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* From the Department of Internal Medicine III (Drs. Grünig, Mereles, Arnold, Benz, Borst, Abushi, and Kübler), Institute of Human Genetics (Drs. Miltenberger-Miltenyi, Bartram, and Janssen), University of Heidelberg, Heidelberg; the Department of Internal Medicine II (Drs. Olschewski and Seeger), University of Giessen, Giessen; the Department of Internal Medicine II (Dr. Winkler), University of Leipzig, Leipzig; and Department of Respiratory Medicine (Dr. Höper), University of Hannover, Hannover, Germany.
Correspondence to: E. Grünig, MD, Department of Cardiology, University Hospital, Bergheimer Str. 58, 69115 Heidelberg, Germany; e-mail: ekkehard_gruenig{at}med.uni-heidelberg.de
The familial
form of primary pulmonary hypertension (PPH) has
been assumed to account for only 6% of cases. We hypothesized that
clinical and genetic assessment of relatives of patients with PPH
reveal a substantially higher proportion of familial cases. One hundred
eight-one relatives of 31 patients with invasively confirmed PPH were
prospectively assessed using Doppler echocardiography (n = 181) and
right-heart catheterization (n = 36) for estimation of pulmonary
artery systolic pressure (PASP) at rest and during supine bicycle
exercise. Linkage analysis was performed in eight families. Manifest
PPH was detected in at least one relative (n = 16) of 29% of the
index patients. Latent PPH with abnormal PASP response to exercise
(
40 mm Hg) was present in at least one relative of another 52% of
the index patients. In the families examined genetically, 39 of 41
relatives with abnormal PASP response to exercise shared the risk
haplotype with the PPH patients. Thus, 81% of the PPH patients had
strong evidence of familial disease. The findings suggest that PPH is
predominantly genetically determined. Family screening of PASP response
to exercise may lead to an earlier diagnosis and more effective
therapy.
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