Volume 114, Issue 1 pp. 226-229

Reduced serum ceruloplasmin levels in hereditary haemochromatosis

Gaetano Cairo

Gaetano Cairo

Istituto di Patologia Generale – IRCCS Ospedale Maggiore, Università di Milano,

Centro di Studio sulla Patologia Cellulare – CNR, Milano, and

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Dario Conte

Dario Conte

Dipartimento di Scienze Mediche – IRCCS Ospedale Maggiore, Università di Milano, Italy

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Laura Bianchi

Laura Bianchi

Istituto di Patologia Generale – IRCCS Ospedale Maggiore, Università di Milano,

Dipartimento di Scienze Mediche – IRCCS Ospedale Maggiore, Università di Milano, Italy

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Mirella Fraquelli

Mirella Fraquelli

Dipartimento di Scienze Mediche – IRCCS Ospedale Maggiore, Università di Milano, Italy

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Stefania Recalcati

Stefania Recalcati

Dipartimento di Scienze Mediche – IRCCS Ospedale Maggiore, Università di Milano, Italy

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First published: 12 January 2002
Citations: 23
Gaetano Cairo, Istituto Patologia Generale, Università di Milano, Via Mangiagalli 31, 20133 Milano, Italy. E-mail: [email protected]

Abstract

As ceruloplasmin (Cp) seems to be involved in iron mobilization, serum Cp levels were measured in 35 patients with hereditary haemochromatosis (HH), 12 with acquired iron overload (AIO) and 36 healthy subjects. Cp was lower in HH patients than in controls (P < 0·001); no difference was found between untreated HH patients and those on a phlebotomy programme (P = 0·07) and between the HH patients carrying the normal and the mutated alleles of the HFE gene (P = 0·8). Cp levels in AIO subjects were significantly higher than in HH patients (P < 0·004) and similar to those of controls (P = 0·2). No differences in albumin, α1 acid glycoprotein and copper serum levels were observed in the three groups.

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