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  1. Article ; Online: Congenital hypothyroidism after newborn screening program reorganization in the Apulia region.

    Simonetti, Simonetta / D'Amato, Gabriele / Esposito, Benedetta / Chiarito, Mariangela / Dentico, Domenico / Lorè, Tania / Cardinali, Roberta / Russo, Silvia / Laforgia, Nicola / Faienza, Maria Felicia

    Italian journal of pediatrics

    2022  Volume 48, Issue 1, Page(s) 131

    Abstract: Background: Congenital hypothyroidism (CH) is the most frequent congenital endocrine disorder. The purpose of the present study was to evaluate the incidence and etiological classification of CH in Apulia in a three-year period according to the ... ...

    Abstract Background: Congenital hypothyroidism (CH) is the most frequent congenital endocrine disorder. The purpose of the present study was to evaluate the incidence and etiological classification of CH in Apulia in a three-year period according to the reorganization of the regional screening program in a single central laboratory, as well as to analyze the growth characteristics and the associated risk factors of the CH newborns diagnosed during the study period.
    Methods: Data derived from the reorganization of the newborn screening program for CH in a single central laboratory that collects dried blood spot (DBS) from 27 Maternity Hospitals are analyzed over a three-year period. Birth weight and length, daily dose of L-T4 at specific key points (3, 6, 12 and 18 months, 2, 2.5 and 3 years) were also obtained from medical records of the CH newborns during the study period and calculated as standard deviation score (SDS).
    Results: The screening program diagnosed 90 newborns with confirmed CH (incidence 1:990; recall rate: 3.6%). In detail, 75.6% newborns had an eutopic thyroid, and 24.4% had thyroid dysgenesis; 33 out of the 90 newborns (36.6%) had one or more risk factors. Among these, the multiple pregnancies are the most important because they tripled the risk of CH. At diagnosis, TSH levels were different between patients with dysgenesis and those with an eutopic thyroid (p = 0.005). Treatment was started at a mean of 18.5 ± 12.8 days of life. The mean starting dose of levothyroxine (L-T4) was 11.38 ± 2.46 μg/kg/day.
    Conclusions: The results of these study show an increase of CH cases in newborns with an eutopic thyroid compared to the traditional classification. The centralization of the screening program allows a closer cooperation between laboratory and clinical centers and facilitates the implementation of appropriate diagnostic evaluations and timely initiation of treatment, with positive effects on the management of the condition.
    MeSH term(s) Congenital Hypothyroidism/diagnosis ; Congenital Hypothyroidism/epidemiology ; Female ; Humans ; Infant, Newborn ; Neonatal Screening ; Pregnancy ; Thyrotropin ; Thyroxine/therapeutic use
    Chemical Substances Thyrotropin (9002-71-5) ; Thyroxine (Q51BO43MG4)
    Language English
    Publishing date 2022-07-29
    Publishing country England
    Document type Journal Article
    ZDB-ID 2088556-8
    ISSN 1824-7288 ; 1720-8424
    ISSN (online) 1824-7288
    ISSN 1720-8424
    DOI 10.1186/s13052-022-01328-0
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Combined isobutyryl-CoA and multiple acyl-CoA dehydrogenase deficiency in a boy with altered riboflavin homeostasis.

    Tummolo, Albina / Leone, Piero / Tolomeo, Maria / Solito, Rita / Mattiuzzo, Matteo / Lepri, Francesca Romana / Lorè, Tania / Cardinali, Roberta / De Giovanni, Donatella / Simonetti, Simonetta / Barile, Maria

    JIMD reports

    2022  Volume 63, Issue 4, Page(s) 276–291

    Abstract: In this report, we describe the case of an 11-year-old boy, who came to our attention for myalgia and muscle weakness, associated with inappetence and vomiting. Hypertransaminasemia was also noted, with ultrasound evidence of hepatomegaly. Biochemical ... ...

    Abstract In this report, we describe the case of an 11-year-old boy, who came to our attention for myalgia and muscle weakness, associated with inappetence and vomiting. Hypertransaminasemia was also noted, with ultrasound evidence of hepatomegaly. Biochemical investigations revealed acylcarnitine and organic acid profiles resembling those seen in MADD, that is, multiple acyl-CoA dehydrogenase deficiencies (OMIM #231680) a rare inherited disorder of fatty acids, amino acids, and choline metabolism. The patient carried a single pathogenetic variant in the
    Language English
    Publishing date 2022-05-07
    Publishing country United States
    Document type Case Reports
    ZDB-ID 2672872-2
    ISSN 2192-8312 ; 2192-8304
    ISSN (online) 2192-8312
    ISSN 2192-8304
    DOI 10.1002/jmd2.12292
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Plasma β-amyloid

    Zecca, Chiara / Tortelli, Rosanna / Panza, Francesco / Arcuti, Simona / Piccininni, Marco / Capozzo, Rosa / Barulli, Maria Rosaria / Barone, Roberta / Cardinali, Roberta / Abbrescia, Daniela / Seripa, Davide / Brescia, Vincenzo / Logroscino, Giancarlo

    Journal of the neurological sciences

    2018  Volume 391, Page(s) 120–126

    Abstract: Background: In clinical practice, the use of plasma β-Amyloid1-42 (Aβ: Methods: Plasma samples were obtained from 245 subjects, with a wide age-range (19-89 years), enrolled at the Unit of Laboratory Medicine of the "Azienda Ospedaliera Cardinale G. ... ...

    Abstract Background: In clinical practice, the use of plasma β-Amyloid1-42 (Aβ
    Methods: Plasma samples were obtained from 245 subjects, with a wide age-range (19-89 years), enrolled at the Unit of Laboratory Medicine of the "Azienda Ospedaliera Cardinale G. Panico" (younger subjects) and from a population-based study on aging (GreatAGE study) (older subjects). Three different age-groups were established: young (≤ 34), adult (35 ≤ age ≤ 64) and old (>64). The Innogenetics Elisa kit for plasma Aβ
    Results: The mean (SD) concentration of plasma Aβ
    Conclusion: The present study proposes reference values for plasma Aβ
    MeSH term(s) Adult ; Aged ; Aged, 80 and over ; Aging/physiology ; Amyloid beta-Peptides/blood ; Biomarkers/blood ; Cognition ; Cohort Studies ; Female ; Humans ; Male ; Middle Aged ; Peptide Fragments/blood ; Reference Values ; Sex Characteristics ; Young Adult
    Chemical Substances Amyloid beta-Peptides ; Biomarkers ; Peptide Fragments ; amyloid beta-protein (1-42)
    Language English
    Publishing date 2018-06-13
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 80160-4
    ISSN 1878-5883 ; 0022-510X ; 0374-8642
    ISSN (online) 1878-5883
    ISSN 0022-510X ; 0374-8642
    DOI 10.1016/j.jns.2018.06.006
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Expanded Newborn Screening in Italy Using Tandem Mass Spectrometry: Two Years of National Experience.

    Ruoppolo, Margherita / Malvagia, Sabrina / Boenzi, Sara / Carducci, Carla / Dionisi-Vici, Carlo / Teofoli, Francesca / Burlina, Alberto / Angeloni, Antonio / Aronica, Tommaso / Bordugo, Andrea / Bucci, Ines / Camilot, Marta / Carbone, Maria Teresa / Cardinali, Roberta / Carducci, Claudia / Cassanello, Michela / Castana, Cinzia / Cazzorla, Chiara / Ciatti, Renzo /
    Ferrari, Simona / Frisso, Giulia / Funghini, Silvia / Furlan, Francesca / Gasperini, Serena / Gragnaniello, Vincenza / Guzzetti, Chiara / La Marca, Giancarlo / La Spina, Luisa / Lorè, Tania / Meli, Concetta / Messina, MariaAnna / Morrone, Amelia / Nardecchia, Francesca / Ortolano, Rita / Parenti, Giancarlo / Pavanello, Enza / Pieragostino, Damiana / Pillai, Sara / Porta, Francesco / Righetti, Francesca / Rossi, Claudia / Rovelli, Valentina / Salina, Alessandro / Santoro, Laura / Sauro, Pina / Schiaffino, Maria Cristina / Simonetti, Simonetta / Vincenzi, Monica / Tarsi, Elisabetta / Uccheddu, Anna Paola

    International journal of neonatal screening

    2022  Volume 8, Issue 3

    Abstract: Newborn screening (NBS) for inborn errors of metabolism is one of the most advanced tools for secondary prevention in medicine, as it allows early diagnosis and prompt treatment initiation. The expanded newborn screening was introduced in Italy between ... ...

    Abstract Newborn screening (NBS) for inborn errors of metabolism is one of the most advanced tools for secondary prevention in medicine, as it allows early diagnosis and prompt treatment initiation. The expanded newborn screening was introduced in Italy between 2016 and 2017 (Law 167/2016; DM 13 October 2016; DPCM 12-1-2017). A total of 1,586,578 infants born in Italy were screened between January 2017 and December 2020. For this survey, we collected data from 15 Italian screening laboratories, focusing on the metabolic disorders identified by tandem mass spectrometry (MS/MS) based analysis between January 2019 and December 2020. Aminoacidemias were the most common inborn errors in Italy, and an equal percentage was observed in detecting organic acidemias and mitochondrial fatty acids beta-oxidation defects. Second-tier tests are widely used in most laboratories to reduce false positives. For example, second-tier tests for methylmalonic acid and homocysteine considerably improved the screening of CblC without increasing unnecessary recalls. Finally, the newborn screening allowed us to identify conditions that are mainly secondary to a maternal deficiency. We describe the goals reached since the introduction of the screening in Italy by exchanging knowledge and experiences among the laboratories.
    Language English
    Publishing date 2022-08-09
    Publishing country Switzerland
    Document type Journal Article
    ISSN 2409-515X
    ISSN (online) 2409-515X
    DOI 10.3390/ijns8030047
    Database MEDical Literature Analysis and Retrieval System OnLINE

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