﻿<?xml version="1.0" encoding="utf-8"?><rss version="2.0"><channel><title>Current Gerontology and Geriatrics Research</title><link>http://www.hindawi.com</link><description>The latest articles from Hindawi Publishing Corporation</description><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright><item><title>Thyroid Function and Cognition during Aging</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/2008/474868</link><description>We summarize here the studies examining the association between thyroid function and
 cognitive performance from an aging perspective. The available data suggest that there may be a continuum
  in which cognitive dysfunction can result from increased or decreased concentrations of thyroid 
  hormones. Clinical and subclinical hypothyroidism as well as hyperthyroidism in middle-aged and elderly 
  adults are both associated with decreased cognitive functioning, especially memory, visuospatial organization, 
  attention, and reaction time.  Mild variations of thyroid function, even within normal limits, can have significant 
  consequences for cognitive function in the elderly. Different cognitive deficits possibly related to thyroid failure 
  do not necessarily follow a consistent pattern, and L-thyroxine treatment may not always completely restore 
  normal functioning in patients with hypothyroidism.  There is little or no consensus in the literature regarding 
  how thyroid function is associated with cognitive performance in the elderly.</description><Author>M. E. B&amp;#233;gin, M. F. Langlois, D. Lorrain, and S. C. Cunnane</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>Personality Characteristics Determine Health-Related 
                        Quality of Life as an Outcome Indicator of Geriatric Inpatient Rehabilitation</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/2008/474618</link><description>Background. The aim of the present study was to investigate the relationships
                    between personality and quality of life during the course of geriatric rehabilitation, against the 
                    background of Cloninger&amp;#39;s biosocial theory of personality. Methods. All 
                    consecutive patients of a geriatric rehabilitation clinic during one year were evaluated at admission 
                    and discharge (N=687) by means of the &amp;#8216;&amp;#8216;Vienna List&amp;#8217;&amp;#8217; (a newly developed questionnaire 
for the assessment of quality of life in patients with severe dementia), and two variants of the Temperament and
 Character Inventory. 
Results. Self-directedness showed the most general and highest impact on quality of life 
and successful rehabilitation. Conclusions. It is probable in old and very old individuals who 
are on their highest level of maturity that the character represents the most important regulatory system in 
the encounter with challenges of daily life, which necessitates rehabilitation.</description><Author>J&amp;#246;rg Richter, Martina Schwarz, and Barbara Bauer</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>Cobalamin Deficiency in Elderly Patients: A Personal View</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/2008/848267</link><description>Cobalamin (vitamin B12) deficiency is particularly common in the elderly (&amp;#x0003E;65 years of age) but is often unrecognized because its clinical manifestations are subtle; however, they are also potentially serious, particularly from a neuropsychiatric and hematological perspective. In the elderly, the main causes of cobalamin deficiency are pernicious anemia and food-cobalamin malabsorption. Food-cobalamin malabsorption syndrome is a disorder characterized by the inability to release cobalamin from food or its binding proteins. This syndrome is usually caused by atrophic gastritis, related or unrelated to Helicobacter pylori infection, and long-term ingestion of antacids and biguanides. Management of cobalamin deficiency with cobalamin injections is currently well documented but new routes of cobalamin administration (oral and nasal) are being studied, especially oral cobalamin therapy for food-cobalamin malabsorption.</description><Author>Emmanuel Andr&amp;#x00E8;s, Thomas Vogel, Laure Federici, Jacques Zimmer, &lt;?layout cmd="newline"?&gt; Ecaterina Ciobanu, and Georges Kaltenbach</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>Deficiency in Poly(ADP-ribose) Polymerase-1 (PARP-1) Accelerates Aging and Spontaneous Carcinogenesis in Mice</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/2008/754190</link><description>Genetic and biochemical studies have shown that PARP-1 and poly(ADP-ribosyl)ation play an important role in DNA repair, genomic stability, cell death, inflammation, telomere maintenance, and suppressing tumorigenesis, suggesting that the homeostasis of poly(ADP-ribosyl)ation and PARP-1 may also play an important role in aging. Here we show that PARP-1-/- mice exhibit a reduction of life span and a significant increase of population aging rate. Analysis of noninvasive parameters, including body weight gain, body temperature, estrous function, behavior, and a number of biochemical indices suggests the acceleration of biological aging in PARP-1-/- mice. The incidence of spontaneous tumors in both PARP-1-/- and PARP-1+/+ groups is similar; however, malignant tumors including uterine tumors, lung adenocarcinomas and hepatocellular carcinomas, develop at a significantly higher frequency in PARP-1-/- mice than PARP-1+/+ mice (72&amp;#37; and 49&amp;#37;, resp.; P&amp;#x003C; .05). In addition, spontaneous tumors appear earlier in PARP-1-/- mice compared to the wild type group. Histopathological studies revealed a wide spectrum of tumors in uterus, ovaries, liver, lungs, mammary gland, soft tissues, and lymphoid organs in both groups of the mice. These results demonstrate that inactivation of DNA repair gene PARP-1 in mice leads to acceleration of aging, shortened life span, and increased spontaneous carcinogenesis.</description><Author>Tatiana S. Piskunova, Maria N. Yurova, Anton I. Ovsyannikov, Anna V. Semenchenko, Mark A. Zabezhinski, Irina G. Popovich, Zhao-Qi Wang, and Vladimir N. Anisimov</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item></channel></rss>