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At least 19 recordsLinked to original sources

Promotion of the use of a thermoplastic material to aid in the identification of unidentified human remains.

There has been a recent effort to promote the use of a thermoplastic bite impression material for the identification of children. The American Board of Forensic Odontology is a certification board for forensic dentists in the United States and Canada. It is the position of the ABFO that this technique is of limited value when used for the dental identification of children. A presentation was made to the Odontology Section of the American Academy of Forensic Sciences in Dallas, Texas, in February 2004. The presentation promoted the use of a thermoplastic material to record the morphology of the human dentition for use by qualified personnel to identify missing persons. Currently, the target population for the recording of this information is children. In addition to recording the morphology of the dentition, the presenter claimed that the material, properly stored after impressing the teeth, could also be used as a source of DNA for identification purposes, as well as a source of the individual's scent to be used by tracking dogs. The weeks and months following this presentation generated significant comments and concerns regarding the information presented amongst members of the ABFO and members of the Odontology Section of AAFS. It was suggested that the ABFO look into this tooth impression method and comment on its validity and usefulness in the identification process. The following comments regarding this method have been formulated following significant input from diplomates of the ABFO. The ABFO is a certifying organization for dentists who wish to become board certified in the field of forensic odontology, and as such, requires its diplomates to maintain significant experience in the use of the human dentition for identification purposes. The ABFO also has a mission to promote and enhance the science of forensic odontology. As the ABFO primarily deals with the dentition, the comments in this paper will be confined to the use of the thermoplastic material as it relates to the dental identification process. Experts in DNA analysis and tracking should address the issues of DNA and scent.

Bites, Human↗

Oral autopsy of unidentified burned human remains. A new procedure.

Forensic dentistry plays an increasingly important role in medicolegal investigation and identification procedures. The oral examination may be difficult because of postmortem changes, especially those of carbonized corpses. We present a new technique of oral autopsy that includes a new means of access to the oral cavity designed for application on unidentified burned human remains. This technique preserves the facial configuration of the cadaver, allowing visual recognition by family members or other persons that is fundamental if the antemortem dental records do not exist or are not available. Also, this technique permits adequate work productivity by the forensic team members and can be used in difficult working conditions, such as mass-disaster scenarios.

Autopsy↗

Identification of missing persons: the Spanish "Phoenix" program.

In 1999, Spain was the first country to officially start a National Program to try to identify cadavers and human remains which could not be identified by the use of traditional forensic approaches. This attempt is called "Phoenix Program". Two independent mitochondrial DNA (mtDNA) databases were generated, which can automatically compare and match identical or similar sequences. One is the Reference Database, with mtDNA sequences from maternal relatives of missing persons, who provide the samples (buccal swabs) voluntarily; the other is the Questioned Database, comprised of mtDNA data of unknown remains and cadavers. Although the first phase of the program (typing of all unidentified human remains) will probably not be completed until December 2003, positive identifications are being made in the interim. To date, more than 1,200 families have contacted Phoenix, and at least 280 reference samples and 48 questioned evidences have been analyzed. When mtDNA matches are found, another independent analysis is performed as a part of the quality control mechanism. Once a match is confirmed (so far in 6 cases), an attempt is made to analyze short tandem repeat (STR) loci. We call for international collaboration to make this effort valuable worldwide.

Cadaver↗

Digital imaging methods as an aid in dental identification of human remains.

The physical comparison of known (K) and questioned (Q) evidence samples is an accepted tool in numerous forensic identification disciplines (1). A subset of this process is the use of antemortem and postmortem dental radiographs to identify unidentified human remains. This method has been generally accepted for decades (2). The outcome is performed with a considerable degree of accuracy, due in part to a finite pool of possible candidates for identification derived via the NCIC database, passenger lists, and law enforcement Missing Persons reports. This paper describes a dental identification comparison protocol that incorporated digital imaging technology in this process. The computer was used to create digital exemplars of the K and Q evidence that were spatially and quantitatively compared (3). The digital mode allowed direct metric and morphologic comparison through the aid of a digital camera, desktop computer, monitor, and printer. The well-known computer program Adobe Photoshop 5.0 (4) was used to process the digital information in two forensic cases described in this paper. It is a commercially available digital imaging editing program that is operated on laptop and desktop computers possessing sufficient chip speed and RAM (Pentium II or equivalent and at least 76MB RAM) to open the large-size files generated by high-resolution digital capture devices. This program accepts raster-based image formats (e.g. .JPG, .BMP). Photoshop is noted for its diverse imaging functions, which allow the computer monitor to be used as a comparison microscope when Q and K sample images are tiled side-by-side and/or superimposed. Two and three-dimensional Q and K evidence samples can be individually digitized and then independently resized to allow two-dimensional comparison. The investigator also has the ability to create magnified images (200% to 300%) when the original digital image has been captured at near photoquality resolution (300 dpi). The visual comparison of physical features on the computer monitor permits a large field of view and robust digital control over image quality. Photographic measurement and enhancement features of Adobe Photoshop mimics and in some circumstances surpasses the historic use of conventional photographic manipulation in forensic casework. This paper presents two cases processed via routine forensic odontology identification protocols. These protocols had minimal results due to limitations described in the case histories. The additional application of digital methods proved useful in the ultimate identification of these human remains.

Adolescent↗

Fluvial transport of human remains in the lower Mississippi River.

The Mississippi River has claimed many lives over the last several decades. A better understanding of the universal dynamics of its fluvial system can help direct the production of a predictive model regarding the transportation of human remains in the river. The model may then be applied to situations where the location and the identification of water victims are necessarily part of the recovery process. Results from the preliminary phase of a longitudinal project involving the transport of human remains in the Mississippi River are presented and represent the analyses of 233 case files of river victims. A provisional model for fluvial transport of human remains in the Mississippi River is proposed and examined. This model indicates that time in the river and distance a body travels are related. Such a model may assist in pinpointing entry location for unidentified human remains found in the river or on its banks. Further, it has the potential to provide local and regional law enforcement agencies, the United States Coast Guard, and other search and rescue organizations with primary search areas when someone is missing in the river. Other results from this study indicate that a relationship exists between the side of the river where victims enter the water and the side of the river where the remains are recovered. Finally, relationships are established between the length of time before recovery of the remains and state of preservation exhibited by those remains. A secondary benefit from this study is a database of river victims that can be used by a variety of different agencies.

Adolescent↗

Clinical investigation of the relationship between Borna disease virus (BDV) infection and schizophrenia in 67 patients in Japan.

The relationship between Borna disease virus (BDV) infection and schizophrenia in the clinical time course was investigated. By nested reverse-transcribed polymerase chain reaction (RT-PCR) and Western blotting, BDV-specific RNA and anti-BDV antibodies were examined in the EDTA-treated blood from 67 schizophrenic patients (according to DSM-III-R) in Japan. A significantly higher proportion (45%) of anti-BDV antibody and/or BDV RNA carriers were found among these 67 schizophrenic patients than in 26 controls (0%). There were no apparent associations of BDV infection with age, age at onset, period of hospitalization, accompanying somatic diseases, a past history of tuberculosis, a history of transfusion, a family history, or doses of psychotropic drugs. It is possible that, at least, BDV infection in schizophrenic patients may not be a nosocomial (hospital-acquired) infection, although the route of BDV infection in humans remains unidentified. More studies on the relationship between BDV infection and clinical psychosomatic features should be performed in order to elucidate the pathogenesis of schizophrenia.

Animals↗

Briefly unidentified: a study of a peculiar source of identification.

In May of 1992, unidentified human remains were received at the C.A. Pound Human Identification Laboratory, University of Florida, Gainesville, Florida for identification. The decedent was identified as a white female in her early sixties between 62 and 63 in. in stature. Significant trauma was observed at various skeletal sites. The identity of the decedent was meant to be obscured due to the decapitation of the head and removal of the lower arms including the hands. Examination of the clothing revealed that the first initial and last name of the decedent had been written in ink inside the label of the underpants. Subsequently, this information was matched with missing persons reports. Identification of the decedent was confirmed by comparison of antemortem and postmortem radiographs.

Clavicle↗

Support for the use of thermoplastic bite impressions to aid in the identification of missing and unknown children.

This paper presents a response to the editorial opinion expressed in the position paper "Promotion of the Use of a Thermoplastic Material to Aid in the Identification of Unidentified Human Remains," published on page 14 of this issue of the JOURNAL OF THE MASSACHUSETTS DENTAL SOCIETY. No references were cited in that paper: Because the mission of the American Board of Forensic Odontology (ABFO) is to "promote and enhance the science of forensic odontology" and realizing that the ABFO Guidelines on bite mark evidence has failed law enforcement in several high-profile cases in the past, it is necessary to publish a referenced response addressing some of the statements that were made in the ABFO article.

Child↗

Racial identification from the midfacial skeleton with special reference to American Indians and whites.

Successful approaches to race determination of unidentified human remains have been developed by anatomists and physical anthropologists, but few quantitative methods are available for distinguishing American Indian crania from those of whites. The leading method in use today is particularly ineffective in its placement of American Indian skulls from the western regions of the United States. Recent development and testing of a new metric method suggests a much more effective technique. The method involves six breadth and projection measurements of the midfacial skeleton, the calculation of three indices, and a simple direct reading of results. The method has the additional advantage of use in the autopsy room with minimal dissection of soft tissue required. Based upon a less extensive test of East Asian and Arctic Mongoloid crania, the method appears to be even more effective in separating them from the sharp featured whites. Larger samples of American blacks and Polynesians are presently under study and these also appear to separate quite readily from whites using the same or similar sectioning values.

Cephalometry↗

Estimation of age at death using cortical histomorphometry of the sternal end of the fourth rib.

Given the often fragmentary nature of unidentified human remains, and the importance of using multiple criteria to estimate age at death, it is essential to have a variety of methods that use different anatomical sampling sites. In this study, osteon population densities (OPDs) were determined from transverse sections removed from an area immediately adjacent to the sternal ends of 60 autopsy rib samples. Regression analysis was performed using age at death as the dependent variable and OPD as the independent variable. The results of a "training set/test set" strategy to evaluate the performance of the histological age predicting model indicates that it provides reasonably reliable and accurate age estimates. A multiple regression model using both OPD and the mean age for a rib's morphological age according to the phase method of Işcan et al. [7,8] is also presented. This later age predicting model is recommended when both methods are applicable.

Adult↗

The detection of morphine and codeine in human teeth: an aid in the identification and study of human skeletal remains.

When studying unidentified putrefied or skeletonised human remains it may be difficult to obtain information on drug habits which may prove important for the construction of a biological profile or lead to hypotheses on the manner of death. The detection of morphine and codeine in teeth from human remains may prove crucial in obtaining such information and thus give forensic odontology and anthropology a further tool for identification. Because teeth can be an important deposit of exogenous substances accumulated both in the pulp and in the calcified tissues, they are an invaluable source of data from a toxicological point of view. The authors therefore tested 3 groups of teeth for morphine and codeine: the first group consisted of artificially aged teeth from individuals known to have died of heroin overdose; the second, of teeth from individuals with no history of drug abuse; the third, of teeth from cases of burnt, putrefied and skeletonised remains found in conditions strongly suggestive of a drug-related death. Results showed that in groups 1 and 3 morphine and codeine could still be identified in the teeth, proving that these tissues may be a reliable source for toxicological information concerning the history of the individual. Further studies are needed to verify whether the substances detected reflect drugs in circulation in an acute phase (and therefore present in blood vessels in the pulp) or whether they represent drugs which have percolated and been stored in dentine and enamel and thus denote a history of drug abuse. Nonetheless this study shows that teeth may be an important source of toxicological information in the forensic scenario.

Adult↗

Evaluation of bone preparation approaches using length-based analysis and targeted sequencing for forensic human identification of historic skeletal remains.

Advances in DNA technology have significantly enhanced the forensic community's ability to develop genetic profiles from unidentified human skeletal remains. However, sampling requires mechanical grinding of hard tissues before DNA isolation. This processing can compromise genetic profiles, particularly in aged bones. We compared the industry-standard pulverization method with an alternative powder-free preparation involving prolonged demineralization and subsequent slicing of 19th-century cortical bone. Data from DNA quantification, STR genotyping, and targeted SNP sequencing were used to evaluate powdered samples versus demineralized slices from paired human bones. Average human DNA yields for pulverized samples and demineralized slices were 0.032&#x2009;ng and 0.692&#x2009;ng, respectively. Demineralized slices recovered more amplifiable DNA than traditional homogenization methods (p&#x2009;<&#x2009;0.05). No pulverized samples produced STR profiles, whereas demineralized slices from the same bone samples yielded partial profiles. Samples underwent DNA repair, library preparation, and hybridization capture using the FORensic Capture Enrichment (FORCE) panel. Applying low-coverage (1X) analysis of high-throughput sequencing (HTS) data, demineralized slices outperformed those prepared by traditional pulverization methods (p&#x2009;<&#x2009;0.05) and substantially increased the information recovered compared with conventional STR analysis methods. Based on HTS data from pulverized samples, DNA fragment length ranged from 27 to 95&#x2009;bp, and FORCE SNP recovery was 33.23%. In contrast, for demineralized slices, DNA fragment length ranged from 85 to 114&#x2009;bp, and FORCE SNP recovery was 83.24%. The required reagents and equipment are typically available in forensic labs, and the workflow outlined herein significantly increases the success of DNA recovery from challenging skeletal samples.

Humans↗

Identification of decomposed human remains by deoxyribonucleic acid (DNA) profiling.

After routine methods failed to establish positive identification of a decomposed homicide victim, deoxyribonucleic acid (DNA) typing techniques using blood from the victim and putative parents of the victim were used. This is the first report in the literature of a case using DNA fingerprinting in a "parentage" context to establish identity of unidentified, decomposed human remains.

DNA↗

Analysis of human sodium iodide symporter gene expression in extrathyroidal tissues and cloning of its complementary deoxyribonucleic acids from salivary gland, mammary gland, and gastric mucosa.

The ability to concentrate iodide is a fundamental property of normally functioning thyroid tissue and represents the first step in the production of thyroid hormones. Iodide uptake has been demonstrated in various extrathyroidal tissues, including salivary gland, gastric mucosa, and lactating mammary gland. Recently, cloning and molecular characterization of the human sodium iodide symporter (hNIS) have been reported; however, the patterns of hNIS gene expression in human tissues have remained unidentified. To examine the profiles of human hNIS gene expression in various normal human tissues, we performed high-stringency Northern blot analysis using a 32P-labeled hNIS-specific complementary DNA (cDNA) probe (nucleotides 1184-1667). To detect rare hNIS transcripts in small tissue samples, RT-PCR was performed with a pair of hNIS-specific oligonucleotide primers designed to amplify a portion (nucleotides 1184-1667) of the hNIS gene. hNIS-specific transcripts were confirmed by Southern hybridization using a digoxigenin-labeled internal hNIS-specific oligonucleotide probe (nucleotides 1460-1477). To monitor cDNA integrity and quantity, and to rule out DNA contamination and illegitimate transcription, all samples were coamplified with two pairs of intron-spanning primers designed to amplify fragments of the human beta-actin and thyroglobulin genes, respectively. Using Northern blot analysis, hNIS transcripts of approximately 4 kb were detected in thyroid gland and parotid gland but not in a broad range of endocrine and nonendocrine tissues. RT-PCR and Southern hybridization revealed hNIS gene expression in thyroid gland, salivary gland, parotid gland, submandibular gland, pituitary gland, pancreas, testis, mammary gland, gastric mucosa, prostate and ovary, adrenal gland, heart, thymus, and lung. By contrast, hNIS transcripts were not detected in normal orbital fibroblasts, colon, and nasopharyngeal mucosa. To further analyze hNIS gene sequences in parotid gland, mammary gland, and gastric mucosa, the EXPAND High Fidelity PCR System and three sets of overlapping NIS oligonucleotide primers were used for amplification and cloning. The resulting PCR products were subcloned into pBluescript-SKII(-)vector, and at least two independent cDNA clones derived from each tissue were subjected to automated sequencing. The nucleotide sequences of hNIS cDNA derived from parotid gland, mammary gland, and gastric mucosa revealed full identity with the recently published human thyroid-derived NIS cDNA sequence. In conclusion, our results demonstrate markedly variable levels of hNIS gene expression in several extrathyroidal tissues. Although the physiological role of hNIS in these tissues awaits further study, our results suggest that the capacity to actively transport iodine may be a feature common to several secretory and endocrine tissues. The diminished capacity to transport and concentrate iodide in extrathyroidal tissues (such as parotid gland, mammary gland, and gastric mucosa), compared with thyroid gland, does not seem to be caused by an altered primary structure of the hNIS cDNA. Variability of NIS gene expression levels in normal extrathyroidal tissues may rather be caused by differences in NIS gene transcriptional activity. Further studies will address this hypothesis and examine the mechanisms of tissue-specific regulation of NIS gene expression.

Blotting, Northern↗

Molecular manipulation of G-protein-coupled receptors: a new avenue into drug discovery.

During the past 10 years or so, associated with the introduction of molecular biology techniques to G protein-coupled receptor (GPCR) research, outstanding progress has been made in understanding the mechanisms of action of these key proteins and their physiological functions. in-vivo manipulation of levels of GPCRs using transgenic and gene knock-out approaches have been particularly successful in assessing the roles of specific GPCRs in animal physiology. Drug discovery is aiming to produce highly specific compounds based on subtle definition of receptor subtypes which can best be studied using heterologous expression of wild type or mutated forms of cDNA or genes encoding these proteins. Furthermore, new therapeutic opportunities may be provided by investigation of orphan receptors, the natural ligands for which remain unidentified. Some human diseases have been shown to be associated with rare mutations of GPCRs and the possibility that widely distributed polymorphisms in GPCR genes may allow selective therapeutic strategies for population subgroups is driving the development of the science of pharmacogenetics.

Animals↗