S, Collins Francis S, Crawford Dana C, Cupples L Adrienne, Cusi Daniele, Danesh John, de Faire Ulf, den Ruijter Hester M, Dominiczak Anna F, Erbel Raimund, Erdmann Jeanette, Eriksson Johan G, Farrall Martin, Felix Stephan B, Ferrannini Ele, Ferrières Jean, Ford Ian, Forouhi Nita G, Forrester Terrence, Franco Oscar H, Gansevoort Ron T, Gejman Pablo V, Gieger Christian, Gottesman Omri, Gudnason Vilmundur, Gyllensten Ulf, Hall Alistair S, Harris Tamara B, Hattersley Andrew T, Hicks Andrew A, Hindorff Lucia A, Hingorani Aroon D, Hofman Albert, Homuth Georg, Hovingh G Kees, Humphries Steve E, Hunt Steven C, Hyppönen Elina, Illig Thomas, Jacobs Kevin B, Jarvelin Marjo-Riitta, Jöckel Karl-Heinz, Johansen Berit, Jousilahti Pekka, Jukema J Wouter, Jula Antti M, Kaprio Jaakko, Kastelein John J P, Keinanen-Kiukaanniemi Sirkka M, Kiemeney Lambertus A, Knekt Paul, Kooner Jaspal S, Kooperberg Charles, Kovacs Peter, Kraja Aldi T, Kumari Meena, Kuusisto Johanna, Lakka Timo A, Langenberg Claudia, Marchand Loic Le, Lehtimäki Terho, Lyssenko Valeriya, Männistö Satu, Marette André, Matise Tara C, McKenzie Colin A, McKnight Barbara, Moll Frans L, Morris Andrew D, Morris Andrew P, Murray Jeffrey C, Nelis Mari, Ohlsson Claes, Oldehinkel Albertine J, Ong Ken K, Madden Pamela A F, Pasterkamp Gerard, Peden John F, Peters Annette, Postma Dirkje S, Pramstaller Peter P, Price Jackie F, Qi Lu, Raitakari Olli T, Rankinen Tuomo, Rao D C, Rice Treva K, Ridker Paul M, Rioux John D, Ritchie Marylyn D, Rudan Igor, Salomaa Veikko, Samani Nilesh J, Saramies Jouko, Sarzynski Mark A, Schunkert Heribert, Schwarz Peter E H, Sever Peter, Shuldiner Alan R, Sinisalo Juha, Stolk Ronald P, Strauch Konstantin, Tönjes Anke, Trégouët David-Alexandre, Tremblay Angelo, Tremoli Elena, Virtamo Jarmo, Vohl Marie-Claude, Völker Uwe, Waeber Gérard, Willemsen Gonneke, Witteman Jacqueline C, Zillikens M Carola, Adair Linda S, Amouyel Philippe, Asselbergs Folkert W, Assimes Themistocles L, Bochud Murielle, Boehm Bernhard O, Boerwinkle Eric, Bornstein Stefan R, Bottinger Erwin P, Bouchard Claude, Cauchi Stéphane, Chambers John C, Chanock Stephen J, Cooper Richard S, de Bakker Paul I W, Dedoussis George, Ferrucci Luigi, Franks Paul W, Froguel Philippe, Groop Leif C, Haiman Christopher A, Hamsten Anders, Hui Jennie, Hunter David J, Hveem Kristian, Kaplan Robert C, Kivimaki Mika, Kuh Diana, Laakso Markku, Liu Yongmei, Martin Nicholas G, März Winfried, Melbye Mads, Metspalu Andres, Moebus Susanne, Munroe Patricia B, Njølstad Inger, Oostra Ben A, Palmer Colin N A, Pedersen Nancy L, Perola Markus, Pérusse Louis, Peters Ulrike, Power Chris, Quertermous Thomas, Rauramaa Rainer, Rivadeneira Fernando, Saaristo Timo E, Saleheen Danish, Sattar Naveed, Schadt Eric E, Schlessinger David, Slagboom P Eline, Snieder Harold, Spector Tim D, Thorsteinsdottir Unnur, Stumvoll Michael, Tuomilehto Jaakko, Uitterlinden André G, Uusitupa Matti, van der Harst Pim, Walker Mark, Wallaschofski Henri, Wareham Nicholas J, Watkins Hugh, Weir David R, Wichmann H-Erich, Wilson James F, Zanen Pieter, Borecki Ingrid B, Deloukas Panos, Fox Caroline S, Heid Iris M, O'Connell Jeffrey R, Strachan David P, Stefansson Kari, van Duijn Cornelia M, Abecasis Gonçalo R, Franke Lude, Frayling Timothy M, McCarthy Mark I, Visscher Peter M, Scherag André, Willer Cristen J, Boehnke Michael, Mohlke Karen L, Lindgren Cecilia M, Beckmann Jacques S, Barroso Inês, North Kari E, Ingelsson Erik, Hirschhorn Joel N, Loos Ruth J F, Speliotes Elizabeth K. Nature. 2015;518(7538):197–206. doi: 10.1038/nature14177. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.New genetic loci link adipose and insulin biology to body fat distribution. Shungin Dmitry, Winkler Thomas W, Croteau-Chonka Damien C, Ferreira Teresa, Locke Adam E, Mägi Reedik, Strawbridge Rona J, Pers Tune H, Fischer Krista, Justice Anne E, Workalemahu Tsegaselassie, Wu Joseph M W, Buchkovich Martin L, Heard-Costa Nancy L, Roman Tamara S, Drong Alexander W, Song Ci, Gustafsson Stefan, Day Felix R, Esko Tonu, Fall Tove, Kutalik Zoltán, Luan Jian'an, Randall Joshua C, Scherag André, Vedantam Sailaja, Wood Andrew R, Chen Jin, Fehrmann Rudolf, Karjalainen Juha, Kahali Bratati, Liu Ching-Ti, Schmidt Ellen M, Absher Devin, Amin Najaf, Anderson Denise, Beekman Marian, Bragg-Gresham Jennifer L, Buyske Steven, Demirkan Ayse, Ehret Georg B, Feitosa Mary F, Goel Anuj, Jackson Anne U, Johnson Toby, Kleber Marcus E, Kristiansson Kati, Mangino Massimo, Leach Irene Mateo, Medina-Gomez Carolina, Palmer Cameron D, Pasko Dorota, Pechlivanis Sonali, Peters Marjolein J, Prokopenko Inga, Stančáková Alena, Sung Yun Ju, Tanaka Toshiko, Teumer Alexander, Van Vliet-Ostaptchouk Jana V, Yengo Loïc, Zhang Weihua, Albrecht Eva, Ärnlöv Johan, Arscott Gillian M, Bandinelli Stefania, Barrett Amy, Bellis Claire, Bennett Amanda J, Berne Christian, Blüher Matthias, Böhringer Stefan, Bonnet Fabrice, Böttcher Yvonne, Bruinenberg Marcel, Carba Delia B, Caspersen Ida H, Clarke Robert, Daw E Warwick, Deelen Joris, Deelman Ewa, Delgado Graciela, Doney Alex Sf, Eklund Niina, Erdos Michael R, Estrada Karol, Eury Elodie, Friedrich Nele, Garcia Melissa E, Giedraitis Vilmantas, Gigante Bruna, Go Alan S, Golay Alain, Grallert Harald, Grammer Tanja B, Gräßler Jürgen, Grewal Jagvir, Groves Christopher J, Haller Toomas, Hallmans Goran, Hartman Catharina A, Hassinen Maija, Hayward Caroline, Heikkilä Kauko, Herzig Karl-Heinz, Helmer Quinta, Hillege Hans L, Holmen Oddgeir, Hunt Steven C, Isaacs Aaron, Ittermann Till, James Alan L, Johansson Ingegerd, Juliusdottir Thorhildur, Kalafati Ioanna-Panagiota, Kinnunen Leena, Koenig Wolfgang, Kooner Ishminder K, Kratzer Wolfgang, Lamina Claudia, Leander Karin, Lee Nanette R, Lichtner Peter, Lind Lars, Lindström Jaana, Lobbens Stéphane, Lorentzon Mattias, Mach François, Magnusson Patrik Ke, Mahajan Anubha, McArdle Wendy L, Menni Cristina, Merger Sigrun, Mihailov Evelin, Milani Lili, Mills Rebecca, Moayyeri Alireza, Monda Keri L, Mooijaart Simon P, Mühleisen Thomas W, Mulas Antonella, Müller Gabriele, Müller-Nurasyid Martina, Nagaraja Ramaiah, Nalls Michael A, Narisu Narisu, Glorioso Nicola, Nolte Ilja M, Olden Matthias, Rayner Nigel W, Renstrom Frida, Ried Janina S, Robertson Neil R, Rose Lynda M, Sanna Serena, Scharnagl Hubert, Scholtens Salome, Sennblad Bengt, Seufferlein Thomas, Sitlani Colleen M, Smith Albert Vernon, Stirrups Kathleen, Stringham Heather M, Sundström Johan, Swertz Morris A, Swift Amy J, Syvänen Ann-Christine, Tayo Bamidele O, Thorand Barbara, Thorleifsson Gudmar, Tomaschitz Andreas, Troffa Chiara, van Oort Floor Va, Verweij Niek, Vonk Judith M, Waite Lindsay L, Wennauer Roman, Wilsgaard Tom, Wojczynski Mary K, Wong Andrew, Zhang Qunyuan, Zhao Jing Hua, Brennan Eoin P, Choi Murim, Eriksson Per, Folkersen Lasse, Franco-Cereceda Anders, Gharavi Ali G, Hedman Åsa K, Hivert Marie-France, Huang Jinyan, Kanoni Stavroula, Karpe Fredrik, Keildson Sarah, Kiryluk Krzysztof, Liang Liming, Lifton Richard P, Ma Baoshan, McKnight Amy J, McPherson Ruth, Metspalu Andres, Min Josine L, Moffatt Miriam F, Montgomery Grant W, Murabito Joanne M, Nicholson George, Nyholt Dale R, Olsson Christian, Perry John Rb, Reinmaa Eva, Salem Rany M, Sandholm Niina, Schadt Eric E, Scott Robert A, Stolk Lisette, Vallejo Edgar E, Westra Harm-Jan, Zondervan Krina T, Amouyel Philippe, Arveiler Dominique, Bakker Stephan Jl, Beilby John, Bergman Richard N, Blangero John, Brown Morris J, Burnier Michel, Campbell Harry, Chakravarti Aravinda, Chines Peter S, Claudi-Boehm Simone, Collins Francis S, Crawford Dana C, Danesh John, de Faire Ulf, de Geus Eco Jc, Dörr Marcus, Erbel Raimund, Eriksson Johan G, Farrall Martin, Ferrannini Ele, Ferrières Jean, Forouhi Nita G, Forrester Terrence, Franco Oscar H, Gansevoort Ron T, Gieger Christian, Gudnason Vilmundur, Haiman Christopher A, Harris Tamara B, Hattersley Andrew T, Heliövaara Markku, Hicks Andrew A, Hingorani Aroon D, Hoffmann Wolfgang, Hofman Albert, Homuth Georg, Humphries Steve E, Hyppönen Elina, Illig Thomas, Jarvelin Marjo-Riitta, Johansen Berit, Jousilahti Pekka, Jula Antti M, Kaprio Jaakko, Kee Frank, Keinanen-Kiukaanniemi Sirkka M, Kooner Jaspal S, Kooperberg Charles, Kovacs Peter, Kraja Aldi T, Kumari Meena, Kuulasmaa Kari, Kuusisto Johanna, Lakka Timo A, Langenberg Claudia, Le Marchand Loic, Lehtimäki Terho, Lyssenko Valeriya, Männistö Satu, Marette André, Matise Tara C, McKenzie Colin A, McKnight Barbara, Musk Arthur W, Möhlenkamp Stefan, Morris Andrew D, Nelis Mari, Ohlsson Claes, Oldehinkel Albertine J, Ong Ken K, Palmer Lyle J, Penninx Brenda W, Peters Annette, Pramstaller Peter P, Raitakari Olli T, Rankinen Tuomo, Rao D C, Rice Treva K, Ridker Paul M, Ritchie Marylyn D, Rudan Igor, Salomaa Veikko, Samani Nilesh J, Saramies Jouko, Sarzynski Mark A, Schwarz Peter Eh, Shuldiner Alan R, Staessen Jan A, Steinthorsdottir Valgerdur, Stolk Ronald P, Strauch Konstantin, Tönjes Anke, Tremblay Angelo, Tremoli Elena, Vohl Marie-Claude, Völker Uwe, Vollenweider Peter, Wilson James F, Witteman Jacqueline C, Adair Linda S, Bochud Murielle, Boehm Bernhard O, Bornstein Stefan R, Bouchard Claude, Cauchi Stéphane, Caulfield Mark J, Chambers John C, Chasman Daniel I, Cooper Richard S, Dedoussis George, Ferrucci Luigi, Froguel Philippe, Grabe Hans-Jörgen, Hamsten Anders, Hui Jennie, Hveem Kristian, Jöckel Karl-Heinz, Kivimaki Mika, Kuh Diana, Laakso Markku, Liu Yongmei, März Winfried, Munroe Patricia B, Njølstad Inger, Oostra Ben A, Palmer Colin Na, Pedersen Nancy L, Perola Markus, Pérusse Louis, Peters Ulrike, Power Chris, Quertermous Thomas, Rauramaa Rainer, Rivadeneira Fernando, Saaristo Timo E, Saleheen Danish, Sinisalo Juha, Slagboom P Eline, Snieder Harold, Spector Tim D, Stefansson Kari, Stumvoll Michael, Tuomilehto Jaakko, Uitterlinden André G, Uusitupa Matti, van der Harst Pim, Veronesi Giovanni, Walker Mark, Wareham Nicholas J, Watkins Hugh, Wichmann H-Erich, Abecasis Goncalo R, Assimes Themistocles L, Berndt Sonja I, Boehnke Michael, Borecki Ingrid B, Deloukas Panos, Franke Lude, Frayling Timothy M, Groop Leif C, Hunter David J, Kaplan Robert C, O'Connell Jeffrey R, Qi Lu, Schlessinger David, Strachan David P, Thorsteinsdottir Unnur, van Duijn Cornelia M, Willer Cristen J, Visscher Peter M, Yang Jian, Hirschhorn Joel N, Zillikens M Carola, McCarthy Mark I, Speliotes Elizabeth K, North Kari E, Fox Caroline S, Barroso Inês, Franks Paul W, Ingelsson Erik, Heid Iris M, Loos Ruth Jf, Cupples L Adrienne, Morris Andrew P, Lindgren Cecilia M, Mohlke Karen L. Nature. 2015;518(7538):187–196. doi: 10.1038/nature14132. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Opening up the "Black Box": metabolic phenotyping and metabolome-wide association studies in epidemiology. Bictash Magda, Ebbels Timothy M, Chan Queenie, Loo Ruey Leng, Yap Ivan K S, Brown Ian J, de Iorio Maria, Daviglus Martha L, Holmes Elaine, Stamler Jeremiah, Nicholson Jeremy K, Elliott Paul. Journal of clinical epidemiology. 2010;63(9):970–9. doi: 10.1016/j.jclinepi.2009.10.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.A genome-wide perspective of genetic variation in human metabolism. Illig Thomas, Gieger Christian, Zhai Guangju, Römisch-Margl Werner, Wang-Sattler Rui, Prehn Cornelia, Altmaier Elisabeth, Kastenmüller Gabi, Kato Bernet S, Mewes Hans-Werner, Meitinger Thomas, de Angelis Martin Hrabé, Kronenberg Florian, Soranzo Nicole, Wichmann H-Erich, Spector Tim D, Adamski Jerzy, Suhre Karsten. Nature genetics. 2010;42(2):137–41. doi: 10.1038/ng.507. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Biological, clinical and population relevance of 95 loci for blood lipids. Teslovich Tanya M, Musunuru Kiran, Smith Albert V, Edmondson Andrew C, Stylianou Ioannis M, Koseki Masahiro, Pirruccello James P, Ripatti Samuli, Chasman Daniel I, Willer Cristen J, Johansen Christopher T, Fouchier Sigrid W, Isaacs Aaron, Peloso Gina M, Barbalic Maja, Ricketts Sally L, Bis Joshua C, Aulchenko Yurii S, Thorleifsson Gudmar, Feitosa Mary F, Chambers John, Orho-Melander Marju, Melander Olle, Johnson Toby, Li Xiaohui, Guo Xiuqing, Li Mingyao, Shin Cho Yoon, Jin Go Min, Jin Kim Young, Lee Jong-Young, Park Taesung, Kim Kyunga, Sim Xueling, Twee-Hee Ong Rick, Croteau-Chonka Damien C, Lange Leslie A, Smith Joshua D, Song Kijoung, Hua Zhao Jing, Yuan Xin, Luan Jian'an, Lamina Claudia, Ziegler Andreas, Zhang Weihua, Zee Robert Y L, Wright Alan F, Witteman Jacqueline C M, Wilson James F, Willemsen Gonneke, Wichmann H-Erich, Whitfield John B, Waterworth Dawn M, Wareham Nicholas J, Waeber Gérard, Vollenweider Peter, Voight Benjamin F, Vitart Veronique, Uitterlinden Andre G, Uda Manuela, Tuomilehto Jaakko, Thompson John R, Tanaka Toshiko, Surakka Ida, Stringham Heather M, Spector Tim D, Soranzo Nicole, Smit Johannes H, Sinisalo Juha, Silander Kaisa, Sijbrands Eric J G, Scuteri Angelo, Scott James, Schlessinger David, Sanna Serena, Salomaa Veikko, Saharinen Juha, Sabatti Chiara, Ruokonen Aimo, Rudan Igor, Rose Lynda M, Roberts Robert, Rieder Mark, Psaty Bruce M, Pramstaller Peter P, Pichler Irene, Perola Markus, Penninx Brenda W J H, Pedersen Nancy L, Pattaro Cristian, Parker Alex N, Pare Guillaume, Oostra Ben A, O'Donnell Christopher J, Nieminen Markku S, Nickerson Deborah A, Montgomery Grant W, Meitinger Thomas, McPherson Ruth, McCarthy Mark I, McArdle Wendy, Masson David, Martin Nicholas G, Marroni Fabio, Mangino Massimo, Magnusson Patrik K E, Lucas Gavin, Luben Robert, Loos Ruth J F, Lokki Marja-Liisa, Lettre Guillaume, Langenberg Claudia, Launer Lenore J, Lakatta Edward G, Laaksonen Reijo, Kyvik Kirsten O, Kronenberg Florian, König Inke R, Khaw Kay-Tee, Kaprio Jaakko, Kaplan Lee M, Johansson Asa, Jarvelin Marjo-Riitta, Janssens A Cecile J W, Ingelsson Erik, Igl Wilmar, Kees Hovingh G, Hottenga Jouke-Jan, Hofman Albert, Hicks Andrew A, Hengstenberg Christian, Heid Iris M, Hayward Caroline, Havulinna Aki S, Hastie Nicholas D, Harris Tamara B, Haritunians Talin, Hall Alistair S, Gyllensten Ulf, Guiducci Candace, Groop Leif C, Gonzalez Elena, Gieger Christian, Freimer Nelson B, Ferrucci Luigi, Erdmann Jeanette, Elliott Paul, Ejebe Kenechi G, Döring Angela, Dominiczak Anna F, Demissie Serkalem, Deloukas Panagiotis, de Geus Eco J C, de Faire Ulf, Crawford Gabriel, Collins Francis S, Chen Yii-der I, Caulfield Mark J, Campbell Harry, Burtt Noel P, Bonnycastle Lori L, Boomsma Dorret I, Boekholdt S Matthijs, Bergman Richard N, Barroso Inês, Bandinelli Stefania, Ballantyne Christie M, Assimes Themistocles L, Quertermous Thomas, Altshuler David, Seielstad Mark, Wong Tien Y, Tai E-Shyong, Feranil Alan B, Kuzawa Christopher W, Adair Linda S, Taylor Herman A, Borecki Ingrid B, Gabriel Stacey B, Wilson James G, Holm Hilma, Thorsteinsdottir Unnur, Gudnason Vilmundur, Krauss Ronald M, Mohlke Karen L, Ordovas Jose M, Munroe Patricia B, Kooner Jaspal S, Tall Alan R, Hegele Robert A, Kastelein John J P, Schadt Eric E, Rotter Jerome I, Boerwinkle Eric, Strachan David P, Mooser Vincent, Stefansson Kari, Reilly Muredach P, Samani Nilesh J, Schunkert Heribert, Cupples L Adrienne, Sandhu Manjinder S, Ridker Paul M, Rader Daniel J, van Duijn Cornelia M, Peltonen Leena, Abecasis Gonçalo R, Boehnke Michael, Kathiresan Sekar. Nature. 2010;466(7307):707–13. doi: 10.1038/nature09270. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Human metabolic individuality in biomedical and pharmaceutical research. Suhre Karsten, Shin So-Youn, Petersen Ann-Kristin, Mohney Robert P, Meredith David, Wägele Brigitte, Altmaier Elisabeth, Deloukas Panos, Erdmann Jeanette, Grundberg Elin, Hammond Christopher J, de Angelis Martin Hrabé, Kastenmüller Gabi, Köttgen Anna, Kronenberg Florian, Mangino Massimo, Meisinger Christa, Meitinger Thomas, Mewes Hans-Werner, Milburn Michael V, Prehn Cornelia, Raffler Johannes, Ried Janina S, Römisch-Margl Werner, Samani Nilesh J, Small Kerrin S, Wichmann H-Erich, Zhai Guangju, Illig Thomas, Spector Tim D, Adamski Jerzy, Soranzo Nicole, Gieger Christian. Nature. 2011;477(7362):54–60. doi: 10.1038/nature10354. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Genome-wide association study identifies multiple loci influencing human serum metabolite levels. Kettunen Johannes, Tukiainen Taru, Sarin Antti-Pekka, Ortega-Alonso Alfredo, Tikkanen Emmi, Lyytikäinen Leo-Pekka, Kangas Antti J, Soininen Pasi, Würtz Peter, Silander Kaisa, Dick Danielle M, Rose Richard J, Savolainen Markku J, Viikari Jorma, Kähönen Mika, Lehtimäki Terho, Pietiläinen Kirsi H, Inouye Michael, McCarthy Mark I, Jula Antti, Eriksson Johan, Raitakari Olli T, Salomaa Veikko, Kaprio Jaakko, Järvelin Marjo-Riitta, Peltonen Leena, Perola Markus, Freimer Nelson B, Ala-Korpela Mika, Palotie Aarno, Ripatti Samuli. Nature genetics. 2012;44(3):269–76. doi: 10.1038/ng.1073. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Body mass index and poststroke mortality. Olsen Tom Skyhøj, Dehlendorff Christian, Petersen Hans Gregers, Andersen Klaus Kaae. Neuroepidemiology. 2008;30(2):93–100. doi: 10.1159/000118945. [DOI] [PubMed] [Google Scholar]
- 21.The impact of body mass index on mortality after stroke. Towfighi Amytis, Ovbiagele Bruce. Stroke. 2009;40(8):2704–8. doi: 10.1161/STROKEAHA.109.550228. [DOI] [PubMed] [Google Scholar]
- 22.Association between obesity and mortality after acute first-ever stroke: the obesity-stroke paradox. Vemmos Konstantinos, Ntaios George, Spengos Konstantinos, Savvari Paraskevi, Vemmou Anastasia, Pappa Theodora, Manios Efstathios, Georgiopoulos George, Alevizaki Maria. Stroke. 2011;42(1):30–6. doi: 10.1161/STROKEAHA.110.593434. [DOI] [PubMed] [Google Scholar]
- 23.Obesity and recurrent vascular risk after a recent ischemic stroke. Ovbiagele Bruce, Bath Philip M, Cotton Daniel, Vinisko Richard, Diener Hans-Christoph. Stroke. 2011;42(12):3397–402. doi: 10.1161/STROKEAHA.111.624957. [DOI] [PubMed] [Google Scholar]
- 24.The obesity paradox in stroke: lower mortality and lower risk of readmission for recurrent stroke in obese stroke patients. Andersen Klaus Kaae, Olsen Tom Skyhøj. International journal of stroke : official journal of the International Stroke Society. 2015;10(1):99–104. doi: 10.1111/ijs.12016. [DOI] [PubMed] [Google Scholar]
- 25.Body mass index, initial neurological severity and long-term mortality in ischemic stroke. Ryu Wi-Sun, Lee Seung-Hoon, Kim Chi Kyung, Kim Beom Joon, Yoon Byung-Woo. Cerebrovascular diseases (Basel, Switzerland) 2011;32(2):170–6. doi: 10.1159/000328250. [DOI] [PubMed] [Google Scholar]
- 26.Favorable functional recovery in overweight ischemic stroke survivors: findings from the China National Stroke Registry. Zhao Lu, Du Wanliang, Zhao Xingquan, Liu Liping, Wang Chunxue, Wang Yilong, Wang Anxin, Liu Gaifen, Wang Yongjun, Xu Yuming. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association. 2014;23(3):e201–6. doi: 10.1016/j.jstrokecerebrovasdis.2013.10.002. [DOI] [PubMed] [Google Scholar]
- 27.Effect of body mass index on stroke rehabilitation. Burke David T, Al-Adawi Samir, Bell Regina B, Easley Kirk, Chen Shou, Burke Daniel P. Archives of physical medicine and rehabilitation. 2014;95(6):1055–9. doi: 10.1016/j.apmr.2014.01.019. [DOI] [PubMed] [Google Scholar]
- 28.[Obesity paradox and functional recovery in first-ever acute ischemic stroke survivors: the PREMIER study]. Chiquete Erwin, Cantú-Brito Carlos, Villarreal-Careaga Jorge, Murillo-Bonilla Luis M, Rangel-Guerra Ricardo, León-Jiménez Carolina, Ochoa-Guzmán Ana, Ramos-Moreno Alma, Arauz Antonio, Barinagarrementeria Fernando, Panduro Arturo, Ruiz-Sandoval José L. Revista de neurologia. 2010;51(12):705–13. [PubMed] [Google Scholar]
- 29.Impact of patient's weight on stroke rehabilitation results. Kalichman Leonid, Rodrigues Biana, Gurvich Diana, Israelov Ziva, Spivak Elina. American journal of physical medicine & rehabilitation. 2007;86(8):650–5. doi: 10.1097/PHM.0b013e318115f41b. [DOI] [PubMed] [Google Scholar]
- 30.Body mass index and hospital discharge outcomes after ischemic stroke. Razinia Tannaz, Saver Jeffrey L, Liebeskind David S, Ali Latisha K, Buck Brian, Ovbiagele Bruce. Archives of neurology. 2007;64(3):388–91. doi: 10.1001/archneur.64.3.388. [DOI] [PubMed] [Google Scholar]
- 31.Incidence and risk factors for subtypes of cerebral infarction in a general population: the Hisayama study. Tanizaki Y, Kiyohara Y, Kato I, Iwamoto H, Nakayama K, Shinohara N, Arima H, Tanaka K, Ibayashi S, Fujishima M. Stroke. 2000;31(11):2616–22. doi: 10.1161/01.str.31.11.2616. [DOI] [PubMed] [Google Scholar]
- 32.Neural injury following stroke: are Toll-like receptors the link between the immune system and the CNS? Downes Catherine E, Crack Peter J. British journal of pharmacology. 2010;160(8):1872–88. doi: 10.1111/j.1476-5381.2010.00864.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.The myeloid cells of the central nervous system parenchyma. Ransohoff Richard M, Cardona Astrid E. Nature. 2010;468(7321):253–62. doi: 10.1038/nature09615. [DOI] [PubMed] [Google Scholar]
- 34.Autoimmune responses to the brain after stroke are associated with worse outcome. Becker Kyra J, Kalil Angela J, Tanzi Pat, Zierath Dannielle K, Savos Anna V, Gee J Michael, Hadwin Jessica, Carter Kelly T, Shibata Dean, Cain Kevin C. Stroke. 2011;42(10):2763–9. doi: 10.1161/STROKEAHA.111.619593. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Peripheral lipopolysaccharide (LPS) challenge promotes microglial hyperactivity in aged mice that is associated with exaggerated induction of both pro-inflammatory IL-1beta and anti-inflammatory IL-10 cytokines. Henry Christopher J, Huang Yan, Wynne Angela M, Godbout Jonathan P. Brain, behavior, and immunity. 2009;23(3):309–17. doi: 10.1016/j.bbi.2008.09.002. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Systemic inflammation switches the inflammatory cytokine profile in CNS Wallerian degeneration. Palin Karine, Cunningham Colm, Forse Penny, Perry V Hugh, Platt Nick. Neurobiology of disease. 2008;30(1):19–29. doi: 10.1016/j.nbd.2007.11.012. [DOI] [PubMed] [Google Scholar]
- 37.Early-life programming of later-life brain and behavior: a critical role for the immune system. Bilbo Staci D, Schwarz Jaclyn M. Frontiers in behavioral neuroscience. 2009;3:14. doi: 10.3389/neuro.08.014.2009. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Systemic inflammation induces acute working memory deficits in the primed brain: relevance for delirium. Murray Carol, Sanderson David J, Barkus Chris, Deacon Robert M J, Rawlins J Nicholas P, Bannerman David M, Cunningham Colm. Neurobiology of aging. 2012;33(3):603–616.e3. doi: 10.1016/j.neurobiolaging.2010.04.002. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39.Central and systemic endotoxin challenges exacerbate the local inflammatory response and increase neuronal death during chronic neurodegeneration. Cunningham Colm, Wilcockson David C, Campion Suzanne, Lunnon Katie, Perry V Hugh. The Journal of neuroscience : the official journal of the Society for Neuroscience. 2005;25(40):9275–84. doi: 10.1523/JNEUROSCI.2614-05.2005. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Age and neuroinflammation: a lifetime of psychoneuroimmune consequences. Godbout Jonathan P, Johnson Rodney W. Neurologic clinics. 2006;24(3):521–38. doi: 10.1016/j.ncl.2006.03.010. [DOI] [PubMed] [Google Scholar]
- 41.Aging, microglial cell priming, and the discordant central inflammatory response to signals from the peripheral immune system. Dilger Ryan N, Johnson Rodney W. Journal of leukocyte biology. 2008;84(4):932–9. doi: 10.1189/jlb.0208108. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Major depression, C-reactive protein, and incident ischemic heart disease in healthy men and women. Surtees Paul G, Wainwright Nicholas W J, Boekholdt S Matthijs, Luben Robert N, Wareham Nicholas J, Khaw Kay-Tee. Psychosomatic medicine. 2008;70(8):850–5. doi: 10.1097/PSY.0b013e318183acd5. [DOI] [PubMed] [Google Scholar]
- 43.The inflammatory & neurodegenerative (I&ND) hypothesis of depression: leads for future research and new drug developments in depression. Maes Michael, Yirmyia Raz, Noraberg Jens, Brene Stefan, Hibbeln Joe, Perini Giulia, Kubera Marta, Bob Petr, Lerer Bernard, Maj Mario. Metabolic brain disease. 2009;24(1):27–53. doi: 10.1007/s11011-008-9118-1. [DOI] [PubMed] [Google Scholar]
- 44.The vascular depression hypothesis: mechanisms linking vascular disease with depression. Taylor W D, Aizenstein H J, Alexopoulos G S. Molecular psychiatry. 2013;18(9):963–74. doi: 10.1038/mp.2013.20. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 45.Neuropsychiatric Adverse Effects of Interferon-alpha: recognition and management. Raison Charles L, Demetrashvili Marina, Capuron Lucile, Miller Andrew H. CNS Drugs. 2005;19(2):105–123. doi: 10.2165/00023210-200519020-00002. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 46.Middle-aged, but not young, rats develop cognitive impairment and cortical neurodegeneration following the four-vessel occlusion/internal carotid artery model of chronic cerebral hypoperfusion. Ferreira Emilene D. Fiuza, Romanini Cássia V., Mori Marco A., de Oliveira Rúbia M. Weffort, Milani Humberto. European Journal of Neuroscience. 2011;34(7):1131-1140. doi: 10.1111/j.1460-9568.2011.07824.x. [DOI] [PubMed] [Google Scholar]
- 47.Neuroinflammation and Comorbidity of Pain and Depression. Walker A. K., Kavelaars A., Heijnen C. J., Dantzer R. Pharmacological Reviews. 2013;66(1):80-101. doi: 10.1124/pr.113.008144. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 48.Depression is an inflammatory disease, but cell-mediated immune activation is the key component of depression. Maes Michael. Progress in Neuro-Psychopharmacology and Biological Psychiatry. 2011;35(3):664-675. doi: 10.1016/j.pnpbp.2010.06.014. [DOI] [PubMed] [Google Scholar]
- 49.Inflammation, Depression and Dementia: Are they Connected? Leonard Brian E. Neurochemical Research. 2007;32(10):1749-1756. doi: 10.1007/s11064-007-9385-y. [DOI] [PubMed] [Google Scholar]
- 50.Neuroinflammation: implications for the pathogenesis and molecular diagnosis of Alzheimer's disease. Rojo Leonel E, Fernández Jorge A, Maccioni Andrea A, Jimenez José M, Maccioni Ricardo B. Archives of medical research. 2008;39(1):1–16. doi: 10.1016/j.arcmed.2007.10.001. [DOI] [PubMed] [Google Scholar]
- 51.Depression and risk of developing dementia. Byers Amy L, Yaffe Kristine. Nature reviews. Neurology. 2011;7(6):323–31. doi: 10.1038/nrneurol.2011.60. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.Rapid disruption of axon-glial integrity in response to mild cerebral hypoperfusion. Reimer Michell M, McQueen Jamie, Searcy Luke, Scullion Gillian, Zonta Barbara, Desmazieres Anne, Holland Philip R, Smith Jessica, Gliddon Catherine, Wood Emma R, Herzyk Pawel, Brophy Peter J, McCulloch James, Horsburgh Karen. The Journal of neuroscience : the official journal of the Society for Neuroscience. 2011;31(49):18185–94. doi: 10.1523/JNEUROSCI.4936-11.2011. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 53.Cerebral hypoperfusion accelerates cerebral amyloid angiopathy and promotes cortical microinfarcts. Okamoto Yoko, Yamamoto Toru, Kalaria Raj N, Senzaki Hideto, Maki Takakuni, Hase Yoshiki, Kitamura Akihiro, Washida Kazuo, Yamada Mahito, Ito Hidefumi, Tomimoto Hidekazu, Takahashi Ryosuke, Ihara Masafumi. Acta neuropathologica. 2012;123(3):381–94. doi: 10.1007/s00401-011-0925-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 54.Diabetes and the risk of multi-system aging phenotypes: a systematic review and meta-analysis. Lu Feng-Ping, Lin Kun-Pei, Kuo Hsu-Ko. PloS one. 2009;4(1):e4144. doi: 10.1371/journal.pone.0004144. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 55.Is Depression a Risk Factor for Dementia or Cognitive Decline? Jorm A.F. Gerontology. 2000;46(4):219-227. doi: 10.1159/000022163. [DOI] [PubMed] [Google Scholar]
- 56.Depression and risk for Alzheimer disease: systematic review, meta-analysis, and metaregression analysis. Ownby Raymond L, Crocco Elizabeth, Acevedo Amarilis, John Vineeth, Loewenstein David. Archives of general psychiatry. 2006;63(5):530–8. doi: 10.1001/archpsyc.63.5.530. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 57.The prevalence of co-morbid depression in adults with Type 2 diabetes: a systematic review and meta-analysis. Ali S, Stone M A, Peters J L, Davies M J, Khunti K. Diabetic medicine : a journal of the British Diabetic Association. 2006;23(11):1165–73. doi: 10.1111/j.1464-5491.2006.01943.x. [DOI] [PubMed] [Google Scholar]
- 58.Association of depression with increased risk of dementia in patients with type 2 diabetes: the Diabetes and Aging Study. Katon Wayne, Lyles Courtney R, Parker Melissa M, Karter Andrew J, Huang Elbert S, Whitmer Rachel A. Archives of general psychiatry. 2012;69(4):410–7. doi: 10.1001/archgenpsychiatry.2011.154. [DOI] [PMC free article] [PubMed] [Google Scholar]

